Atıflar

Toplam Atıf Sayısı: 285

 

2009 Yılı (6 adet)

2008 Yılı (4 adet)

2007 Yılı (1 adet)

2006 Yılı (15 adet)

2005 Yılı (43 adet)

2004 Yılı (14 adet)

2003 Yılı (21 adet)

2002 Yılı (4 adet)

2001 Yılı (2 adet)

2000 Yılı (151 adet)

1999 Yılı (10 adet)

1998 Yılı (2 adet)

1997 Yılı (4 adet)

1995 Yılı (8 adet)

2009 Yılı (6 adet)

 

I- Analysis of PTEN gene mutations in a Turkish patient with Cowden syndrome. Soysal Y, Tate G, Polat C, Polat N, Aktepe F, Sivaci Y, Imirzalioglu N. Genet Test Mol Biomarkers. 2009 Aug; 13 (4): 547-51.

 

Atıf sayısı: 1

1. Thyroid Pathology in PTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity Laury AR, Bongiovanni M, Tille JC, et al. THYROID Volume: 21 Issue: 2 Pages: 135-144 Published: Feb 2011.

 

II- Thyroid Pathology in PTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity Laury AR, Bongiovanni M, Tille JC, et al. THYROID Volume: 21 Issue: 2 Pages: 135-144 Published: Feb 2011.

 

Atıf sayısı: 2

1.VARIEGATED-LIKE MOSAICISM AND RING SYNDROME IN A r(4) BOY. APPRAISAL OF 38 PATIENTS WITH A FAIRLY COMPLETE RING 4 Dominguez MG, Barros-Nunez P, Gonzalez-Ramos IA, et al. GENETIC COUNSELING Volume: 21 Issue:4 Pages: 411-422 Published: 2010.

 

2.Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes Liehr T, Karamysheva T, Merkas M, et al. CURRENT GENOMICS Volume: 11 Issue: 6 Pages: 432-439 Published: Sep 2010.

 

III-Characterization of Double Ring Chromosome 4 Mosaicism Associated With Bilateral Hip Dislocation, Cortical Dysgenesis, and Epilepsy

Author(s): Soysal Yasemin; Balci Sevim; Hekimler Kuyas; et al.

Source: AMERICAN JOURNAL OF MEDICAL GENETICS PART A Volume: 149A Issue: 12 Pages: 2782-2787 Published: 2009.

 

Atıf sayısı: 3

 

1-Title: Ring 21 Chromosome Presenting With Epilepsy and Intellectual Disability: Clinical Report and Review of the Literature

Author(s): Specchio Nicola; Carotenuto Antonio; Trivisano Marina; et al.

Source: AMERICAN JOURNAL OF MEDICAL GENETICS PART A Volume: 155A Issue: 4 Pages: 911-914  DOI: 10.1002/ajmg.a.33899 Published: Apr 2011.

 

2-Title: Somatic Mosaicism in Cases with Small Supernumerary Marker Chromosomes

Author(s): Liehr Thomas; Karamysheva Tatyana; Merkas Martina; et al.

Source: CURRENT GENOMICS Volume: 11 Issue: 6 Pages: 432-439 DOI: 10.2174/138920210793176029 Published: Sep 2010.

 

3-Title: VARIEGATED-LIKE MOSAICISM AND RING SYNDROME IN A r(4) BOY. APPRAISAL OF 38 PATIENTS WITH A FAIRLY COMPLETE RING 4

Author(s): Dominguez M. G.; Barros-Nunez P.; Gonzalez-Ramos I. A.; et al.

Source: GENETIC COUNSELIN Volume: 21 Issue: 4 Pages: 411-422 Published: 2010.

 

2008 Yılı (4 adet)

 

III-Effect of Helicobacter pylori infection and eradication therapy on interleukin-6 levels in patients with Familial Mediterranean Fever. Ozel AM, Demirturk L, Aydogdu A, et al. INTERNATIONAL JOURNAL OF CLINICAL PRACTICE Volume: 62 Issue: 5 754-761, 2008.

 

Atıf sayısı: 4

 

1. Helicobacters and Extragastric Diseases. Pellicano R, Franceschi F, Saracco G, et al. HELICOBACTER Volume: 14 Pages: 58-68 Supplement: Suppl. 1, 2009.

 

2. Familial Mediterranean Fever: A review for clinical management Fonnesu C, Cerquaglia C, Giovinale M, et al. JOINT BONE SPINE Volume: 76 Issue: 3 Pages: 227-233, 2009.

 

3. Familial mediterranean fever: A review for clinical management | [La maladie périodique] Fonnesu, C., Cerquaglia, C., Giovinale, M. et al., Revue du Rhumatisme (Edition Francaise) 76 (5), pp. 382-389 2009.

 

4. Long term changes in platelet counts after H. pylori eradication in non-ITP patients Matsukawa Y, Iwamoto M, Kato K, et al. PLATELETS Volume: 21 Issue: 8 Pages: 628-631 Published: 2010.

 

2007 Yılı (1 adet)

 

IV-Clinical and intraoral findings of a patient with tricho-rhino-phalangeal syndrome type I Karacay, S., Saygun, I., Tunca, Y., Imirzalioglu, N., Guvenc, G. Journal of Indian Society of Pedodontics and Preventive Dentistry 25 (1), 43-45, 2007.

 

Atıf sayısı: 1

 

1. Tricho-rhino-phalanqeal syndrome with supernumerary teeth. Kantaputra, P., Miletich, I., Lüdecke, H.-J. Et al. Journal of Dental Research 87 (11), pp. 1027-1031, 2008.

 

2006 Yılı (15 adet)

 

V-Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD). Samli H, Samli MM, Yilmaz E, et al. ARCHIVES OF ANDROLOGY Volume: 52 Issue: 6 Pages: 471-477, 2006.

 

Atıf sayısı: 4

 

1. The genetic basis of male reproductive failure Oates RD UROLOGIC CLINICS OF NORTH AMERICA Volume: 35 Issue: 2 Pages: 257, 2008.

 

2. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens. Sakamoto H, Yajima T, Suzuki K, et al.

INTERNATIONAL JOURNAL OF UROLOGY Volume: 15 Issue: 3 Pages: 270-271, 2008.

 

3. Clinical evaluation of the infertile male with respect to genetic etiologies Oates RD SYSTEMS BIOLOGY IN REPRODUCTIVE MEDICINE Volume: 57 Issue: 1-2 Pages: 72-77 Published: Feb 2011.

 

4. Strategies for clinicians: Unraveling the genetic basis of severe male factor infertility Oates, R.D.  2011 Sexuality, Reproduction and Menopause 9 (1), pp. 25-30.

 

VI-Genetic anomalies detected in patients with non-obstructive azoospermia and oligozoospermia. Samli H, Samli MM, Solak M, et al. ARCHIVES OF ANDROLOGY Volume: 52 Issue: 4 Pages: 263-267, 2006.

 

Atıf sayısı: 8

 

1. Cytogenetic abnormalities detected in patients with non-obstructive azoospermia and severe oligozoospermia. Kosar PA, Ozcelik N, Kosar A JOURNAL OF ASSISTED REPRODUCTION AND GENETICS Volume: 27 Issue: 1 Pages: 17-21, 2010.

 

2. Androgen receptor gene CAG and GGN polymorphisms in infertile Nigerian men. Akinloye O, Gromoll J, Nieschlag E, et al. JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION Volume: 32 Issue: 10 Pages: 797-804, 2009.

 

3. Genetic anomalies in patients with severe oligozoospermia and azoospermia in eastern Turkey: a prospective study Ceylan GG, Ceylan C, Elyas H GENETICS AND MOLECULAR RESEARCH Volume: 8 Issue: 3 Pages: 915-922, 2009.

 

4. Cytogenetic Evaluation of Infertile Men: A Retrospective Study Ceylan GG, Ceylan C

TURKIYE KLINIKLERI TIP BILIMLERI DERGISI Volume: 29 Issue: 1 Pages: 176-179,2009.

 

5. Cytogenetic abnormalities in 179 cases with male infertility in Western Region of Turkey: Report and review Akgul M, Ozkinay F, Ercal D, et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS Volume: 26 Issue: 2-3 Pages: 119-122, 2009.

 

6. Evaluation of the azoospermic male FERTILITY AND STERILITY Volume: 90 Pages: S74-S77 Supplement: Suppl. 3, 2008.

 

7. Clinical study on 212 azoospermia patients without chromosomal abnormality Hong, K., Jiang, H., Bai, Q., Zhao, L., Yuan, R., Chen, Q., Ma, L. 2008 Chinese Journal of Andrology 22 (11), pp. 47-50.

 

8. The genetic bases of andrological subfertility | [Genetische grundlagen der andrologischen subfertilität] Vogt, P.H. 2007 Gynakologische Endokrinologie 5 (1), pp. 13-20.

 

VII- Investigating the in vitro effect of taurine on the infant lymphocytes by sister chromatid exchange Ergun MA, Soysal Y, Kismet E, et al. PEDIATRICS INTERNATIONAL Volume: 48 Issue: 3 Pages: 284-286, 2006.

 

Atıf sayısı: 3

 

1. Protective efficiacy of taurine against pulmonary edema progression: experimental study Yucel O, Kunak ZI, Macit E, et al. JOURNAL OF CARDIOTHORACIC SURGERY Volume: 3 Article Number: 57, 2008.

 

2. Which mechanisms are involved in taurine-dependent granulocytic immune response or amino- and alpha-keto acid homeostasis? Mulling J, Nickolaus KA, Matejec R, et al. AMINO ACIDS Volume: 34 Issue: 2 Pages: 257-270, 2008.

 

3. Sulfur-containing antioxidants increase in vitro several functions of lymphocytes from mice Author(s): De la Fuente Monica; Hernanz Angel; Viniegra Salvador; et al.

 

Source: INTERNATIONAL IMMUNOPHARMACOLOGY Volume: 11 Issue: 6 Pages: 661-669 DOI: 10.1016/j.intimp.2011.01.008 Published: Jun 2011.

 

2005 Yılı (43 adet)

 

VIII-The vitamin D receptor fok1 start codon polymorphism and bone mineral density in male hypogonadotrophic hypogonadism Bolu, S.E., Suer, F.E.O., Deniz, F., Ückaya, G., Imirzalioglu, N., Kutlu, M. 2005 Journal of Endocrinological Investigation 28 (9), pp. 810-814.

 

Atıf sayısı: 1

 

1. Molecular genetic studies of gene identification for osteoporosis Guo, Y., Yang, T.-L., Pan, F., Xu, X.-H., Dong, S.-S., Deng, H.-W. 2008 Expert Review of Endocrinology and Metabolism 3 (2), pp. 223-267.

 

IX-The cell based dressing with living allogenic keratinocytes in the treatment of foot ulcers: a case study Bayram Y, Deveci M, Imirzalioglu N, et al. BRITISH JOURNAL OF PLASTIC SURGERY Volume: 58 Issue: 7 Pages: 988-996, 2005.

 

Atıf sayısı: 9

 

1. Diagnosis, Treatment, Follow Up and Prevention of the Diabetic Foot Morbach S, Muller E, Reike H, et al. DIABETOLOGIE UND STOFFWECHSEL Volume: 4 Issue: 5 Pages: 301-325, 2009.

 

2. Functional and phenotypic characterization of human keratinocytes expanded in microcarrier culture Borg DJ, Dawson RA, Leavesley DI, et al. JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A Volume: 88A Issue: 1 Pages: 184-194, 2009.

 

3. Unresolved issues in the management of ulcers of the foot in diabetes Jeffcoate WJ, Lipsky BA, Berendt AR, et al. DIABETIC MEDICINE Volume: 25 Issue: 12 Pages: 1380-1389, 2008.

 

4. A systematic review of the effectiveness of interventions to enhance the healing of chronic ulcers of the foot in diabetes Hinchliffe RJ, Valk GD, Apelqvist J, et al. DIABETES-METABOLISM RESEARCH AND REVIEWS Volume: 24 Pages: S119-S144 Supplement: Suppl. 1, 2008.

 

5. Skin replacement therapies for diabetic foot ulcers – Systematic review and meta-analysis Blozik E, Scherer M DIABETES CARE Volume: 31 Issue: 4 Pages: 693-694, 2008.

 

6. Dressings and topical agents for arterial leg ulcers Nelson EA, Bradley MDCOCHRANE DATABASE OF SYSTEMATIC REVIEWS Issue: 1 Article Number: CD001836, 2007.

 

7. Microcarriers in the engineering of cartilage and bone Malda J, Frondoza CGTRENDS IN BIOTECHNOLOGY Volume: 24 Issue: 7 Pages: 299-304, 2006.

 

8. Preparing Engineered Tissues in vitro by Macroporous Microcarriers Tang, Q., Zhou, Y., Chen, F., Tan, W. 2008 Chinese Journal of Biotechnology 24 (1), pp. 74-82.

 

9. Retrospective Review of Free Gracilis Muscle Flaps in the Management of Nonhealing Diabetic Foot Ulceration Osiogo, F.O., Lai, C.-S., Wang, W.-H., Chye, Y.-F., Lin, S.-D. 2006 Journal of Foot and Ankle Surgery 45 (4), pp. 252-260.

 

X-MEFV gene is a probable susceptibility gene for Behcet’s disease Imirzalioglu N, Dursun A, Tastan B, et al. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY Volume: 34 Issue: 1 Pages: 56-58, 2005.

 

Atıf sayısı: 33

 

1. Evaluation of common mutations in the Mediterranean fever gene in Multiple Sclerosis patients: Is it a susceptibility gene? Unal A, Dursun A, Emre U, et al. JOURNAL OF THE NEUROLOGICAL SCIENCES Volume: 294 Issue: 1-2 Pages: 38-42, 2010.

 

2. Genetics of vasculitis Monach PA, Merkel PA CURRENT OPINION IN RHEUMATOLOGY Volume: 22 Issue: 2 Pages: 157-163, 2010.

 

3. Behcet’s Disease: Current Aspects in the Etiopathogenesis Akman A, Alpsoy ETURKDERM-ARCHIVES OF THE TURKISH DERMATOLOGY AND VENEROLOGY Volume: 43 Pages: 32-38 Supplement: Suppl. 2 2009.

 

4. Prevalence and significance of MEFV gene mutations in a cohort of patients with rheumatoid arthritis Koca SS, Etem EO, Isik B, et al. JOINT BONE SPINE Volume: 77 Issue: 1 Pages: 32-35, 2010.

 

5. Behcet’s disease – a contemporary review Mendes D, Correia M, Barbedo M, et al. JOURNAL OF AUTOIMMUNITY Volume: 32 Issue: 3-4 Special Issue: Sp. Iss. SI Pages: 178-188, 2009.

 

6. Common MEFV mutations and polymorphisms in an elderly population: an association with E148Q polymorphism and rheumatoid factor levels Turanli ET, Beger T, Erdincler D, et al. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY Volume: 27 Issue: 2 Pages: 340-343, 2009.

 

7. MEFV mutations in Japanese rheumatoid arthritis patients Migita K, Nakamura T, Maeda Y, et al. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY Volume: 26 Issue: 6 Pages: 1091-1094 Nov-Dec, 2008.

 

8. Auto-inflammatory syndromes and oral health Scully C, Hodgson T, Lachmann HORAL DISEASES Volume: 14 Issue: 8 Pages: 690-699 Nov, 2008.

 

9. Molecular analysis of MEFV gene mutations among Palestinian patients with Behcet’s disease Ayesh S, Abu-Rmaileh H, Nassar S, et al. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY Volume: 37 Issue: 5 Pages: 370-374, 2008.

 

10. Autoinflammatory diseases: Mimics of Autoimmunity or part of its spectrum? Case presentation Kiss MHB, Magalhaes CS JOURNAL OF CLINICAL IMMUNOLOGY Volume: 28 Pages: S84-S89 Supplement: Suppl. 1 May, 2008.

 

11. Chronic GVHD as an autoimmune disease Tyndall A, Dazzi F BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY Volume: 21 Issue: 2 Pages: 281-289 Jun, 2008

 

12. Behcet’s disease: Ocular effects and treatment Deuter CME, Kotter I, Wallace GR, et al. PROGRESS IN RETINAL AND EYE RESEARCH Volume: 27 Issue: 1 Pages: 111-136 Jan, 2008.

 

13. Familial Mediterranean fever in northwest of Iran (Ardabil): the first global report from Iran Salehzadeh F, Emami D, Zolfegari AA, et al. TURKISH JOURNAL OF PEDIATRICS Volume: 50 Issue: 1 Pages: 40-44 Jan-Feb 2008.

 

14. The rate of pyrin mutations in critically ill patients with systemic inflammatory response syndrome and sepsis: A pilot study Koc B, Oktenli C, Bulucu F, et al.  JOURNAL OF RHEUMATOLOGY Volume: 34 Issue: 10 Pages: 2070-2074 Oct, 2007.

 

15. Behcet disease in adult druzes in north Israel – The influence of ethnic origin on disease expression and severity Rozenbaum M, Boulman N, Slobodin G, et al. JCR-JOURNAL OF CLINICAL RHEUMATOLOGY Volume: 13 Issue: 3 Pages: 124-127 Jun, 2007.

 

16. Juvenile Behcet’s disease: Highlighting neuropsychiatric manifestations and putative genetic mechanisms Panicker JN, Vinayan KP, Moosa NVA, et al. CLINICAL NEUROLOGY AND NEUROSURGERY Volume: 109 Issue: 5 Pages: 436-438 Jun, 2007.

 

17. Common FMF alleles may predispose to development of Behcet’s disease with increased risk for venous thrombosis Rabinovich E, Shinar Y, Leiba M, et al. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY Volume: 36 Issue: 1 Pages: 48-52 Jan-Feb, 2007.

 

18. Behcet’s disease and familial Mediterranean fever Takeno M, Ishigatsubo Y INTERNAL MEDICINE Volume: 45 Issue: 13 Pages: 805-806, 2006.

 

19. Pathophysiology of Behcet’s disease Amoura Z, Guillaume M, Caillat-Zucman S, et al. REVUE DE MEDECINE INTERNE Volume: 27 Issue: 11 Pages: 843-853 Nov, 2006.

 

20. Genetic analysis of MEFV gene pyrin domain in patients with Behcet’s disease Dursun A., Durakbasi-Dursun HG, Zamani AG, et al. MEDIATORS OF INFLAMMATION Article Number: 41783, 2006.

 

21. Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever Volume: 65 Issue: 9 Pages: 1154-1157 Sep, 2006.

 

22. CATERPILLERs, pyrin and hereditary immunological disorders Ting JPY, Kastner DL, Hoffman HM NATURE REVIEWS IMMUNOLOGY Volume: 6 Issue: 3 Pages: 183-195 Mar, 2006.

 

23. Familial Mediterranean fever and the other autoinflammatory syndromes: evaluation of the patient with recurrent fever Samuels J, Ozen S CURRENT OPINION IN RHEUMATOLOGY Volume: 18 Issue: 1 Pages: 108-117 Jan, 2006.

 

24. Familial autoinflammatory diseases: genetics, pathogenesis and treatment Stojanov S, Kastner DL CURRENT OPINION IN RHEUMATOLOGY Volume: 17 Issue: 5 Pages: 586-599 Sep, 2005.

 

25. Pediatric Behcet’s Disease and Thromboses Krupa B, Cimaz R, Ozen S, et al. JOURNAL OF RHEUMATOLOGY Volume: 38 Issue: 2 Pages: 387-390 Published: Feb, 2011.

 

26. Familial Mediterranean fever: An association with non-alcoholic fatty liver diseaseRimar, D., Rosner, I., Rozenbaum, M., Zuckerman, E. 2011  Clinical Rheumatology 30 (7), pp. 987-991.

 

27. Familial mediterranean fever-a review  Shohat, M., Halpern, G.J.  2011  Genetics in Medicine 13 (6), pp. 487-498.

 

28. Prevalence of MEFV gene mutations and their clinical correlations in Turkish children with Henoch-Schönlein purpura  Bayram, C., Demircin, G., Erdoǧan, Ö., Bülbül, M., Çaltik, A., Akyüz, S.G. 2011  Acta Paediatrica, International Journal of Paediatrics 100 (5), pp. 745-749.

 

29. The genetics of vasculitides | [Genetischer Hintergrund der Vaskulitiden]  Holle, J.U., Wieczorek, S., Epplen, J.T., Gross, W.L. 2011  Zeitschrift fur Rheumatologie 70 (3), pp. 198-204.

 

30. Mediterranean fever (MEFV) gene mutation frequency is not increased in adults with rheumatic heart disease  Simsek, I., Koz, C., Basar, N., Sari, I., Erdem, H., Pay, S., Kisacik, B., (…), Dinc, A.  2011  Clinical Rheumatology 30 (4), pp. 491-495.

 

31. The Familial Mediterranean Fever Gene as a Modifier of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenopathy Syndrome  Berkun, Y., Levy, R., Hurwitz, A., Meir-Harel, M., Lidar, M., Livneh, A., Padeh, S.  2011  Seminars in Arthritis and Rheumatism 40 (5), pp. 467-472.

 

32. Pediatric Behçet’s disease and thromboses  Krupa, B., Cimaz, R., Ozen, S., Fischbach, M., Cochat, P., Koné-Paut, I.  2011  Journal of Rheumatology 38 (2), pp. 387-390.

 

33. Research progress on genetics of Behcet’s disease  Xue, T.-J., Zhou, Z.-T. 2010  Journal of Shanghai Jiaotong University Medical Science) 30 (9), pp. 1160-1163.

 

2004 Yılı (14 adet)

 

XI-HLA-DR B1 and DQ B1 polymorphisms in patients with coronary artery ectasia Akdemir R, Ozhan H, Gunduz H, et al. ACTA CARDIOLOGICA Volume: 59 Issue: 5 Pages: 499-502  Oct, 2004.

 

Atıf sayısı: 9

 

1. From positive remodelling to coronary artery ectasia. Is coronary artery aneurysm a benign form of coronary disease? | [Od pozytywnego remodelingu do tȩtniakowatego poszerzenia ttnic wieńcowych. Czy tȩtniaki wieńcowe to łagodna forma choroby wieńcowej?]

Araszkiewicz, A., Grygier, M., Lesiak, M., Grajek, S.2009  Kardiologia Polska 67 (12), pp. 1390-139.

 

2. Coronary Artery Ectasia Lin, C.-T., Chen, C.-W., Lin, T.-K., Lin, C.-L. 2008  Tzu Chi Medical Journal 20 (4), pp. 270-274.

 

3. Coronary artery ectasia: A case report and review of literature Hegazy, A.M.  2008Kuwait Medical Journal 40 (1), pp. 59-63.

 

4. Coronary artery ectasia – Is it time for a reappraisal? Ramappa, P., Kottam, A., Kuivanemi, H., Thatai, D.  2007 Clinical Cardiology 30 (5), pp. 214-217.

 

5. Ethnicity may be a reason for lipid changes and high Lp(a) levels in rheumatoid arthritis Cesur, M., Ozbalkan, Z., Temel, M.A., Karaarslan, Y. 2007  Clinical Rheumatology 26 (3), pp. 355-361.

 

6. Endogenous versus exogenous fatty acid availability affects lysosomal acidity and MHC class II expression Schweitzer, S.C., Reding, A.M., Patton, H.M., Sullivan, T.P., Stubbs, C.E., Villalobos-Menuey, E., Huber, S.A., Newell, M.K. 2006  Journal of Lipid Research 47 (11), pp. 2525-2537.

 

7. Coronary artery aneurysm: A review Pahlavan, P.S., Niroomand, F.2006  Clinical Cardiology 29 (10), pp. 439-443.

 

8. Clinical follow-up of a woman with diffuse coronary ectasia and coronaro-left ventricular fistulae Prattichizzo, F., Franzoni, F., Galetta, F. 2006  Minerva Cardioangiologica 54 (2), pp. 273-275.

 

9. An unpleasant surprise in the setting of primary percutaneous coronary intervention: Diffuse and severe vessel ectasia with acute thrombosis of the distal right coronary artery in a patient with acute inferior myocardial infarction Milazzo, D., Caramanno, G., Innocente, P., La Mantia, R., Vaccaro, I.  2005  Italian Heart Journal 6 (4), pp. 353-356.

 

XII- Complete atrioventricular block in Becker muscular dystrophy Akdemir, R., Ozhan, H., Gunduz, H., Yazici, M., Erbilen, E., Uyan, C., Imirzalioglu, N.  2004  New Zealand Medical Journal 117 (1194).

 

Atıf sayısı: 3

 

1. Cardiac involvement in Becker muscular dystrophy Finsterer, J., Stöllberger, C. 2008 Canadian Journal of Cardiology 24 (10), pp. 786-792.

 

2. Wolff-Parkinson-White syndrome as initial manifestation of Becker muscular dystrophy Finsterer, J., Stöllberger, C., Quasthoff, S. 2008 Herz 33 (4), pp. 307-310.

 

3. Complete AV block and cardiac syncope in a patient with Duchenne muscular dystrophy Altekin, R.E., Yanikoglu, A., Ucar, M., Ermis, C. 2011 Journal of Cardiology Cases 3 (2), pp. e68-e70.

 

XIII-Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G. Köseoglu V, Kismet E, Soysal Y, Ulucan H, Dündaröz R, Imirzalioglu N, Gökçay E. Pediatr Int. 2004 Aug; 46(4):415-8.

 

Atıf sayısı: 2

 

1. Cytogenetic Genotoxicity of Amoxicillin Istifli ES, Topaktas M ENVIRONMENTAL AND MOLECULAR MUTAGENESIS Volume: 51 Issue: 3 Pages: 222-228 Published: Apr, 2010.

 

2. Investigation of DNA damage in lymphocytes exposed to benzathine penicillin G (vol 46, pg 597, 2004) Koseoglu V, Kismet E, Soysal Y, et al. PEDIATRICS INTERNATIONAL Volume: 46 Issue: 6 Pages: 756-756 Published: Dec, 2004.

 

2003 Yılı (21 adet)

 

XIV- Essential palatal myoclonus in monozygotic male twins Kutukcu Y, Imirzalioglu N, Odabasi Z, et al. JOURNAL OF NEUROLOGY Volume: 250 Issue: 7 Pages: 885-886  Jul, 2003.

 

Atıf sayısı:3

 

1. Objective tinnitus due to essential palatal tremor in a 5-year-old MacDonald JT PEDIATRIC NEUROLOGY  Volume: 36  Issue: 3 Pages: 175-176 Mar, 2007.

 

2. Treatment of essential palatal myoclonus in a 10-year-old girl with botulinum neurotoxin Krause E, Leunig A, Klopstock T, et al. OTOLOGY & NEUROTOLOGY Volume: 27 Issue: 5 Pages: 672-675 Aug, 2006.

 

3. Myoclonus: current concepts and recent advances Caviness JN, Brown PLANCET NEUROLOGY Volume: 3 Issue: 10 Pages: 598-607 Oct, 2004.

 

XV-Fetal chromosomal analysis of pregnancies following intracytoplasmic sperm injection with amniotic tissue culture  Samli, H., Solak, M., Imirzalioǧlu, N., Beyatli, Y., Şimşek, S., Kahraman, S.  2003  Prenatal Diagnosis 23 (10), pp. 847-850.

 

Atıf sayısı: 8

 

1. X pentasomy in an intracytoplasmic sperm injection pregnancy detected by nuchal translucency testing Cheng, P.-J., Chueh, H.-Y., Shaw, S.-W., Hsu, J.-J., Hsieh, T.-T., Soong, Y.-K. 2008  Fetal Diagnosis and Therapy 24 (3), pp. 299-303.

 

2. Prenatal testing among women pregnant after assisted reproductive techniques in Denmark 1995-2000: A national cohort study Gjerris, A.C., Loft, A., Pinborg, A., Christiansen, M., Tabor, A.  2008  Human Reproduction 23 (7), pp. 1545-1552.

 

3. Intracytoplasmic sperm injection: An assisted reproductive technique and its outcome to overcome infertility Sarkar, N.N.  2007 Journal of Obstetrics and Gynaecology 27 (4), pp. 347-353.

 

4. Interchromosomal effect in sperm of males with translocations: Report of 6 cases and review of the literature Douet-Guilbert, N., Bris, M.-J.L., Amice, V., Marchetti, C., Delobel, B., Amice, J., Braekeleer, M.D., Morel, F.   2005  International Journal of Andrology 28 (6), pp. 372-379.

 

5. Perinatal complications of assisted reproduction Aboulghar, M.A. 2005 Croatian Medical Journal 46 (5), pp. 751-756.

 

6. Benefits and challenges brought by improved results from in vitro fertilization Jansen, R.P.S. 2005 Internal Medicine Journal 35 (2), pp. 108-117.

 

7. Prenatal karyotypes of fetuses conceived by intracytoplasmic sperm injection Jozwiak, E.A., Ulug, U., Mesut, A., Erden, H.F., Bahçeci, M. 2004 Fertility and Sterility 82 (3), pp. 628-633.

 

8. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics Liehr T, Weise A INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE Volume: 19 Issue: 5 Pages: 719-731 Published: May, 2007.

 

XVI- New heritable fragile site at 15q13 in both members of a nonconsanguineous couple.

Karadeniz NN, Tunca Y, Imirzalioglu N AMERICAN JOURNAL OF MEDICAL GENETICS PART A Volume: 118A Issue: 3 Pages: 290-292 Apr 30, 2003.

 

Atıf sayısı: 5

 

1. Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones Mrasek, K., Schoder, C., Teichmann, A.-C., et al 2010 International Journal of Oncology 36 (4), pp. 929-940.

 

2. Cytogenetics: Past, present and future Kannan, T.P., Zilfalil, B.A. 2009  Malaysian Journal of Medical Sciences 16 (2), pp. 4-9.

 

3. Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites Burrow, A.A., Williams, L.E., Pierce, L.C.T., Wang, Y.-H.  2009  BMC Genomics 10, art. no. 59.

 

4. A new heritable fragile site at 15q13 in a three-generation family Zamani, A.G., Durakbasi-Dursun, H.G., Acar, A. 2007  Cytogenetic and Genome Research 116 (4), pp. 252-255.

 

5. Rare fragile sites Sutherland, G.R.2003 Cytogenetic and Genome Research 100 (1-4), pp. 77-84

 

XVII- Prolongation of skin xenograft survival with modified cultured fibroblasts Isik S, Er E, Soysal Y, et al. PLASTIC AND RECONSTRUCTIVE SURGERY Volume: 111 Issue: 1 Pages: 275-282 Jan, 2003.

 

Atıf sayısı: 5

 

1. Fibroblast sheets co-cultured with endothelial progenitor cells improve cardiac function of infarcted hearts Kobayashi H, Shimizu T, Yamato M, et al. JOURNAL OF ARTIFICIAL ORGANS Volume: 11 Issue: 3 Pages: 141-147 Sep, 2008.

 

2.Adult neural stem and progenitor cells modified to secrete GDNF can protect, migrate and integrate after intracerebral transplantation in rats with transient forebrain ischemia Kameda M, Shingo T, Takahashi K, et al.EUROPEAN JOURNAL OF NEUROSCIENCE Volume: 26 Issue: 6 Pages: 1462-1478 Sep, 2007.

 

3.Local expression of indoleamine 2,3-dioxygenase protects engraftment of xenogeneic skin substitute Li YY, Tredget EE, Ghaffari A, et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY Volume: 126 Issue: 1 Pages: 128-136 Jan, 2006.

 

4.Development and maintenance of donor-specific chimerism in semi-allogenic and fully major histocompatibility complex mismatched facial allograft transplants Siemionow M, Demir Y, Mukherjee A, et al.TRANSPLANTATION Volume: 79 Issue: 5 Pages: 558-567 Mar 15, 2005.

 

5.Tolerance induction in composite facial allograft transplantation in the rat model Demir Y, Ozmen S, Klimczak A, et al. PLASTIC AND RECONSTRUCTIVE SURGERY Volume: 114 Issue: 7 Pages: 1790-1801 Dec, 2004.

 

2002 Yılı (4 adet)

 

XVIII- Ebstein’s anomaly in siblings: an original observation Uyan C, Yazici M, Uyan AP, et al. INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING Volume: 18 Issue: 6 Pages: 435-438 Dec, 2002.

 

Atıf sayısı: 4

 

1. Clinical and echocardiographic features of Ebstein’s malformation in Sudanese patients Ali SKM, Nimeri NAGM CARDIOLOGY IN THE YOUNG Volume: 16 Issue: 2 Pages: 147-151 Apr, 2006.

 

2. Ebstein anomaly and duplication of the distal arm of chromosome 15: Report of two patients Miller MS, Rao PN, Dudovitz RN, et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A Volume: 139A Issue: 2 Pages: 141-145 Dec 1, 2005.

 

3. Ebstein anomaly in a meerkat (Suricata suricatta) Chai N, Chetboul V, Carlos C, et al. JOURNAL OF ZOO AND WILDLIFE MEDICINE Volume: 35 Issue: 4 Pages: 546-548 Dec, 2004.

 

4. Ebstein’s anomaly in adults – Response Mulder BJM INTERNATIONAL JOURNAL OF CARDIOVASCULAR IMAGING Volume: 18 Issue: 6 Pages: 439-441 Dec, 2002.

 

2001 Yılı (2 adet)

 

XIX-The effects of folic acid application on IL-1beta levels of human gingival fibroblasts stimulated by phenytoin and TNFalpha in vitro: a preliminary study. Doǧan, A., Tunca, Y., Ozdemir, A., Sengül, A., Imirzalioǧlu, N. 2001 Journal of oral science 43 (4), pp. 255-260.

 

Atıf sayısı: 2

 

1. Effect of phenytoin on collagen accumulation by human gingival fibroblasts exposed to TNF-α in vitro Kato, T., Okahashi, N., Ohno, T., Inaba, H., Kawai, S., Amano, A.2006 Oral Diseases 12 (2), pp. 156-162.

 

2. Folic acid and homocysteine affect neural crest and neuroepithelial cell outgrowth and differentiation in vitro Boot, M.J., Steegers-Theunissen, R.P.M., Poelmann, R.E., Van Iperen, L., Lindemans, J., Gittenberger-de Groot, A.C.  2003  Developmental Dynamics 227 (2), pp. 301-308.

 

2000 Yılı (151 adet)

 

XX-Relationship between granular cytoplasm of oocytes and pregnancy outcome following intracytoplasmic sperm injection Kahraman S, Yakin K, Donmez E, et al.HUMAN REPRODUCTION  Volume: 15 Issue: 11 Pages: 2390-2393 Published: Nov, 2000.

 

Atıf sayısı: 52

 

1. Portrait of an oocyte: Our obscure origin  Gosden, R., Lee, B. 2010 Journal of Clinical Investigation 120 (4), pp. 973-983.

 

2. Morphological criteria of oocyte quality | [Oocitu{ogonek} kokybės morfologiniai požymiai]  Lasiene, K., Vitkus, A., Valančiute, A., Lasys, V.2009  Medicina 45 (7), pp. 574-583.

 

3. Are there non-invasive markers in human oocytes that can predict pregnancy outcome? Kilani, S., Cooke, S., Kan, A., Chapman, M. 2009  Reproductive BioMedicine Online 18 (5), pp. 674-680.

 

4. Intracytoplasmic morphological abnormalities in human oocytes  Otsuki, J. 2009 Journal of Mammalian Ova Research 26 (1), pp. 26-31.

 

5. Relationship between first polar body morphology before intracytoplasmic sperm injection and fertilization rate, cleavage rate, and embryo quality Navarro, P.A., de Araújo, M.M., de Araújo, C.M., Rocha, M., dos Reis, R., Martins, W.  2009  International Journal of Gynecology and Obstetrics 104 (3), pp. 226-229.

 

6. Significance of metaphase II human oocyte morphology on ICSI outcome Rienzi, L., Ubaldi, F.M., Iacobelli, M., Minasi, M.G., Romano, S., Ferrero, S., Sapienza, F., (…), Greco, E. 2008  Fertility and Sterility 90 (5), pp. 1692-1700.

 

7. Effect of a woman’s smoking status on oocyte, zygote, and day 3 pre-embryo quality in in vitro fertilization and embryo transfer program  Gruber, I., Just, A., Birner, M., Lösch, A. 2008 Fertility and Sterility 90 (4), pp. 1249-1252.

 

8. Morphological Selection of Gametes  Ubaldi, F., Rienzi, L. 2008  Placenta 29 (SUPPL.2), pp. 115-120

 

9. Severe cytoplasmic abnormalities of the oocyte decrease cryosurvival and subsequent embryonic development of cryopreserved embryos Balaban, B., Ata, B., Isiklar, A., Yakin, K., Urman, B.  2008  Human Reproduction 23 (8), pp. 1778-1785.

 

10. First polar body morphology and fertilization rate, cleavage rate, and embryo quality | [Morfologia do primeiro corpúsculo polar e taxas de fertilização, clivagem e qualidade embrionária] De Araújo, M.C.P.M., De Araújo, M., De Araújo, C.H.M., Rocha, M.G., Martins, W.D.P., Dos Reis, R.M., Ferriani, R.A., (…), Navarro, S.  2008 Revista Brasileira de Ginecologia e Obstetricia 30 (7), pp. 360-365.

 

11. The predictors of clinical fertilization in IVF cycles Esmailzadeh, S., Faramarzi, M., Farsi, M. 2008  Acta Medica Iranica 46 (2), pp. 87-94.

 

12. Blood clots in the cumulus-oocyte complex predict poor oocyte quality and post-fertilization development  Ebner, T., Moser, M., Shebl, O., Sommergruber, M., Yaman, C., Tews, G.2008  Reproductive BioMedicine Online 16 (6), pp. 801-807.

 

13. Comparison of oocyte quality and intracytoplasmic sperm injection outcome in women with isolated polycystic ovaries or polycystic ovarian syndrome Sahu, B., Ozturk, O., Ranierri, M., Serhal, P.  2008  Archives of Gynecology and Obstetrics 277 (3), pp. 239-244.

 

14. Oocyte dysmorphism is not associated with aneuploidy in the developing embryo Yakin, K., Balaban, B., Isiklar, A., Urman, B. 2007 Fertility and Sterility 88 (4), pp. 811-816.

 

15. Molecular methods for selection of the ideal oocyte Patrizio, P., Fragouli, E., Bianchi, V., Borini, A., Wells, D. 2007 Reproductive BioMedicine Online 15 (3), art. no. 2813, pp. 346-353.

 

16. Evaluation of oocyte quality: Morphological, cellular and molecular predictors Wang, Q., Sun, Q.-Y. 2007  Reproduction, Fertility and Development 19 (1), pp. 1-12.

 

17. Donor oocyte dysmorphisms and their influence on fertilization and embryo quality Ten, J., Mendiola, J., Vioque, J., de Juan, J., Bernabeu, R.2007  Reproductive BioMedicine Online 14 (1), art. no. 2519, pp. 40-48.

 

18.Meiotic spindle presence and oocyte morphology do not predict clinical ICSI outcomes: A study of 967 transferred embryos Chamayou, S., Ragolia, C., Alecci, C., Storaci, G., Maglia, E., Russo, E., Guglielmino, A.   2006  Reproductive BioMedicine Online 13 (5), art. no. 2403, pp. 661-667.

 

19. Relationship between oocyte morphology and fertilization rate after ICSI | [Associação entre morfologia do ovócito e taxa de fertilização após ICSI] Aggelis, A., Faúndes, D., Mattos, A., Petta, C., Neves, P.A., Faúndes, A.   2006  Revista Brasileira de Ginecologia e Obstetricia 28 (4), pp. 220-226.

 

20. Ultrastructural Dynamics of Human Reproduction, from Ovulation to Fertilization and Early Embryo Development1 Familiari, G., Heyn, R., Relucenti, M., Nottola, S.A., Sathananthan, A.H.  2006  International Review of Cytology 249, pp. 53-141.

 

21.Embryo aneuploidy screening for repeated implantation failure and unexplained recurrent miscarriage Findikli, N., Kahraman, S., Saglam, Y., Beyazyurek, C., Sertyel, S., Karlikaya, G., Karagozoglu, H., Aygun, B.   2006  Reproductive BioMedicine Online 13 (1), art. no. 2220, pp. 38-46.

 

22.Effect of oocyte morphology on embryo development and implantation Balaban, B., Urman, B.  2006  Reproductive BioMedicine Online 12 (5), art. no. 2133, pp. 608-615.

 

23.Is oocyte morphology prognostic of embryo developmental potential after ICSI? Ebner, T., Moser, M., Tews, G.2006  Reproductive BioMedicine Online 12 (4), art. no. 2190, pp. 507-512.

 

24.The importance of oocyte morphology with regard to further developmental capacity | [Die bedeutung der morphologie der oozyte hinsichtlich ihres weiteren entwicklungspotentials]  Ebner, Th., Moser, M., Tews, G.   2006  Journal fur Reproduktionsmedizin und endokrinologie 3 (1), pp. 17-23.

 

25.Oocyte and embryo quality: Is their morphology a good criterion? | [Qualité ovocytaire et embryonnaire: La morphologie est-elle un bon critère?]  Hamamah, S. 2005 Journal de Gynecologie Obstetrique et Biologie de la Reproduction 34 (7 II), pp. 5S38-5S41.

26.Early pronuclear breakdown is a good indicator of embryo quality and viability Fancsovits, P., Toth, L., Takacs, Z.F., Murber, A., Papp, Z., Urbancsek, J.  2005 Fertility and Sterility 84 (4), pp. 881-887.

 

27. Occurrence and developmental consequences of vacuoles throughout preimplantation development Ebner, T., Moser, M., Sommergruber, M., Gaiswinkler, U., Shebl, O., Jesacher, K., Tews, G.2005  Fertility and Sterility 83 (6), pp. 1635-1640.

 

28.Role of oocyte morphology on fertilization and embryo formation in assisted reproductive techniques Khalili, M.A., Sultan, A.-M., Mojibian, M.2005 Middle East Fertility Society Journal 10 (1), pp. 72-77.

 

29.Significance of morphological attributes of the early embryo Rienzi, L., Ubaldi, F., Iacobelli, M., Romano, S., Minasi, M.G., Ferrero, S., Sapienza, F., (…), Greco, E.2005 Reproductive BioMedicine Online 10 (5), pp. 669-681.

 

30.First polar body morphology before ICSI is not related to embryo quality or pregnancy rate Ciotti, P.M., Notarangelo, L., Morselli-Labate, A.M., Felletti, V., Porcu, E., Venturo