Ekim M - Search Results

1

The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype.

Tekin M, Kavaz A, Berberoğlu M, Fitoz S, Ekim M, Ocal G, Akar N. Tekin M, et al. Among authors: ekim m. Am J Med Genet A. 2004 Oct 15;130A(3):284-7. doi: 10.1002/ajmg.a.30291. Am J Med Genet A. 2004. PMID: 15378538 Review.

2

Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients.

Ozçakar ZB, Cengiz FB, Cakar N, Uncu N, Kara N, Acar B, Yüksel S, Ekim M, Tekin M, Yalçinkaya F. Ozçakar ZB, et al. Among authors: ekim m. Pediatr Nephrol. 2006 Aug;21(8):1093-6. doi: 10.1007/s00467-006-0116-4. Epub 2006 Jun 30. Pediatr Nephrol. 2006. PMID: 16810518

3

The effect of colchicine on physical growth in children with familial mediterranean fever.

Ozçakar ZB, Kadioğlu G, Siklar Z, Kavaz A, Nur Aksanal F, Berberoğlu M, Ekim M, Ocal G, Yalçinkaya F. Ozçakar ZB, et al. Among authors: ekim m. Eur J Pediatr. 2010 Jul;169(7):825-8. doi: 10.1007/s00431-009-1120-z. Epub 2009 Dec 17. Eur J Pediatr. 2010. PMID: 20016916

4

A germline PTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus.

Tekin M, Hişmi BO, Fitoz S, Yalçinkaya F, Ekim M, Kansu A, Ertem M, Deda G, Tutar E, Arsan S, Zhou XP, Pilarski R, Eng C, Akar N. Tekin M, et al. Among authors: ekim m. Am J Med Genet A. 2006 Jul 1;140(13):1472-5. doi: 10.1002/ajmg.a.31273. Am J Med Genet A. 2006. PMID: 16752378 No abstract available.

5

The effect of plasminogen activator inhibitor-1 -675 4G/5G polymorphism on familial Mediterranean fever (FMF) disease.

Ozel Demiralp D, Ekim M, Akar N. Ozel Demiralp D, et al. Among authors: ekim m. Clin Appl Thromb Hemost. 2009 Jul-Aug;15(4):443-7. doi: 10.1177/1076029608325540. Epub 2008 Nov 24. Clin Appl Thromb Hemost. 2009. PMID: 19033264 Free article.

6

Hypertension and hypokalemia in a 15-year-old boy: question.

Ozçakar ZB, Fitöz S, Kavaz A, Burgu B, Soygür T, Akpınar E, Ekim M, Sertçelik A, Yalçınkaya F. Ozçakar ZB, et al. Among authors: ekim m. Pediatr Nephrol. 2010 Dec;25(12):2443-7. doi: 10.1007/s00467-009-1438-9. Epub 2010 Feb 9. Pediatr Nephrol. 2010. PMID: 20143099 No abstract available.

7

HPSE2 mutations in urofacial syndrome, non-neurogenic neurogenic bladder and lower urinary tract dysfunction.

Bulum B, Özçakar ZB, Duman D, Cengiz FB, Kavaz A, Burgu B, Baskın E, Çakar N, Soygür T, Ekim M, Tekin M, Yalçınkaya F. Bulum B, et al. Among authors: ekim m. Nephron. 2015;130(1):54-8. doi: 10.1159/000381465. Epub 2015 Apr 28. Nephron. 2015. PMID: 25924634

8

Soluble transferrin receptor is not a reliable marker of iron deficiency in pediatric CAPD patients.

Bakkaloglu SA, Ekim M, Tümer N, Akar N, Uysal Z. Bakkaloglu SA, et al. Among authors: ekim m. Perit Dial Int. 2002 Sep-Oct;22(5):621-5. Perit Dial Int. 2002. PMID: 12455576 No abstract available.

9

Serum amyloid A1 and tumor necrosis factor-alpha alleles in Turkish familial Mediterranean fever patients with and without amyloidosis.

Akar N, Hasipek M, Akar E, Ekim M, Yalçinkaya F, Cakar N. Akar N, et al. Among authors: ekim m. Amyloid. 2003 Mar;10(1):12-6. doi: 10.3109/13506120308995251. Amyloid. 2003. PMID: 12762136

10

Nutcracker syndrome with urolithiasis.

Altugan FS, Ekim M, Fitöz S, Ozçakar ZB, Burgu B, Yalçınkaya F, Soygür T. Altugan FS, et al. Among authors: ekim m. J Pediatr Urol. 2010 Oct;6(5):519-21. doi: 10.1016/j.jpurol.2010.05.014. Epub 2010 Jul 2. J Pediatr Urol. 2010. PMID: 20594917

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