Baris I - Search Results

1

High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease.

Bilir B, Yapici Z, Yalcinkaya C, Baris I, Carvalho CM, Bartnik M, Ozes B, Eraksoy M, Lupski JR, Battaloglu E. Bilir B, et al. Among authors: baris i. Clin Genet. 2013 Jan;83(1):66-72. doi: 10.1111/j.1399-0004.2012.01846.x. Epub 2012 Feb 20. Clin Genet. 2013. PMID: 22283455 Free PMC article.

2

Frequency of the 35delG mutation in the connexin 26 gene in Turkish hearing-impaired patients.

Bariş I, Kilinç MO, Tolun A. Bariş I, et al. Clin Genet. 2001 Dec;60(6):452-5. doi: 10.1034/j.1399-0004.2001.600608.x. Clin Genet. 2001. PMID: 11846738

3

Clinicopathological and genetic study of early-onset demyelinating neuropathy.

Parman Y, Battaloglu E, Baris I, Bilir B, Poyraz M, Bissar-Tadmouri N, Williams A, Ammar N, Nelis E, Timmerman V, De Jonghe P, Najafov A, Deymeer F, Serdaroglu P, Brophy PJ, Said G. Parman Y, et al. Among authors: baris i. Brain. 2004 Nov;127(Pt 11):2540-50. doi: 10.1093/brain/awh275. Epub 2004 Oct 6. Brain. 2004. PMID: 15469949

4

A large family with Charcot-Marie-Tooth Type 1a and Type 2 diabetes mellitus.

Koç F, Sarica Y, Yerdelen D, Baris I, Battaloglu E, Sert M. Koç F, et al. Among authors: baris i. Int J Neurosci. 2006 Feb;116(2):103-14. doi: 10.1080/00207450500341431. Int J Neurosci. 2006. PMID: 16393877

5

A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis.

Baris I, Arisoy AE, Smith A, Agostini M, Mitchell CS, Park SM, Halefoglu AM, Zengin E, Chatterjee VK, Battaloglu E. Baris I, et al. J Clin Endocrinol Metab. 2006 Oct;91(10):4183-7. doi: 10.1210/jc.2006-0405. Epub 2006 Aug 1. J Clin Endocrinol Metab. 2006. PMID: 16882747

6

Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: a case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade.

Bayrak AO, Battaloglu E, Turker H, Baris I, Oztas G. Bayrak AO, et al. Among authors: baris i. Brain Dev. 2009 Jun;31(6):445-8. doi: 10.1016/j.braindev.2008.07.002. Epub 2008 Aug 29. Brain Dev. 2009. PMID: 18760885

7

A multiplexed ARMS-PCR approach for the detection of common MECP2 mutations.

Baris I, Battaloglu E. Baris I, et al. Genet Test Mol Biomarkers. 2009 Feb;13(1):19-22. doi: 10.1089/gtmb.2008.0051. Genet Test Mol Biomarkers. 2009. PMID: 19309269

8

Multiplex detection of common mutations in the Connexin-26 gene.

Baris I, Köksal V. Baris I, et al. Genet Test. 2003 Spring;7(1):63-5. doi: 10.1089/109065703321560967. Genet Test. 2003. PMID: 12820705

9

Clinical and Molecular Findings in a Turkish Family Who Had a (c.869- 1G>A) Splicing Variant in PSEN1 Gene with A Rare Condition: The Variant Alzheimer's Disease with Spastic Paraparesis.

Doğan M, Eröz R, Tecellioğlu M, Gezdirici A, Çevik B, Barış İ. Doğan M, et al. Among authors: baris i. Curr Alzheimer Res. 2022;19(3):223-235. doi: 10.2174/1567205019666220414101251. Curr Alzheimer Res. 2022. PMID: 35430993 Review.

10

Association between gene polymorphisms in TIM1, TSLP, IL18R1 and childhood asthma in Turkish population.

Mete F, Ozkaya E, Aras S, Koksal V, Etlik O, Baris I. Mete F, et al. Among authors: baris i. Int J Clin Exp Med. 2014 Apr 15;7(4):1071-7. eCollection 2014. Int J Clin Exp Med. 2014. PMID: 24955184 Free PMC article.

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