Gundesli H[au] - Search Results

Year	Number of Results
2009	3
2010	2
2011	1
2013	1
2014	1
2023	1
2024	0

1

The Versatility of Plectin in Cancer: A Pan-Cancer Analysis on Potential Diagnostic and Prognostic Impacts of Plectin Isoforms.

Gundesli H, Kori M, Arga KY. Gundesli H, et al. OMICS. 2023 Jun;27(6):281-296. doi: 10.1089/omi.2023.0053. Epub 2023 Jun 1. OMICS. 2023. PMID: 37262182

2

A dystroglycan mutation associated with limb-girdle muscular dystrophy.

Hara Y, Balci-Hayta B, Yoshida-Moriguchi T, Kanagawa M, Beltrán-Valero de Bernabé D, Gündeşli H, Willer T, Satz JS, Crawford RW, Burden SJ, Kunz S, Oldstone MB, Accardi A, Talim B, Muntoni F, Topaloğlu H, Dinçer P, Campbell KP. Hara Y, et al. Among authors: gundesli h. N Engl J Med. 2011 Mar 10;364(10):939-46. doi: 10.1056/NEJMoa1006939. N Engl J Med. 2011. PMID: 21388311 Free PMC article.

3

Pitfall of identifying a disease locus by using low-resolution SNP arrays.

Gundesli H, Cirak S, Dincer P. Gundesli H, et al. J Mol Genet Med. 2010;5:264-5. Epub 2011 Nov 22. J Mol Genet Med. 2010. PMID: 22190979 Free PMC article. No abstract available.

4

A novel desmin mutation leading to autosomal recessive limb-girdle muscular dystrophy: distinct histopathological outcomes compared with desminopathies.

Cetin N, Balci-Hayta B, Gundesli H, Korkusuz P, Purali N, Talim B, Tan E, Selcen D, Erdem-Ozdamar S, Dincer P. Cetin N, et al. Among authors: gundesli h. J Med Genet. 2013 Jul;50(7):437-43. doi: 10.1136/jmedgenet-2012-101487. Epub 2013 May 18. J Med Genet. 2013. PMID: 23687351

5

Mutation in exon 1f of PLEC, leading to disruption of plectin isoform 1f, causes autosomal-recessive limb-girdle muscular dystrophy.

Gundesli H, Talim B, Korkusuz P, Balci-Hayta B, Cirak S, Akarsu NA, Topaloglu H, Dincer P. Gundesli H, et al. Am J Hum Genet. 2010 Dec 10;87(6):834-41. doi: 10.1016/j.ajhg.2010.10.017. Epub 2010 Nov 25. Am J Hum Genet. 2010. PMID: 21109228 Free PMC article.

6

Mutation in TOR1AIP1 encoding LAP1B in a form of muscular dystrophy: a novel gene related to nuclear envelopathies.

Kayman-Kurekci G, Talim B, Korkusuz P, Sayar N, Sarioglu T, Oncel I, Sharafi P, Gundesli H, Balci-Hayta B, Purali N, Serdaroglu-Oflazer P, Topaloglu H, Dincer P. Kayman-Kurekci G, et al. Among authors: gundesli h. Neuromuscul Disord. 2014 Jul;24(7):624-33. doi: 10.1016/j.nmd.2014.04.007. Epub 2014 May 2. Neuromuscul Disord. 2014. PMID: 24856141

7

Eosinophilic myositis in calpainopathy: could immunosuppression of the eosinophilic myositis alter the early natural course of the dystrophic disease?

Oflazer PS, Gundesli H, Zorludemir S, Sabuncu T, Dincer P. Oflazer PS, et al. Among authors: gundesli h. Neuromuscul Disord. 2009 Apr;19(4):261-3. doi: 10.1016/j.nmd.2009.01.010. Epub 2009 Mar 13. Neuromuscul Disord. 2009. PMID: 19285864

8

Use of SNP array analysis to identify a novel TRIM32 mutation in limb-girdle muscular dystrophy type 2H.

Cossée M, Lagier-Tourenne C, Seguela C, Mohr M, Leturcq F, Gundesli H, Chelly J, Tranchant C, Koenig M, Mandel JL. Cossée M, et al. Among authors: gundesli h. Neuromuscul Disord. 2009 Apr;19(4):255-60. doi: 10.1016/j.nmd.2009.02.003. Epub 2009 Mar 19. Neuromuscul Disord. 2009. PMID: 19303295

9

[Distribution of Enterobius vermicularis among the schoolchildren of two primary schools with different social-economic status in the Ankara province].

Hazir C, Gündeşli H, Ozkirim A, Keskin N. Hazir C, et al. Among authors: gundesli h. Turkiye Parazitol Derg. 2009;33(1):54-8. Turkiye Parazitol Derg. 2009. PMID: 19367548 Turkish.

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