Parman Y - Search Results

1

Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features.

Çakar A, Şahin E, Tezel S, Candayan A, Samancı B, Battaloğlu E, Başak AN, Bilgiç B, Hanağası H, Durmuş H, Parman Y. Çakar A, et al. Among authors: parman y. Acta Neurol Belg. 2022 Aug;122(4):939-945. doi: 10.1007/s13760-021-01721-2. Epub 2021 Jun 8. Acta Neurol Belg. 2022. PMID: 34101140

2

Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients.

Bissar-Tadmouri N, Parman Y, Boutrand L, Deymeer F, Serdaroglu P, Vandenberghe A, Battaloglu E. Bissar-Tadmouri N, et al. Among authors: parman y. Clin Genet. 2000 Nov;58(5):396-402. doi: 10.1034/j.1399-0004.2000.580511.x. Clin Genet. 2000. PMID: 11140841

3

Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene.

Bissar-Tadmouri N, Nelis E, Züchner S, Parman Y, Deymeer F, Serdaroglu P, De Jonghe P, Van Gerwen V, Timmerman V, Schröder JM, Battaloglu E. Bissar-Tadmouri N, et al. Among authors: parman y. Neurology. 2004 May 11;62(9):1522-5. doi: 10.1212/01.wnl.0000123253.57555.3a. Neurology. 2004. PMID: 15136675

4

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. Brain. 2004 Nov;127(Pt 11):2540-50. doi: 10.1093/brain/awh275. Epub 2004 Oct 6. Brain. 2004. PMID: 15469949

5

Iatrogenic botulism after botulinum toxin type A injections.

Coban A, Matur Z, Hanagasi HA, Parman Y. Coban A, et al. Among authors: parman y. Clin Neuropharmacol. 2010 May;33(3):158-60. doi: 10.1097/WNF.0b013e3181d479e0. Clin Neuropharmacol. 2010. PMID: 20150804

6

Sensorimotor neuropathy associated with endometrioid endometrial carcinoma.

Durmuş H, Tüzün E, Içöz S, Akman-Demir G, Parman Y. Durmuş H, et al. Among authors: parman y. Eur J Obstet Gynecol Reprod Biol. 2010 Jun;150(2):216-7. doi: 10.1016/j.ejogrb.2010.02.014. Epub 2010 Mar 1. Eur J Obstet Gynecol Reprod Biol. 2010. PMID: 20189709 No abstract available.

7

Oculopharyngodistal myopathy is a distinct entity: clinical and genetic features of 47 patients.

Durmus H, Laval SH, Deymeer F, Parman Y, Kiyan E, Gokyigiti M, Ertekin C, Ercan I, Solakoglu S, Karcagi V, Straub V, Bushby K, Lochmüller H, Serdaroglu-Oflazer P. Durmus H, et al. Among authors: parman y. Neurology. 2011 Jan 18;76(3):227-35. doi: 10.1212/WNL.0b013e318207b043. Neurology. 2011. PMID: 21242490

8

Nerve conduction studies in Charcot-Marie-Tooth disease in a cohort from Turkey.

Deymeer F, Matur Z, Poyraz M, Battaloglu E, Oflazer-Serdaroglu P, Parman Y. Deymeer F, et al. Among authors: parman y. Muscle Nerve. 2011 May;43(5):657-64. doi: 10.1002/mus.21932. Epub 2011 Mar 14. Muscle Nerve. 2011. PMID: 21404297

9

ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population.

Lahut S, Ömür Ö, Uyan Ö, Ağım ZS, Özoğuz A, Parman Y, Deymeer F, Oflazer P, Koç F, Özçelik H, Auburger G, Başak AN. Lahut S, et al. Among authors: parman y. PLoS One. 2012;7(8):e42956. doi: 10.1371/journal.pone.0042956. Epub 2012 Aug 20. PLoS One. 2012. PMID: 22916186 Free PMC article.

10

Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia.

Zimoń M, Baets J, Almeida-Souza L, De Vriendt E, Nikodinovic J, Parman Y, Battaloğlu E, Matur Z, Guergueltcheva V, Tournev I, Auer-Grumbach M, De Rijk P, Petersen BS, Müller T, Fransen E, Van Damme P, Löscher WN, Barišić N, Mitrovic Z, Previtali SC, Topaloğlu H, Bernert G, Beleza-Meireles A, Todorovic S, Savic-Pavicevic D, Ishpekova B, Lechner S, Peeters K, Ooms T, Hahn AF, Züchner S, Timmerman V, Van Dijck P, Rasic VM, Janecke AR, De Jonghe P, Jordanova A. Zimoń M, et al. Among authors: parman y. Nat Genet. 2012 Oct;44(10):1080-3. doi: 10.1038/ng.2406. Epub 2012 Sep 9. Nat Genet. 2012. PMID: 22961002

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