Serdaroglu P - Search Results

1

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: serdaroglu p. Neurology. 2004 May 11;62(9):1522-5. doi: 10.1212/01.wnl.0000123253.57555.3a. Neurology. 2004. PMID: 15136675

2

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

3

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: serdaroglu p. Clin Genet. 2000 Nov;58(5):396-402. doi: 10.1034/j.1399-0004.2000.580511.x. Clin Genet. 2000. PMID: 11140841

4

Natural history of SMA IIIb: muscle strength decreases in a predictable sequence and magnitude.

Deymeer F, Serdaroglu P, Parman Y, Poda M. Deymeer F, et al. Among authors: serdaroglu p. Neurology. 2008 Aug 26;71(9):644-9. doi: 10.1212/01.wnl.0000324623.89105.c4. Neurology. 2008. PMID: 18725590

5

DNA analysis in Turkish Duchenne/Becker muscular dystrophy families.

Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Kuseyri F, Ozdemir C, Apak M, Tolun A. Battaloğlu E, et al. Among authors: serdaroglu p. Hum Genet. 1992 Aug;89(6):635-9. doi: 10.1007/BF00221954. Hum Genet. 1992. PMID: 1355068

6

Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene.

Middleton L, Ohno K, Christodoulou K, Brengman J, Milone M, Neocleous V, Serdaroğlu P, Deymeer F, Ozdemir C, Mubaidin A, Horany K, Al-Shehab A, Mavromatis I, Mylonas I, Tsingis M, Zamba E, Pantzaris M, Kyriallis K, Engel AG. Middleton L, et al. Among authors: serdaroglu p. Neurology. 1999 Sep 22;53(5):1076-82. doi: 10.1212/wnl.53.5.1076. Neurology. 1999. PMID: 10496269

7

Two novel mutations in the MPZ gene coding region in Charcot-Marie-Tooth type 1 patients of Turkish origin: S54P, [I30del; GVYI29ins].

Bissar-Tadmouri N, Gulsen-Parman Y, Latour P, Deymeer F, Serdaroglu P, Vandenberghe A, Battaloglu E. Bissar-Tadmouri N, et al. Among authors: serdaroglu p. Hum Mutat. 1999 Nov;14(5):449. doi: 10.1002/(SICI)1098-1004(199911)14:5<449::AID-HUMU17>3.0.CO;2-H. Hum Mutat. 1999. PMID: 10533074 No abstract available.

8

Clinical comparison of anti-MuSK- vs anti-AChR-positive and seronegative myasthenia gravis.

Deymeer F, Gungor-Tuncer O, Yilmaz V, Parman Y, Serdaroglu P, Ozdemir C, Vincent A, Saruhan-Direskeneli G. Deymeer F, et al. Among authors: serdaroglu p. Neurology. 2007 Feb 20;68(8):609-11. doi: 10.1212/01.wnl.0000254620.45529.97. Neurology. 2007. PMID: 17310034

9

HLA-DQ polymorphism in Turkish patients with myasthenia gravis.

Saruhan-Direskeneli G, Kiliç A, Parman Y, Serdaroğlu P, Deymeer F. Saruhan-Direskeneli G, et al. Among authors: serdaroglu p. Hum Immunol. 2006 Apr-May;67(4-5):352-8. doi: 10.1016/j.humimm.2006.02.039. Epub 2006 Apr 7. Hum Immunol. 2006. PMID: 16720217

10

Carrier detection by DNA analysis in Duchenne muscular dystrophy families.

Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Ozdemir C, Kuseyri F, Apak MY, Tolun A. Battaloğlu E, et al. Among authors: serdaroglu p. Turk J Pediatr. 1992 Apr-Jun;34(2):79-92. Turk J Pediatr. 1992. PMID: 1440954

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