Serdaroglu P - Search Results

1

Molecular and clinical study of two myotonic dystrophy homozygotes.

Akbas F, Serdaroglu P, Deymeer F, Aysal F, Erginel-Unaltuna N. Akbas F, et al. Among authors: serdaroglu p. J Med Genet. 2001 Nov;38(11):E40. doi: 10.1136/jmg.38.11.e40. J Med Genet. 2001. PMID: 11694554 Free PMC article. No abstract available.

2

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

3

Familial infantile myasthenia: confusion in terminology.

Deymeer F, Serdaroğlu P, Ozdemir C. Deymeer F, et al. Among authors: serdaroglu p. Neuromuscul Disord. 1999 May;9(3):129-30. doi: 10.1016/s0960-8966(99)00004-8. Neuromuscul Disord. 1999. PMID: 10382904 No abstract available.

4

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

5

Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians.

Onengüt S, Kavaslar GN, Battaloğlu E, Serdaroğlu P, Deymeer F, Ozdemir C, Calafell F, Tolun A. Onengüt S, et al. Among authors: serdaroglu p. Ann Hum Genet. 2000 Jan;64(Pt 1):33-40. doi: 10.1017/S0003480000007934. Ann Hum Genet. 2000. PMID: 11388892

6

Segmental distribution of muscle weakness in SMA III: implications for deterioration in muscle strength with time.

Deymeer F, Serdaroğlu P, Poda M, Gülşen-Parman Y, Ozçelik T, Ozdemir C. Deymeer F, et al. Among authors: serdaroglu p. Neuromuscul Disord. 1997 Dec;7(8):521-8. doi: 10.1016/s0960-8966(97)00113-2. Neuromuscul Disord. 1997. PMID: 9447610 Clinical Trial.

7

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

8

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

9

Identification of a one-basepair deletion in exon 6 of the dystrophin gene.

Kavaslar GN, Telatar M, Serdaroglu P, Deymeer F, Ozdemir C, Tolun A. Kavaslar GN, et al. Among authors: serdaroglu p. Hum Mutat. 1995;6(1):85-6. doi: 10.1002/humu.1380060116. Hum Mutat. 1995. PMID: 7550238 No abstract available.

10

The use of botulinum toxin in localizing neuromyotonia to the terminal branches of the peripheral nerve.

Deymeer F, Oge AE, Serdaroğlu P, Yazici J, Ozdemir C, Baslo A. Deymeer F, et al. Among authors: serdaroglu p. Muscle Nerve. 1998 May;21(5):643-6. doi: 10.1002/(sici)1097-4598(199805)21:5<643::aid-mus12>3.0.co;2-w. Muscle Nerve. 1998. PMID: 9572245

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