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Results: 1-8 |
Results: 8
The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases
Authors: Plante-Bordeneuve, V Parman, Y Guiochon-Mantel, A Alj, Y Deymeer, F Serdaroglu, P Eraksoy, M Said, G
Citation: V. Plante-bordeneuve et al., The range of chronic demyelinating neuropathy of infancy: a clinico-pathological and genetic study of 15 unrelated cases, J NEUROL, 248(9), 2001, pp. 795-803
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
Authors: Plaster, NM Tawil, R Tristani-Firouzi, M Canun, S Bendahhou, S Tsunoda, A Donaldson, MR Iannaccone, ST Brunt, E Barohn, R Clark, J Deymeer, F George, AL Fish, FA Hahn, A Nitu, A Ozdemir, C Serdaroglu, P Subramony, SH Wolfe, G Fu, YH Ptacek, LJ
Citation: Nm. Plaster et al., Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome, CELL, 105(4), 2001, pp. 511-519
Juvenile and late-onset myasthenia gravis
Authors: Deymeer, F Serdaroglu, P Ozdemir, C
Citation: F. Deymeer et al., Juvenile and late-onset myasthenia gravis, MG CLIN NEU, 18, 2000, pp. 113-127
Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type I and HNPP patients
Authors: Bissar-Tadmouri, N Parman, Y Boutrand, L Deymeer, F Serdaroglu, P Vandenberghe, A Battaloglu, E
Citation: N. Bissar-tadmouri et al., Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type I and HNPP patients, CLIN GENET, 58(5), 2000, pp. 396-402
Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians
Authors: Onengut, S Kavaslar, GN Battaloglu, E Serdaroglu, P Deymeer, F Ozdemir, C Calafell, F Tolun, A
Citation: S. Onengut et al., Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians, ANN HUM GEN, 64, 2000, pp. 33-40
Familial infantile myasthenia: confusion in terminology
Authors: Deymeer, F Serdaroglu, P Ozdemir, C
Citation: F. Deymeer et al., Familial infantile myasthenia: confusion in terminology, NEUROMUSC D, 9(3), 1999, pp. 129-130
Electrical myotonia in heterozygous carriers of recessive myotonia congenita
Authors: Deymeer, F Lehmann-Horn, F Serdaroglu, P Cakirkaya, S Benz, S Rudel, R Ozdemir, C
Citation: F. Deymeer et al., Electrical myotonia in heterozygous carriers of recessive myotonia congenita, MUSCLE NERV, 22(1), 1999, pp. 123-125
Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene
Authors: Middleton, L Ohno, K Christodoulou, K Brengman, J Milone, M Neocleous, V Serdaroglu, 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
Citation: L. Middleton et al., Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene, NEUROLOGY, 53(5), 1999, pp. 1076-1082
Risultati: 1-8 |