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Results:
1-15
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Results: 15
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
Authors:
Urganci, N
Erkan, T
Serdaroglu, P
Ozcelik, G
Dogan, S
Kayaalp, N
Citation: N. Urganci et al., A rare cause of high transaminasemia: Autosomal muscle dystrophy with gamma sarcoglycan, J PED GASTR, 32(3), 2001, pp. 327-329
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
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
Authors:
Celet, B
Akman-Demir, G
Serdaroglu, P
Yentur, SP
Tasci, B
van Noort, JM
Eraksoy, M
Saruhan-Direskeneli, G
Citation: B. Celet et al., Anti-a alpha B-crystallin immunoreactivity in inflammatory nervous system diseases, J NEUROL, 247(12), 2000, pp. 935-939
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
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
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
Authors:
Oktem-Tanor, O
Baykan-Kurt, B
Gurvit, IH
Akman-Demir, G
Serdaroglu, P
Citation: O. Oktem-tanor et al., Neuropsychological follow-up of 12 patients with neuro-Behcet disease, J NEUROL, 246(2), 1999, pp. 113-119
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
Authors:
Coban, O
Bahar, S
Akman-Demir, G
Tasci, B
Yurdakul, S
Yazici, H
Serdaroglu, P
Citation: O. Coban et al., Masked assessment of MRI findings: is it possible to differentiate neuro-Behcet's disease from other central nervous system diseases? (vol 41, pg 255, 1999), NEURORADIOL, 41(7), 1999, pp. 550-550
Authors:
Coban, O
Bahar, S
Akman-Demir, G
Tasci, B
Yurdakul, S
Yazici, H
Serdaroglu, P
Citation: O. Coban et al., Masked assessment of MRI findings: is it possible to differentiate neuro-Behcet's disease from other central nervous system, NEURORADIOL, 41(4), 1999, pp. 255-260
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
Authors:
Erdogru, T
Kocak, T
Serdaroglu, P
Kadioglu, A
Tellaloglu, S
Citation: T. Erdogru et al., Evaluation and therapeutic approaches of voiding and erectile dysfunction in neurological Behcet's syndrome, J UROL, 162(1), 1999, pp. 147-153
Authors:
Akman-Demir, G
Serdaroglu, P
Tasci, B
Citation: G. Akman-demir et al., Clinical patterns of neurological involvement in Behcet's disease: evaluation of 200 patients, BRAIN, 122, 1999, pp. 2171-2181
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