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Results: 6

Authors: MIDDLETON L OHNO K CHRISTODOULOU K BRENGMAN J NEOCLEOUS V DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A JORDAN A MAVROMATIS I MYLONAS I EVOLI A TSINGIS M ZAMBA E KYRIALLIS K ENGEL A
Citation: L. Middleton et al., CONGENITAL MYASTHENIC SYNDROMES (CMS) LINKED TO CHROMOSOME 17P ARE CAUSED BY DEFECTS IN ACETYLCHOLINE-RECEPTOR (ACHR) EPSILON-SUBUNIT GENE, Neurology, 50(4), 1998, pp. 67003-67003

Authors: ALSHEHAB A JOHNSEN R KAKULAS BA
Citation: A. Alshehab et al., IMMUNOCYTOCHEMICAL STUDIES OF THE CYTOSKELETON IN CONGENITAL PROGRESSIVE OVINE MUSCULAR-DYSTROPHY (OD), Brain pathology, 7(4), 1997, pp. 1373-1373

Authors: CHRISTODOULOU K TSINGIS M DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A BAIRACTARIS C MAVROMATIS I MYLONAS I EVOLI A KYRIALLIS K MIDDLETON LT
Citation: K. Christodoulou et al., MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA (CONGENITAL MYASTHENIC SYNDROME TYPE IA) GENE TO CHROMOSOME 17P WITH EVIDENCE OF GENETIC HOMOGENEITY, Human molecular genetics, 6(4), 1997, pp. 635-640

Authors: CHRISTODOULOU K TSINGIS M DEYMEER F SERDAROGLU P OZDEMIR C ALSHEHAB A BAIRACTARIS C MAVROMATIS I MYLONAS I EVOLI A KYRIALLIS K MIDDLETON LT
Citation: K. Christodoulou et al., MAPPING OF THE FAMILIAL INFANTILE MYASTHENIA GENE TO CHROMOSOME 17P, Neurology, 48(6), 1997, pp. 3-3

Authors: KYRIALLIS K CHRISTODOULOU K ALSHEHAB A BARBA V MYLONAS Y MAVROMATIS J SERDAROGLU P OZCELIK T DEYMMER F OZDEMIR C MIDDLETON LT
Citation: K. Kyriallis et al., FAMILIAL INFANTILE MYASTHENIA IN EASTERN MEDITERRANEAN COUNTRIES, Neurology, 46(2), 1996, pp. 4089-4089

Authors: ALDIN ASN ELKHATEEB M KURDI A MUBAIDIN A WRIEKAT A ALSHEHAB A KHALIL RW
Citation: Asn. Aldin et al., MULTIPLE-SCLEROSIS IN ARABS IN JORDAN, Journal of the neurological sciences, 131(2), 1995, pp. 144-149
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