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Results: 1-10 |
Results: 10
MARKED CLINICAL HETEROGENEITY IN MITOCHONDRIAL-DNA DEPLETION SYNDROME
Authors: CASTAGNA AE SHOUBRIDGE E ROBINSON BH TEIN L
Citation: Ae. Castagna et al., MARKED CLINICAL HETEROGENEITY IN MITOCHONDRIAL-DNA DEPLETION SYNDROME, Annals of neurology, 44(3), 1998, pp. 43-43
CELL-SPECIFICITY OF THE MOLECULAR DEFECT IN FRIEDREICH ATAXIA
Authors: PANDOLFO M MONTERMINI L COVA L OHSHIMA K JIRALERSPONG S SHOUBRIDGE E KAPLAN J
Citation: M. Pandolfo et al., CELL-SPECIFICITY OF THE MOLECULAR DEFECT IN FRIEDREICH ATAXIA, Annals of neurology, 44(3), 1998, pp. 122-122
PREVALENCE OF MTDNA MUTATIONS ASSOCIATED WITH LEBERS HEREDITARY OPTICNEUROPATHY (LHON) IN FAMILIAL MS AND MS PATIENTS WITH PROMINENT OPTICNEUROPATHY
Authors: FRANCIS GS SHOUBRIDGE E FU K ARNAOUTELIS R
Citation: Gs. Francis et al., PREVALENCE OF MTDNA MUTATIONS ASSOCIATED WITH LEBERS HEREDITARY OPTICNEUROPATHY (LHON) IN FAMILIAL MS AND MS PATIENTS WITH PROMINENT OPTICNEUROPATHY, Neurology, 50(4), 1998, pp. 3057-3057
LEHERS HEREDITARY OPTIC NEUROPATHY PRESENTING AS DEMYELINATING (MS-LIKE) DISEASE OF THE CENTRAL-NERVOUS-SYSTEM
Authors: HORVATH R LOCHMULLER H SHOUBRIDGE E KARCAGI V KOMOLY S
Citation: R. Horvath et al., LEHERS HEREDITARY OPTIC NEUROPATHY PRESENTING AS DEMYELINATING (MS-LIKE) DISEASE OF THE CENTRAL-NERVOUS-SYSTEM, Neurology, 50(4), 1998, pp. 4120-4120
EXPRESSION OF NITRIC-OXIDE SYNTHASE (NOS) ISOFORMS IN SKELETAL-MUSCLEOF PATIENTS WITH MITOCHONDRIAL DISEASE
Authors: HORVATH R LOCHMULLER H KARPATI G SHOUBRIDGE E
Citation: R. Horvath et al., EXPRESSION OF NITRIC-OXIDE SYNTHASE (NOS) ISOFORMS IN SKELETAL-MUSCLEOF PATIENTS WITH MITOCHONDRIAL DISEASE, Neurology, 48(3), 1997, pp. 6143-6143
TRABECULAR MYOPATHY - A DISTINCTIVE CLINICOPATHOLOGICAL ENTITY WITH MARKED OVEREXPRESSION OF VIMENTIN IN MUSCLE
Authors: WELLER B LOCHMULLER H CARPENTER S SHOUBRIDGE E ALLEN C KARPATI G
Citation: B. Weller et al., TRABECULAR MYOPATHY - A DISTINCTIVE CLINICOPATHOLOGICAL ENTITY WITH MARKED OVEREXPRESSION OF VIMENTIN IN MUSCLE, Neurology, 48(3), 1997, pp. 31003-31003
AGING AND MUSCLE MITOCHONDRIAL ABNORMALITIES - REPLY
Authors: KARPATI G SHOUBRIDGE E
Citation: G. Karpati et E. Shoubridge, AGING AND MUSCLE MITOCHONDRIAL ABNORMALITIES - REPLY, Annals of neurology, 38(2), 1995, pp. 274-274
INVESTIGATION OF THE ROLE OF THE MYOTONIC-DYSTROPHY KINASE (DMK) IN THE DIFFERENTIATION OF CULTURED MYOBLASTS
Authors: SABOURIN LA TSILFIDIS CT STORBECK C WARING J NARANG M MAHER P PUYMYRAT JM KARPATI G SHOUBRIDGE E KORNELUK RG
Citation: La. Sabourin et al., INVESTIGATION OF THE ROLE OF THE MYOTONIC-DYSTROPHY KINASE (DMK) IN THE DIFFERENTIATION OF CULTURED MYOBLASTS, Journal of cellular biochemistry, 1994, pp. 531-531
MYOBLAST TRANSFER IN DUCHENNE MUSCULAR-DYSTROPHY
Authors: KARPATI G AJDUKOVIC D ARNOLD D GLEDHILL RB GUTTMANN R HOLLAND P KOCH PA SHOUBRIDGE E SPENCE D VANASSE M WATTERS GV ABRAHAMOWICZ M DUFF C WORTON RG
Citation: G. Karpati et al., MYOBLAST TRANSFER IN DUCHENNE MUSCULAR-DYSTROPHY, Annals of neurology, 34(1), 1993, pp. 8-17
FAMILIAL MYOPATHY WITH CONSPICUOUS DEPLETION OF MITOCHONDRIA IN MUSCLE-FIBERS - A NEW SYNDROME
Authors: GENGE A SHOUBRIDGE E CARPENTER S ARNOLD D JACOB P KARPATI G
Citation: A. Genge et al., FAMILIAL MYOPATHY WITH CONSPICUOUS DEPLETION OF MITOCHONDRIA IN MUSCLE-FIBERS - A NEW SYNDROME, Neurology, 43(4), 1993, pp. 403-403
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