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American Journal of Medical Genetics|January 30, 1995
Duchenne muscular dystrophy and myotonic dystrophy in the same patientA L Dubrovsky, A L Taratuto, G Sevlever, et al.
European Journal of Neurology|May 20, 2003
Memory deficits and retrieval processes in ALSM C Mantovan, L Baggio, G Dalla Barba, et al.
Neurology|April 14, 2004
Large-scale disruption of microtubule pathways in morphologically normal human spastin muscleA Molon, S Di Giovanni, Y W Chen, et al.
American Journal of Medical Genetics|June 28, 1996
Genetic counseling of isolated carriers of Duchenne muscular dystrophyE P Hoffman, E Pegoraro, P Scacheri, et al.
Neurology|July 1, 1997
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque familyS Capellari, C Vital, P Parchi, et al.
Fetal Diagnosis and Therapy|March 1, 1995
In utero fetal muscle biopsy alters diagnosis and carrier risks in Duchenne and Becker muscular dystrophyM I Evans, E L Krivchenia, M P Johnson, et al.
Human Molecular Genetics|May 20, 1999
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expressionZ Korade-Mirnics, J Tarleton, S Servidei, et al.
Neuro-Degenerative Diseases|June 11, 2011
Genetic variation in KIFAP3 is associated with an upper motor neuron-predominant phenotype in amyotrophic lateral sclerosisV Orsetti, E Pegoraro, V Cima, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 1, 2014
Italian recommendations for Lambert-Eaton myasthenic syndrome (LEMS) managementA Evoli, R Liguori, A Romani, et al.
Neurology|September 29, 2004
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophyP Prandini, A Berardinelli, M Fanin, et al.
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