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Muscle & Nerve|April 9, 1998
Sarcolemmal excitability in myotonic dystrophy: assessment through surface EMGC Chisari, C D'Alessandro, M L Manca, et al.Collegium Antropologicum|July 26, 2002
Bayesian approach to searching for susceptibility genes: Gc2 and EsD1 alleles and multiple sclerosisM Di Bacco, D Luiselli, M L Manca, et al.The Cochrane Database of Systematic Reviews|October 21, 2006
Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron diseaseS E Langmore, E J Kasarskis, M L Manca, et al.Neuromuscular Disorders : NMD|March 11, 2000
Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathiesG Siciliano, M L Manca, M Renna, et al.Clinical Genetics|August 31, 1999
Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitationG Siciliano, A Tessa, M Renna, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathiesG Siciliano, M Mancuso, L Pasquali, et al.Journal of the Neurological Sciences|October 26, 2001
Impaired oxidative metabolism in exercising muscle from ALS patientsG Siciliano, E Pastorini, L Pasquali, et al.Australian Veterinary Journal|October 28, 2017
Elevated serum creatinine and hyponatraemia as prognostic factors in canine acute pancreatitisV Marchetti, E Gori, I Lippi, et al.Tissue Antigens|August 1, 1989
The absence of 21-OH A and C4 B genes is a constant characteristic of the "Sardinian" HLA extended haplotype A30 Cw5 B18 BfF1 DR3 DRw52 DQw2C Carcassi, R Porcella, M L Manca, et al.The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Response to a single dose of human chorionic gonadotropin in prepubertal boysV Toscano, R Balducci, M V Adamo, et al.Pageof 5