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A Berardinelli

Showing results (11-20 of 34) with videos related to

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Functional Neurology|February 21, 2002
Pelizaeus-Merzbacher disease: electrophysiological study of two sibs with the classic form and of their relativesE Alfonsi, A M Clerici, I Costi, et al.
Italian Journal of Neurological Sciences|May 1, 1995
Prospective study of gross motor development in children with SMA type IIR Bono, M Inverno, G Botteon, et al.
Muscle & Nerve|August 22, 2000
A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophyM D Bonifati, G Ruzza, P Bonometto, et al.
Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|June 20, 1998
The efficacy of noninvasive mechanical ventilation on nocturnal hypoxaemia in Duchenne's muscular dystrophyF Fanfulla, A Berardinelli, G Gualtieri, et al.
Journal of Medical Genetics|May 1, 1996
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophyR Tupler, A Berardinelli, L Barbierato, et al.
Acta Diabetologica|November 18, 2003
Measurement of skeletal muscle mass in Duchenne muscular dystrophy: use of 24-h creatinine excretionD Franciotta, M C Zanardi, L Albertotti, et al.
Neuropediatrics|June 1, 1995
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changesE Mercuri, L Dubowitz, A Berardinelli, 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.
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Functional Neurology|February 21, 2002
Pelizaeus-Merzbacher disease: electrophysiological study of two sibs with the classic form and of their relativesE Alfonsi, A M Clerici, I Costi, et al.
Italian Journal of Neurological Sciences|May 1, 1995
Prospective study of gross motor development in children with SMA type IIR Bono, M Inverno, G Botteon, et al.
Muscle & Nerve|August 22, 2000
A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophyM D Bonifati, G Ruzza, P Bonometto, et al.
Monaldi Archives for Chest Disease = Archivio Monaldi Per Le Malattie Del Torace|June 20, 1998
The efficacy of noninvasive mechanical ventilation on nocturnal hypoxaemia in Duchenne's muscular dystrophyF Fanfulla, A Berardinelli, G Gualtieri, et al.
Journal of Medical Genetics|May 1, 1996
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophyR Tupler, A Berardinelli, L Barbierato, et al.
Acta Diabetologica|November 18, 2003
Measurement of skeletal muscle mass in Duchenne muscular dystrophy: use of 24-h creatinine excretionD Franciotta, M C Zanardi, L Albertotti, et al.
Neuropediatrics|June 1, 1995
Minor neurological and perceptuo-motor deficits in children with congenital muscular dystrophy: correlation with brain MRI changesE Mercuri, L Dubowitz, A Berardinelli, 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.
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.
Pageof 4