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F Muntoni

Showing results (61-70 of 275) with videos related to

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European Journal of Human Genetics : EJHG|April 11, 2000
Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardationH Jin, R J Gardner, R Viswesvaraiah, et al.
Supplements to Clinical Neurophysiology|August 19, 2005
Immunopathology and molecular genetics of dystrophinopathiesS C Brown, S Torelli, C Jimenez, et al.
Italian Journal of Neurological Sciences|April 1, 1994
Toxic effect of intraventricular interferon-alpha in subacute sclerosing panencephalitisC Cianchetti, A L Fratta, F Muntoni, et al.
Heart (British Cardiac Society)|January 3, 2006
Cardiac tissue velocities and strain rate in the early detection of myocardial dysfunction of asymptomatic boys with Duchenne's muscular dystrophy: relationship to clinical outcomeN Giatrakos, M Kinali, D Stephens, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotypeK Talbot, N R Rodrigues, J Ignatius, et al.
Neuromuscular Disorders : NMD|November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritanceA Y Manzur, C A Sewry, J Ziprin, et al.
Brain & Development|May 1, 1996
Clinical and EEG findings in eleven patients affected by mitochondrial encephalomyopathy with MERRF-MELAS overlapG Serra, R Piccinnu, M Tondi, et al.
Neuromuscular Disorders : NMD|January 1, 1997
Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodiesS Manilal, C A Sewry, N Man, et al.
Neuropediatrics|January 4, 2005
Bone mineral density in a paediatric spinal muscular atrophy populationM Kinali, L M Banks, E Mercuri, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?A-M Lamhonwah, R Onizuka, S E Olpin, et al.
Pageof 28

Showing results (61-70 of 275) with videos related to

Sort By:
Pageof 28
European Journal of Human Genetics : EJHG|April 11, 2000
Two novel members of the interleukin-1 receptor gene family, one deleted in Xp22.1-Xp21.3 mental retardationH Jin, R J Gardner, R Viswesvaraiah, et al.
Supplements to Clinical Neurophysiology|August 19, 2005
Immunopathology and molecular genetics of dystrophinopathiesS C Brown, S Torelli, C Jimenez, et al.
Italian Journal of Neurological Sciences|April 1, 1994
Toxic effect of intraventricular interferon-alpha in subacute sclerosing panencephalitisC Cianchetti, A L Fratta, F Muntoni, et al.
Heart (British Cardiac Society)|January 3, 2006
Cardiac tissue velocities and strain rate in the early detection of myocardial dysfunction of asymptomatic boys with Duchenne's muscular dystrophy: relationship to clinical outcomeN Giatrakos, M Kinali, D Stephens, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotypeK Talbot, N R Rodrigues, J Ignatius, et al.
Neuromuscular Disorders : NMD|November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritanceA Y Manzur, C A Sewry, J Ziprin, et al.
Brain & Development|May 1, 1996
Clinical and EEG findings in eleven patients affected by mitochondrial encephalomyopathy with MERRF-MELAS overlapG Serra, R Piccinnu, M Tondi, et al.
Neuromuscular Disorders : NMD|January 1, 1997
Diagnosis of X-linked Emery-Dreifuss muscular dystrophy by protein analysis of leucocytes and skin with monoclonal antibodiesS Manilal, C A Sewry, N Man, et al.
Neuropediatrics|January 4, 2005
Bone mineral density in a paediatric spinal muscular atrophy populationM Kinali, L M Banks, E Mercuri, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?A-M Lamhonwah, R Onizuka, S E Olpin, et al.
Pageof 28