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F Muntoni

Showing results (81-90 of 275) with videos related to

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Human Genetics|August 1, 1993
Identification of a novel T-insertion polymorphism at the DMD locusF Muntoni, M Cau, R Congiu, et al.
FEBS Letters|April 27, 2001
Overexpressed human survival motor neurone isoforms, SMNDeltaexon7 and SMN+exon7, both form intranuclear gems but differ in cytoplasmic distributionE Dodds, M G Dunckley, R G Roberts, et al.
Neuromuscular Disorders : NMD|March 10, 2015
Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1)C A Sewry, J L Holton, D J Dick, et al.
Neuropediatrics|February 1, 1995
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin statusE Mercuri, F Muntoni, A Berardinelli, et al.
Neuromuscular Disorders : NMD|November 11, 2025
Respiratory management in spinal muscular atrophy: development of a global outcome measureL Edel, M Civitello, F Muntoni, et al.
Clinical Radiology|January 19, 2002
Magnetic resonance imaging assessment of infantile myofibromatosisS J Counsell, C Devile, E Mercuri, et al.
Neuropediatrics|May 31, 2003
Occipito-temporal polymicrogyria and subclinical muscular dystrophyZ Zolkipli, L Hartley, S Brown, et al.
Neuromuscular Disorders : NMD|April 30, 1999
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imagingJ Philpot, F Cowan, J Pennock, et al.
European Neurology|January 1, 1992
Polymerase chain reaction analysis for specific HTLV-1 sequences from cerebrospinal fluid and peripheral blood cells in Sardinian multiple sclerosis patientsM G Marrosu, A P Mazzoleni, S Galantuomo, et al.
European Journal of Pharmacology|October 27, 1987
Stress-induced insomnia: opioid-dopamine interactionsW Fratta, M Collu, M C Martellotta, et al.
Pageof 28

Showing results (81-90 of 275) with videos related to

Sort By:
Pageof 28
Human Genetics|August 1, 1993
Identification of a novel T-insertion polymorphism at the DMD locusF Muntoni, M Cau, R Congiu, et al.
FEBS Letters|April 27, 2001
Overexpressed human survival motor neurone isoforms, SMNDeltaexon7 and SMN+exon7, both form intranuclear gems but differ in cytoplasmic distributionE Dodds, M G Dunckley, R G Roberts, et al.
Neuromuscular Disorders : NMD|March 10, 2015
Zebra body myopathy is caused by a mutation in the skeletal muscle actin gene (ACTA1)C A Sewry, J L Holton, D J Dick, et al.
Neuropediatrics|February 1, 1995
Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin statusE Mercuri, F Muntoni, A Berardinelli, et al.
Neuromuscular Disorders : NMD|November 11, 2025
Respiratory management in spinal muscular atrophy: development of a global outcome measureL Edel, M Civitello, F Muntoni, et al.
Clinical Radiology|January 19, 2002
Magnetic resonance imaging assessment of infantile myofibromatosisS J Counsell, C Devile, E Mercuri, et al.
Neuropediatrics|May 31, 2003
Occipito-temporal polymicrogyria and subclinical muscular dystrophyZ Zolkipli, L Hartley, S Brown, et al.
Neuromuscular Disorders : NMD|April 30, 1999
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imagingJ Philpot, F Cowan, J Pennock, et al.
European Neurology|January 1, 1992
Polymerase chain reaction analysis for specific HTLV-1 sequences from cerebrospinal fluid and peripheral blood cells in Sardinian multiple sclerosis patientsM G Marrosu, A P Mazzoleni, S Galantuomo, et al.
European Journal of Pharmacology|October 27, 1987
Stress-induced insomnia: opioid-dopamine interactionsW Fratta, M Collu, M C Martellotta, et al.
Pageof 28