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Human Genetics
|
August 1, 1993
Identification of a novel T-insertion polymorphism at the DMD locus
F 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 distribution
E 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 status
E Mercuri, F Muntoni, A Berardinelli, et al.
Neuromuscular Disorders : NMD
|
November 11, 2025
Respiratory management in spinal muscular atrophy: development of a global outcome measure
L Edel, M Civitello, F Muntoni, et al.
Clinical Radiology
|
January 19, 2002
Magnetic resonance imaging assessment of infantile myofibromatosis
S J Counsell, C Devile, E Mercuri, et al.
Neuropediatrics
|
May 31, 2003
Occipito-temporal polymicrogyria and subclinical muscular dystrophy
Z 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 imaging
J 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 patients
M G Marrosu, A P Mazzoleni, S Galantuomo, et al.
European Journal of Pharmacology
|
October 27, 1987
Stress-induced insomnia: opioid-dopamine interactions
W Fratta, M Collu, M C Martellotta, et al.
Page
of 28
Search research articles
Search
Showing results (81-90 of 275) with videos related to
Sort By:
Page
of 28
Human Genetics
|
August 1, 1993
Identification of a novel T-insertion polymorphism at the DMD locus
F 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 distribution
E 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 status
E Mercuri, F Muntoni, A Berardinelli, et al.
Neuromuscular Disorders : NMD
|
November 11, 2025
Respiratory management in spinal muscular atrophy: development of a global outcome measure
L Edel, M Civitello, F Muntoni, et al.
Clinical Radiology
|
January 19, 2002
Magnetic resonance imaging assessment of infantile myofibromatosis
S J Counsell, C Devile, E Mercuri, et al.
Neuropediatrics
|
May 31, 2003
Occipito-temporal polymicrogyria and subclinical muscular dystrophy
Z 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 imaging
J 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 patients
M G Marrosu, A P Mazzoleni, S Galantuomo, et al.
European Journal of Pharmacology
|
October 27, 1987
Stress-induced insomnia: opioid-dopamine interactions
W Fratta, M Collu, M C Martellotta, et al.
Page
of 28