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Developmental Medicine and Child Neurology
|
June 1, 1985
Chromosome 15 in Prader-Willi syndrome
C N Fear, D E Mutton, A C Berry, et al.
Pediatrics
|
September 1, 1988
Predictive value of early continuous electroencephalogram monitoring in ventilated preterm infants with intraventricular hemorrhage
J Connell, L de Vries, R Oozeer, et al.
The Journal of Pediatrics
|
August 4, 1999
Optimality score for the neurologic examination of the infant at 12 and 18 months of age
L Haataja, E Mercuri, R Regev, et al.
Neuromuscular Disorders : NMD
|
July 1, 1995
Expression of laminin subunits in congenital muscular dystrophy
C A Sewry, J Philpot, D Mahony, et al.
Society of General Physiologists Series
|
January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4
J Wang, V Dubowitz, F Lehmann-Horn, et al.
Neuromuscular Disorders : NMD
|
August 26, 1998
Fifty year follow-up of a patient with central core disease shows slow but definite progression
P J Lamont, V Dubowitz, D N Landon, et al.
Journal of Medical Genetics
|
November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy
S Hodgson, K Hart, S Abbs, et al.
Muscle & Nerve
|
November 1, 1980
Polymyositis--an immunofluorescence study on the distribution of collagen types
V C Duance, C M Black, V Dubowitz, et al.
Journal of the Neurological Sciences
|
January 1, 1982
Collagen types in neuromuscular diseases
H R Stephens, V C Duance, M J Dunn, 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.
Page
of 35
Search research articles
Search
Showing results (261-270 of 349) with videos related to
Sort By:
Page
of 35
Developmental Medicine and Child Neurology
|
June 1, 1985
Chromosome 15 in Prader-Willi syndrome
C N Fear, D E Mutton, A C Berry, et al.
Pediatrics
|
September 1, 1988
Predictive value of early continuous electroencephalogram monitoring in ventilated preterm infants with intraventricular hemorrhage
J Connell, L de Vries, R Oozeer, et al.
The Journal of Pediatrics
|
August 4, 1999
Optimality score for the neurologic examination of the infant at 12 and 18 months of age
L Haataja, E Mercuri, R Regev, et al.
Neuromuscular Disorders : NMD
|
July 1, 1995
Expression of laminin subunits in congenital muscular dystrophy
C A Sewry, J Philpot, D Mahony, et al.
Society of General Physiologists Series
|
January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4
J Wang, V Dubowitz, F Lehmann-Horn, et al.
Neuromuscular Disorders : NMD
|
August 26, 1998
Fifty year follow-up of a patient with central core disease shows slow but definite progression
P J Lamont, V Dubowitz, D N Landon, et al.
Journal of Medical Genetics
|
November 1, 1989
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy
S Hodgson, K Hart, S Abbs, et al.
Muscle & Nerve
|
November 1, 1980
Polymyositis--an immunofluorescence study on the distribution of collagen types
V C Duance, C M Black, V Dubowitz, et al.
Journal of the Neurological Sciences
|
January 1, 1982
Collagen types in neuromuscular diseases
H R Stephens, V C Duance, M J Dunn, 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.
Page
of 35