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Archives of Disease in Childhood
|
April 1, 1989
Clinical and EEG response to anticonvulsants in neonatal seizures
J Connell, R Oozeer, L de Vries, et al.
The Journal of Pediatrics
|
October 1, 1985
Hearing threshold in preterm and term infants by auditory brainstem response
S Lary, G Briassoulis, L de Vries, et al.
Human Genetics
|
October 30, 1999
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?
M D'Alessandro, I Naom, A Ferlini, et al.
Journal of the Neurological Sciences
|
November 1, 1988
Dystrophin and nebulin in the muscular dystrophies
K Patel, T Voit, M J Dunn, et al.
Neurology
|
July 1, 1981
An X-linked disease of the nervous system with disordered copper metabolism and features differing from Menkes disease
R H Haas, A Robinson, K Evans, et al.
The Journal of Pediatrics
|
July 1, 1981
Neurologic signs in neonatal intraventricular hemorrhage: a correlation with real-time ultrasound
L M Dubowitz, M I Levene, A Morante, et al.
Neuromuscular Disorders : NMD
|
March 1, 1994
Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy
C A Sewry, A Sansome, K Matsumura, et al.
Physiotherapy
|
June 1, 1981
Effect of exercise in Duchenne muscular dystrophy
O M Scott, S A Hyde, C Goddard, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance
A Y Manzur, C A Sewry, J Ziprin, et al.
Neuropathology and Applied Neurobiology
|
August 1, 1994
Expression of utrophin (dystrophin-related protein) during regeneration and maturation of skeletal muscle in canine X-linked muscular dystrophy
L A Wilson, B J Cooper, L Dux, et al.
Page
of 35
Search research articles
Search
Showing results (231-240 of 349) with videos related to
Sort By:
Page
of 35
Archives of Disease in Childhood
|
April 1, 1989
Clinical and EEG response to anticonvulsants in neonatal seizures
J Connell, R Oozeer, L de Vries, et al.
The Journal of Pediatrics
|
October 1, 1985
Hearing threshold in preterm and term infants by auditory brainstem response
S Lary, G Briassoulis, L de Vries, et al.
Human Genetics
|
October 30, 1999
Is there selection in favour of heterozygotes in families with merosin-deficient congenital muscular dystrophy?
M D'Alessandro, I Naom, A Ferlini, et al.
Journal of the Neurological Sciences
|
November 1, 1988
Dystrophin and nebulin in the muscular dystrophies
K Patel, T Voit, M J Dunn, et al.
Neurology
|
July 1, 1981
An X-linked disease of the nervous system with disordered copper metabolism and features differing from Menkes disease
R H Haas, A Robinson, K Evans, et al.
The Journal of Pediatrics
|
July 1, 1981
Neurologic signs in neonatal intraventricular hemorrhage: a correlation with real-time ultrasound
L M Dubowitz, M I Levene, A Morante, et al.
Neuromuscular Disorders : NMD
|
March 1, 1994
Deficiency of the 50 kDa dystrophin-associated glycoprotein and abnormal expression of utrophin in two south Asian cousins with variable expression of severe childhood autosomal recessive muscular dystrophy
C A Sewry, A Sansome, K Matsumura, et al.
Physiotherapy
|
June 1, 1981
Effect of exercise in Duchenne muscular dystrophy
O M Scott, S A Hyde, C Goddard, et al.
Neuromuscular Disorders : NMD
|
November 26, 1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance
A Y Manzur, C A Sewry, J Ziprin, et al.
Neuropathology and Applied Neurobiology
|
August 1, 1994
Expression of utrophin (dystrophin-related protein) during regeneration and maturation of skeletal muscle in canine X-linked muscular dystrophy
L A Wilson, B J Cooper, L Dux, et al.
Page
of 35