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E M Brett

Showing results (61-70 of 74) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Journal of Medical Genetics|September 1, 1989
Moebius' syndrome with unilateral cerebellar hypoplasiaM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1989
Autosomal recessive microcephaly, mental retardation with nonpigmentary retinopathy and a distinctive electroretinogramM G Harbord, S R Lambert, A Kriss, et al.
Archives of Neurology|November 1, 1986
Total and free serum concentrations of carbamazepine and carbamazepine-10,11-epoxide in children with epilepsyO A Agbato, A A Elyas, P N Patsalos, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenaseT C Gibbs, J Payan, E M Brett, et al.
Neuropediatrics|August 1, 1989
Early onset leukodystrophy with distinct facial features in 2 siblingsM G Harbord, J P Finn, M A Hall-Craggs, et al.
Journal of Child Neurology|April 1, 1993
Alexander's disease: clues to diagnosisC L Pridmore, M Baraitser, B Harding, et al.
Journal of Medical Genetics|October 1, 1989
Central nervous system malformations in Mohr's syndromeW Reardon, M G Harbord, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1987
Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight casesV T Ramaekers, B D Lake, B Harding, et al.
Archives of Disease in Childhood|October 1, 1973
Late onset GM2-gangliosidosis. Clinical, pathological, and biochemical studies on 8 patientsE M Brett, R B Ellis, L Haas, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.
Journal of Medical Genetics|September 1, 1989
Moebius' syndrome with unilateral cerebellar hypoplasiaM G Harbord, J P Finn, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1989
Autosomal recessive microcephaly, mental retardation with nonpigmentary retinopathy and a distinctive electroretinogramM G Harbord, S R Lambert, A Kriss, et al.
Archives of Neurology|November 1, 1986
Total and free serum concentrations of carbamazepine and carbamazepine-10,11-epoxide in children with epilepsyO A Agbato, A A Elyas, P N Patsalos, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenaseT C Gibbs, J Payan, E M Brett, et al.
Neuropediatrics|August 1, 1989
Early onset leukodystrophy with distinct facial features in 2 siblingsM G Harbord, J P Finn, M A Hall-Craggs, et al.
Journal of Child Neurology|April 1, 1993
Alexander's disease: clues to diagnosisC L Pridmore, M Baraitser, B Harding, et al.
Journal of Medical Genetics|October 1, 1989
Central nervous system malformations in Mohr's syndromeW Reardon, M G Harbord, M A Hall-Craggs, et al.
Neuropediatrics|August 1, 1987
Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight casesV T Ramaekers, B D Lake, B Harding, et al.
Archives of Disease in Childhood|October 1, 1973
Late onset GM2-gangliosidosis. Clinical, pathological, and biochemical studies on 8 patientsE M Brett, R B Ellis, L Haas, et al.
Pageof 8