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E M Brett

Showing results (31-40 of 74) with videos related to

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Neuropediatrics|November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndromeK Tomiwa, M Baraitser, E M Brett, et al.
Archives of Disease in Childhood|August 1, 1978
Neurological abnormalities in patients treated for hypothyroidism from early lifeR Macfaul, S Dorner, E M Brett, et al.
Journal of Medical Genetics|March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysisC Pridmore, M Baraitser, E M Brett, et al.
Journal of Medical Genetics|July 1, 1988
Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migrationJ A Hurst, M Markiewicz, D Kumar, et al.
Transactions of the American Neurological Association|January 1, 1974
Heterogeneity in two families with central core diseaseE M Brett, J A Morgan-Hughes, B D Lake
Lancet (London, England)|December 5, 1987
Rett's syndrome and ornithine carbamoyltransferase deficiencyS Thomas, M Hjelm, V Oberholzer, et al.
Neuropediatrics|November 1, 1981
The possible adjuvant role of bordetella pertussis and pertussis vaccine in causing severe encephalopathic illness: a presentation of three case historiesN P Cavanagh, E M Brett, W C Marshall, et al.
Journal of Mental Deficiency Research|December 1, 1979
The Börjeson-Forssman-Lehmann syndrome: a new caseR M Veall, E M Brett, T M Rivinus, et al.
Developmental Medicine and Child Neurology|December 1, 1984
Correlation between plasma carbamazepine-10,11-epoxide concentration and drug side-effects in children with epilepsyJ F Schoeman, A A Elyas, E M Brett, et al.
Acta Neuropathologica|August 31, 1977
Comparative ultrastructural observations on peripheral nerve abnormalities in the late infantile, juvenile and late onset forms of metachromatic leukodystrophyP K Thomas, R H King, R S Kocen, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Neuropediatrics|November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndromeK Tomiwa, M Baraitser, E M Brett, et al.
Archives of Disease in Childhood|August 1, 1978
Neurological abnormalities in patients treated for hypothyroidism from early lifeR Macfaul, S Dorner, E M Brett, et al.
Journal of Medical Genetics|March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysisC Pridmore, M Baraitser, E M Brett, et al.
Journal of Medical Genetics|July 1, 1988
Unknown syndrome: Hirschsprung's disease, microcephaly, and iris coloboma: a new syndrome of defective neuronal migrationJ A Hurst, M Markiewicz, D Kumar, et al.
Transactions of the American Neurological Association|January 1, 1974
Heterogeneity in two families with central core diseaseE M Brett, J A Morgan-Hughes, B D Lake
Lancet (London, England)|December 5, 1987
Rett's syndrome and ornithine carbamoyltransferase deficiencyS Thomas, M Hjelm, V Oberholzer, et al.
Neuropediatrics|November 1, 1981
The possible adjuvant role of bordetella pertussis and pertussis vaccine in causing severe encephalopathic illness: a presentation of three case historiesN P Cavanagh, E M Brett, W C Marshall, et al.
Journal of Mental Deficiency Research|December 1, 1979
The Börjeson-Forssman-Lehmann syndrome: a new caseR M Veall, E M Brett, T M Rivinus, et al.
Developmental Medicine and Child Neurology|December 1, 1984
Correlation between plasma carbamazepine-10,11-epoxide concentration and drug side-effects in children with epilepsyJ F Schoeman, A A Elyas, E M Brett, et al.
Acta Neuropathologica|August 31, 1977
Comparative ultrastructural observations on peripheral nerve abnormalities in the late infantile, juvenile and late onset forms of metachromatic leukodystrophyP K Thomas, R H King, R S Kocen, et al.
Pageof 8