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Neuropediatrics
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November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndrome
K 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 life
R Macfaul, S Dorner, E M Brett, et al.
Journal of Medical Genetics
|
March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysis
C 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 migration
J A Hurst, M Markiewicz, D Kumar, et al.
Transactions of the American Neurological Association
|
January 1, 1974
Heterogeneity in two families with central core disease
E M Brett, J A Morgan-Hughes, B D Lake
Lancet (London, England)
|
December 5, 1987
Rett's syndrome and ornithine carbamoyltransferase deficiency
S 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 histories
N 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 case
R 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 epilepsy
J 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 leukodystrophy
P K Thomas, R H King, R S Kocen, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 74) with videos related to
Sort By:
Page
of 8
Neuropediatrics
|
November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndrome
K 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 life
R Macfaul, S Dorner, E M Brett, et al.
Journal of Medical Genetics
|
March 1, 1992
Distal spinal muscular atrophy with vocal cord paralysis
C 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 migration
J A Hurst, M Markiewicz, D Kumar, et al.
Transactions of the American Neurological Association
|
January 1, 1974
Heterogeneity in two families with central core disease
E M Brett, J A Morgan-Hughes, B D Lake
Lancet (London, England)
|
December 5, 1987
Rett's syndrome and ornithine carbamoyltransferase deficiency
S 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 histories
N 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 case
R 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 epilepsy
J 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 leukodystrophy
P K Thomas, R H King, R S Kocen, et al.
Page
of 8