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Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1996
Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families
M A Ahmed, E Reid, A Cooke, et al.
Archives of Disease in Childhood
|
January 6, 1999
Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric reflux
S M Zuberi, J B Stephenson, A F Azmy, et al.
Archives of Disease in Childhood
|
August 1, 1977
Hereditary coproporphyria and epilepsy
A B Houston, M J Brodie, M R Moore, et al.
Developmental Medicine and Child Neurology
|
July 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one family
C M Brewer, B J Fredericks, J M Pont, et al.
Neuropediatrics
|
June 1, 1997
Batten disease in the west of Scotland 1974-1995 including five cases of the juvenile form with granular osmiophilic deposits
Y J Crow, J L Tolmie, A G Howatson, et al.
Archives of Disease in Childhood
|
September 1, 1988
Hyperventilation in the awake state: potentially treatable component of Rett syndrome
D P Southall, A M Kerr, E Tirosh, et al.
Archives of Disease in Childhood
|
March 1, 1989
Intracranial pressure monitoring in a group of critically ill children
G Balakrishnan, C H Skeoch, J B Stephenson, et al.
Archives of Disease in Childhood
|
January 1, 1994
The Prader-Willi syndrome
M D Donaldson, C E Chu, A Cooke, et al.
The British Journal of Ophthalmology
|
June 1, 1997
A novel pattern of oculocerebral malformation
B J Clark, W R Lee, D Doyle, et al.
Journal of Medical Genetics
|
January 1, 1994
Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues
P M Matthews, J Hopkin, R M Brown, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 110) with videos related to
Sort By:
Page
of 11
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 1, 1996
Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families
M A Ahmed, E Reid, A Cooke, et al.
Archives of Disease in Childhood
|
January 6, 1999
Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric reflux
S M Zuberi, J B Stephenson, A F Azmy, et al.
Archives of Disease in Childhood
|
August 1, 1977
Hereditary coproporphyria and epilepsy
A B Houston, M J Brodie, M R Moore, et al.
Developmental Medicine and Child Neurology
|
July 1, 1996
X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one family
C M Brewer, B J Fredericks, J M Pont, et al.
Neuropediatrics
|
June 1, 1997
Batten disease in the west of Scotland 1974-1995 including five cases of the juvenile form with granular osmiophilic deposits
Y J Crow, J L Tolmie, A G Howatson, et al.
Archives of Disease in Childhood
|
September 1, 1988
Hyperventilation in the awake state: potentially treatable component of Rett syndrome
D P Southall, A M Kerr, E Tirosh, et al.
Archives of Disease in Childhood
|
March 1, 1989
Intracranial pressure monitoring in a group of critically ill children
G Balakrishnan, C H Skeoch, J B Stephenson, et al.
Archives of Disease in Childhood
|
January 1, 1994
The Prader-Willi syndrome
M D Donaldson, C E Chu, A Cooke, et al.
The British Journal of Ophthalmology
|
June 1, 1997
A novel pattern of oculocerebral malformation
B J Clark, W R Lee, D Doyle, et al.
Journal of Medical Genetics
|
January 1, 1994
Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues
P M Matthews, J Hopkin, R M Brown, et al.
Page
of 11