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J B Stephenson

Showing results (81-90 of 110) with videos related to

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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 familiesM A Ahmed, E Reid, A Cooke, et al.
Archives of Disease in Childhood|January 6, 1999
Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric refluxS M Zuberi, J B Stephenson, A F Azmy, et al.
Archives of Disease in Childhood|August 1, 1977
Hereditary coproporphyria and epilepsyA 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 familyC 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 depositsY 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 syndromeD 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 childrenG Balakrishnan, C H Skeoch, J B Stephenson, et al.
Archives of Disease in Childhood|January 1, 1994
The Prader-Willi syndromeM D Donaldson, C E Chu, A Cooke, et al.
The British Journal of Ophthalmology|June 1, 1997
A novel pattern of oculocerebral malformationB 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 tissuesP M Matthews, J Hopkin, R M Brown, et al.
Pageof 11

Showing results (81-90 of 110) with videos related to

Sort By:
Pageof 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 familiesM A Ahmed, E Reid, A Cooke, et al.
Archives of Disease in Childhood|January 6, 1999
Hyperammonaemic encephalopathy after a subureteric injection for vesicoureteric refluxS M Zuberi, J B Stephenson, A F Azmy, et al.
Archives of Disease in Childhood|August 1, 1977
Hereditary coproporphyria and epilepsyA 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 familyC 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 depositsY 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 syndromeD 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 childrenG Balakrishnan, C H Skeoch, J B Stephenson, et al.
Archives of Disease in Childhood|January 1, 1994
The Prader-Willi syndromeM D Donaldson, C E Chu, A Cooke, et al.
The British Journal of Ophthalmology|June 1, 1997
A novel pattern of oculocerebral malformationB 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 tissuesP M Matthews, J Hopkin, R M Brown, et al.
Pageof 11