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B D Lake

Showing results (111-120 of 136) with videos related to

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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.
Pediatric Research|September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiencyA A Morris, C V Lascelles, S E Olpin, et al.
Gut|November 1, 1992
Gastric antral dysrhythmias in children with chronic idiopathic intestinal pseudoobstructionS P Devane, A M Ravelli, W M Bisset, et al.
European Journal of Pediatrics|March 1, 1987
Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometryP T Clayton, B D Lake, N A Hall, et al.
Brain : a Journal of Neurology|December 1, 1985
Acid maltase deficiency in adults. Diagnosis and management in five casesP S Trend, C M Wiles, G T Spencer, 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.
The British Journal of Dermatology|April 1, 1994
Neutral lipid storage disease. Case report and lipid studiesM R Judge, D J Atherton, R Salvayre, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
An adult with a non-neuronopathic form of Niemann-Pick C diseaseA H Fensom, A R Grant, S J Steinberg, et al.
Archives of Disease in Childhood|February 1, 1992
Persistent gastrointestinal symptoms after correction of malrotationS P Devane, R Coombes, V V Smith, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1972
A case of G M2 gangliosidosis of late onsetP Buxton, J N Cumings, R B Ellis, et al.
Pageof 14

Showing results (111-120 of 136) with videos related to

Sort By:
Pageof 14
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.
Pediatric Research|September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiencyA A Morris, C V Lascelles, S E Olpin, et al.
Gut|November 1, 1992
Gastric antral dysrhythmias in children with chronic idiopathic intestinal pseudoobstructionS P Devane, A M Ravelli, W M Bisset, et al.
European Journal of Pediatrics|March 1, 1987
Plasma bile acids in patients with peroxisomal dysfunction syndromes: analysis by capillary gas chromatography-mass spectrometryP T Clayton, B D Lake, N A Hall, et al.
Brain : a Journal of Neurology|December 1, 1985
Acid maltase deficiency in adults. Diagnosis and management in five casesP S Trend, C M Wiles, G T Spencer, 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.
The British Journal of Dermatology|April 1, 1994
Neutral lipid storage disease. Case report and lipid studiesM R Judge, D J Atherton, R Salvayre, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
An adult with a non-neuronopathic form of Niemann-Pick C diseaseA H Fensom, A R Grant, S J Steinberg, et al.
Archives of Disease in Childhood|February 1, 1992
Persistent gastrointestinal symptoms after correction of malrotationS P Devane, R Coombes, V V Smith, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1972
A case of G M2 gangliosidosis of late onsetP Buxton, J N Cumings, R B Ellis, et al.
Pageof 14