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Neuropediatrics
|
August 1, 1987
Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases
V T Ramaekers, B D Lake, B Harding, et al.
Pediatric Research
|
September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiency
A A Morris, C V Lascelles, S E Olpin, et al.
Gut
|
November 1, 1992
Gastric antral dysrhythmias in children with chronic idiopathic intestinal pseudoobstruction
S 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 spectrometry
P 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 cases
P 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 patients
E 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 studies
M 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 disease
A H Fensom, A R Grant, S J Steinberg, et al.
Archives of Disease in Childhood
|
February 1, 1992
Persistent gastrointestinal symptoms after correction of malrotation
S 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 onset
P Buxton, J N Cumings, R B Ellis, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 136) with videos related to
Sort By:
Page
of 14
Neuropediatrics
|
August 1, 1987
Diagnostic difficulties in infantile neuroaxonal dystrophy. A clinicopathological study of eight cases
V T Ramaekers, B D Lake, B Harding, et al.
Pediatric Research
|
September 4, 1998
Hepatic mitochondrial 3-hydroxy-3-methylglutaryl-coenzyme a synthase deficiency
A A Morris, C V Lascelles, S E Olpin, et al.
Gut
|
November 1, 1992
Gastric antral dysrhythmias in children with chronic idiopathic intestinal pseudoobstruction
S 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 spectrometry
P 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 cases
P 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 patients
E 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 studies
M 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 disease
A H Fensom, A R Grant, S J Steinberg, et al.
Archives of Disease in Childhood
|
February 1, 1992
Persistent gastrointestinal symptoms after correction of malrotation
S 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 onset
P Buxton, J N Cumings, R B Ellis, et al.
Page
of 14