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Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
April 11, 2001
Variability of blood-brain ratios of phenylalanine in typical patients with phenylketonuria
A Rupp, R Kreis, J Zschocke, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1993
Bile acid metabolism in three patients with mevalonic aciduria due to mevalonate kinase deficiency
K M Gibson, F Stellaard, G F Hoffmann, et al.
Bulletin of the World Health Organization
|
January 1, 1996
The prevalence of epilepsy follows the distribution of onchocerciasis in a west Ugandan focus
C Kaiser, W Kipp, G Asaba, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. I. Clinical review
D Rating, F Hanefeld, H Siemes, et al.
Neuropediatrics
|
April 25, 2000
2-ketoglutarate dehydrogenase deficiency with intermittent 2-ketoglutaric aciduria
R J Dunckelmann, F Ebinger, A Schulze, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
March 18, 2003
[Pigmented retinopathy as a presenting sign of mitochondrial encephalomyopathy without external ophthalmoplegia]
S Staudt, A M Joussen, D Rating, et al.
Medical and Pediatric Oncology
|
January 1, 1980
Changes of CSF-protein pattern in children with acute lymphoblastic leukemia during prophylactic CNS therapy (Berlin protocol)
H Siemes, D Rating, M Siegert, et al.
Bulletin De La Societe De Pathologie Exotique (1990)
|
February 24, 2001
Clinical and electro-clinical classification of epileptic seizure in west Uganda
C Kaiser, C Benninger, G Asaba, et al.
European Journal of Pediatrics
|
August 1, 1998
Therapeutic trial of arginine restriction in creatine deficiency syndrome
A Schulze, E Mayatepek, P Bachert, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Physiology and pathophysiology of organic acids in cerebrospinal fluid
G F Hoffmann, W Meier-Augenstein, S Stöckler, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 96) with videos related to
Sort By:
Page
of 10
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
April 11, 2001
Variability of blood-brain ratios of phenylalanine in typical patients with phenylketonuria
A Rupp, R Kreis, J Zschocke, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 31, 1993
Bile acid metabolism in three patients with mevalonic aciduria due to mevalonate kinase deficiency
K M Gibson, F Stellaard, G F Hoffmann, et al.
Bulletin of the World Health Organization
|
January 1, 1996
The prevalence of epilepsy follows the distribution of onchocerciasis in a west Ugandan focus
C Kaiser, W Kipp, G Asaba, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. I. Clinical review
D Rating, F Hanefeld, H Siemes, et al.
Neuropediatrics
|
April 25, 2000
2-ketoglutarate dehydrogenase deficiency with intermittent 2-ketoglutaric aciduria
R J Dunckelmann, F Ebinger, A Schulze, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
March 18, 2003
[Pigmented retinopathy as a presenting sign of mitochondrial encephalomyopathy without external ophthalmoplegia]
S Staudt, A M Joussen, D Rating, et al.
Medical and Pediatric Oncology
|
January 1, 1980
Changes of CSF-protein pattern in children with acute lymphoblastic leukemia during prophylactic CNS therapy (Berlin protocol)
H Siemes, D Rating, M Siegert, et al.
Bulletin De La Societe De Pathologie Exotique (1990)
|
February 24, 2001
Clinical and electro-clinical classification of epileptic seizure in west Uganda
C Kaiser, C Benninger, G Asaba, et al.
European Journal of Pediatrics
|
August 1, 1998
Therapeutic trial of arginine restriction in creatine deficiency syndrome
A Schulze, E Mayatepek, P Bachert, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
Physiology and pathophysiology of organic acids in cerebrospinal fluid
G F Hoffmann, W Meier-Augenstein, S Stöckler, et al.
Page
of 10