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Annals of Neurology
|
June 18, 1998
Identical mitochondrial DNA in monozygotic twins with discordant adrenoleukodystrophy phenotype
E Wilichowski, A Ohlenbusch, G C Korenke, et al.
Pediatric Research
|
December 1, 1979
Effects of riboflavin on Gunn rats under phototherapy
L Ballowitz, A Bunjamin, F Hanefeld, et al.
Brain & Development
|
January 1, 1986
Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome)
R Heyer, J Ehrich, H H Goebel, et al.
Biology of the Neonate
|
January 1, 1978
Sephadex-gel filtration (SGF) in infant and adult Gunn rats
L Ballowitz, F Hanefeld, R Jerofke, et al.
Journal of Medical Genetics
|
August 6, 2002
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution
F Laccone, B Zoll, P Huppke, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. II. Biochemical findings
C Jakobs, J Kneer, D Rating, et al.
Clinical Neuropathology
|
May 1, 1991
Wernicke's encephalopathy in a child with acute lymphoblastic leukemia treated with polychemotherapy
W Brück, H J Christen, H Lakomek, et al.
Neuropediatrics
|
October 1, 1996
Localized proton magnetic resonance spectroscopy of cerebral metabolic disturbances in children with neuronal ceroid lipofuscinosis
K Brockmann, P J Pouwels, H J Christen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 9, 1981
Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolism
C Jakobs, M Bojasch, E Mönch, et al.
Neuropediatrics
|
August 1, 1983
Cranial computed tomography of 64 children in continuous complete remission of leukemia I: relations to therapy in modalities
E Habermalz, H J Habermalz, U Stephani, et al.
Page
of 20
Search research articles
Search
Showing results (111-120 of 197) with videos related to
Sort By:
Page
of 20
Annals of Neurology
|
June 18, 1998
Identical mitochondrial DNA in monozygotic twins with discordant adrenoleukodystrophy phenotype
E Wilichowski, A Ohlenbusch, G C Korenke, et al.
Pediatric Research
|
December 1, 1979
Effects of riboflavin on Gunn rats under phototherapy
L Ballowitz, A Bunjamin, F Hanefeld, et al.
Brain & Development
|
January 1, 1986
Congenital muscular dystrophy with cerebral and ocular malformations (cerebro-oculo-muscular syndrome)
R Heyer, J Ehrich, H H Goebel, et al.
Biology of the Neonate
|
January 1, 1978
Sephadex-gel filtration (SGF) in infant and adult Gunn rats
L Ballowitz, F Hanefeld, R Jerofke, et al.
Journal of Medical Genetics
|
August 6, 2002
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution
F Laccone, B Zoll, P Huppke, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
4-Hydroxybutyric aciduria: a new inborn error of metabolism. II. Biochemical findings
C Jakobs, J Kneer, D Rating, et al.
Clinical Neuropathology
|
May 1, 1991
Wernicke's encephalopathy in a child with acute lymphoblastic leukemia treated with polychemotherapy
W Brück, H J Christen, H Lakomek, et al.
Neuropediatrics
|
October 1, 1996
Localized proton magnetic resonance spectroscopy of cerebral metabolic disturbances in children with neuronal ceroid lipofuscinosis
K Brockmann, P J Pouwels, H J Christen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 9, 1981
Urinary excretion of gamma-hydroxybutyric acid in a patient with neurological abnormalities. The probability of a new inborn error of metabolism
C Jakobs, M Bojasch, E Mönch, et al.
Neuropediatrics
|
August 1, 1983
Cranial computed tomography of 64 children in continuous complete remission of leukemia I: relations to therapy in modalities
E Habermalz, H J Habermalz, U Stephani, et al.
Page
of 20