Search research articles
Contact Us
Filters
Showing results (141-150 of 186) with videos related to
Page
of 19
Sort By:
Clinical Chemistry
|
May 1, 1995
Standardized method for high-resolution 1H-NMR of cerebrospinal fluid
R A Wevers, U Engelke, U Wendel, et al.
AJR. American Journal of Roentgenology
|
July 20, 2001
MR imaging of bone marrow in glycogen storage disease type IB in children and young adults
A Scherer, V Engelbrecht, G Neises, et al.
Neurology
|
March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency
K Hyland, I Smith, T Bottiglieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1996
Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset
R Gold, U Bogdahn, L Kappos, et al.
European Journal of Pediatrics
|
April 1, 1986
Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)
I Lombeck, U Wendel, J Versieck, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorder
H Przyrembel, U Wendel, K Becker, et al.
Lancet (London, England)
|
March 23, 1991
Colony-stimulating factors for neutropenia in glycogen storage disease Ib
H Schroten, U Wendel, S Burdach, et al.
Journal of Bioenergetics and Biomembranes
|
April 1, 1996
Importance of mitochondrial transmembrane processes in human mitochondriopathies
M Huizing, V DePinto, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine disease
U Langenbeck, U Wendel, A Mench-Hoinowski, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 8, 1975
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies
H Przyrembel, D Bachmann, I Lombeck, et al.
Page
of 19
Search research articles
Search
Showing results (141-150 of 186) with videos related to
Sort By:
Page
of 19
Clinical Chemistry
|
May 1, 1995
Standardized method for high-resolution 1H-NMR of cerebrospinal fluid
R A Wevers, U Engelke, U Wendel, et al.
AJR. American Journal of Roentgenology
|
July 20, 2001
MR imaging of bone marrow in glycogen storage disease type IB in children and young adults
A Scherer, V Engelbrecht, G Neises, et al.
Neurology
|
March 1, 1988
Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency
K Hyland, I Smith, T Bottiglieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 1, 1996
Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset
R Gold, U Bogdahn, L Kappos, et al.
European Journal of Pediatrics
|
April 1, 1986
Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)
I Lombeck, U Wendel, J Versieck, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 16, 1976
Glutaric aciduria type II: report on a previously undescribed metabolic disorder
H Przyrembel, U Wendel, K Becker, et al.
Lancet (London, England)
|
March 23, 1991
Colony-stimulating factors for neutropenia in glycogen storage disease Ib
H Schroten, U Wendel, S Burdach, et al.
Journal of Bioenergetics and Biomembranes
|
April 1, 1996
Importance of mitochondrial transmembrane processes in human mitochondriopathies
M Huizing, V DePinto, W Ruitenbeek, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine disease
U Langenbeck, U Wendel, A Mench-Hoinowski, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 8, 1975
Alpha-ketoadipic aciduria, a new inborn error of lysine metabolism; biochemical studies
H Przyrembel, D Bachmann, I Lombeck, et al.
Page
of 19