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The Journal of Pediatrics
|
November 1, 1986
Lithium for treatment of neutropenia in glycogen storage disease type Ib
B Koletzko, U Wendel, H J Bremer
Journal of Chromatography. B, Biomedical Applications
|
July 12, 1996
Determination of R- and S-3-methyl-2-oxopentanoate enantiomers in human plasma: suitable method for label enrichment analysis
P Schadewaldt, U Wendel, H W Hammen
Pediatric Research
|
September 1, 1975
Maple syrup urine disease: analysis of branched chain ketoacid decarboxylation in cultured fibroblasts
U Wendel, H Wentrup, H W Rüdiger
Journal of Inherited Metabolic Disease
|
January 1, 1988
Odd-numbered long-chain fatty acid contents in erythrocyte membrane phospholipids in patients with an impaired propionate utilization
U Wendel, E Diekmann, M D Laryea
The Journal of Pediatrics
|
January 1, 1987
Inflammatory bowel disease in glycogen storage disease type Ib
U Wendel, H J Bremer, B Willberg
The New England Journal of Medicine
|
May 5, 1983
Maple-syrup-urine disease
U Wendel, I Lombeck, H J Bremer
Geburtshilfe Und Frauenheilkunde
|
December 1, 1990
[Diagnostic differentiation between precocious puberty and premature thelarche using ultrasonography and the stimulated LH/FSH quotient]
V Pelzer, M Von Ditfurth, U Wendel
Monatsschrift Fur Kinderheilkunde
|
January 1, 1974
[Biochemical diagnosis of mucopolysaccharidoses in cell culture (author's transl)]
U Wendel, H W Rüdiger, E Passarge
Pediatric Cardiology
|
November 29, 2002
Cardiomyopathy and pericardial effusion in infancy point to a fatty acid b-oxidation defect after exclusion of an underlying infection
U Spiekerkoetter, T Tenenbaum, A Heusch, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1984
[Initiation of treatment following screening for phenylketonuria]
M Mahle, H Schmidt, P Lutz, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 186) with videos related to
Sort By:
Page
of 19
The Journal of Pediatrics
|
November 1, 1986
Lithium for treatment of neutropenia in glycogen storage disease type Ib
B Koletzko, U Wendel, H J Bremer
Journal of Chromatography. B, Biomedical Applications
|
July 12, 1996
Determination of R- and S-3-methyl-2-oxopentanoate enantiomers in human plasma: suitable method for label enrichment analysis
P Schadewaldt, U Wendel, H W Hammen
Pediatric Research
|
September 1, 1975
Maple syrup urine disease: analysis of branched chain ketoacid decarboxylation in cultured fibroblasts
U Wendel, H Wentrup, H W Rüdiger
Journal of Inherited Metabolic Disease
|
January 1, 1988
Odd-numbered long-chain fatty acid contents in erythrocyte membrane phospholipids in patients with an impaired propionate utilization
U Wendel, E Diekmann, M D Laryea
The Journal of Pediatrics
|
January 1, 1987
Inflammatory bowel disease in glycogen storage disease type Ib
U Wendel, H J Bremer, B Willberg
The New England Journal of Medicine
|
May 5, 1983
Maple-syrup-urine disease
U Wendel, I Lombeck, H J Bremer
Geburtshilfe Und Frauenheilkunde
|
December 1, 1990
[Diagnostic differentiation between precocious puberty and premature thelarche using ultrasonography and the stimulated LH/FSH quotient]
V Pelzer, M Von Ditfurth, U Wendel
Monatsschrift Fur Kinderheilkunde
|
January 1, 1974
[Biochemical diagnosis of mucopolysaccharidoses in cell culture (author's transl)]
U Wendel, H W Rüdiger, E Passarge
Pediatric Cardiology
|
November 29, 2002
Cardiomyopathy and pericardial effusion in infancy point to a fatty acid b-oxidation defect after exclusion of an underlying infection
U Spiekerkoetter, T Tenenbaum, A Heusch, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde
|
November 1, 1984
[Initiation of treatment following screening for phenylketonuria]
M Mahle, H Schmidt, P Lutz, et al.
Page
of 19