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Molecular and Cellular Biochemistry
|
October 6, 1997
Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complex
F J Trijbels, W Ruitenbeek, M Huizing, et al.
Klinische Padiatrie
|
January 1, 1986
[The intermediate form of maple syrup disease]
O Rittinger, C Bachmann, T Irnberger, et al.
European Journal of Pediatrics
|
February 1, 2000
Odd-numbered long-chain fatty acids in propionic acidaemia
W Sperl, C Murr, D Skladal, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2008
Severe neurological crisis in a patient with hereditary tyrosinaemia type I after interruption of NTBC treatment
J-U Schlump, C Perot, K Ketteler, et al.
European Journal of Pediatrics
|
September 1, 1981
Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia
C R Bartram, H Przyrembel, U Wendel, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
April 1, 1986
[Cranial computed tomography in maple syrup urine disease]
T Irnberger, E Plöchl, O Rittinger, et al.
Neuropediatrics
|
September 13, 2006
Acute neuronopathic Gaucher disease complicated by fatal gastrointestinal bleeding
B Hoffmann, B Schwahn, C B Knobbe, et al.
European Journal of Pediatrics
|
June 1, 1980
Peritoneal dialysis in maple-syrup-urine disease: studies on branched-chain amino and keto acids
U Wendel, K Becker, H Przyrembel, et al.
Helvetica Paediatrica Acta
|
March 1, 1983
Multiple acyl-Co A dehydrogenation deficiency (MADD) in a boy with nonketotic hypoglycemia, hepatomegaly, muscle hypotonia and cardiomyopathy. Detection of N-isovalerylglutamic acid and its monoamide
A Niederwieser, B Steinmann, U Exner, et al.
Clinical Chemistry
|
January 1, 1997
Pitfalls in measuring plasma cholesterol in the Smith-Lemli-Opitz syndrome
P E Jira, J G de Jong, F S Janssen-Zijlstra, et al.
Page
of 19
Search research articles
Search
Showing results (131-140 of 186) with videos related to
Sort By:
Page
of 19
Molecular and Cellular Biochemistry
|
October 6, 1997
Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complex
F J Trijbels, W Ruitenbeek, M Huizing, et al.
Klinische Padiatrie
|
January 1, 1986
[The intermediate form of maple syrup disease]
O Rittinger, C Bachmann, T Irnberger, et al.
European Journal of Pediatrics
|
February 1, 2000
Odd-numbered long-chain fatty acids in propionic acidaemia
W Sperl, C Murr, D Skladal, et al.
Journal of Inherited Metabolic Disease
|
May 27, 2008
Severe neurological crisis in a patient with hereditary tyrosinaemia type I after interruption of NTBC treatment
J-U Schlump, C Perot, K Ketteler, et al.
European Journal of Pediatrics
|
September 1, 1981
Glycogenosis type Ib complicated by severe granulocytopenia resembling inherited neutropenia
C R Bartram, H Przyrembel, U Wendel, et al.
Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin
|
April 1, 1986
[Cranial computed tomography in maple syrup urine disease]
T Irnberger, E Plöchl, O Rittinger, et al.
Neuropediatrics
|
September 13, 2006
Acute neuronopathic Gaucher disease complicated by fatal gastrointestinal bleeding
B Hoffmann, B Schwahn, C B Knobbe, et al.
European Journal of Pediatrics
|
June 1, 1980
Peritoneal dialysis in maple-syrup-urine disease: studies on branched-chain amino and keto acids
U Wendel, K Becker, H Przyrembel, et al.
Helvetica Paediatrica Acta
|
March 1, 1983
Multiple acyl-Co A dehydrogenation deficiency (MADD) in a boy with nonketotic hypoglycemia, hepatomegaly, muscle hypotonia and cardiomyopathy. Detection of N-isovalerylglutamic acid and its monoamide
A Niederwieser, B Steinmann, U Exner, et al.
Clinical Chemistry
|
January 1, 1997
Pitfalls in measuring plasma cholesterol in the Smith-Lemli-Opitz syndrome
P E Jira, J G de Jong, F S Janssen-Zijlstra, et al.
Page
of 19