Search research articles
Contact Us
Filters
Showing results (241-250 of 543) with videos related to
Page
of 55
Sort By:
Clinical Chemistry
|
December 10, 1999
Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency
C Bräutigam, G C Steenbergen-Spanjers, G F Hoffmann, et al.
The American Journal of Clinical Nutrition
|
August 13, 1998
Role of cobalamin intake and atrophic gastritis in mild cobalamin deficiency in older Dutch subjects
D Z van Asselt, L C de Groot, W A van Staveren, et al.
Clinical Chemistry
|
September 11, 1998
Biochemical hallmarks of tyrosine hydroxylase deficiency
C Bräutigam, R A Wevers, R J Jansen, et al.
Journal of Inherited Metabolic Disease
|
May 13, 2022
Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
Brechtje Hoegen, Juliet E Hampstead, Udo F H Engelke, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2007
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia
Eva Morava, Renate Zeevaert, Eckhard Korsch, et al.
Molecular Genetics and Metabolism
|
June 24, 2008
Pericardial and abdominal fluid accumulation in congenital disorder of glycosylation type Ia
Gerben Truin, Mailys Guillard, Dirk J Lefeber, et al.
Journal of Inherited Metabolic Disease
|
September 10, 2005
Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder
L J M Spaapen, J A Bakker, S B van der Meer, et al.
The Journal of Clinical Investigation
|
August 1, 1994
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil
A A Benders, J H Veerkamp, A Oosterhof, et al.
Journal of Proteome Research
|
December 13, 2005
Serial isoelectric focusing as an effective and economic way to obtain maximal resolution and high-throughput in 2D-based comparative proteomics of scarce samples: proof-of-principle
Murtada H Farhoud, Hans J C T Wessels, Ron A Wevers, et al.
Muscle & Nerve
|
October 1, 1986
Improvement of screening in exertional myalgia with a standardized ischemic forearm test
S P Sinkeler, R A Wevers, E M Joosten, et al.
Page
of 55
Search research articles
Search
Showing results (241-250 of 543) with videos related to
Sort By:
Page
of 55
Clinical Chemistry
|
December 10, 1999
Biochemical and molecular genetic characteristics of the severe form of tyrosine hydroxylase deficiency
C Bräutigam, G C Steenbergen-Spanjers, G F Hoffmann, et al.
The American Journal of Clinical Nutrition
|
August 13, 1998
Role of cobalamin intake and atrophic gastritis in mild cobalamin deficiency in older Dutch subjects
D Z van Asselt, L C de Groot, W A van Staveren, et al.
Clinical Chemistry
|
September 11, 1998
Biochemical hallmarks of tyrosine hydroxylase deficiency
C Bräutigam, R A Wevers, R J Jansen, et al.
Journal of Inherited Metabolic Disease
|
May 13, 2022
Application of metabolite set enrichment analysis on untargeted metabolomics data prioritises relevant pathways and detects novel biomarkers for inherited metabolic disorders
Brechtje Hoegen, Juliet E Hampstead, Udo F H Engelke, et al.
European Journal of Human Genetics : EJHG
|
March 16, 2007
A common mutation in the COG7 gene with a consistent phenotype including microcephaly, adducted thumbs, growth retardation, VSD and episodes of hyperthermia
Eva Morava, Renate Zeevaert, Eckhard Korsch, et al.
Molecular Genetics and Metabolism
|
June 24, 2008
Pericardial and abdominal fluid accumulation in congenital disorder of glycosylation type Ia
Gerben Truin, Mailys Guillard, Dirk J Lefeber, et al.
Journal of Inherited Metabolic Disease
|
September 10, 2005
Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder
L J M Spaapen, J A Bakker, S B van der Meer, et al.
The Journal of Clinical Investigation
|
August 1, 1994
Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil
A A Benders, J H Veerkamp, A Oosterhof, et al.
Journal of Proteome Research
|
December 13, 2005
Serial isoelectric focusing as an effective and economic way to obtain maximal resolution and high-throughput in 2D-based comparative proteomics of scarce samples: proof-of-principle
Murtada H Farhoud, Hans J C T Wessels, Ron A Wevers, et al.
Muscle & Nerve
|
October 1, 1986
Improvement of screening in exertional myalgia with a standardized ischemic forearm test
S P Sinkeler, R A Wevers, E M Joosten, et al.
Page
of 55