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Journal of Child Neurology
|
December 11, 1999
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter
M S van der Knaap, R A Wevers, S Kure, et al.
The British Journal of Ophthalmology
|
November 21, 2008
Ophthalmological abnormalities in children with congenital disorders of glycosylation type I
E Morava, H N Wosik, J Sykut-Cegielska, et al.
Annals of Neurology
|
October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic study
O Bandmann, E M Valente, P Holmans, et al.
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
|
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.
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.
Biochimica Et Biophysica Acta
|
October 19, 1999
beta-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brain
S Grünewald, K Huyben, J G de Jong, et al.
Page
of 23
Search research articles
Search
Showing results (131-140 of 222) with videos related to
Sort By:
Page
of 23
Journal of Child Neurology
|
December 11, 1999
Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter
M S van der Knaap, R A Wevers, S Kure, et al.
The British Journal of Ophthalmology
|
November 21, 2008
Ophthalmological abnormalities in children with congenital disorders of glycosylation type I
E Morava, H N Wosik, J Sykut-Cegielska, et al.
Annals of Neurology
|
October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic study
O Bandmann, E M Valente, P Holmans, et al.
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
|
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.
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.
Biochimica Et Biophysica Acta
|
October 19, 1999
beta-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brain
S Grünewald, K Huyben, J G de Jong, et al.
Page
of 23