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A Wevers

Showing results (191-200 of 543) with videos related to

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Plos One|April 28, 2010
Ovarian cyst fluid of serous ovarian tumors contains large quantities of the brain amino acid N-acetylaspartateEva Kolwijck, Ron A Wevers, Udo F Engelke, et al.
BMC Neurology|May 12, 2017
A diagnostic biomarker profile for fibromyalgia syndrome based on an NMR metabolomics study of selected patients and controlsBontle G Malatji, Helgard Meyer, Shayne Mason, et al.
Annals of Clinical Biochemistry|January 25, 2003
Proteomics and neuromuscular diseases: theoretical concept and first resultsL P van den Heuvel, M H Farhoud, R A Wevers, et al.
Brain Research. Molecular Brain Research|April 14, 2000
Quantitative assessment of nicotinic acetylcholine receptor proteins in the cerebral cortex of Alzheimer patientsL Burghaus, U Schütz, U Krempel, et al.
Biochimica Et Biophysica Acta. General Subjects|January 10, 2020
CLPB (caseinolytic peptidase B homolog), the first mitochondrial protein refoldase associated with human diseaseDagmara Mróz, Hubert Wyszkowski, Tomasz Szablewski, et al.
Neuropediatrics|April 1, 1997
Dihydropyrimidinase deficiency, a progressive neurological disorder?C W Putman, J J Rotteveel, R A Wevers, et al.
Acta Neurologica Scandinavica|July 21, 1998
Cerebrospinal fluid methylmalonic acid concentrations in neurological patients with low and normal serum cobalamin concentrationsD Z van Asselt, M H Karlietis, P J Poels, et al.
Annals of Human Genetics|March 14, 2001
Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonismR J Swaans, P Rondot, W O Renier, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 22, 2004
[From gene to disease; dopamine-beta-hydroxylase deficiency and orthostatic hypotension]J Deinum, A H van den Meiracker, F Boomsma, et al.
Mitochondrion|August 12, 2009
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 childrenEva Morava, Ulrike Steuerwald, Rosalba Carrozzo, et al.
Pageof 55

Showing results (191-200 of 543) with videos related to

Sort By:
Pageof 55
Plos One|April 28, 2010
Ovarian cyst fluid of serous ovarian tumors contains large quantities of the brain amino acid N-acetylaspartateEva Kolwijck, Ron A Wevers, Udo F Engelke, et al.
BMC Neurology|May 12, 2017
A diagnostic biomarker profile for fibromyalgia syndrome based on an NMR metabolomics study of selected patients and controlsBontle G Malatji, Helgard Meyer, Shayne Mason, et al.
Annals of Clinical Biochemistry|January 25, 2003
Proteomics and neuromuscular diseases: theoretical concept and first resultsL P van den Heuvel, M H Farhoud, R A Wevers, et al.
Brain Research. Molecular Brain Research|April 14, 2000
Quantitative assessment of nicotinic acetylcholine receptor proteins in the cerebral cortex of Alzheimer patientsL Burghaus, U Schütz, U Krempel, et al.
Biochimica Et Biophysica Acta. General Subjects|January 10, 2020
CLPB (caseinolytic peptidase B homolog), the first mitochondrial protein refoldase associated with human diseaseDagmara Mróz, Hubert Wyszkowski, Tomasz Szablewski, et al.
Neuropediatrics|April 1, 1997
Dihydropyrimidinase deficiency, a progressive neurological disorder?C W Putman, J J Rotteveel, R A Wevers, et al.
Acta Neurologica Scandinavica|July 21, 1998
Cerebrospinal fluid methylmalonic acid concentrations in neurological patients with low and normal serum cobalamin concentrationsD Z van Asselt, M H Karlietis, P J Poels, et al.
Annals of Human Genetics|March 14, 2001
Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonismR J Swaans, P Rondot, W O Renier, et al.
Nederlands Tijdschrift Voor Geneeskunde|October 22, 2004
[From gene to disease; dopamine-beta-hydroxylase deficiency and orthostatic hypotension]J Deinum, A H van den Meiracker, F Boomsma, et al.
Mitochondrion|August 12, 2009
Dystonia and deafness due to SUCLA2 defect; Clinical course and biochemical markers in 16 childrenEva Morava, Ulrike Steuerwald, Rosalba Carrozzo, et al.
Pageof 55