His primary scientific interests are in Internal medicine, Endocrinology, Mutation, Genetics and Biochemistry. His Internal medicine research incorporates elements of Gastroenterology, Missense mutation, Compound heterozygosity and Pathology. His work in Missense mutation addresses issues such as Mucopolysaccharidosis III, which are connected to fields such as Sanfilippo syndrome.
His Endocrinology study combines topics from a wide range of disciplines, such as Central nervous system disease and Cerebrospinal fluid. His Mutation study incorporates themes from Dystonia, Molecular biology, Cutis laxa, Intracellular and Hypotonia. In his work, Cerebrotendinous Xanthomatosis is strongly intertwined with Genotype, which is a subfield of Phenotype.
Ron A. Wevers mostly deals with Internal medicine, Endocrinology, Pathology, Biochemistry and Genetics. His Internal medicine research is multidisciplinary, relying on both Gastroenterology and Dystonia. His Endocrinology research is multidisciplinary, incorporating perspectives in Homovanillic acid and Epilepsy.
His specific area of interest is Pathology, where Ron A. Wevers studies Cutis laxa. Biochemistry is often connected to Molecular biology in his work. His work in Mutation, Gene, Missense mutation and Exon is related to Genetics.
His primary areas of investigation include Internal medicine, Endocrinology, Metabolomics, Biochemistry and Pathology. As a part of the same scientific study, Ron A. Wevers usually deals with the Internal medicine, concentrating on Gastroenterology and frequently concerns with Renal function. His Endocrinology study frequently draws connections between adjacent fields such as 3-Methylglutaconic Aciduria.
His Metabolomics research incorporates themes from Metabolite, Computational biology and Metabolic pathway. The various areas that Ron A. Wevers examines in his Pathology study include Limb-girdle muscular dystrophy, Encephalopathy and Compound heterozygosity. His study in Bioinformatics is interdisciplinary in nature, drawing from both Mutation, Status epilepticus, Genetic testing and Global developmental delay.
Ron A. Wevers focuses on Genetics, Internal medicine, Biochemistry, Endocrinology and Bioinformatics. His work in the fields of Exome sequencing, Missense mutation and Exon overlaps with other areas such as Premature aging. The Internal medicine study combines topics in areas such as Gastroenterology, Aureus infection, Staphylococcus aureus and Pathology.
His study connects Dystrophy and Endocrinology. His Bioinformatics research integrates issues from Tandem mass spectrometry, Phenotype, Molecule, Analytical chemistry and Epilepsy. His biological study spans a wide range of topics, including Bacteria, Enzyme, Glutathione peroxidase and Odor.
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The frequency of lysosomal storage diseases in The Netherlands
B.J.H.M. Poorthuis;R.A. Wevers;W.J. Kleijer;J.E.M. Groener.
Human Genetics (1999)
Performance of near-infrared spectroscopy in measuring local O(2) consumption and blood flow in skeletal muscle.
Mireille C. P. Van Beekvelt;Willy N. J. M. Colier;Ron A. Wevers;Baziel G. M. Van Engelen.
Journal of Applied Physiology (2001)
Mitochondrial creatine kinase: a key enzyme of aerobic energy metabolism
Markus Wyss;Jan Smeitink;Ron A. Wevers;Theo Wallimann.
Biochimica et Biophysica Acta (1992)
Adipose tissue thickness affects in vivo quantitative near-IR spectroscopy in human skeletal muscle.
M. C. P. Van Beekvelt;M. S. Borghuis;B. G. M. Van Engelen;R. A. Wevers.
Clinical Science (2001)
Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.
Uwe Kornak;Ellen Reynders;Aikaterini Dimopoulou;Jeroen Van Reeuwijk.
Nature Genetics (2008)
Glucose transporter-1 deficiency syndrome: The expanding clinical and genetic spectrum of a treatable disorder
Wilhelmina G. Leen;Joerg Klepper;Marcel M. Verbeek;Maike Leferink.
Brain (2010)
Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man
Karin Tuschl;Peter T. Clayton;Sidney M. Gospe;Shamshad Gulab.
American Journal of Human Genetics (2012)
SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
Vincent Cantagrel;Dirk J. Lefeber;Bobby G. Ng;Ziqiang Guan.
Cell (2010)
Role of cobalamin intake and atrophic gastritis in mild cobalamin deficiency in older Dutch subjects.
D.Z.B. van Asselt;C.P.G.M. de Groot;W.A. van Staveren;H.J.M. Blom.
The American Journal of Clinical Nutrition (1998)
Elevated plasma chitotriosidase activity in various lysosomal storage disorders.
Yufeng Guo;Wang He;A. M. Boer;R. A. Wevers.
Journal of Inherited Metabolic Disease (1995)
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