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M.D., PH.D.,
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Wevers Ron A.
WEVERS R. A.
Wevers R. A.
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r.wevers@cukz.umcn.nl
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R. A.
Ron A.
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http://hub.abes.fr/bmj/periodical/jmedgenet/2004/volume_41/issue_7/B3598D6B61A67CBEE053120B220A90C5/authorship/9
http://hub.abes.fr/bmj/periodical/jnnp/2006/volume_77/issue_1/B35A821677714C40E053120B220AF6DD/authorship/6
http://hub.abes.fr/bmj/periodical/jnnp/1993/volume_56/issue_7/B35A3ACB6BDD41C6E053120B220A637A/authorship/2
http://hub.abes.fr/bmj/periodical/jnnp/1988/volume_51/issue_10/B35A2023E0D9769BE053120B220A767E/authorship/5
http://hub.abes.fr/bmj/periodical/jmedgenet/2004/volume_41/issue_4/B3598D6B61497CBEE053120B220A90C5/authorship/9
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http://hub.abes.fr/bmj/periodical/jmedgenet/1996/volume_33/issue_8/B35966E2257E6AB5E053120B220AFD24/authorship/4
http://hub.abes.fr/oup/periodical/glycob/2005/volume_15/issue_12/101093glycobcwj017/authorship/7
http://hub.abes.fr/oup/periodical/bjaint/1992/volume_69/issue_1/101093bja69129/authorship/5
http://hub.abes.fr/oup/periodical/brainj/2007/volume_130/issue_3/101093brainawl389/authorship/19
http://hub.abes.fr/bmj/periodical/jnnp/1994/volume_57/issue_2/B35A3ACB6D0041C6E053120B220A637A/authorship/1
http://hub.abes.fr/oup/periodical/brainj/2010/volume_133/issue_6/101093brainawq087/authorship/32
http://hub.abes.fr/oup/periodical/brainj/1986/volume_109/issue_6/101093brain10961087/authorship/4
http://hub.abes.fr/oup/periodical/brainj/1999/volume_122/issue_8/101093brain12281589/authorship/7
http://hub.abes.fr/oup/periodical/brainj/2000/volume_123/issue_5/101093brain1235908/authorship/5
http://hub.abes.fr/oup/periodical/hmg/2004/volume_13/issue_22/101093hmgddh303/authorship/17
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http://hub.abes.fr/springer/periodical/439/1996/volume_98/issue_6/B927DD9E82125D90E053120B220A1EA8/authorship/7
http://hub.abes.fr/springer/periodical/10545/1995/volume_18/issue_6/B8DD76546CE52FF1E053120B220A8ECF/authorship/4
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Elevated plasma chitotriosidase activity in various lysosomal storage disorders
Cerebrospinal fluid homocysteine and the cobalamin status of the brain
Paediatric cerebrotendinous xanthomatosis
Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis
FACTORS AFFECTING MAGNITUDE AND TIME COURSE OF NEUROMUSCULAR BLOCK PRODUCED BY SUXAMETHONIUM
SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness
Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis
THE SECOND WIND PHENOMENON IN McARDLE'S DISEASE
β-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities
Isolated (biotin-resistant) 3-methylcrotonyl-CoA carboxylase deficiency: four sibs devoid of pathology
Short aramid-fiber reinforced ultra-high molecular weight polyethylene
Beta-mannosidosis and ethanolaminuria in a female patient
Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria
Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis
Ischaemic forearm testing in a patient with Ca2+-ATPase deficiency
Diagnosis of a new case of trimethylaminuria using direct proton NMR spectroscopy of urine
Decreased vitamin B12 and folate levels in cerebrospinal fluid and serum of multiple sclerosis patients after high-dose intravenous methylprednisolone
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