Aad Verrips


Ontology type: schema:Person     


Person Info

NAME

Aad

SURNAME

Verrips

Publications in SciGraph latest 50 shown

  • 2018-07 Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosis in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2018-06 Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study in JOURNAL OF NEUROLOGY
  • 2017 ALG13-CDG with Infantile Spasms in a Male Patient Due to a De Novo ALG13 Gene Mutation in JIMD REPORTS, VOLUME 40
  • 2016 14 Perifeer-neurologische aandoeningen in KINDERFYSIOTHERAPIE
  • 2016-01 Hepatotoxicity due to chenodeoxycholic acid supplementation in an infant with cerebrotendinous xanthomatosis: implications for treatment in EUROPEAN JOURNAL OF PEDIATRICS
  • 2015-12 It is in his eyes in ACTA NEUROLOGICA BELGICA
  • 2015-09 Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-09 Further delineation of the KBG syndrome caused by ANKRD11 aberrations in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2015-03 Hematopoietic cell transplantation does not prevent myelopathy in X-linked adrenoleukodystrophy: a retrospective study in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2014-10 Severe Hypomagnesaemia Causing Reversible Cerebellopathy in THE CEREBELLUM
  • 2013-07 Pure adult-onset Spastic Paraplegia caused by a novel mutation in the KIAA0196 (SPG8) gene in JOURNAL OF NEUROLOGY
  • 2013-02 Hoofdpijn bij kinderen en tieners in BIJBLIJVEN
  • 2012-09 Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study in JOURNAL OF NEUROLOGY
  • 2011-01 A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann–Sträussler–Scheinker disease phenotype: comparison with similar cases from the literature in ACTA NEUROPATHOLOGICA
  • 2009-04 A previously healthy 11-year-old girl with behavioural disturbances, desquamation of the skin and loss of teeth in EUROPEAN JOURNAL OF PEDIATRICS
  • 2009-04 Neuroborreliose bij kinderen, herkenning en diagnostiek in TIJDSCHRIFT VOOR KINDERGENEESKUNDE
  • 2004-01 Spinal phenotype of cerebrotendinous xanthomatosis in JOURNAL OF NEUROLOGY
  • 2002-11 Mutations in the sterol 27-hydoxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2002-10 Acute gedissemineerde encefalomyelitis (adem) op de kinderleeftijd: klinisch spectrum en therapie in TIJDSCHRIFT VOOR KINDERGENEESKUNDE
  • 2001-10 Neuroleptic malignant syndrome during zuclopenthixol therapy in X-linked cerebral adrenoleukodystrophy in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2001-04 Dermoïdcyste op het hoofd; denk aan cerebrale uitbreiding in TIJDSCHRIFT VOOR KINDERGENEESKUNDE
  • 2000-11 Bile acid deconjugation by Lactobacilli and its effects in patients with a short small bowel in JOURNAL OF GASTROENTEROLOGY
  • 1998-03 Treatment and follow-up of children with cerebrotendinous xanthomatosis in EUROPEAN JOURNAL OF PEDIATRICS
  • 1997-07 Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis in HUMAN GENETICS
  • 1996-11 Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis in HUMAN GENETICS
  • 1993-05 Cerebrospinal fluid homocysteine and the cobalamin status of the brain in JOURNAL OF INHERITED METABOLIC DISEASE
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