| Document Date: 2014-07-11 07:50:10
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Company COL4A1 / Smit A.E. / Kia / Kushner S.A. / Brooks A.S. / D Krab L.C. / Krab L.C. / Balgobind B.V. / Pop A.S. / / Country Netherlands / / Facility Tuberous Sclerosis Complex / / IndustryTerm treatment of fragile X syndrome / diffusion tensor imaging / Treatment of neurodevelopmental disorders / enteric nervous systems / gene products / gene product / / MedicalCondition Microcephaly / distal limb deficiency / muscular dystrophy / neuroaxonal injury / hydrocephalus / split notochord syndrome / Endocrinologic disorders / Krabbe disease / complex developmental disorder / seizures / increased autism / Movement disorder / arterial tortuosity syndrome / developmental disorders / bladder cancer / X mental retardation / KBG syndrome / infantile spasms / polyneuropathy / Prader-Willi syndrome / X syndrome / malonyl-CoA decarboxylase deficiency / Absence epilepsy / Lung disease / hydranencephaly / Adolescents With Autism Spectrum Disorder / distinctive X-linked mental retardation / tuberous sclerosis / infantile diabetes / pervasive developmental disorder / pervasive developmental disorders / neuronal migration disorder / autism spectrum disorders / neurodevelopmental disorders / cerebral palsy / ADHD / mental retardation / cognitive diseases / peripheral nerve sheath tumors / Hereditary / Costello Syndrome / cardiomyopathy / neurofibromatosis type / neurofibromatosis type I / disease / periventricular nodular heterotopia / cerebral infarction / galactosylceramidase deficiency / UBE3A causing Angelman syndrome / anxiety disorders / autism / pediatric T-ALL / Minor disease / tumour / aneurysms / type 1 lissencephaly / neurofibromatosis / Seizure / perisylvian polymicrogyria / tuberous sclerosis complex / Angelman syndrome / early onset insulin-dependent diabetes mellitus / optic pathway gliomas / fragile X-associated tremor/ataxia syndrome / incontinentia pigmenti / polydactyly / smallvessel disease / epilepsy / sleep disorders / meningitis / Asymmetric polymicrogyria / human disease / TORC1-dependent epilepsy / / MedicalTreatment counseling / counselling / / Organization International Society of Psychiatric Genetics / British Epilepsy Association / Two / Academy of Sciences DOI / / Person Arch Neurol / Ann Neurol / Halley / Van Der Vaart / Ned Tijdschr Geneeskd / Mancini / Acta Genet Med Gemellol / / Position model for mental retardation / D.J. / Teacher / Hunter / / Product Simvastatin / LG PC12 Radio / / PublishedMedium European Journal of Human Genetics / / Technology Genomics / neuroscience / Genetic engineering / apoptosis / MRI / genotype / drug development / /
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Neurofibromatose Erasmus MC/ ENCORE publicaties: Van Der Vaart, T. et al[removed]Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo