prof. Helene Verhelst
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STXBP1 encephalopathy : a neurodevelopmental disorder including epilepsy
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Therapeutic plasma exchange in children with acute autoimmune central nervous system disorders
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- Conference Paper
- C3
- open access
Intensive therapeutic plasma exchange in children with acute autoimmune neurological disorders
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- Journal Article
- A1
- open access
Polymicrogyria with dysmorphic basal ganglia? Think tubulin!
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Lambert-Eaton myasthenic syndrome in a 13-year-old girl with Xp11.22-p11.23 duplication
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Colon enemas for fecal incontinence in patients with spina bifida
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Expanding the spectrum of MERS type 2 lesions, a particular form of encephalitis
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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders
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- Conference Paper
- C3
- open access
Achieving anal pseudo-continence by colonic irrigations in patients with spina bifida
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- Journal Article
- A1
- open access
Colon transit time and anorectal manometry in children and young adults with spina bifida
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- Journal Article
- A1
- open access
First line management of prolonged convulsive seizures in children and adults : good practice points
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Temps du transit colique chez l'enfant atteint de dysraphisme ouvert
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Hypocretin-1 deficiency in a girl with ROHHAD syndrome
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Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review
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- Conference Paper
- C3
- open access
Developing a modified 'quality of life' questionnaire for children with spina bifida
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Colon enemas in patients with spina bifida: practical approach
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TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria
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Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster
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Palatal insufficiency as isolated sign of GQ1b antibody syndrome
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Hashimoto encephalopathy and antibodies against dimethylargininase-1: a rare cause of cognitive decline in a pediatric Down's syndrome patient