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Acta Paediatrica (Oslo, Norway : 1992)|March 27, 2007
Health-related-quality-of-life in obese adolescents is decreased and inversely related to BMIM de Beer, G H Hofsteenge, H M Koot, et al.Neuropediatrics|November 1, 1989
Schilder's diffuse sclerosis: case study with three years' follow-up and neuro-imagingP G Barth, M M Derix, M C de Krom, et al.Neurology|January 1, 1996
Peripheral nerve abnormalities in adrenomyeloneuropathy: a clinical and electrodiagnostic studyB M van Geel, J H Koelman, P G Barth, et al.Developmental Medicine and Child Neurology|August 1, 1990
Diagnostic features and clinical signs of 21 patients with lissencephaly type 1J F de Rijk-van Andel, W F Arts, P G Barth, et al.Neurology|January 5, 2002
Late onset white matter disease in peroxisome biogenesis disorderP G Barth, J Gootjes, H Bode, et al.Journal of Computer Assisted Tomography|March 1, 1995
Central cortico-subcortical involvement: a distinct pattern of brain damage caused by perinatal and postnatal asphyxia in term infantsR P Rademakers, M S van der Knaap, B Verbeeten, et al.Neuropadiatrie|May 1, 1980
Congenital muscular dystrophy and cerebral dysgenesis in a Dutch familyJ B Krijgsman, P G Barth, F C Stam, et al.Journal of Inherited Metabolic Disease|July 17, 1999
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)P G Barth, R J Wanders, P Vreken, et al.Journal of Neurology|February 1, 1992
Hereditary protein S deficiency presenting with cerebral sinus thrombosis in an adolescent girlJ H Koelman, C M Bakker, W C Plandsoen, et al.Journal of the Neurological Sciences|June 1, 1990
Inherited syndrome of microcephaly, dyskinesia and pontocerebellar hypoplasia: a systemic atrophy with early onsetP G Barth, G F Vrensen, H B Uylings, et al.Pageof 23