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Clinical Genetics|January 1, 1987
A male infant with holoprosencephaly, associated with ring chromosome 21D C Aronson, M C Jansweijer, J M Hoovers, et al.Neurology|December 1, 1994
Predominance of the adrenomyeloneuropathy phenotype of X-linked adrenoleukodystrophy in The Netherlands: a survey of 30 kindredsB M van Geel, J Assies, G J Weverling, et al.Brain : a Journal of Neurology|April 29, 1999
Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contracturesG J Jöbsis, J M Boers, P G Barth, et al.Brain & Development|March 1, 1995
Epidermal nevus syndrome with isolated enlargement of one temporal lobe: a case reportV I Kwa, J H Smitt, B W Verbeeten, et al.American Journal of Medical Genetics|March 15, 1996
Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studiesP G Barth, R J Wanders, R B Schutgens, et al.European Journal of Pediatrics|January 1, 1994
Clinical and biochemical characteristics of peroxisomal disorders: an updateR J Wanders, P G Barth, R B Schutgens, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapyB M van Geel, J Assies, R J Wanders, et al.Acta Paediatrica (Oslo, Norway : 1992)|March 25, 1998
Psychological responses to the needle-free Medi-Jector or the multidose Disetronic injection pen in human growth hormone therapyG H Verrips, R A Hirasing, M Fekkes, et al.Acta Neuropathologica|August 1, 1996
Histopathology of an infantile-onset spongiform leukoencephalopathy with a discrepantly mild clinical courseM S van der Knaap, P G Barth, G F Vrensen, et al.Neuromuscular Disorders : NMD|January 1, 1994
Cultured human muscle cells and respiratory chain deficienciesN H Herzberg, P A Bolhuis, C van den Bogert, et al.Pageof 23