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American Journal of Medical Genetics|May 3, 1996
Diffuse polymicrogyria associated with an unusual pattern of multiple congenital anomalies including turribrachycephaly and hypogenitalismR D Cohn, G Gillessen-Kaesbach, W B Dobyns, et al.
Brain & Development|July 7, 1999
MRI abnormalities in neurofibromatosis type 1 (NF1): a study of men and miceT Rosenbaum, V Engelbrecht, W Krölls, et al.
Rheumatology International|November 4, 2000
Relapsing polychondritis in childhood--case report and short reviewS Knipp, H Bier, G Horneff, et al.
Human Molecular Genetics|December 15, 2000
Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulationsE Serra, T Rosenbaum, U Winner, et al.
Neuropediatrics|August 26, 1998
Paraneoplastic limbic encephalitis in two teenage girlsT Rosenbaum, J Gärtner, D Körholz, et al.
Acta Paediatrica (Oslo, Norway : 1992)|January 1, 1994
Multisystem triglyceride storage disorder without ichthyosis in two siblingsR Wessalowski, H Schroten, E Neuen-Jacob, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 11, 2001
Interdisciplinary treatment in pediatric patients with malignant CNS tumorsA M Messing-Jünger, G Janssen, H Pape, et al.
Human Molecular Genetics|September 26, 2000
Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophyR Herrmann, V Straub, M Blank, et al.
Neuropediatrics|May 1, 1988
Emery-Dreifuss muscular dystrophy: disease spectrum and differential diagnosisT Voit, O Krogmann, H G Lenard, et al.
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