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Journal of Child Neurology|April 1, 1993
Alexander's disease: clues to diagnosisC L Pridmore, M Baraitser, B Harding, et al.Neuropediatrics|May 1, 1991
Pelizaeus-Merzbacher disease: classical or connatal?I E Scheffer, M Baraitser, J Wilson, et al.Neuropediatrics|August 1, 1990
Megalencephaly with dysmyelination, spasticity, ataxia, seizures and distinctive neurophysiological findings in two siblingsM G Harbord, A Harden, B Harding, et al.Journal of Medical Genetics|October 1, 1989
Central nervous system malformations in Mohr's syndromeW Reardon, M G Harbord, M A Hall-Craggs, et al.Clinical Dysmorphology|April 1, 1992
Alopecia, mental retardation, epilepsy and microcephaly in two cousinsC Pridmore, M Baraitser, E M BrettClinical Genetics|February 1, 1986
A family with congenital suprabulbar paresis (Worster-Drought syndrome)M A Patton, M Baraitser, E M BrettClinical Genetics|October 1, 1983
Greig cephalopolysyndactyly: report of 13 affected individuals in three familiesM Baraitser, R M Winter, E M BrettDevelopmental Medicine and Child Neurology|October 1, 1991
Severe microcephaly associated with congenital varicella infectionI E Scheffer, M Baraitser, E M BrettNeuropediatrics|November 1, 1987
The use of a computerised database for the diagnosis of a rare neurological syndromeK Tomiwa, M Baraitser, E M Brett, et al.American Journal of Medical Genetics|December 11, 1996
Hemihypertrophy, hemimegalencephaly, and polydactylyW Reardon, B Harding, R M Winter, et al.Pageof 56