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Archives of Pathology & Laboratory Medicine|February 1, 1984
Granulomatous coronary arteritisH M Payan, E F GilbertNeuropediatrics|November 9, 2000
Polymicrogyria and motor neuropathy in Micro syndromeM C Nassogne, B Henrot, C Saint-Martin, et al.Pediatric Neurology|February 1, 1994
Childhood stroke and lupus anticoagulantJ C Olson, R J Konkol, J C Gill, et al.American Journal of Medical Genetics|September 1, 1985
Syndromes with lissencephaly. II: Walker-Warburg and cerebro-oculo-muscular syndromes and a new syndrome with type II lissencephalyW B Dobyns, J B Kirkpatrick, H M Hittner, et al.Journal of Child Neurology|October 8, 1999
Clinical nosologic and genetic aspects of Joubert and related syndromesP F Chance, L Cavalier, D Satran, et al.American Journal of Medical Genetics|September 1, 1985
Deficiency of chromosome 8p21.1----8pter: case report and review of the literatureW B Dobyns, G W Dewald, R O Carlson, et al.Journal of Neurology|October 1, 1996
Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type IL Pavone, A Fiumara, R Barone, et al.Neurology|April 1, 1997
Rapid-onset dystonia-parkinsonism in a second familyA Brashear, D DeLeon, S B Bressman, et al.Clinical Genetics|March 1, 1976
Autosomal recessive syndrome of pseudogliomantous blindness, osteoporosis and mild mental retardationG Neuhäuser, E G Kaveggia, J M OpitzZeitschrift Fur Kinderheilkunde|September 11, 1975
Studies of malformation syndromes of man XXXVIII: The BD syndrome. A "new" multiple congenital anomalies/mental retardation syndrome with athetoid cerebral palsyG Neuhäuser, E G Kaveggia, J M OpitzPageof 40