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American Journal of Medical Genetics|October 16, 1996
Retinitis pigmentosa in a young man with Noonan syndrome: further evidence that Noonan syndrome (NS) and the cardio-facio-cutaneous syndrome (CFC) are variable manifestations of the same entity?M E Lorenzetti, J P FrynsAnnales De Genetique|January 1, 1996
Facial asymmetry, cardio-vascular anomalies and adducted thumbs as unusual symptoms in Dubowitz syndrome?A Vogels, M E Lorenzetti, P Gillis, et al.Journal of Gastroenterology and Hepatology|November 1, 1990
Oesophageal and ileal ulceration in Behçet's diseaseM E Lorenzetti, I J Forbes, I C Roberts-ThomsonAnnali Dell'Istituto Superiore Di Sanita|January 1, 1994
[The association between hypothyroidism and other congenital defects. The experience of the National Registry in 1987-1992]P Balestrazzi, M Sorcini, M E Grandolfo, et al.American Journal of Medical Genetics|January 11, 1996
Micromelic dwarfism with cone epiphyses, metaphyseal dysplasia, and vertebral segmentation defectsJ P Fryns, M E Lorenzetti, P Maroteaux, et al.The Clinical Journal of Pain|December 1, 1991
Placebo-controlled trial of dexamethasone for chronic biliary pain after cholecystectomyM E Lorenzetti, I C Roberts-Thomson, P R Pannall, et al.Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|June 27, 2001
[Care recommendations for type 1 neurofibromatosis]A Donadio, L Garavelli, M E Lorenzetti, et al.Journal of Child Neurology|June 8, 2001
Seckel's syndrome and malformations of cortical development: report of three new cases and review of the literatureG Capovilla, M E Lorenzetti, A Montagnini, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2001
A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic studyG Capovilla, G Rubboli, F Beccaria, et al.Pageof 1