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Neuropediatrics|September 26, 2001
Closely related Swedish Rett Syndrome females - none with MECP2 mutation revealedF Xiang, Y Stenbom, M Anvret, et al.European Child & Adolescent Psychiatry|May 1, 1998
Lamotrigine in Rett syndrome: treatment experience from a pilot studyY Stenbom, B Tonnby, B HagbergActa Paediatrica (Oslo, Norway : 1992)|March 10, 2000
Head growth in Rett syndromeG Hagberg, Y Stenbom, I Witt EngerströmBrain & Development|December 12, 2001
Head growth in Rett syndromeG Hagberg, Y Stenbom, I W EngerströmNeuropediatrics|April 1, 1995
Gross motor disability and head growth in Rett syndrome--a preliminary reportY Stenbom, I W Engerström, G HagbergNeuromuscular Disorders : NMD|July 17, 1999
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21F Xiang, P Nicolao, F Chapon, et al.Journal of Medical Genetics|April 4, 2000
Mutation screening in Rett syndrome patientsF Xiang, S Buervenich, P Nicolao, et al.American Journal of Human Genetics|March 3, 1999
Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2qP Nicolao, F Xiang, L G Gunnarsson, et al.Human Mutation|April 24, 2001
Identification of four novel polymorphisms in the calcitonin/alpha-CGRP (CALCA) gene and an investigation of their possible associations with Parkinson disease, schizophrenia, and manic depressionS Buervenich, F Xiang, O Sydow, et al.Pageof 18