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Lancet (London, England)|September 21, 2002
Randomised controlled study of early pulsed dye laser treatment of uncomplicated childhood haemangiomas: results of a 1-year analysisKapila Batta, Helen M Goodyear, Celia Moss, et al.
Pediatric Nephrology (Berlin, Germany)|July 20, 2007
End-stage renal failure in adolescence with Sjögren's syndrome autoantibodies SSA and SSBSally Johnson, Sally-Anne Hulton, Marie-Anne Brundler, et al.
Pediatric Dermatology|June 12, 2014
Hereditary vitamin D-resistant rickets presenting as alopeciaGenevieve Casey, Tess McPherson, Usha Kini, et al.
Pediatric Dermatology|June 12, 2010
Links between granuloma annulare, necrobiosis lipoidica diabeticorum and childhood diabetes: a matter of time?James E Davison, Alison Davies, Celia Moss, et al.
American Journal of Human Genetics|October 7, 2008
A connective tissue disorder caused by mutations of the lysyl hydroxylase 3 geneAntti M Salo, Helen Cox, Peter Farndon, et al.
Developmental Medicine and Child Neurology|June 25, 2009
Degos disease: a new simulator of non-accidental injuryCelia Moss, Evangeline Wassmer, Geoff Debelle, et al.
Journal of Human Genetics|August 28, 2015
Setleis syndrome due to inheritance of the 1p36.22p36.21 duplication: evidence for lack of penetranceBeom Hee Lee, Christos Kasparis, Brenden Chen, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 21, 2013
Multiple cerebral abscesses in Papillon-Lefèvre syndromeHari Krishnan Kanthimathinathan, Fiona Browne, Roberto Ramirez, et al.
American Journal of Medical Genetics. Part A|September 5, 2003
Deletion of the SLUG (SNAI2) gene results in human piebaldismManuel Sánchez-Martín, Jesús Pérez-Losada, Arancha Rodríguez-García, et al.
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