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Journal of Inherited Metabolic Disease|February 3, 2011
Sub-pleural bullous changes in two adults with Mucopolysaccharidosis type I (Hurler-Scheie)Michel C Tchan, Nicole Graf, David O Sillence
Pediatric Radiology|August 27, 2002
Gracile bone dysplasiasKazimierz Kozlowski, John Masel, David O Sillence, et al.
Sleep & Breathing = Schlaf & Atmung|January 13, 2011
Respiratory events and obstructive sleep apnea in children with achondroplasia: investigation and treatment outcomesShahla Afsharpaiman, David O Sillence, Mehrdad Sheikhvatan, et al.
Pediatric Rheumatology Online Journal|January 7, 2009
The differential diagnosis of children with joint hypermobility: a review of the literatureLouise J Tofts, Elizabeth J Elliott, Craig Munns, et al.
Orphanet Journal of Rare Diseases|July 19, 2024
Letter to the editor: Re: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classificationRaymond Dalgleish, Dimitra Micha, Andrea Superti-Furga, et al.
Journal of Paediatrics and Child Health|November 14, 2006
Neonatal severe hyperparathyroidism: an important clue to the aetiologyMichael T Gabbett, Kristi Jones, Christopher T Cowell, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|October 17, 2014
Cognitive and psychological functioning in Fabry diseaseLinda Sigmundsdottir, Michel C Tchan, Alex A Knopman, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 8, 2013
Left atrial enlargement and reduced atrial compliance occurs early in Fabry cardiomyopathyAnita C Boyd, Queenie Lo, Kerry Devine, et al.
American Journal of Medical Genetics. Part A|January 6, 2005
Three patients with terminal deletions within the subtelomeric region of chromosome 9qKatherine R Neas, Janine M Smith, Nicole Chia, et al.
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