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Case Reports in Pediatrics|November 13, 2014
Neonatal pulmonary hemosiderosisBoris Limme, Ramona Nicolescu, Jean-Paul MissonClinical Dysmorphology|September 15, 2004
Hypertrichosis, Fallot tetralogy, growth and developmental delayAlain Verloes, Martial Massin, Anne-Catherine Fransolet, et al.Neuropediatrics|February 23, 2018
Phenotype-Genotype Correlation in Children with Neurofibromatosis Type 1Christophe Barrea, Sandrine Vaessen, Saskia Bulk, et al.Annales De Genetique|December 9, 2003
Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?Alain Verloes, Jean-Paul Misson, Philippe Gillet, et al.Neuropediatrics|May 6, 2016
Horner Syndrome in Children: A Clinical Condition with Serious Underlying DiseaseChristophe Barrea, Tiphaine Vigouroux, Joe Karam, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 3, 2004
Spontaneous arachnoid cyst rupture in a previously asymptomatic child: a case reportAnne-Lise M L Poirrier, Issa Ngosso-Tetanye, Micheline Mouchamps, et al.Journal of Tropical Pediatrics|December 17, 2013
Evaluation of adherence to a convulsion management protocol for children in RwandaCélestin Kaputu-Kalala-Malu, Jean D'Amour Birindabagabo, Timothy David Walker, et al.American Journal of Medical Genetics. Part A|August 5, 2010
Temple-Baraitser syndrome: a rare and possibly unrecognized conditionAdeline Jacquinet, Marion Gérard, Michael T Gabbett, et al.Acta Neurologica Belgica|September 18, 2008
Management of diffuse glioma in children: a retrospective study of 27 cases and review of literatureCaroline Piette, Manuel Deprez, Jacques Born, et al.BMC Palliative Care|May 24, 2018
Building Bridges, Paediatric Palliative Care in Belgium: A secondary data analysis of annual paediatric liaison team reports from 2010 to 2014Marie Friedel, Bénédicte Brichard, Christine Fonteyne, et al.Pageof 2