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European Journal of Pediatrics|June 1, 1990
Alobar holoprosencephaly, diabetes insipidus and coloboma without craniofacial abnormalities: a case reportS Van Gool, F de Zegher, L S de Vries, et al.European Journal of Pediatrics|October 1, 1988
Spontaneous healing of Langerhans cell histiocytosis (histiocytosis X)L Corbeel, E Eggermont, J Desmyter, et al.Helvetica Paediatrica Acta|January 1, 1979
Unilateral galactocoele in a male infantM Vanderschueren-Lodeweyckx, M L Gielen, E Eggermont, et al.Neuropediatrics|August 1, 1984
Gamma-aminobutyric acid-transaminase deficiency: a newly recognized inborn error of neurotransmitter metabolismJ Jaeken, P Casaer, P de Cock, et al.Archives of Disease in Childhood|February 1, 1975
Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspectsL Corbeel, K Tada, J P Colombo, et al.Helvetica Paediatrica Acta|August 1, 1984
The thyroid-system function in preterm infants of postmenstrual ages of 31 weeks or less: evidence for a "transient lazy thyroid system"E Eggermont, M Vanderschueren-Lodeweyckx, P De Nayer, et al.American Journal of Medical Genetics|July 1, 1990
Restrictive dermopathy with distinct morphological abnormalitiesM Van Hoestenberghe, E Legius, W Vandevoorde, et al.Human Genetics|January 25, 1979
A new chromosome anomaly in acute lymphoblastic leukemia (ALL)H Van den Berghe, G David, A Broeckaert-Van Orshoven, et al.Acta Gastro-Enterologica Belgica|January 6, 2026
Correlating Quality of Life with Point-of-Care Intestinal Ultrasound in Inflammatory Bowel Disease (CUALITY Study)V Parra Izquierdo, K Ernest Suarez, M Argollo, et al.Human Genetics|September 1, 1990
Association between XV2c/CS7/KM19/D9 haplotypes and the delta F508 mutation. A study of 57 Belgian familiesH Cuppens, E Legius, P Cabello, et al.Pageof 14