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Journal of Inherited Metabolic Disease|April 22, 2008
Serum prolactin as a tool for the follow-up of treated DHPR-deficient patientsD Concolino, G Muzzi, M Rapsomaniki, et al.Archives of Disease in Childhood|November 1, 1996
Delayed gastric emptying: a novel gastrointestinal finding in Turner's syndromeA Staiano, M Salerno, S Di Maio, et al.Beneficial Microbes|September 11, 2018
Mind the gut: probiotics in paediatric neurogastroenterologyS Salvatore, L Pensabene, O Borrelli, et al.Current Gene Therapy|April 6, 2018
Genetics and Gene Therapy in Hunter DiseaseS Sestito, F Falvo, C Scozzafava, et al.American Journal of Medical Genetics. Part A|August 25, 2010
Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: delineation of the phenotypeD Concolino, G Roversi, G L Muzzi, et al.Revista De Gastroenterologia De Mexico (English)|April 7, 2018
Overlap between functional abdominal pain disorders and organic diseases in childrenA H Langshaw, J M Rosen, L Pensabene, et al.Seizure|June 30, 2006
Electroclinical evolution in ring chromosome 20 epilepsy syndrome: a case with severe phenotypic features followed for 25 yearsF A de Falco, P Olivieri, A de Falco, et al.Journal of Inherited Metabolic Disease|November 5, 1997
Phenylketonuria in Italy: distinct distribution pattern of three mutations of the phenylalanine hydroxylase geneV Guzzetta, G Bonapace, I Dianzani, et al.Clinical Genetics|August 29, 2013
Intrafamilial phenotypic variability in four families with Anderson-Fabry diseaseM Rigoldi, D Concolino, A Morrone, et al.European Journal of Medical Genetics|October 6, 2011
A de novo 8q22.2-24.3 duplication in a patient with mild phenotypeD Concolino, M A Iembo, M T Moricca, et al.Pageof 6