L de Sanctis - JoVE Visualize

Showing results (11-20 of 31) with videos related to

Pageof 4

Sort By:

Clinical Nephrology|January 5, 2002

Cystinuria phenotyping by oral lysine and arginine loadingL de Sanctis, G Bonetti, M Bruno, et al.

Hormone Research in Paediatrics|September 26, 2012

Thyroid abnormalities in children and adolescents with McCune-Albright syndromeD Tessaris, A Corrias, P Matarazzo, et al.

International Journal of Immunopathology and Pharmacology|June 11, 2011

Prognostic implication of high risk human papillomavirus E6 and E7 mRNA in patients with intraepithelial lesions of the cervix in relationship to ageA Frega, L Lorenzon, M R Giovagnoli, et al.

Journal of Pediatric Endocrinology & Metabolism : JPEM|January 1, 1997

Growth hormone treatment in irradiated children with brain tumorsA Corrias, P Picco, S Einaudi, et al.

Journal of Medical Genetics|January 7, 2005

New insights into cystinuria: 40 new mutations, genotype-phenotype correlation, and digenic inheritance causing partial phenotypeM Font-Llitjós, M Jiménez-Vidal, L Bisceglia, et al.

European Journal of Human Genetics : EJHG|January 1, 1995

Characterization of phenylketonuria alleles in the Italian populationI Dianzani, S Giannattasio, L de Sanctis, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995

Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuriaM J Calonge, V Volpini, L Bisceglia, et al.

Journal of Endocrinological Investigation|March 30, 2007

GH secretion in a cohort of children with pseudohypoparathyroidism type IaL de Sanctis, J Bellone, M Salerno, et al.

Journal of Endocrinological Investigation|June 23, 2009

Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.

Italian Journal of Pediatrics|November 23, 2016

Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoptionL de Sanctis, F Giachero, G Mantovani, et al.

Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:

Pageof 4

Clinical Nephrology|January 5, 2002

Cystinuria phenotyping by oral lysine and arginine loadingL de Sanctis, G Bonetti, M Bruno, et al.

Hormone Research in Paediatrics|September 26, 2012

Thyroid abnormalities in children and adolescents with McCune-Albright syndromeD Tessaris, A Corrias, P Matarazzo, et al.

International Journal of Immunopathology and Pharmacology|June 11, 2011

Prognostic implication of high risk human papillomavirus E6 and E7 mRNA in patients with intraepithelial lesions of the cervix in relationship to ageA Frega, L Lorenzon, M R Giovagnoli, et al.

Journal of Pediatric Endocrinology & Metabolism : JPEM|January 1, 1997

Growth hormone treatment in irradiated children with brain tumorsA Corrias, P Picco, S Einaudi, et al.

Journal of Medical Genetics|January 7, 2005

New insights into cystinuria: 40 new mutations, genotype-phenotype correlation, and digenic inheritance causing partial phenotypeM Font-Llitjós, M Jiménez-Vidal, L Bisceglia, et al.

European Journal of Human Genetics : EJHG|January 1, 1995

Characterization of phenylketonuria alleles in the Italian populationI Dianzani, S Giannattasio, L de Sanctis, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995

Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuriaM J Calonge, V Volpini, L Bisceglia, et al.

Journal of Endocrinological Investigation|March 30, 2007

GH secretion in a cohort of children with pseudohypoparathyroidism type IaL de Sanctis, J Bellone, M Salerno, et al.

Journal of Endocrinological Investigation|June 23, 2009

Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesisA M Ferrara, L De Sanctis, G Rossi, et al.

Italian Journal of Pediatrics|November 23, 2016

Genetic and epigenetic alterations in the GNAS locus and clinical consequences in Pseudohypoparathyroidism: Italian common healthcare pathways adoptionL de Sanctis, F Giachero, G Mantovani, et al.

Pageof 4