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Showing results (151-160 of 177) with videos related to

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Diabetes Research and Clinical Practice|April 10, 2010
Computer use, free time activities and metabolic control in patients with type 1 diabetesD Benevento, C Bizzarri, D Pitocco, et al.
Clinical Endocrinology|January 13, 2006
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative studyA Cassio, A Corrias, S Gualandi, et al.
The British Journal of Dermatology|May 23, 2012
Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysisG Cirillo, R Marini, S Ito, et al.
Clinical Genetics|March 18, 2006
Succinic semialdehyde dehydrogenase deficiency: clinical, biochemical and molecular characterization of a new patient with severe phenotype and a novel mutationP Blasi, F Palmerio, S Caldarola, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 7, 2014
Functional and structural analysis of four novel mutations of CYP21A2 gene in Italian patients with 21-hydroxylase deficiencyA Massimi, M Malaponti, L Federici, et al.
Journal of Endocrinological Investigation|March 26, 2008
Young elite athletes of different sport disciplines present with an increase in pulsatile secretion of growth hormone compared with non-elite athletes and sedentary subjectsG Ubertini, A Grossi, D Colabianchi, et al.
Journal of Endocrinological Investigation|July 14, 2016
Adherence in children with growth hormone deficiency treated with r-hGH and the easypod™ deviceS Loche, M Salerno, P Garofalo, et al.
Brain : a Journal of Neurology|July 1, 1997
Neurophysiological abnormalities in adrenoleukodystrophy carriers. Evidence of different degrees of central nervous system involvementD Restuccia, V Di Lazzaro, M Valeriani, et al.
European Journal of Neurology|October 9, 2018
Natural history of a cohort of ABCD1 variant female carriersT Schirinzi, G Vasco, C Aiello, et al.
Journal of Endocrinological Investigation|May 20, 2023
Quality of life in children and adolescents with growth hormone deficiency and their caregivers: an Italian surveyM Maghnie, M Orso, B Polistena, et al.
Pageof 18

Showing results (151-160 of 177) with videos related to

Sort By:
Pageof 18
Diabetes Research and Clinical Practice|April 10, 2010
Computer use, free time activities and metabolic control in patients with type 1 diabetesD Benevento, C Bizzarri, D Pitocco, et al.
Clinical Endocrinology|January 13, 2006
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative studyA Cassio, A Corrias, S Gualandi, et al.
The British Journal of Dermatology|May 23, 2012
Lack of red hair phenotype in a North-African obese child homozygous for a novel POMC null mutation: nonsense-mediated decay RNA evaluation and hair pigment chemical analysisG Cirillo, R Marini, S Ito, et al.
Clinical Genetics|March 18, 2006
Succinic semialdehyde dehydrogenase deficiency: clinical, biochemical and molecular characterization of a new patient with severe phenotype and a novel mutationP Blasi, F Palmerio, S Caldarola, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|May 7, 2014
Functional and structural analysis of four novel mutations of CYP21A2 gene in Italian patients with 21-hydroxylase deficiencyA Massimi, M Malaponti, L Federici, et al.
Journal of Endocrinological Investigation|March 26, 2008
Young elite athletes of different sport disciplines present with an increase in pulsatile secretion of growth hormone compared with non-elite athletes and sedentary subjectsG Ubertini, A Grossi, D Colabianchi, et al.
Journal of Endocrinological Investigation|July 14, 2016
Adherence in children with growth hormone deficiency treated with r-hGH and the easypod™ deviceS Loche, M Salerno, P Garofalo, et al.
Brain : a Journal of Neurology|July 1, 1997
Neurophysiological abnormalities in adrenoleukodystrophy carriers. Evidence of different degrees of central nervous system involvementD Restuccia, V Di Lazzaro, M Valeriani, et al.
European Journal of Neurology|October 9, 2018
Natural history of a cohort of ABCD1 variant female carriersT Schirinzi, G Vasco, C Aiello, et al.
Journal of Endocrinological Investigation|May 20, 2023
Quality of life in children and adolescents with growth hormone deficiency and their caregivers: an Italian surveyM Maghnie, M Orso, B Polistena, et al.
Pageof 18