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Bruno Donadille

Showing results (11-20 of 33) with videos related to

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Frontiers in Endocrinology|January 20, 2022
Molecular and Cellular Bases of Lipodystrophy SyndromesJamila Zammouri, Camille Vatier, Emilie Capel, et al.
European Journal of Medical Genetics|March 19, 2022
Quality of life and mental health of adolescents and adults with Silver-Russell syndromeMélissa Burgevin, Agnès Lacroix, Karine Bourdet, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failureAzzedine Aboura, Claire Dupas, Gérard Tachdjian, et al.
Plos One|January 20, 2023
Executive functioning in adolescents and adults with Silver-Russell syndromeMélissa Burgevin, Agnès Lacroix, Fanny Ollivier, et al.
Orphanet Journal of Rare Diseases|July 16, 2013
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndromeBruno Donadille, Pascal D'Anella, Martine Auclair, et al.
The Journal of Clinical Endocrinology and Metabolism|August 23, 2007
New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndromeAurélie Decaudain, Marie-Christine Vantyghem, Bruno Guerci, et al.
European Journal of Medical Genetics|February 10, 2018
Harmonising phenomics information for a better interoperability in the rare disease fieldSylvie Maiella, Annie Olry, Marc Hanauer, et al.
European Journal of Endocrinology|April 9, 2008
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiencyZeina Chakhtoura, Anne Bachelot, Dinane Samara-Boustani, et al.
European Journal of Endocrinology|October 28, 2022
Prevalence and characteristics of gonadoblastoma in a retrospective multi-center study with follow-up investigations of 70 patients with Turner syndrome and a 45,X/46,XY karyotypeDaphné Karila, Bruno Donadille, Juliane Léger, et al.
Orphanet Journal of Rare Diseases|November 5, 2021
Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseasesWafa Kallali, Claude Messiaen, Roumaisah Saïdi, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Frontiers in Endocrinology|January 20, 2022
Molecular and Cellular Bases of Lipodystrophy SyndromesJamila Zammouri, Camille Vatier, Emilie Capel, et al.
European Journal of Medical Genetics|March 19, 2022
Quality of life and mental health of adolescents and adults with Silver-Russell syndromeMélissa Burgevin, Agnès Lacroix, Karine Bourdet, et al.
The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failureAzzedine Aboura, Claire Dupas, Gérard Tachdjian, et al.
Plos One|January 20, 2023
Executive functioning in adolescents and adults with Silver-Russell syndromeMélissa Burgevin, Agnès Lacroix, Fanny Ollivier, et al.
Orphanet Journal of Rare Diseases|July 16, 2013
Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndromeBruno Donadille, Pascal D'Anella, Martine Auclair, et al.
The Journal of Clinical Endocrinology and Metabolism|August 23, 2007
New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndromeAurélie Decaudain, Marie-Christine Vantyghem, Bruno Guerci, et al.
European Journal of Medical Genetics|February 10, 2018
Harmonising phenomics information for a better interoperability in the rare disease fieldSylvie Maiella, Annie Olry, Marc Hanauer, et al.
European Journal of Endocrinology|April 9, 2008
Impact of total cumulative glucocorticoid dose on bone mineral density in patients with 21-hydroxylase deficiencyZeina Chakhtoura, Anne Bachelot, Dinane Samara-Boustani, et al.
European Journal of Endocrinology|October 28, 2022
Prevalence and characteristics of gonadoblastoma in a retrospective multi-center study with follow-up investigations of 70 patients with Turner syndrome and a 45,X/46,XY karyotypeDaphné Karila, Bruno Donadille, Juliane Léger, et al.
Orphanet Journal of Rare Diseases|November 5, 2021
Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseasesWafa Kallali, Claude Messiaen, Roumaisah Saïdi, et al.
Pageof 4