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Karine Aouchiche

Showing results (1-10 of 18) with videos related to

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European Journal of Medical Genetics|May 21, 2026
Novelty and idiosyncrasy: the clay feet of rare disease descriptionsKarine Aouchiche, Paul Guerry, Alexandre Fabre
Endocrine|January 5, 2022
Teriparatide administration by the Omnipod pump: preliminary experience from two cases with refractory hypoparathyroidismKarine Aouchiche, Rachel Reynaud, Vincent Amodru, et al.
Hormone Research in Paediatrics|March 20, 2026
A Review of Pituitary Duplication and First Report of Associated Precocious Puberty in a BoyKarine Aouchiche, Mirjam Dirlewanger, Mehul Dattani, et al.
Clinical Endocrinology|August 19, 2025
Sucessful Transition in Rare Endocrine Diseases: Patient Experiences in a French Reference CentreKarine Aouchiche, Thierry Brue, Emeline Marquant, et al.
Clinical Endocrinology|December 16, 2024
CSNK2B Mutation: A Rare Cause of IGHDKarine Aouchiche, Pauline Romanet, Anne Barlier, et al.
Annales D'Endocrinologie|June 6, 2026
Pituitary Developmental Gene Defects and Their Contribution to Growth Hormone DeficiencyKarine Aouchiche, Rachel Reynaud, Theo Charnay, et al.
Annales D'Endocrinologie|March 30, 2026
Facts and news about growth hormone replacement therapy in adultsThierry Brue, Karine Aouchiche, Nicolas Sahakian, et al.
Annales D'Endocrinologie|May 8, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Primary Care Diabetes|June 30, 2023
Assessment of a new home-based care pathway for children newly diagnosed with type 1 diabetesLaetitia Gauche, Rémi Laporte, Delphine Bernoux, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
European Journal of Medical Genetics|May 21, 2026
Novelty and idiosyncrasy: the clay feet of rare disease descriptionsKarine Aouchiche, Paul Guerry, Alexandre Fabre
Endocrine|January 5, 2022
Teriparatide administration by the Omnipod pump: preliminary experience from two cases with refractory hypoparathyroidismKarine Aouchiche, Rachel Reynaud, Vincent Amodru, et al.
Hormone Research in Paediatrics|March 20, 2026
A Review of Pituitary Duplication and First Report of Associated Precocious Puberty in a BoyKarine Aouchiche, Mirjam Dirlewanger, Mehul Dattani, et al.
Clinical Endocrinology|August 19, 2025
Sucessful Transition in Rare Endocrine Diseases: Patient Experiences in a French Reference CentreKarine Aouchiche, Thierry Brue, Emeline Marquant, et al.
Clinical Endocrinology|December 16, 2024
CSNK2B Mutation: A Rare Cause of IGHDKarine Aouchiche, Pauline Romanet, Anne Barlier, et al.
Annales D'Endocrinologie|June 6, 2026
Pituitary Developmental Gene Defects and Their Contribution to Growth Hormone DeficiencyKarine Aouchiche, Rachel Reynaud, Theo Charnay, et al.
Annales D'Endocrinologie|March 30, 2026
Facts and news about growth hormone replacement therapy in adultsThierry Brue, Karine Aouchiche, Nicolas Sahakian, et al.
Annales D'Endocrinologie|May 8, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: A retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Annales D'Endocrinologie|March 21, 2026
Genotype-phenotype correlation and challenges in mutation detection in McCune-Albright syndrome: a retrospective study of a French cohortCamille Giannetti, Karine Aouchiche, Arnaud Lagarde, et al.
Primary Care Diabetes|June 30, 2023
Assessment of a new home-based care pathway for children newly diagnosed with type 1 diabetesLaetitia Gauche, Rémi Laporte, Delphine Bernoux, et al.
Pageof 2