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Showing results (161-170 of 169) with videos related to

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The Australian and New Zealand Journal of Psychiatry|February 20, 2016
Ketamine augmentation for outpatients with treatment-resistant depression: Preliminary evidence for two-step intravenous dose escalationCristina Cusin, Dawn Flosnik Ionescu, Kara Jean Pavone, et al.
The Journal of Clinical Endocrinology and Metabolism|November 2, 2022
Genotype-phenotype Description of Vitamin D-dependent Rickets 1A: CYP27B1 p.(Ala129Thr) Variant Induces a Milder DiseaseMarie-Noëlle Méaux, Jérôme Harambat, Anya Rothenbuhler, et al.
Plos One|October 29, 2024
Genital infections in high-risk human papillomavirus positive Paraguayan women aged 30-64 with and without cervical lesionsAlanis Arévalos, Adriana Valenzuela, Pamela Mongelós, et al.
Diabetes Care|July 8, 1998
Factors associated with glycemic control. A cross-sectional nationwide study in 2,579 French children with type 1 diabetes. The French Pediatric Diabetes GroupM Rosilio, J B Cotton, M C Wieliczko, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Evaluation of gonadal function in 107 intersex patients by means of serum antimüllerian hormone measurementR A Rey, C Belville, C Nihoul-Fékété, et al.
European Journal of Endocrinology|December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric populationYasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
Endocrine Connections|January 6, 2023
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in FranceEstelle Bonnet, Mathias Winter, Delphine Mallet, et al.
Human Molecular Genetics|February 12, 2015
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfectaMathilde Huckert, Corinne Stoetzel, Supawich Morkmued, et al.
Journal of Medical Genetics|October 28, 2015
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementMegana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.
Pageof 17

Showing results (161-170 of 169) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 169 results.
The Australian and New Zealand Journal of Psychiatry|February 20, 2016
Ketamine augmentation for outpatients with treatment-resistant depression: Preliminary evidence for two-step intravenous dose escalationCristina Cusin, Dawn Flosnik Ionescu, Kara Jean Pavone, et al.
The Journal of Clinical Endocrinology and Metabolism|November 2, 2022
Genotype-phenotype Description of Vitamin D-dependent Rickets 1A: CYP27B1 p.(Ala129Thr) Variant Induces a Milder DiseaseMarie-Noëlle Méaux, Jérôme Harambat, Anya Rothenbuhler, et al.
Plos One|October 29, 2024
Genital infections in high-risk human papillomavirus positive Paraguayan women aged 30-64 with and without cervical lesionsAlanis Arévalos, Adriana Valenzuela, Pamela Mongelós, et al.
Diabetes Care|July 8, 1998
Factors associated with glycemic control. A cross-sectional nationwide study in 2,579 French children with type 1 diabetes. The French Pediatric Diabetes GroupM Rosilio, J B Cotton, M C Wieliczko, et al.
The Journal of Clinical Endocrinology and Metabolism|February 18, 1999
Evaluation of gonadal function in 107 intersex patients by means of serum antimüllerian hormone measurementR A Rey, C Belville, C Nihoul-Fékété, et al.
European Journal of Endocrinology|December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric populationYasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
Endocrine Connections|January 6, 2023
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in FranceEstelle Bonnet, Mathias Winter, Delphine Mallet, et al.
Human Molecular Genetics|February 12, 2015
Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfectaMathilde Huckert, Corinne Stoetzel, Supawich Morkmued, et al.
Journal of Medical Genetics|October 28, 2015
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvementMegana K Prasad, Véronique Geoffroy, Serge Vicaire, et al.
Pageof 17