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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 17, 2024
Endocrine management of transgender adolescents: Expert consensus of the french society of pediatric endocrinology and diabetology working group
François Brezin, Kanetee Busiah, Clara Leroy, et al.
Diabetes Care
|
April 11, 2020
Long-term Metabolic and Socioeducational Outcomes of Transient Neonatal Diabetes: A Longitudinal and Cross-sectional Study
Fleur Le Bourgeois, Jacques Beltrand, Baz Baz, et al.
Diabetes Care
|
December 24, 2015
Erratum. Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations. Diabetes Care 2015;38:2033-2041
Jacques Beltrand, Caroline Elie, Kanetee Busiah, et al.
Journal of the Endocrine Society
|
July 2, 2025
Prevalence of Differences of Sex Development Among Pediatric Endocrine Care Centers in Switzerland From 2000 to 2019
Sara Metzger, Christine Aebi-Ochsner, Kanetee Busiah, et al.
Diabetes Care
|
October 7, 2015
Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations
Jacques Beltrand, Caroline Elie, Kanetee Busiah, et al.
The Journal of Biological Chemistry
|
May 20, 2011
Disruption of a novel Kruppel-like transcription factor p300-regulated pathway for insulin biosynthesis revealed by studies of the c.-331 INS mutation found in neonatal diabetes mellitus
Amélie Bonnefond, Gwen Lomberk, Navtej Buttar, et al.
Molecular Genetics and Metabolism
|
January 14, 2024
Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study
Kanetee Busiah, Célina Roda, Anne-Sophie Crosnier, et al.
European Journal of Endocrinology
|
December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population
Yasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
The Lancet. Diabetes & Endocrinology
|
March 14, 2014
Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected]
Kanetee Busiah, Séverine Drunat, Laurence Vaivre-Douret, et al.
American Journal of Human Genetics
|
August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy
Florence Habarou, Yamina Hamel, Tobias B Haack, et al.
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Search research articles
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Showing results (31-40 of 42) with videos related to
Sort By:
Page
of 5
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
November 17, 2024
Endocrine management of transgender adolescents: Expert consensus of the french society of pediatric endocrinology and diabetology working group
François Brezin, Kanetee Busiah, Clara Leroy, et al.
Diabetes Care
|
April 11, 2020
Long-term Metabolic and Socioeducational Outcomes of Transient Neonatal Diabetes: A Longitudinal and Cross-sectional Study
Fleur Le Bourgeois, Jacques Beltrand, Baz Baz, et al.
Diabetes Care
|
December 24, 2015
Erratum. Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations. Diabetes Care 2015;38:2033-2041
Jacques Beltrand, Caroline Elie, Kanetee Busiah, et al.
Journal of the Endocrine Society
|
July 2, 2025
Prevalence of Differences of Sex Development Among Pediatric Endocrine Care Centers in Switzerland From 2000 to 2019
Sara Metzger, Christine Aebi-Ochsner, Kanetee Busiah, et al.
Diabetes Care
|
October 7, 2015
Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations
Jacques Beltrand, Caroline Elie, Kanetee Busiah, et al.
The Journal of Biological Chemistry
|
May 20, 2011
Disruption of a novel Kruppel-like transcription factor p300-regulated pathway for insulin biosynthesis revealed by studies of the c.-331 INS mutation found in neonatal diabetes mellitus
Amélie Bonnefond, Gwen Lomberk, Navtej Buttar, et al.
Molecular Genetics and Metabolism
|
January 14, 2024
Pubertal origin of growth retardation in inborn errors of protein metabolism: A longitudinal cohort study
Kanetee Busiah, Célina Roda, Anne-Sophie Crosnier, et al.
European Journal of Endocrinology
|
December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population
Yasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
The Lancet. Diabetes & Endocrinology
|
March 14, 2014
Neuropsychological dysfunction and developmental defects associated with genetic changes in infants with neonatal diabetes mellitus: a prospective cohort study [corrected]
Kanetee Busiah, Séverine Drunat, Laurence Vaivre-Douret, et al.
American Journal of Human Genetics
|
August 1, 2017
Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy
Florence Habarou, Yamina Hamel, Tobias B Haack, et al.
Page
of 5