Search research articles
Contact Us
Filters
Showing results (191-200 of 207) with videos related to
Page
of 21
Sort By:
European Journal of Endocrinology
|
June 26, 2019
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene
Giuseppa Patti, Saverio Scianguetta, Domenico Roberti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2025
Clinical course of COVID-19 in children with Adrenal Insufficiency: Results from National Data
Donatella Capalbo, Cristina Moracas, Laura Guazzarotti, et al.
Italian Journal of Pediatrics
|
October 26, 2014
Inter-society consensus document on treatment and prevention of bronchiolitis in newborns and infants
Eugenio Baraldi, Marcello Lanari, Paolo Manzoni, et al.
American Journal of Human Genetics
|
March 3, 2015
Mutations in the NHEJ component XRCC4 cause primordial dwarfism
Jennie E Murray, Mirjam van der Burg, Hanna IJspeert, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 16, 2022
Safety and Efficacy of Lonapegsomatropin in Children With Growth Hormone Deficiency: enliGHten Trial 2-Year Results
Aristides K Maniatis, Samuel J Casella, Ulhas M Nadgir, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2024
The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022
Novella Rapini, Maurizio Delvecchio, Mafalda Mucciolo, et al.
JCI Insight
|
March 23, 2018
Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes
Ciriana Orabona, Giada Mondanelli, Maria T Pallotta, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2008
The Italian National Survey for Prader-Willi syndrome: an epidemiologic study
Graziano Grugni, Antonino Crinò, Laura Bosio, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Ahmed Khattab, Shozeb Haider, Ameet Kumar, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 27, 2025
MCT8 Deficiency in Females
Stefan Groeneweg, Ferdy S van Geest, Floor van der Most, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 207) with videos related to
Sort By:
Page
of 21
European Journal of Endocrinology
|
June 26, 2019
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene
Giuseppa Patti, Saverio Scianguetta, Domenico Roberti, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 7, 2025
Clinical course of COVID-19 in children with Adrenal Insufficiency: Results from National Data
Donatella Capalbo, Cristina Moracas, Laura Guazzarotti, et al.
Italian Journal of Pediatrics
|
October 26, 2014
Inter-society consensus document on treatment and prevention of bronchiolitis in newborns and infants
Eugenio Baraldi, Marcello Lanari, Paolo Manzoni, et al.
American Journal of Human Genetics
|
March 3, 2015
Mutations in the NHEJ component XRCC4 cause primordial dwarfism
Jennie E Murray, Mirjam van der Burg, Hanna IJspeert, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 16, 2022
Safety and Efficacy of Lonapegsomatropin in Children With Growth Hormone Deficiency: enliGHten Trial 2-Year Results
Aristides K Maniatis, Samuel J Casella, Ulhas M Nadgir, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 26, 2024
The Changing Landscape of Neonatal Diabetes Mellitus in Italy Between 2003 and 2022
Novella Rapini, Maurizio Delvecchio, Mafalda Mucciolo, et al.
JCI Insight
|
March 23, 2018
Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1in juvenile diabetes
Ciriana Orabona, Giada Mondanelli, Maria T Pallotta, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2008
The Italian National Survey for Prader-Willi syndrome: an epidemiologic study
Graziano Grugni, Antonino Crinò, Laura Bosio, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 24, 2017
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Ahmed Khattab, Shozeb Haider, Ameet Kumar, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 27, 2025
MCT8 Deficiency in Females
Stefan Groeneweg, Ferdy S van Geest, Floor van der Most, et al.
Page
of 21