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Frontiers in Endocrinology
|
May 19, 2025
Developing a congenital hyperinsulinism prioritized research agenda: a patient-driven international collaborative research network
Tai L S Pasquini, Indraneel Banerjee, Henrik Thybo Christesen, et al.
Ebiomedicine
|
May 25, 2026
Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNA
Jasmin J Bennett, Thomas W Laver, Jonna M E Männistö, et al.
Annals of Neurology
|
October 24, 1997
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families
L Almasy, S B Bressman, D Raymond, et al.
Genome Research
|
May 1, 1997
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium
L J Ozelius, J Hewett, P Kramer, et al.
Neurology
|
October 23, 2002
Phenotypic features of myoclonus-dystonia in three kindreds
D O Doheny, M F Brin, C E Morrison, et al.
American Journal of Medical Genetics. Part A
|
February 6, 2019
Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations
Katheryn Grand, Christina Gonzalez-Gandolfi, Amanda M Ackermann, et al.
Annals of Neurology
|
March 15, 2000
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia
C Klein, N Gurvich, M Sena-Esteves, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 12, 2018
Correction: "Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals"
Kai Lee Yap, Amy E Knight Johnson, David Fischer, et al.
Hormone Research in Paediatrics
|
November 26, 2025
EndoCompass Project: Research Roadmap for Diabetes, Obesity, and Metabolism
Chantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
European Journal of Endocrinology
|
October 17, 2025
EndoCompass project: research roadmap for diabetes, obesity, and metabolism
Chantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
Page
of 18
Search research articles
Search
Showing results (171-180 of 180) with videos related to
Sort By:
Page
of 18
You have reached the last page of results.
This site can display upto 180 results.
Frontiers in Endocrinology
|
May 19, 2025
Developing a congenital hyperinsulinism prioritized research agenda: a patient-driven international collaborative research network
Tai L S Pasquini, Indraneel Banerjee, Henrik Thybo Christesen, et al.
Ebiomedicine
|
May 25, 2026
Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNA
Jasmin J Bennett, Thomas W Laver, Jonna M E Männistö, et al.
Annals of Neurology
|
October 24, 1997
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families
L Almasy, S B Bressman, D Raymond, et al.
Genome Research
|
May 1, 1997
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium
L J Ozelius, J Hewett, P Kramer, et al.
Neurology
|
October 23, 2002
Phenotypic features of myoclonus-dystonia in three kindreds
D O Doheny, M F Brin, C E Morrison, et al.
American Journal of Medical Genetics. Part A
|
February 6, 2019
Hyperinsulinemic hypoglycemia in seven patients with de novo NSD1 mutations
Katheryn Grand, Christina Gonzalez-Gandolfi, Amanda M Ackermann, et al.
Annals of Neurology
|
March 15, 2000
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia
C Klein, N Gurvich, M Sena-Esteves, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 12, 2018
Correction: "Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 10 affected individuals"
Kai Lee Yap, Amy E Knight Johnson, David Fischer, et al.
Hormone Research in Paediatrics
|
November 26, 2025
EndoCompass Project: Research Roadmap for Diabetes, Obesity, and Metabolism
Chantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
European Journal of Endocrinology
|
October 17, 2025
EndoCompass project: research roadmap for diabetes, obesity, and metabolism
Chantal Mathieu, Manuela Meireles, Uberto Pagotto, et al.
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of 18