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Proceedings of the National Academy of Sciences of the United States of America
|
April 29, 1999
Association of a missense change in the D2 dopamine receptor with myoclonus dystonia
C Klein, M F Brin, P Kramer, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 22, 2018
Islet Hormone and Incretin Secretion in Cystic Fibrosis after Four Months of Ivacaftor Therapy
Andrea Kelly, Diva D De Leon, Saba Sheikh, et al.
Journal of Forensic Sciences
|
August 24, 2017
A Molecular Method to Detect Wound Cells in Bloodstains Resultant of Sharp Force Injuries for Crime Scene Reconstruction
Donald J Johnson, David E Raymond, Cynthia Chen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 16, 2026
Functional evaluation of pancreatic islets from patients with Beckwith-Wiedemann syndrome and congenital hyperinsulinism
Christine A Juliana, Changhong Li, Jinghua Chai, et al.
The Physiologist
|
February 1, 1991
Changes in recruitment of rhesus soleus and gastrocnemius muscles following a 14 day spaceflight
J A Hodgson, S C Bodine-Fowler, R R Roy, et al.
Hormone Research in Paediatrics
|
April 14, 2026
Natural History of the Hyperinsulinism Hyperammonemia Syndrome - A Retrospective Review Incorporating Patient-centered Data
Elizabeth Rosenfeld, Olivia Taylor, Lauren M Mitteer, et al.
Hormone Research in Paediatrics
|
July 16, 2023
Novel Use of Dasiglucagon, a Soluble Glucagon Analog, for the Treatment of Hyperinsulinemic Hypoglycemia Secondary to Suspected Insulinoma: A Case Report
Dana Reynolds, Lauren M Mitteer, Winifred Sigal, et al.
Frontiers in Endocrinology
|
September 8, 2025
Real-world experience with the use of diazoxide among people living with congenital hyperinsulinism and their caregivers
Tai L S Pasquini, Kristen E Rohli, Fiona J Almeida, et al.
Annals of Neurology
|
November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation
S B Bressman, D de Leon, P L Kramer, et al.
Annals of Neurology
|
February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
P L Kramer, D de Leon, L Ozelius, et al.
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of 18
Search research articles
Search
Showing results (121-130 of 180) with videos related to
Sort By:
Page
of 18
Proceedings of the National Academy of Sciences of the United States of America
|
April 29, 1999
Association of a missense change in the D2 dopamine receptor with myoclonus dystonia
C Klein, M F Brin, P Kramer, et al.
American Journal of Respiratory and Critical Care Medicine
|
August 22, 2018
Islet Hormone and Incretin Secretion in Cystic Fibrosis after Four Months of Ivacaftor Therapy
Andrea Kelly, Diva D De Leon, Saba Sheikh, et al.
Journal of Forensic Sciences
|
August 24, 2017
A Molecular Method to Detect Wound Cells in Bloodstains Resultant of Sharp Force Injuries for Crime Scene Reconstruction
Donald J Johnson, David E Raymond, Cynthia Chen, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 16, 2026
Functional evaluation of pancreatic islets from patients with Beckwith-Wiedemann syndrome and congenital hyperinsulinism
Christine A Juliana, Changhong Li, Jinghua Chai, et al.
The Physiologist
|
February 1, 1991
Changes in recruitment of rhesus soleus and gastrocnemius muscles following a 14 day spaceflight
J A Hodgson, S C Bodine-Fowler, R R Roy, et al.
Hormone Research in Paediatrics
|
April 14, 2026
Natural History of the Hyperinsulinism Hyperammonemia Syndrome - A Retrospective Review Incorporating Patient-centered Data
Elizabeth Rosenfeld, Olivia Taylor, Lauren M Mitteer, et al.
Hormone Research in Paediatrics
|
July 16, 2023
Novel Use of Dasiglucagon, a Soluble Glucagon Analog, for the Treatment of Hyperinsulinemic Hypoglycemia Secondary to Suspected Insulinoma: A Case Report
Dana Reynolds, Lauren M Mitteer, Winifred Sigal, et al.
Frontiers in Endocrinology
|
September 8, 2025
Real-world experience with the use of diazoxide among people living with congenital hyperinsulinism and their caregivers
Tai L S Pasquini, Kristen E Rohli, Fiona J Almeida, et al.
Annals of Neurology
|
November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation
S B Bressman, D de Leon, P L Kramer, et al.
Annals of Neurology
|
February 1, 1990
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34
P L Kramer, D de Leon, L Ozelius, et al.
Page
of 18