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Diabetologia
|
November 8, 2015
Use of insulin pump therapy in children and adolescents with type 1 diabetes and its impact on metabolic control: comparison of results from three large, transatlantic paediatric registries
Jennifer L Sherr, Julia M Hermann, Fiona Campbell, et al.
Diabetes Care
|
August 19, 2015
Rates of diabetic ketoacidosis: international comparison with 49,859 pediatric patients with type 1 diabetes from England, Wales, the U.S., Austria, and Germany
David M Maahs, Julia M Hermann, Naomi Holman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 2018
A New Multisystem Disorder Caused by the Gαs Mutation p.F376V
Heike Biebermann, Gunnar Kleinau, Dirk Schnabel, et al.
Human Molecular Genetics
|
March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism
Michael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2014
Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3)
Angela Rogers, M Andrew Nesbit, Fadil M Hannan, et al.
Kidney International
|
October 26, 2024
Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c
Max Brunkhorst, Lena Brunkhorst, Helge Martens, et al.
The Journal of Investigative Dermatology
|
October 6, 2023
GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calcium Indices and Microvascular Neurocalcification
Nicole Knöpfel, Davide Zecchin, Hanna Richardson, et al.
Journal of the Endocrine Society
|
July 14, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK
Federica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
American Journal of Human Genetics
|
August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay
Ronit Marom, Lindsay C Burrage, Rossella Venditti, et al.
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of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Diabetologia
|
November 8, 2015
Use of insulin pump therapy in children and adolescents with type 1 diabetes and its impact on metabolic control: comparison of results from three large, transatlantic paediatric registries
Jennifer L Sherr, Julia M Hermann, Fiona Campbell, et al.
Diabetes Care
|
August 19, 2015
Rates of diabetic ketoacidosis: international comparison with 49,859 pediatric patients with type 1 diabetes from England, Wales, the U.S., Austria, and Germany
David M Maahs, Julia M Hermann, Naomi Holman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 13, 2018
A New Multisystem Disorder Caused by the Gαs Mutation p.F376V
Heike Biebermann, Gunnar Kleinau, Dirk Schnabel, et al.
Human Molecular Genetics
|
March 2, 2010
Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism
Michael R Bowl, Samantha M Mirczuk, Irina V Grigorieva, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 9, 2014
Mutational analysis of the adaptor protein 2 sigma subunit (AP2S1) gene: search for autosomal dominant hypocalcemia type 3 (ADH3)
Angela Rogers, M Andrew Nesbit, Fadil M Hannan, et al.
Kidney International
|
October 26, 2024
Presentation and outcome in carriers of pathogenic variants in SLC34A1 and SLC34A3 encoding sodium-phosphate transporter NPT 2a and 2c
Max Brunkhorst, Lena Brunkhorst, Helge Martens, et al.
The Journal of Investigative Dermatology
|
October 6, 2023
GNAQ/GNA11 Mosaicism Is Associated with Abnormal Serum Calcium Indices and Microvascular Neurocalcification
Nicole Knöpfel, Davide Zecchin, Hanna Richardson, et al.
Journal of the Endocrine Society
|
July 14, 2021
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK
Federica Buonocore, Avinaash Maharaj, Younus Qamar, et al.
American Journal of Human Genetics
|
August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay
Ronit Marom, Lindsay C Burrage, Rossella Venditti, et al.
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of 4