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The Journal of Clinical Endocrinology and Metabolism
|
October 7, 2016
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline
Rebecca J Brown, David Araujo-Vilar, Pik To Cheung, et al.
American Journal of Human Genetics
|
June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations
Jennifer J Johnston, Katie L Lewis, David Ng, et al.
Medicine
|
March 18, 2008
Predictors of acquired lipodystrophy in juvenile-onset dermatomyositis and a gradient of severity
April Bingham, Gulnara Mamyrova, Kristina I Rother, et al.
The American Journal of Clinical Nutrition
|
December 10, 2020
NIH Workshop Report: sensory nutrition and disease
Danielle R Reed, Amber L Alhadeff, Gary K Beauchamp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 2, 2018
Safety and efficacy of low-dose sirolimus in the PIK3CA-related overgrowth spectrum
Victoria E R Parker, Kim M Keppler-Noreuil, Laurence Faivre, et al.
The Journal of Clinical Investigation
|
February 2, 2016
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production
Anja Brehm, Yin Liu, Afzal Sheikh, et al.
The Journal of Clinical Investigation
|
November 3, 2015
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production
Anja Brehm, Yin Liu, Afzal Sheikh, et al.
The Journal of Clinical Investigation
|
April 13, 2018
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies
Gina A Montealegre Sanchez, Adam Reinhardt, Suzanne Ramsey, et al.
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of 13
Search research articles
Search
Showing results (121-130 of 128) with videos related to
Sort By:
Page
of 13
You have reached the last page of results.
This site can display upto 128 results.
The Journal of Clinical Endocrinology and Metabolism
|
October 7, 2016
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline
Rebecca J Brown, David Araujo-Vilar, Pik To Cheung, et al.
American Journal of Human Genetics
|
June 6, 2015
Individualized iterative phenotyping for genome-wide analysis of loss-of-function mutations
Jennifer J Johnston, Katie L Lewis, David Ng, et al.
Medicine
|
March 18, 2008
Predictors of acquired lipodystrophy in juvenile-onset dermatomyositis and a gradient of severity
April Bingham, Gulnara Mamyrova, Kristina I Rother, et al.
The American Journal of Clinical Nutrition
|
December 10, 2020
NIH Workshop Report: sensory nutrition and disease
Danielle R Reed, Amber L Alhadeff, Gary K Beauchamp, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 2, 2018
Safety and efficacy of low-dose sirolimus in the PIK3CA-related overgrowth spectrum
Victoria E R Parker, Kim M Keppler-Noreuil, Laurence Faivre, et al.
The Journal of Clinical Investigation
|
February 2, 2016
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production
Anja Brehm, Yin Liu, Afzal Sheikh, et al.
The Journal of Clinical Investigation
|
November 3, 2015
Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production
Anja Brehm, Yin Liu, Afzal Sheikh, et al.
The Journal of Clinical Investigation
|
April 13, 2018
JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies
Gina A Montealegre Sanchez, Adam Reinhardt, Suzanne Ramsey, et al.
Page
of 13