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JAMA Dermatology
|
June 12, 2024
Skin Manifestations of VEXAS Syndrome and Associated Genotypes
Isabella J Tan, Marcela A Ferrada, Serene Ahmad, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
December 16, 2015
Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome
Anja K Büscher, Bodo B Beck, Anette Melk, et al.
Plos One
|
November 16, 2018
Long-term effects of smallpox vaccination on expression of the HIV-1 co-receptor CCR5 in women
K B Beck, B L Hønge, J S Olesen, et al.
Kidney International Reports
|
May 20, 2021
Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo Signaling
Francesca Fabretti, Nikolai Tschernoster, Florian Erger, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
September 21, 2025
Clinical Manifestations of VEXAS Syndrome Across a Broad Spectrum of UBA1 Mutation Burden
Meghan Anderson, Defne Ercelen, Ashley Richardson, et al.
Journal of Clinical Medicine
|
February 27, 2026
PAXIS: A Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Phase 2 Study (Part 1) Followed by an Open-Label Period (Part 2) to Assess the Efficacy and Safety of Pacritinib in Patients with VEXAS Syndrome
David B Beck, Maël Heiblig, Sinisa Savic, et al.
Rheumatology (Oxford, England)
|
March 29, 2024
Description of a novel splice site variant in UBA1 gene causing VEXAS syndrome
Daniela Ospina Cardona, Ignasi Rodriguez-Pinto, Sonia Iosim, et al.
The Journal of Molecular Diagnostics : JMD
|
April 10, 2022
Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted Sequencing
Nikolai Tschernoster, Florian Erger, Patrick R Walsh, et al.
Kidney International
|
November 6, 2019
Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up
Sander F Garrelfs, Gill Rumsby, Hessel Peters-Sengers, et al.
Frontiers in Neuroscience
|
November 16, 2020
Human iPSC-Derived Neuronal Cells From <i>CTBP1</i>-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene Networks
S Vijayalingam, Uthayashanker R Ezekiel, Fenglian Xu, et al.
Page
of 72
Search research articles
Search
Showing results (621-630 of 718) with videos related to
Sort By:
Page
of 72
JAMA Dermatology
|
June 12, 2024
Skin Manifestations of VEXAS Syndrome and Associated Genotypes
Isabella J Tan, Marcela A Ferrada, Serene Ahmad, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
December 16, 2015
Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid-Resistant Nephrotic Syndrome
Anja K Büscher, Bodo B Beck, Anette Melk, et al.
Plos One
|
November 16, 2018
Long-term effects of smallpox vaccination on expression of the HIV-1 co-receptor CCR5 in women
K B Beck, B L Hønge, J S Olesen, et al.
Kidney International Reports
|
May 20, 2021
Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo Signaling
Francesca Fabretti, Nikolai Tschernoster, Florian Erger, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
September 21, 2025
Clinical Manifestations of VEXAS Syndrome Across a Broad Spectrum of UBA1 Mutation Burden
Meghan Anderson, Defne Ercelen, Ashley Richardson, et al.
Journal of Clinical Medicine
|
February 27, 2026
PAXIS: A Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Phase 2 Study (Part 1) Followed by an Open-Label Period (Part 2) to Assess the Efficacy and Safety of Pacritinib in Patients with VEXAS Syndrome
David B Beck, Maël Heiblig, Sinisa Savic, et al.
Rheumatology (Oxford, England)
|
March 29, 2024
Description of a novel splice site variant in UBA1 gene causing VEXAS syndrome
Daniela Ospina Cardona, Ignasi Rodriguez-Pinto, Sonia Iosim, et al.
The Journal of Molecular Diagnostics : JMD
|
April 10, 2022
Unraveling Structural Rearrangements of the CFH Gene Cluster in Atypical Hemolytic Uremic Syndrome Patients Using Molecular Combing and Long-Fragment Targeted Sequencing
Nikolai Tschernoster, Florian Erger, Patrick R Walsh, et al.
Kidney International
|
November 6, 2019
Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up
Sander F Garrelfs, Gill Rumsby, Hessel Peters-Sengers, et al.
Frontiers in Neuroscience
|
November 16, 2020
Human iPSC-Derived Neuronal Cells From <i>CTBP1</i>-Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene Networks
S Vijayalingam, Uthayashanker R Ezekiel, Fenglian Xu, et al.
Page
of 72