Search research articles
Contact Us
Filters
Showing results (371-380 of 606) with videos related to
Page
of 61
Sort By:
Human Mutation
|
July 26, 2012
ALX4 gain-of-function mutations in nonsyndromic craniosynostosis
Garima Yagnik, Apar Ghuman, Sundon Kim, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
May 11, 2016
Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal Period
Yair J Blumenfeld, Alexis S Davis, Susan R Hintz, et al.
The Journal of Allergy and Clinical Immunology
|
August 13, 2021
Developing a standardized approach for assessing mast cells and eosinophils on tissue biopsies: A Work Group Report of the AAAAI Allergic Skin Diseases Committee
Nives Zimmermann, J Pablo Abonia, Stephen C Dreskin, et al.
The British Journal of Dermatology
|
February 17, 2024
Benralizumab does not elicit therapeutic effect in patients with chronic spontaneous urticaria: results from the phase IIb multinational randomized double-blind placebo-controlled ARROYO trial
Sabine Altrichter, Ana Maria Giménez-Arnau, Jonathan A Bernstein, et al.
The Journal of Allergy and Clinical Immunology
|
July 22, 2015
Defects of B-cell terminal differentiation in patients with type-1 Kabuki syndrome
Andrew W Lindsley, Howard M Saal, Thomas A Burrow, et al.
Nature Communications
|
December 10, 2015
Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant
Enrico Leipold, Andrea Hanson-Kahn, Miya Frick, et al.
American Journal of Medical Genetics. Part A
|
August 18, 2017
Clinical and molecular characterization of de novo loss of function variants in HNRNPU
Magalie S Leduc, Hsiao-Tuan Chao, Chunjing Qu, et al.
Human Mutation
|
September 24, 2017
Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype
Li Chen, Philip J Jensik, Joseph T Alaimo, et al.
JAMA Dermatology
|
February 18, 2026
Dupilumab in Patients With Chronic Spontaneous Urticaria: Phase 3 LIBERTY-CSU CUPID Randomized Clinical Trials
Thomas B Casale, Sarbjit S Saini, Moshe Ben-Shoshan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 8, 2022
A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network
Rebecca C Spillmann, Queenie K-G Tan, Chloe Reuter, et al.
Page
of 61
Search research articles
Search
Showing results (371-380 of 606) with videos related to
Sort By:
Page
of 61
Human Mutation
|
July 26, 2012
ALX4 gain-of-function mutations in nonsyndromic craniosynostosis
Garima Yagnik, Apar Ghuman, Sundon Kim, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine
|
May 11, 2016
Prenatally Diagnosed Cases of Binder Phenotype Complicated by Respiratory Distress in the Immediate Postnatal Period
Yair J Blumenfeld, Alexis S Davis, Susan R Hintz, et al.
The Journal of Allergy and Clinical Immunology
|
August 13, 2021
Developing a standardized approach for assessing mast cells and eosinophils on tissue biopsies: A Work Group Report of the AAAAI Allergic Skin Diseases Committee
Nives Zimmermann, J Pablo Abonia, Stephen C Dreskin, et al.
The British Journal of Dermatology
|
February 17, 2024
Benralizumab does not elicit therapeutic effect in patients with chronic spontaneous urticaria: results from the phase IIb multinational randomized double-blind placebo-controlled ARROYO trial
Sabine Altrichter, Ana Maria Giménez-Arnau, Jonathan A Bernstein, et al.
The Journal of Allergy and Clinical Immunology
|
July 22, 2015
Defects of B-cell terminal differentiation in patients with type-1 Kabuki syndrome
Andrew W Lindsley, Howard M Saal, Thomas A Burrow, et al.
Nature Communications
|
December 10, 2015
Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant
Enrico Leipold, Andrea Hanson-Kahn, Miya Frick, et al.
American Journal of Medical Genetics. Part A
|
August 18, 2017
Clinical and molecular characterization of de novo loss of function variants in HNRNPU
Magalie S Leduc, Hsiao-Tuan Chao, Chunjing Qu, et al.
Human Mutation
|
September 24, 2017
Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype
Li Chen, Philip J Jensik, Joseph T Alaimo, et al.
JAMA Dermatology
|
February 18, 2026
Dupilumab in Patients With Chronic Spontaneous Urticaria: Phase 3 LIBERTY-CSU CUPID Randomized Clinical Trials
Thomas B Casale, Sarbjit S Saini, Moshe Ben-Shoshan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 8, 2022
A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network
Rebecca C Spillmann, Queenie K-G Tan, Chloe Reuter, et al.
Page
of 61