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American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs
Tess Levy, Cristan Farmer, Siddharth Srivastava, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 6, 2018
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis
Cole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
December 20, 2023
Once-Daily Oral Berotralstat for Long-Term Prophylaxis of Hereditary Angioedema: The Open-Label Extension of the APeX-2 Randomized Trial
Sorena Kiani-Alikhan, Richard Gower, Timothy Craig, et al.
Biorxiv : the Preprint Server for Biology
|
June 12, 2025
Biomni: A General-Purpose Biomedical AI Agent
Kexin Huang, Serena Zhang, Hanchen Wang, et al.
Human Molecular Genetics
|
September 24, 2021
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, et al.
Journal of Inherited Metabolic Disease
|
July 2, 2024
MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deterioration
Nicole Hammann, Dominic Lenz, Alyssa Bianzano, et al.
Orphanet Journal of Rare Diseases
|
February 16, 2021
Long-term health-related quality of life in patients treated with subcutaneous C1-inhibitor replacement therapy for the prevention of hereditary angioedema attacks: findings from the COMPACT open-label extension study
William R Lumry, Bruce Zuraw, Marco Cicardi, et al.
The Journal of Allergy and Clinical Immunology
|
April 29, 2014
The diagnosis and management of acute and chronic urticaria: 2014 update
Jonathan A Bernstein, David M Lang, David A Khan, et al.
Advances in Therapy
|
June 12, 2025
Sustained Effectiveness, Tolerability, and Safety of Long-Term Prophylaxis with Lanadelumab in Hereditary Angioedema: The Prospective, Phase 4, Noninterventional EMPOWER Real-World Study
Jonathan A Bernstein, Stephen D Betschel, Paula J Busse, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
February 3, 2018
Health-Related Quality of Life with Subcutaneous C1-Inhibitor for Prevention of Attacks of Hereditary Angioedema
William R Lumry, Timothy Craig, Bruce Zuraw, et al.
Page
of 61
Search research articles
Search
Showing results (451-460 of 606) with videos related to
Sort By:
Page
of 61
American Journal on Intellectual and Developmental Disabilities
|
August 26, 2025
Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs
Tess Levy, Cristan Farmer, Siddharth Srivastava, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 6, 2018
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis
Cole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
December 20, 2023
Once-Daily Oral Berotralstat for Long-Term Prophylaxis of Hereditary Angioedema: The Open-Label Extension of the APeX-2 Randomized Trial
Sorena Kiani-Alikhan, Richard Gower, Timothy Craig, et al.
Biorxiv : the Preprint Server for Biology
|
June 12, 2025
Biomni: A General-Purpose Biomedical AI Agent
Kexin Huang, Serena Zhang, Hanchen Wang, et al.
Human Molecular Genetics
|
September 24, 2021
Strong evidence for genotype-phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium
Tess Levy, Jennifer H Foss-Feig, Catalina Betancur, et al.
Journal of Inherited Metabolic Disease
|
July 2, 2024
MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deterioration
Nicole Hammann, Dominic Lenz, Alyssa Bianzano, et al.
Orphanet Journal of Rare Diseases
|
February 16, 2021
Long-term health-related quality of life in patients treated with subcutaneous C1-inhibitor replacement therapy for the prevention of hereditary angioedema attacks: findings from the COMPACT open-label extension study
William R Lumry, Bruce Zuraw, Marco Cicardi, et al.
The Journal of Allergy and Clinical Immunology
|
April 29, 2014
The diagnosis and management of acute and chronic urticaria: 2014 update
Jonathan A Bernstein, David M Lang, David A Khan, et al.
Advances in Therapy
|
June 12, 2025
Sustained Effectiveness, Tolerability, and Safety of Long-Term Prophylaxis with Lanadelumab in Hereditary Angioedema: The Prospective, Phase 4, Noninterventional EMPOWER Real-World Study
Jonathan A Bernstein, Stephen D Betschel, Paula J Busse, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
February 3, 2018
Health-Related Quality of Life with Subcutaneous C1-Inhibitor for Prevention of Attacks of Hereditary Angioedema
William R Lumry, Timothy Craig, Bruce Zuraw, et al.
Page
of 61