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American Journal of Rhinology & Allergy
|
September 20, 2024
Association Between Smell Loss, Disease Burden, and Dupilumab Efficacy in Chronic Rhinosinusitis with Nasal Polyps
Zachary M Soler, Zara M Patel, Joaquim Mullol, et al.
Epigenomics
|
October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns
Mohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 13, 2025
Refining Aicardi Syndrome diagnostic Criteria: an expert-based consensus using a modified Delphi approach
Silvia Masnada, Valentina De Giorgis, Umberto Carugo, et al.
The Lancet. Respiratory Medicine
|
October 1, 2025
Dupilumab versus omalizumab in patients with chronic rhinosinusitis with nasal polyps and coexisting asthma (EVEREST): a multicentre, randomised, double-blind, head-to-head phase 4 trial
Eugenio De Corso, G Walter Canonica, Enrico Heffler, et al.
Human Mutation
|
September 10, 2015
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability
Detelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, et al.
European Journal of Human Genetics : EJHG
|
December 24, 2009
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
Anna Hackett, Patrick S Tarpey, Andrea Licata, et al.
The British Journal of Dermatology
|
May 24, 2022
Biomarkers of systemic treatment response in people with psoriasis: a scoping review
Mark Corbett, Ravi Ramessur, David Marshall, et al.
The British Journal of Dermatology
|
April 28, 2022
Biomarkers of disease progression in people with psoriasis: a scoping review
Ravi Ramessur, Mark Corbett, David Marshall, et al.
Human Molecular Genetics
|
July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency
Chuan Tan, Chloe Shard, Enzo Ranieri, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
February 16, 2023
Accelerating Food Allergy Research: Need for a Data Commons
Ruchi S Gupta, Shruti Sehgal, Mark Wlodarski, et al.
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of 9
Search research articles
Search
Showing results (61-70 of 82) with videos related to
Sort By:
Page
of 9
American Journal of Rhinology & Allergy
|
September 20, 2024
Association Between Smell Loss, Disease Burden, and Dupilumab Efficacy in Chronic Rhinosinusitis with Nasal Polyps
Zachary M Soler, Zara M Patel, Joaquim Mullol, et al.
Epigenomics
|
October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns
Mohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 13, 2025
Refining Aicardi Syndrome diagnostic Criteria: an expert-based consensus using a modified Delphi approach
Silvia Masnada, Valentina De Giorgis, Umberto Carugo, et al.
The Lancet. Respiratory Medicine
|
October 1, 2025
Dupilumab versus omalizumab in patients with chronic rhinosinusitis with nasal polyps and coexisting asthma (EVEREST): a multicentre, randomised, double-blind, head-to-head phase 4 trial
Eugenio De Corso, G Walter Canonica, Enrico Heffler, et al.
Human Mutation
|
September 10, 2015
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability
Detelina Grozeva, Keren Carss, Olivera Spasic-Boskovic, et al.
European Journal of Human Genetics : EJHG
|
December 24, 2009
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
Anna Hackett, Patrick S Tarpey, Andrea Licata, et al.
The British Journal of Dermatology
|
May 24, 2022
Biomarkers of systemic treatment response in people with psoriasis: a scoping review
Mark Corbett, Ravi Ramessur, David Marshall, et al.
The British Journal of Dermatology
|
April 28, 2022
Biomarkers of disease progression in people with psoriasis: a scoping review
Ravi Ramessur, Mark Corbett, David Marshall, et al.
Human Molecular Genetics
|
July 1, 2015
Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency
Chuan Tan, Chloe Shard, Enzo Ranieri, et al.
The Journal of Allergy and Clinical Immunology. in Practice
|
February 16, 2023
Accelerating Food Allergy Research: Need for a Data Commons
Ruchi S Gupta, Shruti Sehgal, Mark Wlodarski, et al.
Page
of 9