Search research articles
Contact Us
Filters
Showing results (201-210 of 287) with videos related to
Page
of 29
Sort By:
The Journal of Clinical Investigation
|
July 30, 2024
Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery
Benjamin J Landis, Benjamin M Helm, Matthew D Durbin, et al.
Gynecologic Oncology
|
July 25, 2018
Patient reported outcomes in evaluation of chemotherapy toxicity in women with gynecologic malignancies: A pilot study
Emily M Webster, William M Burke, Hannah M Ware, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
July 24, 2023
Distinct CRTH2+CD161+ (peTh2) memory CD4+ T-cell cytokine profiles in food allergy and eosinophilic gastrointestinal disorders
Michelle A Makiya, Thomas Brown, Nicole Holland, et al.
Plos One
|
June 2, 2023
Spatial variation and antecedent sea surface temperature conditions influence Hawaiian intertidal community structure
Rebecca J Ward, T Erin Cox, Anuschka Faucci, et al.
Molecular Genetics & Genomic Medicine
|
November 26, 2024
Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Benjamin M Helm, Lindsey R Helvaty, Erin Conboy, et al.
The Journal of Allergy and Clinical Immunology
|
August 31, 2013
Marked and persistent eosinophilia in the absence of clinical manifestations
Yun-Yun K Chen, Paneez Khoury, JeanAnne M Ware, et al.
Pediatric Research
|
January 7, 2026
Variant burden and severity of cardiomyopathy in patients with DMD-related Duchenne muscular dystrophy
Gabrielle C Geddes, Stephanie M Ware, Tae-Hwi Schwantes-An, et al.
Allergy
|
January 23, 2016
Clinical features predict responsiveness to imatinib in platelet-derived growth factor receptor-alpha-negative hypereosinophilic syndrome
P Khoury, R Desmond, A Pabon, et al.
Clinical Dysmorphology
|
September 14, 2020
Chromosome 4q28.3q32.3 duplication in a patient with lymphatic malformations, craniosynostosis, and dysmorphic features
Eric S Traub, Sarah E Sheppard, Yoav Dori, et al.
Heart Rhythm
|
September 28, 2014
Novel Timothy syndrome mutation leading to increase in CACNA1C window current
Nicole J Boczek, Erin M Miller, Dan Ye, et al.
Page
of 29
Search research articles
Search
Showing results (201-210 of 287) with videos related to
Sort By:
Page
of 29
The Journal of Clinical Investigation
|
July 30, 2024
Early ascertainment of genetic diagnoses clarifies impact on medium-term survival following neonatal congenital heart surgery
Benjamin J Landis, Benjamin M Helm, Matthew D Durbin, et al.
Gynecologic Oncology
|
July 25, 2018
Patient reported outcomes in evaluation of chemotherapy toxicity in women with gynecologic malignancies: A pilot study
Emily M Webster, William M Burke, Hannah M Ware, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
July 24, 2023
Distinct CRTH2+CD161+ (peTh2) memory CD4+ T-cell cytokine profiles in food allergy and eosinophilic gastrointestinal disorders
Michelle A Makiya, Thomas Brown, Nicole Holland, et al.
Plos One
|
June 2, 2023
Spatial variation and antecedent sea surface temperature conditions influence Hawaiian intertidal community structure
Rebecca J Ward, T Erin Cox, Anuschka Faucci, et al.
Molecular Genetics & Genomic Medicine
|
November 26, 2024
Performance of Dysmorphology-Based Screening for Genetic Disorders in Pediatric Congenital Heart Disease Supports Wider Genetic Testing
Benjamin M Helm, Lindsey R Helvaty, Erin Conboy, et al.
The Journal of Allergy and Clinical Immunology
|
August 31, 2013
Marked and persistent eosinophilia in the absence of clinical manifestations
Yun-Yun K Chen, Paneez Khoury, JeanAnne M Ware, et al.
Pediatric Research
|
January 7, 2026
Variant burden and severity of cardiomyopathy in patients with DMD-related Duchenne muscular dystrophy
Gabrielle C Geddes, Stephanie M Ware, Tae-Hwi Schwantes-An, et al.
Allergy
|
January 23, 2016
Clinical features predict responsiveness to imatinib in platelet-derived growth factor receptor-alpha-negative hypereosinophilic syndrome
P Khoury, R Desmond, A Pabon, et al.
Clinical Dysmorphology
|
September 14, 2020
Chromosome 4q28.3q32.3 duplication in a patient with lymphatic malformations, craniosynostosis, and dysmorphic features
Eric S Traub, Sarah E Sheppard, Yoav Dori, et al.
Heart Rhythm
|
September 28, 2014
Novel Timothy syndrome mutation leading to increase in CACNA1C window current
Nicole J Boczek, Erin M Miller, Dan Ye, et al.
Page
of 29