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Molecular Pharmaceutics
|
February 21, 2023
Photochemical Internalization Using Natural Anticancer Drugs, Antimetabolites, and Nanoformulations: A Systematic Study against Breast and Pancreatic Cancer Cell Lines
Christopher Barnett, Fanny Joubert, Alexandra Iliopoulou, et al.
Case Reports in Cardiology
|
March 5, 2020
Plaque Rupture-Induced Myocardial Infarction and Mechanical Circulatory Support in Alpha-Gal Allergy
Sohab S Radwan, Gauravpal Gill, Amre Ghazzal, et al.
Molecular Syndromology
|
June 22, 2018
Atypical Skin Manifestations in <i>FGFR2</i>-Related Craniosynostosis Syndromes Broaden the Phenotypic Spectrum
Shannon LeBlanc, David David, Alison Colley, et al.
Journal of Pediatric Surgery
|
July 4, 2009
Looking past the lump: genetic aspects of inguinal hernia in children
Christopher Barnett, Jacob C Langer, Aleksander Hinek, et al.
Clinical Imaging
|
March 7, 2022
Metastatic melanoma in the breast and axilla: A case report
Christopher Barnett, Nishi Mehta, William S Towne, et al.
American Journal of Medical Genetics. Part A
|
April 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer risk
Shannon LeBlanc, Dildeepa Naveen, Eric Haan, et al.
Experimental Gerontology
|
March 31, 2004
Effects of a reduced oxygen tension culture system on human T cell clones as a function of in vitro age
Orla Duggan, Paul Hyland, Kathryn Annett, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 22, 2004
Elimination of an immunodominant CD4+ T cell epitope in human IFN-beta does not result in an in vivo response directed at the subdominant epitope
V Peter Yeung, Judy Chang, Jeff Miller, et al.
Pediatric Dermatology
|
September 10, 2019
Novel KIT mutation presenting as marked lentiginosis
Alain K Tran, Annette Pearce, Marcos López-Sánchez, et al.
The Journal of Craniofacial Surgery
|
September 21, 2020
Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome
Sarut Chaisrisawadisuk, Elie Hammam, Cindy J Molloy, et al.
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Search research articles
Search
Showing results (11-20 of 72) with videos related to
Sort By:
Page
of 8
Molecular Pharmaceutics
|
February 21, 2023
Photochemical Internalization Using Natural Anticancer Drugs, Antimetabolites, and Nanoformulations: A Systematic Study against Breast and Pancreatic Cancer Cell Lines
Christopher Barnett, Fanny Joubert, Alexandra Iliopoulou, et al.
Case Reports in Cardiology
|
March 5, 2020
Plaque Rupture-Induced Myocardial Infarction and Mechanical Circulatory Support in Alpha-Gal Allergy
Sohab S Radwan, Gauravpal Gill, Amre Ghazzal, et al.
Molecular Syndromology
|
June 22, 2018
Atypical Skin Manifestations in <i>FGFR2</i>-Related Craniosynostosis Syndromes Broaden the Phenotypic Spectrum
Shannon LeBlanc, David David, Alison Colley, et al.
Journal of Pediatric Surgery
|
July 4, 2009
Looking past the lump: genetic aspects of inguinal hernia in children
Christopher Barnett, Jacob C Langer, Aleksander Hinek, et al.
Clinical Imaging
|
March 7, 2022
Metastatic melanoma in the breast and axilla: A case report
Christopher Barnett, Nishi Mehta, William S Towne, et al.
American Journal of Medical Genetics. Part A
|
April 18, 2020
CDH1-related blepharocheilodontic syndrome is associated with diffuse gastric cancer risk
Shannon LeBlanc, Dildeepa Naveen, Eric Haan, et al.
Experimental Gerontology
|
March 31, 2004
Effects of a reduced oxygen tension culture system on human T cell clones as a function of in vitro age
Orla Duggan, Paul Hyland, Kathryn Annett, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
May 22, 2004
Elimination of an immunodominant CD4+ T cell epitope in human IFN-beta does not result in an in vivo response directed at the subdominant epitope
V Peter Yeung, Judy Chang, Jeff Miller, et al.
Pediatric Dermatology
|
September 10, 2019
Novel KIT mutation presenting as marked lentiginosis
Alain K Tran, Annette Pearce, Marcos López-Sánchez, et al.
The Journal of Craniofacial Surgery
|
September 21, 2020
Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome
Sarut Chaisrisawadisuk, Elie Hammam, Cindy J Molloy, et al.
Page
of 8