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Annals of Neurology
|
February 3, 2004
Cerebral palsy is characterized by protein mediators in cord serum
Tuula Kaukola, Ebenezer Satyaraj, Dhavalkumar D Patel, et al.
Clinical Immunology (Orlando, Fla.)
|
March 29, 2014
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients
Sonia Caracciolo, Daniele Moratto, Mauro Giacomelli, et al.
Pediatric Pulmonology
|
March 11, 2014
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia
Johanna M Huusko, Mari Mahlman, Minna K Karjalainen, et al.
NPJ Genomic Medicine
|
April 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine
|
March 28, 2024
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action
Vaidehi Jobanputra, Brock Schroeder, Heidi L Rehm, et al.
NPJ Genomic Medicine
|
May 27, 2021
Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine
|
May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
The Journal of Emergency Medicine
|
November 8, 2011
Discriminative value of inflammatory biomarkers for suspected sepsis
Ephraim L Tsalik, L Brett Jaggers, Seth W Glickman, et al.
Genome Medicine
|
March 17, 2023
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning
Bennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, et al.
Human Mutation
|
April 8, 2015
Alström Syndrome: Mutation Spectrum of ALMS1
Jan D Marshall, Jean Muller, Gayle B Collin, et al.
Page
of 18
Search research articles
Search
Showing results (71-80 of 171) with videos related to
Sort By:
Page
of 18
Annals of Neurology
|
February 3, 2004
Cerebral palsy is characterized by protein mediators in cord serum
Tuula Kaukola, Ebenezer Satyaraj, Dhavalkumar D Patel, et al.
Clinical Immunology (Orlando, Fla.)
|
March 29, 2014
Expansion of CCR4+ activated T cells is associated with memory B cell reduction in DOCK8-deficient patients
Sonia Caracciolo, Daniele Moratto, Mauro Giacomelli, et al.
Pediatric Pulmonology
|
March 11, 2014
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasia
Johanna M Huusko, Mari Mahlman, Minna K Karjalainen, et al.
NPJ Genomic Medicine
|
April 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine
|
March 28, 2024
Advancing access to genome sequencing for rare genetic disorders: recent progress and call to action
Vaidehi Jobanputra, Brock Schroeder, Heidi L Rehm, et al.
NPJ Genomic Medicine
|
May 27, 2021
Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
NPJ Genomic Medicine
|
May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury, et al.
The Journal of Emergency Medicine
|
November 8, 2011
Discriminative value of inflammatory biomarkers for suspected sepsis
Ephraim L Tsalik, L Brett Jaggers, Seth W Glickman, et al.
Genome Medicine
|
March 17, 2023
Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning
Bennet Peterson, Edgar Javier Hernandez, Charlotte Hobbs, et al.
Human Mutation
|
April 8, 2015
Alström Syndrome: Mutation Spectrum of ALMS1
Jan D Marshall, Jean Muller, Gayle B Collin, et al.
Page
of 18