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Journal of Clinical Medicine
|
December 23, 2022
Incidence and Severity of Community- and Hospital-Acquired Hyponatremia in Pediatrics
J M Rius-Peris, P Tambe, M Chilet Sáez, et al.
Revista De Salud Publica (Bogota, Colombia)
|
May 16, 2007
[Displaced and local children's alimentary patterns and nutritional state in Piedecuesta, Colombia]
Edna M Gamboa-Delgado, Nahyr López-Barbosa, Lina M Vera-Cala, et al.
Journal of Clinical Microbiology
|
October 23, 2015
Evaluation of the Lyra Direct Strep Assay To Detect Group A Streptococcus and Group C and G Beta-Hemolytic Streptococcus from Pharyngeal Specimens
Bobby L Boyanton, Elizabeth M Darnell, Anne E Prada, et al.
Nephron
|
March 30, 2025
Further Clinical and Biochemical Phenotype of GLA p.A143T: A Fabry Disease Newborn Screening Experience
Allison M Paltzer, Allegra M Quadri, Carly Rasmussen, et al.
American Journal of Medical Genetics. Part A
|
October 3, 2025
A Collaborative Approach to Pediatric Genetic Evaluation in the Era of Genomic Medicine
Sarah Jurgensmeyer Langas, Allison Goetsch Weisman, Valerie Allegretti, et al.
Developmental Biology
|
March 29, 2021
A role for sustained MAPK activity in the mouse ventral telencephalon
Mary Jo Talley, Diana Nardini, Shenyue Qin, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2011
Lethal presentation of neurofibromatosis and Noonan syndrome
Carlos E Prada, Yuri A Zarate, Sean Hagenbuch, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2024
Presentation of ichthyosis after substrate reduction therapy in Gaucher type 1
Jack Herbster, Carlos E Prada, Carly A Rasmussen, et al.
Frontiers in Cell and Developmental Biology
|
July 5, 2021
Generation of a Mouse Model to Study the Noonan Syndrome Gene <i>Lztr1</i> in the Telencephalon
Mary Jo Talley, Diana Nardini, Nisha Shabbir, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2023
Clinical and ocular abnormalities in DEGCAGS syndrome-Developmental delay with gastrointestinal, cardiovascular, genitourinary, and skeletal abnormalities
Syed M Ali, Dua A AlMasri, Carlos E Prada, et al.
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of 16
Search research articles
Search
Showing results (41-50 of 155) with videos related to
Sort By:
Page
of 16
Journal of Clinical Medicine
|
December 23, 2022
Incidence and Severity of Community- and Hospital-Acquired Hyponatremia in Pediatrics
J M Rius-Peris, P Tambe, M Chilet Sáez, et al.
Revista De Salud Publica (Bogota, Colombia)
|
May 16, 2007
[Displaced and local children's alimentary patterns and nutritional state in Piedecuesta, Colombia]
Edna M Gamboa-Delgado, Nahyr López-Barbosa, Lina M Vera-Cala, et al.
Journal of Clinical Microbiology
|
October 23, 2015
Evaluation of the Lyra Direct Strep Assay To Detect Group A Streptococcus and Group C and G Beta-Hemolytic Streptococcus from Pharyngeal Specimens
Bobby L Boyanton, Elizabeth M Darnell, Anne E Prada, et al.
Nephron
|
March 30, 2025
Further Clinical and Biochemical Phenotype of GLA p.A143T: A Fabry Disease Newborn Screening Experience
Allison M Paltzer, Allegra M Quadri, Carly Rasmussen, et al.
American Journal of Medical Genetics. Part A
|
October 3, 2025
A Collaborative Approach to Pediatric Genetic Evaluation in the Era of Genomic Medicine
Sarah Jurgensmeyer Langas, Allison Goetsch Weisman, Valerie Allegretti, et al.
Developmental Biology
|
March 29, 2021
A role for sustained MAPK activity in the mouse ventral telencephalon
Mary Jo Talley, Diana Nardini, Shenyue Qin, et al.
American Journal of Medical Genetics. Part A
|
May 14, 2011
Lethal presentation of neurofibromatosis and Noonan syndrome
Carlos E Prada, Yuri A Zarate, Sean Hagenbuch, et al.
American Journal of Medical Genetics. Part A
|
August 5, 2024
Presentation of ichthyosis after substrate reduction therapy in Gaucher type 1
Jack Herbster, Carlos E Prada, Carly A Rasmussen, et al.
Frontiers in Cell and Developmental Biology
|
July 5, 2021
Generation of a Mouse Model to Study the Noonan Syndrome Gene <i>Lztr1</i> in the Telencephalon
Mary Jo Talley, Diana Nardini, Nisha Shabbir, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2023
Clinical and ocular abnormalities in DEGCAGS syndrome-Developmental delay with gastrointestinal, cardiovascular, genitourinary, and skeletal abnormalities
Syed M Ali, Dua A AlMasri, Carlos E Prada, et al.
Page
of 16