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AIDS Care
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September 30, 2025
Awareness, acceptance, and impact of undetectable equals untransmittable (U = U) among people living with HIV across Canada
Alex Tran, James R Watson, Jason M Lo Hog Tian, et al.
Cancer
|
December 8, 2016
Synuclein-γ in uterine serous carcinoma impacts survival: An NRG Oncology/Gynecologic Oncology Group study
Abigail D Winder, Kruti P Maniar, Jian-Jun Wei, et al.
Journal of Child Neurology
|
June 25, 2020
Management of Infantile Spasms During the COVID-19 Pandemic
Zachary M Grinspan, John R Mytinger, Fiona M Baumer, et al.
Cell Host & Microbe
|
February 12, 2022
Mutations in SARS-CoV-2 variants of concern link to increased spike cleavage and virus transmission
Alba Escalera, Ana S Gonzalez-Reiche, Sadaf Aslam, et al.
Mitochondrion
|
July 30, 2013
Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, et al.
Neurology
|
March 12, 2026
International Consensus on the Evaluation and Management of Hypothalamic Hamartomas: Results From a Modified Delphi Survey
Nathan T Cohen, Xiaotong Li, Madison M Berl, et al.
Journal of Inherited Metabolic Disease
|
November 17, 2020
Consensus guidelines for the diagnosis and management of pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency
Curtis R Coughlin, Laura A Tseng, Jose E Abdenur, et al.
The Lancet. Diabetes & Endocrinology
|
December 21, 2023
Bringing an end to diabetes stigma and discrimination: an international consensus statement on evidence and recommendations
Jane Speight, Elizabeth Holmes-Truscott, Matthew Garza, et al.
Molecular Genetics and Metabolism
|
June 22, 2023
Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes
Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, et al.
American Journal of Human Genetics
|
April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
Heather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
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of 68
Search research articles
Search
Showing results (661-670 of 674) with videos related to
Sort By:
Page
of 68
AIDS Care
|
September 30, 2025
Awareness, acceptance, and impact of undetectable equals untransmittable (U = U) among people living with HIV across Canada
Alex Tran, James R Watson, Jason M Lo Hog Tian, et al.
Cancer
|
December 8, 2016
Synuclein-γ in uterine serous carcinoma impacts survival: An NRG Oncology/Gynecologic Oncology Group study
Abigail D Winder, Kruti P Maniar, Jian-Jun Wei, et al.
Journal of Child Neurology
|
June 25, 2020
Management of Infantile Spasms During the COVID-19 Pandemic
Zachary M Grinspan, John R Mytinger, Fiona M Baumer, et al.
Cell Host & Microbe
|
February 12, 2022
Mutations in SARS-CoV-2 variants of concern link to increased spike cleavage and virus transmission
Alba Escalera, Ana S Gonzalez-Reiche, Sadaf Aslam, et al.
Mitochondrion
|
July 30, 2013
Practice patterns of mitochondrial disease physicians in North America. Part 1: diagnostic and clinical challenges
Sumit Parikh, Amy Goldstein, Mary Kay Koenig, et al.
Neurology
|
March 12, 2026
International Consensus on the Evaluation and Management of Hypothalamic Hamartomas: Results From a Modified Delphi Survey
Nathan T Cohen, Xiaotong Li, Madison M Berl, et al.
Journal of Inherited Metabolic Disease
|
November 17, 2020
Consensus guidelines for the diagnosis and management of pyridoxine-dependent epilepsy due to α-aminoadipic semialdehyde dehydrogenase deficiency
Curtis R Coughlin, Laura A Tseng, Jose E Abdenur, et al.
The Lancet. Diabetes & Endocrinology
|
December 21, 2023
Bringing an end to diabetes stigma and discrimination: an international consensus statement on evidence and recommendations
Jane Speight, Elizabeth Holmes-Truscott, Matthew Garza, et al.
Molecular Genetics and Metabolism
|
June 22, 2023
Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes
Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, et al.
American Journal of Human Genetics
|
April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis
Heather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Page
of 68