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Intensive Care Medicine
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January 12, 2026
Temporary mechanical support in fulminant myocarditis: prognostic factors and clinical implications from the FULLMOON study
Matthieu Schmidt, Maharajah Ponnaiah, Florent Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 6, 2018
Putting genome-wide sequencing in neonates into perspective
Pleuntje J van der Sluijs, Emmelien Aten, Daniela Q C M Barge-Schaapveld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 7, 2021
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
Daniel L Polla, Mohammad Ali Farazi Fard, Zahra Tabatabaei, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making
Daphne J Smits, Federico Ferraro, Mark Drost, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 25, 2019
Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia
Lieke H H Meeter, Rebecca M E Steketee, Dina Salkovic, et al.
Nature Communications
|
March 16, 2022
Tau deposition patterns are associated with functional connectivity in primary tauopathies
Nicolai Franzmeier, Matthias Brendel, Leonie Beyer, et al.
Plos One
|
September 13, 2019
The epidemiological signature of influenza B virus and its B/Victoria and B/Yamagata lineages in the 21st century
Saverio Caini, Gabriela Kusznierz, Verònica Vera Garate, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 16, 2025
Missense variants in <i>TUBA4A</i> cause myo-tubulinopathies
Mridul Johari, Chiara Folland, Yoshihiko Saito, et al.
HGG Advances
|
September 24, 2025
Routine RNA-based analysis of potential splicing variants facilitates genomic diagnostics and reveals limitations of in silico prediction tools
Mark Drost, Jordy Dekker, Federico Ferraro, et al.
Brain : a Journal of Neurology
|
September 15, 2023
TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions
Hashem Almousa, Sara A Lewis, Somayeh Bakhtiari, et al.
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of 108
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Showing results (1061-1070 of 1,079) with videos related to
Sort By:
Page
of 108
Intensive Care Medicine
|
January 12, 2026
Temporary mechanical support in fulminant myocarditis: prognostic factors and clinical implications from the FULLMOON study
Matthieu Schmidt, Maharajah Ponnaiah, Florent Huang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 6, 2018
Putting genome-wide sequencing in neonates into perspective
Pleuntje J van der Sluijs, Emmelien Aten, Daniela Q C M Barge-Schaapveld, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 7, 2021
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder
Daniel L Polla, Mohammad Ali Farazi Fard, Zahra Tabatabaei, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2025
Nanopore long-read sequencing for the critically ill facilitates ultrarapid diagnostics and urgent clinical decision making
Daphne J Smits, Federico Ferraro, Mark Drost, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 25, 2019
Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia
Lieke H H Meeter, Rebecca M E Steketee, Dina Salkovic, et al.
Nature Communications
|
March 16, 2022
Tau deposition patterns are associated with functional connectivity in primary tauopathies
Nicolai Franzmeier, Matthias Brendel, Leonie Beyer, et al.
Plos One
|
September 13, 2019
The epidemiological signature of influenza B virus and its B/Victoria and B/Yamagata lineages in the 21st century
Saverio Caini, Gabriela Kusznierz, Verònica Vera Garate, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 16, 2025
Missense variants in <i>TUBA4A</i> cause myo-tubulinopathies
Mridul Johari, Chiara Folland, Yoshihiko Saito, et al.
HGG Advances
|
September 24, 2025
Routine RNA-based analysis of potential splicing variants facilitates genomic diagnostics and reveals limitations of in silico prediction tools
Mark Drost, Jordy Dekker, Federico Ferraro, et al.
Brain : a Journal of Neurology
|
September 15, 2023
TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions
Hashem Almousa, Sara A Lewis, Somayeh Bakhtiari, et al.
Page
of 108