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The New England Journal of Medicine
|
October 30, 2009
Human dectin-1 deficiency and mucocutaneous fungal infections
Bart Ferwerda, Gerben Ferwerda, Theo S Plantinga, et al.
British Journal of Cancer
|
July 15, 2016
FAM19A4 methylation analysis in self-samples compared with cervical scrapes for detecting cervical (pre)cancer in HPV-positive women
Roosmarijn Luttmer, Lise M A De Strooper, Maaike G Dijkstra, et al.
Acta Neuropathologica
|
March 31, 2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
Jan Verheijen, Tobi Van den Bossche, Julie van der Zee, et al.
American Journal of Human Genetics
|
October 24, 2003
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy
Jan Senderek, Carsten Bergmann, Claudia Stendel, et al.
Nature
|
August 25, 2017
Epitaxy of advanced nanowire quantum devices
Sasa Gazibegovic, Diana Car, Hao Zhang, et al.
Lancet (London, England)
|
September 6, 2014
Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years: 4-year interim follow-up of the phase 3, double-blind, randomised controlled VIVIANE study
S Rachel Skinner, Anne Szarewski, Barbara Romanowski, et al.
Neurobiology of Aging
|
November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
Jan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Intensive Care Medicine Experimental
|
September 18, 2022
Development and validation of an early warning model for hospitalized COVID-19 patients: a multi-center retrospective cohort study
Jim M Smit, Jesse H Krijthe, Andrei N Tintu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 20, 2016
Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency
Simone Olgiati, Matej Skorvanek, Marialuisa Quadri, et al.
Nature Communications
|
October 7, 2024
Transcript errors generate amyloid-like proteins in huwman cells
Claire S Chung, Yi Kou, Sarah J Shemtov, et al.
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of 101
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Showing results (971-980 of 1,005) with videos related to
Sort By:
Page
of 101
The New England Journal of Medicine
|
October 30, 2009
Human dectin-1 deficiency and mucocutaneous fungal infections
Bart Ferwerda, Gerben Ferwerda, Theo S Plantinga, et al.
British Journal of Cancer
|
July 15, 2016
FAM19A4 methylation analysis in self-samples compared with cervical scrapes for detecting cervical (pre)cancer in HPV-positive women
Roosmarijn Luttmer, Lise M A De Strooper, Maaike G Dijkstra, et al.
Acta Neuropathologica
|
March 31, 2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
Jan Verheijen, Tobi Van den Bossche, Julie van der Zee, et al.
American Journal of Human Genetics
|
October 24, 2003
Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy
Jan Senderek, Carsten Bergmann, Claudia Stendel, et al.
Nature
|
August 25, 2017
Epitaxy of advanced nanowire quantum devices
Sasa Gazibegovic, Diana Car, Hao Zhang, et al.
Lancet (London, England)
|
September 6, 2014
Efficacy, safety, and immunogenicity of the human papillomavirus 16/18 AS04-adjuvanted vaccine in women older than 25 years: 4-year interim follow-up of the phase 3, double-blind, randomised controlled VIVIANE study
S Rachel Skinner, Anne Szarewski, Barbara Romanowski, et al.
Neurobiology of Aging
|
November 18, 2017
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
Jan Verheijen, Julie van der Zee, Ilse Gijselinck, et al.
Intensive Care Medicine Experimental
|
September 18, 2022
Development and validation of an early warning model for hospitalized COVID-19 patients: a multi-center retrospective cohort study
Jim M Smit, Jesse H Krijthe, Andrei N Tintu, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 20, 2016
Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency
Simone Olgiati, Matej Skorvanek, Marialuisa Quadri, et al.
Nature Communications
|
October 7, 2024
Transcript errors generate amyloid-like proteins in huwman cells
Claire S Chung, Yi Kou, Sarah J Shemtov, et al.
Page
of 101