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Olbrich

Showing results (961-970 of 999) with videos related to

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Clinical EEG and Neuroscience|September 25, 2020
Special Report on the Impact of the COVID-19 Pandemic on Clinical EEG and Research and Consensus Recommendations for the Safe Use of EEGSalvatore Campanella, Kemal Arikan, Claudio Babiloni, et al.
F1000Research|October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunitiesIsrael Amirav, Mary Roduta Roberts, Huda Mussaffi, et al.
Plos Genetics|August 28, 2018
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertilityAsaf Ta-Shma, Rim Hjeij, Zeev Perles, et al.
Respiratory Medicine|October 4, 2016
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practicesRevital Abitbul, Israel Amirav, Hannah Blau, et al.
Translational Psychiatry|October 8, 2021
Altered resting-state functional connectome in major depressive disorder: a mega-analysis from the PsyMRI consortiumNooshin Javaheripour, Meng Li, Tara Chand, et al.
American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, et al.
The Pediatric Infectious Disease Journal|February 4, 2021
Distinct Laboratory and Clinical Features of Secondary Hemophagocytic Lymphohistiocytosis in Pediatric Visceral Leishmaniasis: A Retrospective Analysis of 127 Children in Andalusia, Spain (2004-2019)María López Marcos, Beatriz Ruiz Sáez, Juan Salvador Vílchez Pérez, et al.
The Journal of General Virology|October 8, 2021
Head-to-head evaluation of seven different seroassays including direct viral neutralisation in a representative cohort for SARS-CoV-2Laura Olbrich, Noemi Castelletti, Yannik Schälte, et al.
Mutation Research. Reviews in Mutation Research|September 28, 2025
Mortality rate and causes of death in inborn errors of immunity: A systematic review and meta-analysisSaba Fekrvand, Zahra Hamidi Esfahani, Mohammadmehdi Yarahmadi, et al.
Human Mutation|December 21, 2012
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein armsDinu Antony, Anita Becker-Heck, Maimoona A Zariwala, et al.
Pageof 100

Showing results (961-970 of 999) with videos related to

Sort By:
Pageof 100
Clinical EEG and Neuroscience|September 25, 2020
Special Report on the Impact of the COVID-19 Pandemic on Clinical EEG and Research and Consensus Recommendations for the Safe Use of EEGSalvatore Campanella, Kemal Arikan, Claudio Babiloni, et al.
F1000Research|October 30, 2016
Collecting clinical data in primary ciliary dyskinesia- challenges and opportunitiesIsrael Amirav, Mary Roduta Roberts, Huda Mussaffi, et al.
Plos Genetics|August 28, 2018
Homozygous loss-of-function mutations in MNS1 cause laterality defects and likely male infertilityAsaf Ta-Shma, Rim Hjeij, Zeev Perles, et al.
Respiratory Medicine|October 4, 2016
Primary ciliary dyskinesia in Israel: Prevalence, clinical features, current diagnosis and management practicesRevital Abitbul, Israel Amirav, Hannah Blau, et al.
Translational Psychiatry|October 8, 2021
Altered resting-state functional connectome in major depressive disorder: a mega-analysis from the PsyMRI consortiumNooshin Javaheripour, Meng Li, Tara Chand, et al.
American Journal of Human Genetics|October 22, 2019
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body AsymmetryJulia Wallmeier, Diana Frank, Amelia Shoemark, et al.
The Pediatric Infectious Disease Journal|February 4, 2021
Distinct Laboratory and Clinical Features of Secondary Hemophagocytic Lymphohistiocytosis in Pediatric Visceral Leishmaniasis: A Retrospective Analysis of 127 Children in Andalusia, Spain (2004-2019)María López Marcos, Beatriz Ruiz Sáez, Juan Salvador Vílchez Pérez, et al.
The Journal of General Virology|October 8, 2021
Head-to-head evaluation of seven different seroassays including direct viral neutralisation in a representative cohort for SARS-CoV-2Laura Olbrich, Noemi Castelletti, Yannik Schälte, et al.
Mutation Research. Reviews in Mutation Research|September 28, 2025
Mortality rate and causes of death in inborn errors of immunity: A systematic review and meta-analysisSaba Fekrvand, Zahra Hamidi Esfahani, Mohammadmehdi Yarahmadi, et al.
Human Mutation|December 21, 2012
Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein armsDinu Antony, Anita Becker-Heck, Maimoona A Zariwala, et al.
Pageof 100