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Peter Bauer

Showing results (391-400 of 585) with videos related to

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Diagnostics (Basel, Switzerland)|July 12, 2020
Rapid Large-Scale COVID-19 Testing During ShortagesChristian Beetz, Volha Skrahina, Toni M Förster, et al.
Orphanet Journal of Rare Diseases|May 3, 2022
Clinical and genetic characterization of a cohort of 97 CLN6 patients tested at a single centerCorina-Marcela Rus, Thomas Weissensteiner, Catarina Pereira, et al.
Parkinson'S Disease|February 3, 2022
Prevalence of Fabry Disease among Patients with Parkinson's DiseaseAlexandra Lackova, Christian Beetz, Sebastian Oppermann, et al.
The Journal of Allergy and Clinical Immunology|July 31, 2012
Molecular spreading and predictive value of preclinical IgE response to Phleum pratense in children with hay feverLaura Hatzler, Valentina Panetta, Susanne Lau, et al.
The Science of the Total Environment|November 2, 2020
Association of early life and acute pollen exposure with lung function and exhaled nitric oxide (FeNO). A prospective study up to adolescence in the GINIplus and LISA cohortKatrina A Lambert, Iana Markevych, Bo-Yi Yang, et al.
Paediatric Respiratory Reviews|October 12, 2002
The development of childhood asthma: lessons from the German Multicentre Allergy Study (MAS)Susanne Lau, Renate Nickel, Bodo Niggemann, et al.
European Journal of Human Genetics : EJHG|May 13, 2010
A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42)Nina A Schlipf, Christian Beetz, Rebecca Schüle, et al.
European Journal of Medical Genetics|June 11, 2022
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular diseaseAnett Marais, Aida M Bertoli-Avella, Christian Beetz, et al.
Human Genetics|September 1, 2023
A founder DBR1 variant causes a lethal form of congenital ichthyosisHanan E Shamseldin, Mukunth Sadagopan, Javier Martini, et al.
European Journal of Human Genetics : EJHG|March 28, 2020
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discoveryHolger Hengel, Rebecca Buchert, Marc Sturm, et al.
Pageof 59

Showing results (391-400 of 585) with videos related to

Sort By:
Pageof 59
Diagnostics (Basel, Switzerland)|July 12, 2020
Rapid Large-Scale COVID-19 Testing During ShortagesChristian Beetz, Volha Skrahina, Toni M Förster, et al.
Orphanet Journal of Rare Diseases|May 3, 2022
Clinical and genetic characterization of a cohort of 97 CLN6 patients tested at a single centerCorina-Marcela Rus, Thomas Weissensteiner, Catarina Pereira, et al.
Parkinson'S Disease|February 3, 2022
Prevalence of Fabry Disease among Patients with Parkinson's DiseaseAlexandra Lackova, Christian Beetz, Sebastian Oppermann, et al.
The Journal of Allergy and Clinical Immunology|July 31, 2012
Molecular spreading and predictive value of preclinical IgE response to Phleum pratense in children with hay feverLaura Hatzler, Valentina Panetta, Susanne Lau, et al.
The Science of the Total Environment|November 2, 2020
Association of early life and acute pollen exposure with lung function and exhaled nitric oxide (FeNO). A prospective study up to adolescence in the GINIplus and LISA cohortKatrina A Lambert, Iana Markevych, Bo-Yi Yang, et al.
Paediatric Respiratory Reviews|October 12, 2002
The development of childhood asthma: lessons from the German Multicentre Allergy Study (MAS)Susanne Lau, Renate Nickel, Bodo Niggemann, et al.
European Journal of Human Genetics : EJHG|May 13, 2010
A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42)Nina A Schlipf, Christian Beetz, Rebecca Schüle, et al.
European Journal of Medical Genetics|June 11, 2022
Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular diseaseAnett Marais, Aida M Bertoli-Avella, Christian Beetz, et al.
Human Genetics|September 1, 2023
A founder DBR1 variant causes a lethal form of congenital ichthyosisHanan E Shamseldin, Mukunth Sadagopan, Javier Martini, et al.
European Journal of Human Genetics : EJHG|March 28, 2020
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discoveryHolger Hengel, Rebecca Buchert, Marc Sturm, et al.
Pageof 59