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International Journal of Molecular Sciences
|
February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher Disease
Tama Dinur, Peter Bauer, Christian Beetz, et al.
European Journal of Human Genetics : EJHG
|
October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach
Jürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
Caries Research
|
May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries Experience
Andrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.
Neurology. Genetics
|
June 30, 2025
A Retrospective Cohort Study of the GLA c.937G > T, p.Asp313Tyr Variant With No Evidence of an Association With Fabry Disease
Tobias Boettcher, Christian Beetz, Daniel Schulze, et al.
NPJ Parkinson'S Disease
|
January 10, 2026
Metabolomic breath landscape analysis unravels lipid biomarker candidates in patients with genetic and idiopathic Parkinson's disease
Madiha Malik, Norbert Brüggemann, Tatiana Usnich, et al.
Allergy
|
December 15, 2020
Long-term effects of hydrolyzed formulae on atopic diseases in the GINI study
Monika Gappa, Birgit Filipiak-Pittroff, Lars Libuda, et al.
Journal of Neurology
|
March 13, 2024
Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literature
Daniel Strunk, Peter Bauer, Kathy Keyvani, et al.
Scientific Reports
|
October 30, 2023
Neuronal progenitor cells-based metabolomics study reveals dysregulated lipid metabolism and identifies putative biomarkers for CLN6 disease
Corina-Marcela Rus, Daniel L Polla, Sebastiano Di Bucchianico, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
October 20, 2005
Diagnostic value of quantitative hepatic copper determination in patients with Wilson's Disease
Peter Ferenci, Petra Steindl-Munda, Wolfgang Vogel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in Germany
Claudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Page
of 59
Search research articles
Search
Showing results (221-230 of 585) with videos related to
Sort By:
Page
of 59
International Journal of Molecular Sciences
|
February 25, 2023
Contribution of Glucosylsphingosine (Lyso-Gb1) to Treatment Decisions in Patients with Gaucher Disease
Tama Dinur, Peter Bauer, Christian Beetz, et al.
European Journal of Human Genetics : EJHG
|
October 13, 2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach
Jürgen Tomiuk, Lutz Bachmann, Claudia Bauer, et al.
Caries Research
|
May 23, 2015
Lactotransferrin Gene Polymorphism Associated with Caries Experience
Andrea D Doetzer, João A Brancher, Giovana D Pecharki, et al.
Neurology. Genetics
|
June 30, 2025
A Retrospective Cohort Study of the GLA c.937G > T, p.Asp313Tyr Variant With No Evidence of an Association With Fabry Disease
Tobias Boettcher, Christian Beetz, Daniel Schulze, et al.
NPJ Parkinson'S Disease
|
January 10, 2026
Metabolomic breath landscape analysis unravels lipid biomarker candidates in patients with genetic and idiopathic Parkinson's disease
Madiha Malik, Norbert Brüggemann, Tatiana Usnich, et al.
Allergy
|
December 15, 2020
Long-term effects of hydrolyzed formulae on atopic diseases in the GINI study
Monika Gappa, Birgit Filipiak-Pittroff, Lars Libuda, et al.
Journal of Neurology
|
March 13, 2024
Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literature
Daniel Strunk, Peter Bauer, Kathy Keyvani, et al.
Scientific Reports
|
October 30, 2023
Neuronal progenitor cells-based metabolomics study reveals dysregulated lipid metabolism and identifies putative biomarkers for CLN6 disease
Corina-Marcela Rus, Daniel L Polla, Sebastiano Di Bucchianico, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association
|
October 20, 2005
Diagnostic value of quantitative hepatic copper determination in patients with Wilson's Disease
Peter Ferenci, Petra Steindl-Munda, Wolfgang Vogel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 18, 2015
Mutations in CIZ1 are not a major cause for dystonia in Germany
Claudia Dufke, Ann-Kathrin Hauser, Marc Sturm, et al.
Page
of 59