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Frontiers in Immunology
|
December 14, 2020
Der p 2.1 Peptide Abrogates House Dust Mites-Induced Asthma Features in Mice and Humanized Mice by Inhibiting DC-Mediated T Cell Polarization
Martin Klein, Luc Colas, Marie-Aude Cheminant, et al.
Journal of Parkinson'S Disease
|
February 18, 2022
Prevalence of Prodromal Symptoms of Parkinson's Disease in the Late Middle-Aged Population
Dareia S Roos, Martin Klein, Dorly J H Deeg, et al.
Clinical and Experimental Rheumatology
|
March 3, 2022
VEXAS syndrome: a report of three cases
Hana Ciferska, Monika Gregová, Martin Klein, et al.
Journal of Neurology
|
September 2, 2025
Olfactory function is longitudinally associated with semantic fluency in Parkinson's disease: a cohort study
Dareia S Roos, Henk W Berendse, Richard L Doty, et al.
Plos One
|
December 3, 2016
Scholarly Context Adrift: Three out of Four URI References Lead to Changed Content
Shawn M Jones, Herbert Van de Sompel, Harihar Shankar, et al.
The Journal of Prosthetic Dentistry
|
August 9, 2011
Analysis of the periimplant tissue of craniofacial implants by sulcus fluid flow rate (SFFR)
Chie Hee Cho, Martin Klein, Ramona Scheufele, et al.
Respiratory Research
|
January 31, 2020
The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
Antoine Moui, Martin Klein, Dorian Hassoun, et al.
Investigative Ophthalmology & Visual Science
|
March 23, 2019
Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations
Lea D Bennett, Georgiana Metz, Martin Klein, et al.
Epilepsy & Behavior : E&B
|
June 27, 2018
The role of mTOR inhibitors in preventing epileptogenesis in patients with TSC: Current evidence and future perspectives
Susanne Schubert-Bast, Felix Rosenow, Karl Martin Klein, et al.
Translational Vision Science & Technology
|
August 22, 2020
Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1)
Lea D Bennett, Martin Klein, Finny T John, et al.
Page
of 40
Search research articles
Search
Showing results (121-130 of 397) with videos related to
Sort By:
Page
of 40
Frontiers in Immunology
|
December 14, 2020
Der p 2.1 Peptide Abrogates House Dust Mites-Induced Asthma Features in Mice and Humanized Mice by Inhibiting DC-Mediated T Cell Polarization
Martin Klein, Luc Colas, Marie-Aude Cheminant, et al.
Journal of Parkinson'S Disease
|
February 18, 2022
Prevalence of Prodromal Symptoms of Parkinson's Disease in the Late Middle-Aged Population
Dareia S Roos, Martin Klein, Dorly J H Deeg, et al.
Clinical and Experimental Rheumatology
|
March 3, 2022
VEXAS syndrome: a report of three cases
Hana Ciferska, Monika Gregová, Martin Klein, et al.
Journal of Neurology
|
September 2, 2025
Olfactory function is longitudinally associated with semantic fluency in Parkinson's disease: a cohort study
Dareia S Roos, Henk W Berendse, Richard L Doty, et al.
Plos One
|
December 3, 2016
Scholarly Context Adrift: Three out of Four URI References Lead to Changed Content
Shawn M Jones, Herbert Van de Sompel, Harihar Shankar, et al.
The Journal of Prosthetic Dentistry
|
August 9, 2011
Analysis of the periimplant tissue of craniofacial implants by sulcus fluid flow rate (SFFR)
Chie Hee Cho, Martin Klein, Ramona Scheufele, et al.
Respiratory Research
|
January 31, 2020
The IL-15 / sIL-15Rα complex modulates immunity without effect on asthma features in mouse
Antoine Moui, Martin Klein, Dorian Hassoun, et al.
Investigative Ophthalmology & Visual Science
|
March 23, 2019
Regional Variations and Intra-/Intersession Repeatability for Scotopic Sensitivity in Normal Controls and Patients With Inherited Retinal Degenerations
Lea D Bennett, Georgiana Metz, Martin Klein, et al.
Epilepsy & Behavior : E&B
|
June 27, 2018
The role of mTOR inhibitors in preventing epileptogenesis in patients with TSC: Current evidence and future perspectives
Susanne Schubert-Bast, Felix Rosenow, Karl Martin Klein, et al.
Translational Vision Science & Technology
|
August 22, 2020
Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1)
Lea D Bennett, Martin Klein, Finny T John, et al.
Page
of 40