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Proceedings of the National Academy of Sciences of the United States of America
|
September 22, 2020
Strain engineering of the charge and spin-orbital interactions in Sr<sub>2</sub>IrO<sub>4</sub>
Eugenio Paris, Yi Tseng, Ekaterina M Pärschke, et al.
Biomedicines
|
October 26, 2024
Prognostic Value of Speckle Tracking Echocardiography-Derived Strain in Unmasking Risk for Arrhythmias in Children with Myocarditis
Nele Rolfs, Cynthia Huber, Bernd Opgen-Rhein, et al.
Annals of Medicine
|
October 18, 2021
Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology
Volha Skrahina, Ulrike Grittner, Christian Beetz, et al.
Leukemia
|
July 7, 2023
Activation of distinct inflammatory pathways in subgroups of LR-MDS
Marie Schneider, Clara Rolfs, Matthias Trumpp, et al.
Nature Communications
|
July 5, 2017
AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability
Aline Brechet, Rebecca Buchert, Jochen Schwenk, et al.
Clinical Genetics
|
February 2, 2018
Expanding the clinical and genetic spectra of NKX6-2-related disorder
C Baldi, A M Bertoli-Avella, N Al-Sannaa, et al.
Journal of Neuropathology and Experimental Neurology
|
June 20, 2002
Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy
Rolf Schröder, Wolfram S Kunz, Fatima Rouan, et al.
Journal of Clinical Medicine
|
October 26, 2024
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 Participants
Sabine Rösner, Luba M Pardo, Aida M Bertoli-Avella, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 14, 2020
The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings
Volha Skrahina, Hanaa Gaber, Eva-Juliane Vollstedt, et al.
Parkinsonism & Related Disorders
|
February 5, 2019
Role of ANO3 mutations in dystonia: A large-scale mutational screening study
Luisa Olschewski, Silvia Jesús, Han-Joon Kim, et al.
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Search research articles
Search
Showing results (571-580 of 632) with videos related to
Sort By:
Page
of 64
Proceedings of the National Academy of Sciences of the United States of America
|
September 22, 2020
Strain engineering of the charge and spin-orbital interactions in Sr<sub>2</sub>IrO<sub>4</sub>
Eugenio Paris, Yi Tseng, Ekaterina M Pärschke, et al.
Biomedicines
|
October 26, 2024
Prognostic Value of Speckle Tracking Echocardiography-Derived Strain in Unmasking Risk for Arrhythmias in Children with Myocarditis
Nele Rolfs, Cynthia Huber, Bernd Opgen-Rhein, et al.
Annals of Medicine
|
October 18, 2021
Hereditary transthyretin-related amyloidosis is frequent in polyneuropathy and cardiomyopathy of no obvious aetiology
Volha Skrahina, Ulrike Grittner, Christian Beetz, et al.
Leukemia
|
July 7, 2023
Activation of distinct inflammatory pathways in subgroups of LR-MDS
Marie Schneider, Clara Rolfs, Matthias Trumpp, et al.
Nature Communications
|
July 5, 2017
AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability
Aline Brechet, Rebecca Buchert, Jochen Schwenk, et al.
Clinical Genetics
|
February 2, 2018
Expanding the clinical and genetic spectra of NKX6-2-related disorder
C Baldi, A M Bertoli-Avella, N Al-Sannaa, et al.
Journal of Neuropathology and Experimental Neurology
|
June 20, 2002
Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy
Rolf Schröder, Wolfram S Kunz, Fatima Rouan, et al.
Journal of Clinical Medicine
|
October 26, 2024
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 Participants
Sabine Rösner, Luba M Pardo, Aida M Bertoli-Avella, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 14, 2020
The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings
Volha Skrahina, Hanaa Gaber, Eva-Juliane Vollstedt, et al.
Parkinsonism & Related Disorders
|
February 5, 2019
Role of ANO3 mutations in dystonia: A large-scale mutational screening study
Luisa Olschewski, Silvia Jesús, Han-Joon Kim, et al.
Page
of 64