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Blood
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June 22, 2019
Differential expression of Plg-R<sub>KT</sub> and its effects on migration of proinflammatory monocyte and macrophage subsets
Barbara Thaler, Nagyung Baik, Philipp J Hohensinner, et al.
Cardiovascular Research
|
May 12, 2025
Proteomic profiling reveals a higher presence of glycolytic enzymes in human atherosclerotic lesions with unfavourable histological characteristics
Kaylin C A Palm, Xiaoke Yin, Ferheen Baig, et al.
Brain : a Journal of Neurology
|
December 1, 2022
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy
Arnaud Jacquier, Julian Theuriet, Fanny Fontaine, et al.
European Journal of Neurology
|
April 16, 2026
Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic Amyotrophy
Julian Theuriet, Isabelle Quadrio, Frédéric Fer, et al.
The Tohoku Journal of Experimental Medicine
|
December 23, 2017
Polymorphisms in ACE and ACTN3 Genes and Blood Pressure Response to Acute Exercise in Elite Male Athletes from Serbia
Tijana S Durmic, Marija D Zdravkovic, Marina N Djelic, et al.
Frontiers in Genetics
|
February 13, 2024
Recurrent "outsider" intronic variation in the <i>SLC5A</i>6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb
Lamisse Mansour-Hendili, Cyril Gitiaux, Madeleine Harion, et al.
Genes
|
February 25, 2022
A National French Consensus on Gene List for the Diagnosis of Charcot-Marie-Tooth Disease and Related Disorders Using Next-Generation Sequencing
Thibaut Benquey, Emmanuelle Pion, Mireille Cossée, et al.
Neuromuscular Disorders : NMD
|
April 15, 2009
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia
Tanya Stojkovic, El Hadi Hammouda, Pascale Richard, et al.
Muscle & Nerve
|
October 7, 2021
Determinants of diaphragm inspiratory motion, diaphragm thickening, and its performance for predicting respiratory restrictive pattern in Duchenne muscular dystrophy
Abdallah Fayssoil, Lee S Nguyen, Tanya Stojkovic, et al.
Neuropathology and Applied Neurobiology
|
April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathy
M Cerino, E Campana-Salort, A Salvi, et al.
Page
of 107
Search research articles
Search
Showing results (891-900 of 1,067) with videos related to
Sort By:
Page
of 107
Blood
|
June 22, 2019
Differential expression of Plg-R<sub>KT</sub> and its effects on migration of proinflammatory monocyte and macrophage subsets
Barbara Thaler, Nagyung Baik, Philipp J Hohensinner, et al.
Cardiovascular Research
|
May 12, 2025
Proteomic profiling reveals a higher presence of glycolytic enzymes in human atherosclerotic lesions with unfavourable histological characteristics
Kaylin C A Palm, Xiaoke Yin, Ferheen Baig, et al.
Brain : a Journal of Neurology
|
December 1, 2022
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy
Arnaud Jacquier, Julian Theuriet, Fanny Fontaine, et al.
European Journal of Neurology
|
April 16, 2026
Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic Amyotrophy
Julian Theuriet, Isabelle Quadrio, Frédéric Fer, et al.
The Tohoku Journal of Experimental Medicine
|
December 23, 2017
Polymorphisms in ACE and ACTN3 Genes and Blood Pressure Response to Acute Exercise in Elite Male Athletes from Serbia
Tijana S Durmic, Marija D Zdravkovic, Marina N Djelic, et al.
Frontiers in Genetics
|
February 13, 2024
Recurrent "outsider" intronic variation in the <i>SLC5A</i>6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb
Lamisse Mansour-Hendili, Cyril Gitiaux, Madeleine Harion, et al.
Genes
|
February 25, 2022
A National French Consensus on Gene List for the Diagnosis of Charcot-Marie-Tooth Disease and Related Disorders Using Next-Generation Sequencing
Thibaut Benquey, Emmanuelle Pion, Mireille Cossée, et al.
Neuromuscular Disorders : NMD
|
April 15, 2009
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget's disease of bone and frontotemporal dementia
Tanya Stojkovic, El Hadi Hammouda, Pascale Richard, et al.
Muscle & Nerve
|
October 7, 2021
Determinants of diaphragm inspiratory motion, diaphragm thickening, and its performance for predicting respiratory restrictive pattern in Duchenne muscular dystrophy
Abdallah Fayssoil, Lee S Nguyen, Tanya Stojkovic, et al.
Neuropathology and Applied Neurobiology
|
April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathy
M Cerino, E Campana-Salort, A Salvi, et al.
Page
of 107