Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Véronique Bissay"'
Autor:
Ann Cordenier, Anja Flamez, Thomy de Ravel, Alexander Gheldof, Luigi Pannone, Carlo De Asmundis, Gudrun Pappaert, Véronique Bissay
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Myotonia congenita is a rare neuromuscular disorder caused by CLCN1 mutations resulting in delayed muscle relaxation. Extramuscular manifestations are not considered to be present in chloride skeletal channelopathies, although recently some cardiac m
Externí odkaz:
https://doaj.org/article/f09725c899704f50b6309cd3fccdbe39
Autor:
Jolien Geers, Maria-Luiza Luchian, Andreea Motoc, Jari De Winter, Bram Roosens, Maria Bjerke, Ann Van Eeckhaut, Mandy M. J. Wittens, Simke Demeester, Ramses Forsyth, Thomy de Ravel, Véronique Bissay, Rik Schots, Frederik H. Verbrugge, Caroline Weytjens, Ilse Weets, Bernard Cosyns, Steven Droogmans
Publikováno v:
The International Journal of Cardiovascular Imaging. 39:585-593
PURPOSE: The aim of the present study was to evaluate the role of ejection fraction (EF), left ventricular (LV) global longitudinal strain (LVGLS) and global constructive work (GCW) as prognostic variables in patients with cardiac amyloidosis (CA). M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52fd1d521f925aaed1693b56997f9311
https://doi.org/10.1007/s10554-022-02762-1
https://doi.org/10.1007/s10554-022-02762-1
Autor:
Nicolas Dubuisson, Sofia Maldonado Slootjes, Véronique Bissay, Antoine Guilmot, Michel Gille, Clémence de Broglie
Publikováno v:
Acta Neurologica Belgica
Acta neurologica Belgica, Vol. 122, no.3, p. 703-707 (2022)
Acta neurologica Belgica, Vol. 06860, no.570, p. 1-5 (2021)
Acta neurologica Belgica, Vol. 122, no.3, p. 703-707 (2022)
Acta neurologica Belgica, Vol. 06860, no.570, p. 1-5 (2021)
Background A growing number of Guillain–Barré syndrome (GBS) and Miller Fisher Syndrome (MFS) cases following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are reported. Nevertheless, this association is still debated, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a4e2b32e6b3182cb13a9c6342c5df13
http://europepmc.org/articles/PMC8412854
http://europepmc.org/articles/PMC8412854
Autor:
Véronique Bissay, Ricardo A. Maselli
Publikováno v:
Journal of clinical neuromuscular disease. 21(1)
INTRODUCTION: Mutations in the Dok-7 gene (DOK7) underlie a congenital myasthenic syndrome (CMS) with a characteristic limb-girdle (LG) pattern of muscle weakness. Multiple clinical findings and a wide clinical heterogeneity have been identified in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5e8f5cd8f597b27204e4b02ddfceac
https://pubmed.ncbi.nlm.nih.gov/31453852
https://pubmed.ncbi.nlm.nih.gov/31453852
Autor:
Sonia Van Dooren, Jacques De Keyser, Dorien Daneels, Sophie Van Malderen, Willy Lissens, Pedro Brugada, Anna Jansen, Gudrun Pappaert, Véronique Bissay, Uschi Peeters, Kathelijn Keymolen
Publikováno v:
European Journal of Human Genetics, 24(3), 400-407. Nature Publishing Group
SCN5A mutations involving the α-subunit of the cardiac voltage-gated muscle sodium channel (NaV1.5) result in different cardiac channelopathies with an autosomal-dominant inheritance such as Brugada syndrome. On the other hand, mutations in SCN4A en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b1f6a14f681baa5854c8cefd74fd8a
https://doi.org/10.1038/ejhg.2015.125
https://doi.org/10.1038/ejhg.2015.125
Autor:
Sophie Van Malderen, Véronique Bissay
Publikováno v:
Acta clinica Belgica. 73(1)
© Acta Clinica Belgica 2017 Objectives: Non-dystrophic myotonia, periodic paralysis and, to a certain extent, myotonic dystrophies are rare hereditary skeletal muscle channelopathies, charactarized by myotonia or episodic muscle weakness. This revie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc394cc87a5670a95c80831c3540d0d5
https://pubmed.ncbi.nlm.nih.gov/29088983
https://pubmed.ncbi.nlm.nih.gov/29088983
Autor:
Wietse Wiels, Stephanie Du Four, Anja Flamez, Rembert Mertens, Véronique Bissay, Jacques De Keyser
Publikováno v:
Acta neurologica Belgica. 118(1)
Tick borne encephalitis (TBE) is an infectious zoonotic disease caused by an RNA virus that is endemic to Central and Eastern Europe, Russia, and large parts of Asia. The tick borne encephalitis virus (TBEV) is transmitted through the saliva of infec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43f2810ae06c64badb9c238d4b649601
https://pubmed.ncbi.nlm.nih.gov/29313244
https://pubmed.ncbi.nlm.nih.gov/29313244
Autor:
Guy Laureys, E. Schmedding, Kathelijn Keymolen, Jacques De Keyser, Willy Lissens, Véronique Bissay
Publikováno v:
Vrije Universiteit Brussel
We describe three Belgian families with a L1436P mutation in the SCN4A gene, causing a sodium channel myotonia with an atypical clinical presentation, characterized by late onset painful cold-aggravated myotonia. These families represent a distinct p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a82193f8d66662441ae0d50a236cd871
https://doi.org/10.1016/j.nmd.2011.05.006
https://doi.org/10.1016/j.nmd.2011.05.006
Publikováno v:
Muscle & Nerve. 38:1653-1657
Different clinical presentations of chronic inflammatory demyelinating polyneuropathy (CIDP) have been described. Fatigue is generally considered to be a secondary sign and is not mentioned as a warning sign for the diagnosis. We present a patient wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea07b59f60281e7971446a5862598ca2
https://doi.org/10.1002/mus.21158
https://doi.org/10.1002/mus.21158
