1
0
0
News
Netzwerk-Profile
OPUS FAU | Suchen
opus4.kobv.de
Myofibrillar instability exacerbated by acute exercise in filaminopathy (2015); Frédéric Chevessier Julia Schuld Zacharias Orfanos Anne-C. Plank Lucie Wolf ...
WikiGenes - Frédéric Chevessier
www.wikigenes.org
Frédéric Chevessier. Max-Planck-Institut für Medizinische Forschung. Heidelberg. Germany. [.de. Name/email consistency: high.
Interessen
Clinical, histological and genetic characterisation of patients with...
jmg.bmj.com
Johann Böhm,1,2,3,4,5 Frédéric Chevessier,6 Catherine Koch,1,2,3,4,5. G Arielle Peche,1,2,3,4,5 Marina Mora,7,8 Lucia Morandi,7 Barbara Pasanisi,7. Isabella ...
Bücher
De la jonction neuromusculaire au reticulum sarcoplasmique:...
books.google.de
Frédéric Chevessier pages. 0 Reviewshttps://books.google.com/books/about/De_la_jonction_neuromusculaire_au_reticu.html?id=nymHtgAACAAJ.
Dokumente zum Namen
Clinical, histological and genetic characterisation of patients with...
www.proquest.com
Johann Böhm,1,2,3,4,5 Frédéric Chevessier,6 Catherine Koch,1,2,3,4,5. G Arielle Peche,1,2,3,4,5 Marina Mora,7,8 Lucia Morandi,7 Barbara Pasanisi,7. Isabella ...
Abstract (Eng) - Synapsis.ru
www.synapsis.ru
Mutations in MUSK cause congenital myasthenic syndrome. Frédéric Chevessier. 1. , Brice Faraut. 2. , Aymeric Ravel-Chapuis. 2. , Pascale Richard. 1,3. , Karen.
Publications | Institut de neurophysiopathologie - UMR ...
inp.univ-amu.fr
⟨hal ⟩ Document type : ART; Johann Böhm, Frédéric Chevessier, André Maues de Paula, Catherine Koch, Shahram Attarian, et al.. Constitutive ...
Wissenschaftliche Veröffentlichungen
Constitutive Activation of the Calcium Sensor STIM1 Causes...
www.sciencedirect.com
Constitutive Activation of the Calcium Sensor STIM1 Causes Tubular-Aggregate Myopathy. Johann Böhm,,,,,; Frédéric Chevessier,,,; André ...
CHEVESSIER | Fondation Bettencourt Schueller
www.fondationbs.org
Génération d'une souris transgénique pour l'analyse d'une mutation humaine dans MuSK induisant un syndrome myasthénique
Thrombin Receptor Induction by Injury-Related Factors in Human...
www.sciencedirect.com
Corinne Mbebi,* Troy Rohn,†,1 Marie-Agne`s Doyennette,* Frédéric Chevessier,* Martine Jandrot-Perrus,‡. Daniel Hantaı,* and Martine Verdie`re-Sahuqué*,§, ...
Forschungsförderung heißt Hoffnung geben | Deutsche Gesellschaft für...
www.dgm.org
Der in der Regel in drei Stufen verliehene Preis wurde einmal an Dr. Frédéric Chevessier von der Universität Erlangen vergeben. Der höchste Preis den ...
Veröffentlichungen allgemein
Publications Authored by Frederic Chevessier | PubFacts
www.pubfacts.com
Publications Authored by Frederic Chevessier
Felix-Jerusalem-Preis | SpringerLink
link.springer.com
V. (DGM) den Felix-Jerusalem-Preis zur Förderung der Forschung auf dem Gebiet der neuromuskulären Erkrankungen an Dr. Frédéric Chevessier, ...
Characterization of a mouse model lacking acetylcholine receptor...
www.youscribe.com
Characterization of a mouse model lacking acetylcholine receptor activity during embryonic development [Elektronische Ressource] / vorgelegt von Pier Giorgio...
Sonstiges
Identification of an agrin mutation that causes congenital myasthenia...
slideplayer.com
... Lausanne Thierry Kuntzer Biozentrum, Basel Markus Rüegg MPI, Heidelberg Frédéric Chevessier Università Cattolica del Sacre Cuore, Rome Andrea ...
Frédéric Chevessier - Tours
www.trombi.com
Retrouve avec Trombi.com - retrouveur d'amis - tes anciens camarades de classe, tes collègues, tes camarades de promotions, tes premiers amours et tes amis...
Frédéric Chevessier
www.infona.pl
Search results for: Frédéric Chevessier ... Christine B. Gurniak, Frédéric Chevessier, Melanie Jokwitz, Friederike Jönsson, more · European ...
Chevessier, Frederic - UF VIVO - University of Florida
vivo.ufl.edu
Frederic Chevessier. ©2019 University of Florida | Terms of Use | Powered by VIVO · About · Contact Us · Help · Privacy Policy · Picked up by 1 news outlets.
A mouse model for congenital myasthenic syndrome due to MuSK...
hal.archives-ouvertes.fr
Frédéric Chevessier, Emmanuelle Girard, Jordi Molgó, Sönke Bartling, Jeanine Koenig, et al.. A mouse model for congenital myasthenic syndrome due to MuSK ...
Altmetric – CASQ1 mutations impair calsequestrin polymerization and...
springeropen.altmetric.com
Johann Böhm, Xavière Lornage, Frederic Chevessier, Catherine Birck, Simona Zanotti, Paola Cudia, Monica Bulla, Florence Granger, Mai ...
A new mouse model for the slow-channel congenital myasthenic...
pure.mpg.de
Autor: Chevessier, Frédéric et al.; Genre: Zeitschriftenartikel; Im Druck veröffentlicht: ; Keywords: Neuromuscular Junction, Slow Channel Congenital...
At a glance - Authentification
api.mycongressonline.net
Christoph Clemen , Florian St_ckigt , Frederic Chevessier , Karl-Heinz Strucksberg , Lilli Winter , Harald Herrmann , Matthias Tôrk , Regine Schneider-Stock ...
Atypical nuclear abnormalities in a patient with Brody disease
www.infona.pl
Frédéric Chevessier. Institut de Myologie, Hôpital de La Salpêtrière, Paris, France; Neuropathologisches Institut, Universitätsklinikum Erlangen, ...
Constitutive Activation of the Calcium Sensor STIM1 Causes...
hal.archives-ouvertes.fr
Johann Böhm 1Frédéric Chevessier 2 André Maues de Paula 3 Catherine Koch 1 Shahram Attarian 4 Claire Feger 5 Daniel Hantaï 6 Pascal Laforêt 7 Karima ...
A new mouse model for the slow-channel congenital myasthenic syndrome...
www.infona.pl
Frédéric Chevessier. Department of Molecular Neurobiology, Max Planck Institute for Medical ResearchHeidelberg, ...
viaf.org
... syndromes myasthéniques congénitaux et les myopathies à agrégats tubulaires / par Frédéric Chevessier, (1) Sudoc [ABES], France ...
Hereditary myopathy with early respiratory failure: Occurrence in...
moh-it.pure.elsevier.com
... Johanna Tommiska and Taneli Raivio and Matthias Tuerk and Philipp G{\"o}litz and Frederic Chevessier and Caroline Sewry and Fiona Norwood and Carola ...
Mutations in GFPT1-related congenital myasthenic syndromes are...
read.qxmd.com
... Sylvie Sukno, Françoise Bouhour, Pascal Laforêt, Bertrand Fontaine, Laure Strochlic, Bruno Eymard, Frédéric Chevessier, Tanya Stojkovic, Sophie Nicole.
Identification of an agrin mutation that causes congenital myasthenia...
www.hal.inserm.fr
We report the case of a congenital myasthenic syndrome due to a mutation in AGRN, the gene encoding agrin, an extracellular matrix molecule released by the...
C9ORF72-ALS: P62- and ubiquitin-aggregation pathology in skeletal...
read.qxmd.com
Matthias Türk, Gerrit Haaker, Lilli Winter, Walter Just, Florian T Nickel, Ralf A Linker, Frédéric Chevessier, Rolf Schröder. Muscle & Nerve 2014, 50 (3):
Neuromuscular endplate pathology in recessive desminopathies |...
n.neurology.org
Frederic Chevessier, PhD. Ursula Schlötzer-. Schrehardt, PhD. Christoph S. Clemen,. MD. Said Hashemolhosseini,. PhD. Rolf Schröder, MD.
(PDF) Clinical, histological and genetic characterisation of patients...
www.academia.edu
Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1
GMS | Joint-Meeting of the German Society for Neuropathology and...
www.egms.de
... Bonn, Germany; Frederic Chevessier - Institute of Neuropathology, Erlangen, Germany; Rudolf Kley - University Hospital Bergmannsheil, ...
mRNA as a Novel Treatment Strategy for Hereditary Spastic Paraplegia...
en.x-mol.com
Hereditary spastic paraplegia type 5 is a neurodegenerative disease caused by loss-of-function mutations in the CYP7B1 gene encoding the oxysterol...
Verwandte Suchanfragen zu Frédéric Chevessier
| Jeanine Koenig |
Personen Vorname "Frédéric" (1566) Name "Chevessier" (2) |
sortiert nach Relevanz / Datum