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Initial Posting: September 5, 2000; Last Revision: January 20, 2022. Clinical characteristics. The dystrophinopathies cover a spectrum of X-linked muscle disease ranging from mild to severe that includes Duchenne muscular dystrophy, Becker[...]Article
Laporte A ; Mariampillai K ; Allenbach Y ; Pasi N ; Donciu V ; Toledano D ; Granger B ; Benveniste O ; Grenier PA ; Boussouar S | Germany | 13/01/2022Article
Last Update: January 9, 2022 (previous version August 14, 2021; August 15, 2020)Article
Crefcoeur LL ; Visser G ; Ferdinandusse S ; Wijburg FA ; Langeveld M ; Sjouke B | United States | 08/01/2022Article
Schreuder AB ; Rossi A ; Grünert SC ; Derks TGJ | 06/01/2022Initial Posting: March 9, 2010; Last Update: January 6, 2022. Clinical characteristics. Glycogen storage disease type III (GSD III) is characterized by variable liver, cardiac muscle, and skeletal muscle involvement. GSD IIIa is the most c[...]Article
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Breillat P ; Mariampillai K ; Legendre P ; Martins P ; Dunogue B ; Charuel JL ; Miyara M ; Goulvestre C ; Paule R ; Vanquaethem H ; Ackermann F ; Benveniste O ; Nunes H ; Mouthon L ; Allenbach Y ; Uzunhan Y | England | 2022Article
Abicht A ; Müller J ; Lochmuller H | 23/12/2021Initial Posting: May 9, 2003; Last Update: December 23, 2021. The purpose of this overview is to increase the awareness of clinicians regarding congenital myasthenic syndromes (CMS) and their genetic causes and management. The following ar[...]Article
Comi GP ; Niks EH ; Cinnante CM ; Kan HE ; Vandenborne K ; Willcocks RJ ; Velardo D ; Ripolone M ; van Benthem JJ ; van de Velde NM ; Nava S ; Ambrosoli L ; Cazzaniga S ; Bettica PU | United States | 16/12/2021Article
Tanboon J ; Inoue M ; Saito Y ; Tachimori H ; Hayashi S ; Noguchi S ; Okiyama N ; Fujimoto M ; Nishino I | United States | 06/12/2021Article
Lundberg IE ; Fujimoto M ; Vencovsky J ; Aggarwal R ; Holmqvist M ; Christopher Stine L ; Mammen AL ; Miller FW | England | 02/12/2021Article
General features This table is published annually in the December issue. Its purpose is to provide the reader of Neuromuscular Disorders with an updated list of monogenic neuromuscular diseases due to a primary defect residing in the nuclear [...]Article
Zoske J ; Schneider U ; Siegert E ; Kleefeld F ; Preusse C ; Stenzel W ; Hahn K | 15/11/2021Article
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Opal P | 14/10/2021Initial Posting: January 9, 2003; Last Update: October 14, 2021. Clinical characteristics. GAN-related neurodegeneration comprises a phenotypic continuum ranging from severe (sometimes called classic giant axonal neuropathy) to milder pure[...]Article
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Veneruso M ; Fiorillo C ; Broda P ; Baratto S ; Traverso M ; Donati A ; Savasta S ; Falsaperla R ; Mancardi MM ; Pedemonte M ; Panicucci C ; Piatelli G ; Pacetti M ; Moscatelli A ; Ramenghi LA ; Nobili L ; Minetti C ; Bruno C | 05/10/2021Article
Pinto WBVR ; Pinto WBVR ; Souza PVS ; Badia BML ; Farias IB ; Albuquerque Filho JMV ; Goncalves EA ; Machado RIL ; Oliveira ASB | Brazil | 10/2021Article
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