نتایج جستجو برای: nondystrophic myotonia

تعداد نتایج: 1472  

Journal: :The Journal of General Physiology 2007
John D. Lueck Ami Mankodi Maurice S. Swanson Charles A. Thornton Robert T. Dirksen

Muscle degeneration and myotonia are clinical hallmarks of myotonic dystrophy type 1 (DM1), a multisystemic disorder caused by a CTG repeat expansion in the 3' untranslated region of the myotonic dystrophy protein kinase (DMPK) gene. Transgenic mice engineered to express mRNA with expanded (CUG)(250) repeats (HSA(LR) mice) exhibit prominent myotonia and altered splicing of muscle chloride chann...

2017
Michela De Bellis Roberta Carbonara Julien Roussel Alessandro Farinato Ada Massari Sabata Pierno Marilena Muraglia Filomena Corbo Carlo Franchini Maria Rosaria Carratù Annamaria De Luca Diana Conte Camerino Jean-François Desaphy

Although the sodium channel blocker, mexiletine, is the first choice drug in myotonia, some myotonic patients remain unsatisfied due to contraindications, lack of tolerability, or incomplete response. More therapeutic options are thus needed for myotonic patients, which require clinical trials based on solid preclinical data. In previous structure-activity relationship studies, we identified tw...

Journal: :Arquivos de neuro-psiquiatria 2002
Umbertina Conti Reed Rubens Reimao Adriana Avila Espindola Fernando Kok Lúcio Gobbo Ferreira Maria Bernardete Dutra Resende Thelma Correia Messias Mary Souza Carvalho Aron Diament Milberto Scaff Suely Kazue Nagahashi Marie

We describe five patients with Schwartz-Jampel syndrome (SJS) examined at the outpatient service for neuromuscular disorders at our Institution from 1996 to 1999 with the objective of emphasizing the characteristic dysmorphic phenotype of SJS and its different clinical forms. Two cases presented SJS-type 1A, two had SJS-type 1B and one manifested SJS-type 2. Two boys with 3 and 13 years of age ...

Journal: :Archives of neurology 1999
R Sasaki H Takano K Kamakura K Kaida A Hirata M Saito H Tanaka S Kuzuhara S Tsuji

BACKGROUND Paramyotonia congenita (PMC) of von Eulenburg is an autosomal dominant muscular disease characterized by exercise- and cold-induced myotonia and weakness. To date, 18 missense mutations in the adult skeletal muscle sodium channel alpha-subunit (SCN4A) gene have been identified to cause a spectrum of muscular diseases, including PMC of von Eulenburg, PMC without cold paralysis, potass...

Journal: :British journal of anaesthesia 1994
S H Russell N P Hirsch

The myotonias are a group of uncommon disorders. All display a characteristic electromyographic picture and some of the disorders have systemic manifestations. They are important to the anaesthetist for several reasons. Anaesthetic and surgical interventions may induce myotonia which, when initiated, may complicate the course of anaesthesia and be difficult to abolish. Furthermore, patients oft...

Journal: :Anaesthesia and Intensive Care 2001

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1988

Journal: :The Boston Medical and Surgical Journal 1908

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