نتایج جستجو برای: charcot marie tooth

تعداد نتایج: 97261  

Journal: :The New England journal of medicine 2010
James R Lupski Jeffrey G Reid Claudia Gonzaga-Jauregui David Rio Deiros David C Y Chen Lynne Nazareth Matthew Bainbridge Huyen Dinh Chyn Jing David A Wheeler Amy L McGuire Feng Zhang Pawel Stankiewicz John J Halperin Chengyong Yang Curtis Gehman Danwei Guo Rola K Irikat Warren Tom Nick J Fantin Donna M Muzny Richard A Gibbs

BACKGROUND Whole-genome sequencing may revolutionize medical diagnostics through rapid identification of alleles that cause disease. However, even in cases with simple patterns of inheritance and unambiguous diagnoses, the relationship between disease phenotypes and their corresponding genetic changes can be complicated. Comprehensive diagnostic assays must therefore identify all possible DNA c...

2009
Camiel Verhamme Rob J de Haan Marinus Vermeulen Frank Baas Marianne de Visser Ivo N van Schaik

BACKGROUND High dose oral ascorbic acid substantially improved myelination and locomotor function in a Charcot-Marie-Tooth type 1A mouse model. A phase II study was warranted to investigate whether high dose ascorbic acid also has such a substantial effect on myelination in Charcot-Marie-Tooth type 1A patients and whether this treatment is safe. METHODS Patients below age 25 years were random...

Journal: :genetics in the 3rd millennium 0
آویسا عباسی avisa abbasi department of genetics, faculty of basic sciences, tarbiat modares university, tehran, iran مجید صادقی زاده majis sadeghizadeh مهرداد به منش mehrdad behmanesh امید آریانی omid ariani مسعود هوشمند masoud houshmand

charcot-marie-tooth disease (cmt) is the most common form of inherited peripheral neuropathy. cmt is genetically and clinically heterogenous group of hereditary motor and sensory neuropathies characterized by areflexia, distal sensory loss and progressive weakness of the distal limb muscles. the x-linked cmt (cmtx) is the second most frequent form of charcot-marie-tooth disease. the dominant cm...

2016
Jasper M Morrow Christopher D J Sinclair Arne Fischmann Pedro M Machado Mary M Reilly Tarek A Yousry John S Thornton Michael G Hanna

BACKGROUND A substantial impediment to progress in trials of new therapies in neuromuscular disorders is the absence of responsive outcome measures that correlate with patient functional deficits and are sensitive to early disease processes. Irrespective of the primary molecular defect, neuromuscular disorder pathological processes include disturbance of intramuscular water distribution followe...

Journal: :Majalah Kedokteran Neurosains Perhimpunan Dokter Spesialis Saraf Indonesia 2020

Journal: :Pediatric Neurology Briefs 2005

Journal: :Clinical and Experimental Neuroimmunology 2020

Journal: :Southern African Journal of Anaesthesia and Analgesia 2006

Journal: :Cochrane Database of Systematic Reviews 2008

Journal: :Pediatric Neurology Briefs 1998

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