Autosomal dominant congenital spinal muscular atrophy – A possible developmental deficiency of motor neurones?-Reference-Cited by-同舟云学术

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Autosomal dominant congenital spinal muscular atrophy – A possible developmental deficiency of motor neurones?

Published:2008-07 Issue:7 Volume:18 Page:530-535
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Reddel S.,Ouvrier R.A.,Nicholson G.,Dierick I.,Irobi J.,Timmerman V.,Ryan M.M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference22 articles.

1. Estimating the number of motor units in a muscle;Daube;J Clin Neurophysiol,1995

2. Unraveling the genetics of distal hereditary motor neuronopathies;Irobi;Neuromolecular Med,2006

3. Chronic neurogenic muscle atrophies of infancy. Their nosological relationship with Werdnig–Hoffmann’s disease;Lugaresi;J Neurol Sci,1966

4. A dominantly inherited lower motor neuron disorder presenting at birth with associated arthrogyposis;Fleury;JNNP,1985

5. Dominant congenital benign spinal muscular atrophy;Frijns;Muscle Nerve,1994

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2. Clinical, Genetic, and Disability Profile of Pediatric Distal Hereditary Motor Neuropathy;Neurology;2020-10-16

3. Neuropathological Hallmarks of Brain Malformations in Extreme Phenotypes Related to DYNC1H1 Mutations;Journal of Neuropathology & Experimental Neurology;2017-03-10

4. Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy;Neurology;2015-01-21

5. Congenital and Early Infantile Neuropathies;Neuromuscular Disorders of Infancy, Childhood, and Adolescence;2015

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