[PDF] from nih.govES Bertini, E Eymard-Pierre, O Boespflug-Tanguy… - 2011 - ncbi.nlm.nih.gov ... Devon RS, Helm JR, Rouleau GA, Leitner Y, Lerman-Sagie T, Lev D, Hayden MR (2003) The first nonsense mutation in alsin results in a homogeneous phenotype of infantile-onset ascending spasticparalysis with bulbar involvement in two siblings. Clin Genet 64:210-5 ... View as HTML
DW Begley, DR Davies, RC Hartley… - … Section F: Structural …, 2011 - scripts.iucr.org ... Glutaric acidemia type 1 is an inherited metabolic disorder which can cause macrocephaly, muscular rigidity, spasticparalysis and other progressive movement disorders in humans. The defects in glutaryl-CoA dehydrogenase ...
C Chen - 2011 - gradworks.umi.com ... at the peripheral neuromuscular junction which results in flaccid paralysis, while TeNT initially binds to peripheral neurons and retrograde traffics to the central nervous system where glycine release is blocked in TeNT intoxicated inhibitory inter-neurons to elicit spasticparalysis. ... Cached
JM Dmetrichuk, C Pendleton, ES Ahn… - Child's Nervous …, 2011 - Springer ... The earliest report to our knowledge of tendon transfer for the symptomatic treatment of cerebral palsy is that of Dr. Robert Jones of England, in 1903 [2]. Jones notably credited Americans with “more serious and consecutive work” in spasticparalysis and further explained that in ... Related articles - All 2 versions
I Enunlu, M Ozansoy… - Biochemical and Biophysical Research …, 2011 - Elsevier ... Abstract. Mutations in Als2 gene cause several autosomal recessive forms of motor neuron diseases including Juvenile Amyotrophic Lateral Sclerosis (JALS), juvenile Primary lateral Sclerosis (PLSJ) and Infantile-onset Ascending Hereditary SpasticParalysis (IAHSP). ...
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