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Year Number of Results
1993 2
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2,344 results

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Page 1
Spinal muscular atrophy.
Lunn MR, Wang CH. Lunn MR, et al. Lancet. 2008 Jun 21;371(9630):2120-33. doi: 10.1016/S0140-6736(08)60921-6. Lancet. 2008. PMID: 18572081 Review.
Spinal muscular atrophy is an autosomal recessive neurodegenerative disease characterised by degeneration of spinal cord motor neurons, atrophy of skeletal muscles, and generalised weakness. ...These and other advances in medical technology have …
Spinal muscular atrophy is an autosomal recessive neurodegenerative disease characterised by degeneration of spinal …
Hirayama disease.
Huang YL, Chen CJ. Huang YL, et al. Neuroimaging Clin N Am. 2011 Nov;21(4):939-50, ix-x. doi: 10.1016/j.nic.2011.07.009. Neuroimaging Clin N Am. 2011. PMID: 22032508 Free article. Review.
Hirayama disease (juvenile muscular atrophy of distal upper extremity) is a cervical myelopathy. Predominantly affecting male adolescents, it is characterized by progressive muscular weakness and atrophy of distal upper limbs, followed by spontaneous a …
Hirayama disease (juvenile muscular atrophy of distal upper extremity) is a cervical myelopathy. Predominantly affecting male …
Spinal muscular atrophy.
Talbot K, Davies KE. Talbot K, et al. Semin Neurol. 2001 Jun;21(2):189-97. doi: 10.1055/s-2001-15264. Semin Neurol. 2001. PMID: 11442327 Review.
The spinal muscular atrophies are a group of mostly inherited disorders selectively affecting the lower motor neuron. ...
The spinal muscular atrophies are a group of mostly inherited disorders selectively affecting the lower motor neuron. . …
Spinal muscular atrophy.
Iannaccone ST, Smith SA, Simard LR. Iannaccone ST, et al. Curr Neurol Neurosci Rep. 2004 Jan;4(1):74-80. doi: 10.1007/s11910-004-0016-6. Curr Neurol Neurosci Rep. 2004. PMID: 14683633 Review.
Spinal muscular atrophy is a common genetic disease of the motor neuron (frequency of eight cases per 100,000 live births) with a high mortality during infancy and no known treatment. ...Rehabilitation and proper management of medical complications have impro …
Spinal muscular atrophy is a common genetic disease of the motor neuron (frequency of eight cases per 100,000 live birt …
Spinal muscular atrophy.
Vitte J, Attali R, Warwar N, Gurt I, Melki J. Vitte J, et al. Adv Exp Med Biol. 2009;652:237-46. doi: 10.1007/978-90-481-2813-6_16. Adv Exp Med Biol. 2009. PMID: 20225030
Spinal muscular atrophies (SMA) are frequent autosomal recessive disorders characterized by degeneration of lower motor neurons. ...
Spinal muscular atrophies (SMA) are frequent autosomal recessive disorders characterized by degeneration of lower motor …
Spinal muscular atrophy.
Cifuentes-Diaz C, Frugier T, Melki J. Cifuentes-Diaz C, et al. Semin Pediatr Neurol. 2002 Jun;9(2):145-50. doi: 10.1053/spen.2002.33801. Semin Pediatr Neurol. 2002. PMID: 12138998 Review.
Spinal muscular atrophies (SMA) are characterized by degeneration of lower motor neurons associated with muscle paralysis and atrophy. ...
Spinal muscular atrophies (SMA) are characterized by degeneration of lower motor neurons associated with muscle paralys …
Spinal muscular atrophy diagnostics.
Prior TW. Prior TW. J Child Neurol. 2007 Aug;22(8):952-6. doi: 10.1177/0883073807305668. J Child Neurol. 2007. PMID: 17761649 Review.
Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the survival motor neuron gene (SMN), which exists in 2 nearly identical copies (SMN1 and SMN2). Exon 7 of SMN1 is homozygously absent in about 95% of spi …
Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the survival moto …
Pathogenesis-targeting therapeutics for spinal and bulbar muscular atrophy (SBMA).
Suzuki K, Kastuno M, Banno H, Sobue G. Suzuki K, et al. Neuropathology. 2009 Aug;29(4):509-16. doi: 10.1111/j.1440-1789.2009.01013.x. Epub 2009 May 22. Neuropathology. 2009. PMID: 19486304 Review.
Spinal and bulbar muscular atrophy (SBMA) is an hereditary, adult-onset, lower motor neuron disease caused by an aberrant elongation of a trinucleotide CAG repeat, which encodes the polyglutamine tract, in the first exon of the androgen receptor (AR) gene. Th …
Spinal and bulbar muscular atrophy (SBMA) is an hereditary, adult-onset, lower motor neuron disease caused by an aberra …
Spinal muscular atrophy type 1: what are the ethics and practicality of respiratory support?
Mitchell I. Mitchell I. Paediatr Respir Rev. 2006;7 Suppl 1:S210-1. doi: 10.1016/j.prrv.2006.04.200. Epub 2006 Jun 5. Paediatr Respir Rev. 2006. PMID: 16798568 Review.
Spinal Muscular Atrophy Type I (SMA I) is the most severe form of SMA. It presents in infancy and without treatment death occurs by 2 years. ...
Spinal Muscular Atrophy Type I (SMA I) is the most severe form of SMA. It presents in infancy and without treatment dea …
Modern management of spinal muscular atrophy.
Iannaccone ST. Iannaccone ST. J Child Neurol. 2007 Aug;22(8):974-8. doi: 10.1177/0883073807305670. J Child Neurol. 2007. PMID: 17761652 Review.
Spinal muscular atrophy is an incurable disease with a frequency of 8 per 100,000 live births. ...
Spinal muscular atrophy is an incurable disease with a frequency of 8 per 100,000 live births. ...
2,344 results