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1993 2
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Showing results for (((spinal) AND muscular) AND atrophy) AND ("2001/01/01"[Date - Publication] : "2011/12/31"[Date - Publication])
Your search for (((pinal) AND muscular) AND astrophy) AND ("2001/01/01"[Date - Publication] : "2011/12/31"[Date - Publication]) retrieved no results
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.
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 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.
Exon 7 of SMN1 is homozygously absent in about 95% of spinal muscular atrophy patients, whereas the loss of SMN2 does not cause spinal muscular atrophy. ...SMN1 dosage testing can be used to determine the SMN1 copy number and to detect …
Exon 7 of SMN1 is homozygously absent in about 95% of spinal muscular atrophy patients, whereas the loss of SMN2 does n …
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.
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: recent advances and future prospects.
Nicole S, Diaz CC, Frugier T, Melki J. Nicole S, et al. Muscle Nerve. 2002 Jul;26(1):4-13. doi: 10.1002/mus.10110. Muscle Nerve. 2002. PMID: 12115944 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 …
Clinical outcome measures in spinal muscular atrophy.
Montes J, Gordon AM, Pandya S, De Vivo DC, Kaufmann P. Montes J, et al. J Child Neurol. 2009 Aug;24(8):968-78. doi: 10.1177/0883073809332702. Epub 2009 Jun 9. J Child Neurol. 2009. PMID: 19509409 Review.
Spinal muscular atrophy is one of the most devastating neurological diseases of childhood. ...Following is an evidence-based review of available clinical outcome measures in spinal muscular atrophy....
Spinal muscular atrophy is one of the most devastating neurological diseases of childhood. ...Following is an evidence- …
Clinical and molecular diagnosis of spinal muscular atrophy.
Panigrahi I, Kesari A, Phadke SR, Mittal B. Panigrahi I, et al. Neurol India. 2002 Jun;50(2):117-22. Neurol India. 2002. PMID: 12134171 Free article. Review.
The spinal muscular atrophies are a group of disorders characterized by flaccid limb weakness. ...
The spinal muscular atrophies are a group of disorders characterized by flaccid limb weakness. ...
Molecular mechanisms of spinal muscular atrophy.
Sumner CJ. Sumner CJ. J Child Neurol. 2007 Aug;22(8):979-89. doi: 10.1177/0883073807305787. J Child Neurol. 2007. PMID: 17761653 Review.
Significant strides have been made during the past decade in the understanding of the molecular mechanisms that lead to the autosomal recessive motor neuron disease spinal muscular atrophy. Genetic studies revealed that spinal muscular atroph …
Significant strides have been made during the past decade in the understanding of the molecular mechanisms that lead to the autosomal recess …
2,344 results