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Year Number of Results
2008 1
2009 35
2010 320
2011 50
2013 1
2015 1
2024 0

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320 results

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Page 1
Motor neuron diversity in development and disease.
Kanning KC, Kaplan A, Henderson CE. Kanning KC, et al. Annu Rev Neurosci. 2010;33:409-40. doi: 10.1146/annurev.neuro.051508.135722. Annu Rev Neurosci. 2010. PMID: 20367447 Review.
Although often considered as a group, spinal motor neurons are highly diverse in terms of their morphology, connectivity, and functional properties and differ significantly in their response to disease. ...For example, glial cell line-derived neurotrophic factor (GDNF) has …
Although often considered as a group, spinal motor neurons are highly diverse in terms of their morphology, connectivity, and functio …
TRPV4-mediated channelopathies.
Verma P, Kumar A, Goswami C. Verma P, et al. Channels (Austin). 2010 Jul-Aug;4(4):319-28. doi: 10.4161/chan.4.4.12905. Epub 2010 Jul 6. Channels (Austin). 2010. PMID: 20676052 Review.
Recently it gained immense medical and clinical interest as several independent studies have demonstrated that mutations in the TRPV4 gene can results in genetic disorders like Brachyolmia, Charcot-Marie-Tooth disease type 2C, Spinal Muscular Atrophy and Here …
Recently it gained immense medical and clinical interest as several independent studies have demonstrated that mutations in the TRPV4 gene c …
Spinal muscular atrophy: diagnosis, treatment and future prospects.
Baioni MT, Ambiel CR. Baioni MT, et al. J Pediatr (Rio J). 2010 Jul-Aug;86(4):261-70. doi: 10.2223/JPED.1988. J Pediatr (Rio J). 2010. PMID: 20711542 Review. English, Portuguese.
OBJECTIVE: To report on recent genetic and molecular discoveries and on future prospects for the treatment of spinal muscular atrophy (SMA), thereby helping healthcare professionals to make a quick diagnosis and provide appropriate and timely therapeutic supp …
OBJECTIVE: To report on recent genetic and molecular discoveries and on future prospects for the treatment of spinal muscular …
Spinal muscular atrophy: mechanisms and therapeutic strategies.
Lorson CL, Rindt H, Shababi M. Lorson CL, et al. Hum Mol Genet. 2010 Apr 15;19(R1):R111-8. doi: 10.1093/hmg/ddq147. Epub 2010 Apr 13. Hum Mol Genet. 2010. PMID: 20392710 Free PMC article. Review.
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder and a leading genetic cause of infantile mortality. ...The clinical features of the disease are caused by specific degeneration of alpha-motor neurons in the spinal cord …
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder and a leading genetic cause of infan …
Perspectives and diagnostic considerations in spinal muscular atrophy.
Prior TW. Prior TW. Genet Med. 2010 Mar;12(3):145-52. doi: 10.1097/GIM.0b013e3181c5e713. Genet Med. 2010. PMID: 20057317 Free article. Review.
Spinal muscular atrophy is an autosomal recessive neurodegenerative disease and the most common genetic cause of infant mortality. The disease results in motor neuron loss and skeletal muscle atrophy. Spinal muscular atrophy is cau …
Spinal muscular atrophy is an autosomal recessive neurodegenerative disease and the most common genetic cause of infant …
Clinical features and molecular mechanisms of spinal and bulbar muscular atrophy (SBMA).
Katsuno M, Banno H, Suzuki K, Adachi H, Tanaka F, Sobue G. Katsuno M, et al. Adv Exp Med Biol. 2010;685:64-74. doi: 10.1007/978-1-4419-6448-9_6. Adv Exp Med Biol. 2010. PMID: 20687495 Review.
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset neurodegenerative disease characterized by slowly progressive muscle weakness and atrophy. ...SBMA exclusively occurs in adult males, whereas both heterozygous and homozygous females are usual …
Spinal and bulbar muscular atrophy (SBMA) is an adult-onset neurodegenerative disease characterized by slowly progressi …
Carrier testing for spinal muscular atrophy.
Gitlin JM, Fischbeck K, Crawford TO, Cwik V, Fleischman A, Gonye K, Heine D, Hobby K, Kaufmann P, Keiles S, MacKenzie A, Musci T, Prior T, Lloyd-Puryear M, Sugarman EA, Terry SF, Urv T, Wang C, Watson M, Yaron Y, Frosst P, Howell RR. Gitlin JM, et al. Genet Med. 2010 Oct;12(10):621-2. doi: 10.1097/GIM.0b013e3181ef6079. Genet Med. 2010. PMID: 20808230 Free PMC article.
Spinal muscular atrophy is the most common fatal hereditary disease among newborns and infants. ...In this article, the meeting participants summarize the discussions and conclude that pan-ethnic carrier screening for spinal muscular atrophy …
Spinal muscular atrophy is the most common fatal hereditary disease among newborns and infants. ...In this article, the …
Spinal muscular atrophy: new and emerging insights from model mice.
Park GH, Kariya S, Monani UR. Park GH, et al. Curr Neurol Neurosci Rep. 2010 Mar;10(2):108-17. doi: 10.1007/s11910-010-0095-5. Curr Neurol Neurosci Rep. 2010. PMID: 20425235 Free PMC article. Review.
Spinal muscular atrophy (SMA) is a common and often fatal neurodegenerative disease that primarily afflicts infants and young children. ...
Spinal muscular atrophy (SMA) is a common and often fatal neurodegenerative disease that primarily afflicts infants and …
Therapeutic approaches to spinal and bulbar muscular atrophy.
Ranganathan S, Fischbeck KH. Ranganathan S, et al. Trends Pharmacol Sci. 2010 Nov;31(11):523-7. doi: 10.1016/j.tips.2010.08.005. Epub 2010 Sep 20. Trends Pharmacol Sci. 2010. PMID: 20863580 Free PMC article. Review.
Spinal and bulbar muscular atrophy is a hereditary motor neuron disease caused by trinucleotide repeat expansion in the androgen receptor gene. ...
Spinal and bulbar muscular atrophy is a hereditary motor neuron disease caused by trinucleotide repeat expansion in the …
Proteasomal and autophagic degradative activities in spinal and bulbar muscular atrophy.
Rusmini P, Bolzoni E, Crippa V, Onesto E, Sau D, Galbiati M, Piccolella M, Poletti A. Rusmini P, et al. Neurobiol Dis. 2010 Nov;40(2):361-9. doi: 10.1016/j.nbd.2010.06.016. Epub 2010 Jul 16. Neurobiol Dis. 2010. PMID: 20621188 Review.
Spinal and bulbar muscular atrophy (SBMA or Kennedy's disease) is a fatal neurodegenerative disease characterized by the selective loss of motor neurons in the bulbar region of the brain and in the anterior horns of the spinal cord. ...SBMA was the fir …
Spinal and bulbar muscular atrophy (SBMA or Kennedy's disease) is a fatal neurodegenerative disease characterized by th …
320 results