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    Results: 1 to 20 of 3129

    1.

    A negatively acting bifunctional RNA increases survival motor neuron both in vitro and in vivo.

    Dickson A, Osman E, Lorson CL.

    Hum Gene Ther. 2008 Nov;19(11):1307-15.PMID: 19848583 [PubMed - indexed for MEDLINE]Related articles

    2.

    Weak hands from a flexed neck.

    Dimberg EL, Rubin DI.

    Neurology. 2009 Sep 22;73(12):996. No abstract available. PMID: 19770478 [PubMed - indexed for MEDLINE]Related articles

    3.

    Anterior and posterior decompressive surgery for progressive amyotrophy associated with cervical spondylosis: a retrospective study of 51 patients.

    Uchida K, Nakajima H, Yayama T, Sato R, Kobayashi S, Kokubo Y, Mwaka ES, Baba H.

    J Neurosurg Spine. 2009 Sep;11(3):330-7.PMID: 19769515 [PubMed - indexed for MEDLINE]Related articles

    4.

    An analysis of disease severity based on SMN2 copy number in adults with spinal muscular atrophy.

    Elsheikh B, Prior T, Zhang X, Miller R, Kolb SJ, Moore D, Bradley W, Barohn R, Bryan W, Gelinas D, Iannaccone S, Leshner R, Mendell JR, Mendoza M, Russman B, Smith S, King W, Kissel JT.

    Muscle Nerve. 2009 Oct;40(4):652-6.PMID: 19760790 [PubMed - indexed for MEDLINE]Related articles

    5.

    A positive modifier of spinal muscular atrophy in the SMN2 gene.

    Prior TW, Krainer AR, Hua Y, Swoboda KJ, Snyder PC, Bridgeman SJ, Burghes AH, Kissel JT.

    Am J Hum Genet. 2009 Sep;85(3):408-13. Epub 2009 Aug 27.PMID: 19716110 [PubMed - indexed for MEDLINE]Related articles

    6.

    Prenatal genetic testing.

    Dolan SM.

    Pediatr Ann. 2009 Aug;38(8):426-30. doi: 10.3928/00904481-20090723-05. No abstract available. PMID: 19711880 [PubMed - indexed for MEDLINE]Related articles

    7.

    Nerve, muscle or bone disease? Look before you leap.

    Muthukrishnan J, Harikumar KV, Sangeeta J, Singh MK, Modi K.

    Singapore Med J. 2009 Aug;50(8):e293-4.PMID: 19710962 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Overexpression of IGF-1 in muscle attenuates disease in a mouse model of spinal and bulbar muscular atrophy.

    Palazzolo I, Stack C, Kong L, Musaro A, Adachi H, Katsuno M, Sobue G, Taylor JP, Sumner CJ, Fischbeck KH, Pennuto M.

    Neuron. 2009 Aug 13;63(3):316-28.PMID: 19679072 [PubMed - indexed for MEDLINE]Related articles

    9.

    IGF-1: elixir for motor neuron diseases.

    Papanikolaou T, Ellerby LM.

    Neuron. 2009 Aug 13;63(3):277-8.PMID: 19679066 [PubMed - indexed for MEDLINE]Related articles

    10.

    Oral administration of the thyrotropin-releasing hormone (TRH) analogue, taltireline hydrate, in spinal muscular atrophy.

    Kato Z, Okuda M, Okumura Y, Arai T, Teramoto T, Nishimura M, Kaneko H, Kondo N.

    J Child Neurol. 2009 Aug;24(8):1010-2.PMID: 19666885 [PubMed - indexed for MEDLINE]Related articles

    11.

    Increased levels of glial cell-derived neurotrophic factor in CSF of infants with SMA.

    Chiaretti A, Leoni C, Barone G, Genovese O, Brahe C, Mariotti P, Conti G.

    Pediatr Neurol. 2009 Sep;41(3):195-9.PMID: 19664536 [PubMed - indexed for MEDLINE]Related articles

    12.

    False homozygous deletions of SMN1 exon 7 using Dra I PCR-RFLP caused by a novel mutation in spinal muscular atrophy.

    Kang SH, Cho SI, Chae JH, Chung KN, Ra EK, Kim SY, Seong MW, Kim JY, Park SS.

    Genet Test Mol Biomarkers. 2009 Aug;13(4):511-3.PMID: 19663601 [PubMed - indexed for MEDLINE]Related articles

    13.

    Gene therapy for neurodegenerative diseases based on lentiviral vectors.

    Nanou A, Azzouz M.

    Prog Brain Res. 2009;175:187-200. Review.PMID: 19660657 [PubMed - indexed for MEDLINE]Related articles

    14.

    Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.

    Renbaum P, Kellerman E, Jaron R, Geiger D, Segel R, Lee M, King MC, Levy-Lahad E.

    Am J Hum Genet. 2009 Aug;85(2):281-9. Epub 2009 Jul 30.PMID: 19646678 [PubMed - indexed for MEDLINE]Related articles

    15.

    HnRNP C1/C2 may regulate exon 7 splicing in the spinal muscular atrophy gene SMN1.

    Irimura S, Kitamura K, Kato N, Saiki K, Takeuchi A, Gunadi, Matsuo M, Nishio H, Lee MJ.

    Kobe J Med Sci. 2009 Mar 10;54(5):E227-36.PMID: 19628962 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Vascular perfusion abnormalities in infants with spinal muscular atrophy.

    Araujo Ade Q, Araujo M, Swoboda KJ.

    J Pediatr. 2009 Aug;155(2):292-4.PMID: 19619755 [PubMed - indexed for MEDLINE]Related articles

    17.

    Fibroblast growth factor-2 regulates the stability of nuclear bodies.

    Bruns AF, van Bergeijk J, Lorbeer C, Nölle A, Jungnickel J, Grothe C, Claus P.

    Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):12747-52. Epub 2009 Jul 17.PMID: 19617559 [PubMed - indexed for MEDLINE]Related articles

    18.

    Spinal angiography and epidural venography in juvenile muscular atrophy of the distal arm "Hirayama disease".

    Elsheikh B, Kissel JT, Christoforidis G, Wicklund M, Kehagias DT, Chiocca EA, Mendell JR.

    Muscle Nerve. 2009 Aug;40(2):206-12.PMID: 19609908 [PubMed - indexed for MEDLINE]Related articles

    19.

    Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects.

    Boon KL, Xiao S, McWhorter ML, Donn T, Wolf-Saxon E, Bohnsack MT, Moens CB, Beattie CE.

    Hum Mol Genet. 2009 Oct 1;18(19):3615-25. Epub 2009 Jul 10.PMID: 19592581 [PubMed - indexed for MEDLINE]Related articles

    20.

    Juvenile muscular atrophy of the distal upper extremity (hirayama disease) in two lanky look-alike brothers.

    Kajikawa H, Kokubo Y, Taniguchi A, Naito Y, Kuzuhara S.

    Neurologist. 2009 Jul;15(4):220-2.PMID: 19590383 [PubMed - indexed for MEDLINE]Related articles

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