These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
141 related articles for article (PubMed ID: 16607426)
21. Spinal muscular atrophy of childhood at the edge of the centuries. Hausmanowa-Petrusewicz I; Jedrzejowska M Funct Neurol; 2001; 16(4 Suppl):247-53. PubMed ID: 11996521 [No Abstract] [Full Text] [Related]
22. Molecular study of spinal muscular atrophy patients with hybrid genes in Bulgaria. Kremensky I; Jankova S; Bochukova E; Uzunova M; Litvinenko I; Jordanova A J Inherit Metab Dis; 1999 May; 22(3):322-6. PubMed ID: 10384397 [No Abstract] [Full Text] [Related]
27. An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene. Parsons DW; McAndrew PE; Monani UR; Mendell JR; Burghes AH; Prior TW Hum Mol Genet; 1996 Nov; 5(11):1727-32. PubMed ID: 8922999 [TBL] [Abstract][Full Text] [Related]
28. Descriptive epidemiology of spinal muscular atrophy type I in Estonia. Vaidla E; Talvik I; Kulla A; Kahre T; Hamarik M; Napa A; Metsvaht T; Piirsoo A; Talvik T Neuroepidemiology; 2006; 27(3):164-8. PubMed ID: 17035693 [TBL] [Abstract][Full Text] [Related]
29. Synthesis and biological evaluation of novel 2,4-diaminoquinazoline derivatives as SMN2 promoter activators for the potential treatment of spinal muscular atrophy. Thurmond J; Butchbach ME; Palomo M; Pease B; Rao M; Bedell L; Keyvan M; Pai G; Mishra R; Haraldsson M; Andresson T; Bragason G; Thosteinsdottir M; Bjornsson JM; Coovert DD; Burghes AH; Gurney ME; Singh J J Med Chem; 2008 Feb; 51(3):449-69. PubMed ID: 18205293 [TBL] [Abstract][Full Text] [Related]
30. Prenatal prediction of spinal muscular atrophy by SMN deletion analysis. Dhamcharee V; Mutirangura A; Tannirandom Y; Jongpiputvanich S; Romyanan O Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():186-7. PubMed ID: 11400766 [TBL] [Abstract][Full Text] [Related]
32. Prenatal diagnosis of spinal muscular atrophy in Chinese by genetic analysis of fetal cells. Wu T; Ding XS; Li WL; Yao J; Deng XX Chin Med J (Engl); 2005 Aug; 118(15):1274-7. PubMed ID: 16117881 [TBL] [Abstract][Full Text] [Related]
33. Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion. García-Cabezas MA; García-Alix A; Martín Y; Gutiérrez M; Hernández C; Rodríguez JI; Morales C Acta Neuropathol; 2004 May; 107(5):475-8. PubMed ID: 14968368 [TBL] [Abstract][Full Text] [Related]
34. Analysis of the mRNA transcripts of the survival motor neuron (SMN) gene in the tissue of an SMA fetus and the peripheral blood mononuclear cells of normals, carriers and SMA patients. Jong YJ; Chang JG; Lin SP; Yang TY; Wang JC; Chang CP; Lee CC; Li H; Hsieh-Li HM; Tsai CH J Neurol Sci; 2000 Feb; 173(2):147-53. PubMed ID: 10675659 [TBL] [Abstract][Full Text] [Related]
35. Congenital bone fractures in spinal muscular atrophy: functional role for SMN protein in bone remodeling. Shanmugarajan S; Swoboda KJ; Iannaccone ST; Ries WL; Maria BL; Reddy SV J Child Neurol; 2007 Aug; 22(8):967-73. PubMed ID: 17761651 [TBL] [Abstract][Full Text] [Related]
36. Transmission ratio distortion in the spinal muscular atrophy locus: data from 314 prenatal tests. Botta A; Tacconelli A; Bagni I; Giardina E; Bonifazi E; Pietropolli A; Clementi M; Novelli G Neurology; 2005 Nov; 65(10):1631-5. PubMed ID: 16301493 [TBL] [Abstract][Full Text] [Related]
37. Molecular analysis of SMN1 and NAIP genes in Egyptian patients with spinal muscular atrophy. Essawi ML; Effat LK; Shanab GM; Al-Ettribi GM; El-Haronui AA; Karim AM Bratisl Lek Listy; 2007; 108(3):133-7. PubMed ID: 17682539 [TBL] [Abstract][Full Text] [Related]