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598 related items for PubMed ID: 17761649
21. Identification of a battery of tests for drug candidate evaluation in the SMNDelta7 neonate model of spinal muscular atrophy. El-Khodor BF, Edgar N, Chen A, Winberg ML, Joyce C, Brunner D, Suárez-Fariñas M, Heyes MP. Exp Neurol; 2008 Jul; 212(1):29-43. PubMed ID: 18455159 [Abstract] [Full Text] [Related]
24. [Quantitative analysis of the genes determining spinal muscular atrophy]. Nagymihály M, Herczegfalvi A, Tímár L, Karcagi V. Ideggyogy Sz; 2009 Nov 30; 62(11-12):390-7. PubMed ID: 20025129 [Abstract] [Full Text] [Related]
25. Prenatal diagnosis for risk of spinal muscular atrophy. Cuscó I, Barceló MJ, Soler C, Parra J, Baiget M, Tizzano E. BJOG; 2002 Nov 30; 109(11):1244-9. PubMed ID: 12452462 [Abstract] [Full Text] [Related]
27. Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system. Shaw SW, Cheng PJ, Chang SD, Lin YT, Hung CC, Chen CP, Su YN. Acta Obstet Gynecol Scand; 2008 Nov 30; 87(9):960-8. PubMed ID: 18720039 [Abstract] [Full Text] [Related]
28. Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome. Voutoufianakis S, Psoni S, Vorgia P, Tsekoura F, Kekou K, Traeger-Synodinos J, Kitsiou S, Kanavakis E, Fryssira H. Eur J Paediatr Neurol; 2007 Jul 30; 11(4):235-9. PubMed ID: 17276711 [Abstract] [Full Text] [Related]
29. Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families. Savas S, Eraslan S, Kantarci S, Karaman B, Acarsoz D, Tükel T, Cogulu O, Ozkinay F, Basaran S, Aydinli K, Yuksel-Apak M, Kirdar B. Prenat Diagn; 2002 Aug 30; 22(8):703-9. PubMed ID: 12210580 [Abstract] [Full Text] [Related]