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9. 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]
10. [Prenatal diagnosis of spinal muscular atrophy (SMA) -- indications, restrictions, interpretation of results]. Jedrzejowska M; Zimowski J; Wiszniewski W; Sielska D; Bal J; Mazurczak T; Hausmanowa-Petrusewicz I; Zaremba J Med Wieku Rozwoj; 2004; 8(3 Pt 2):651-61. PubMed ID: 15858238 [TBL] [Abstract][Full Text] [Related]
11. Rapid genetic diagnosis and prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography. Zhu HY; Wu LQ; Pan Q; Tang BS; Liang DS; Long ZG; Dai HP; Xia K; Xia JH Chin Med J (Engl); 2006 Jul; 119(14):1222-5. PubMed ID: 16863617 [No Abstract] [Full Text] [Related]
15. Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy. Beattie CE; Carrel TL; McWhorter ML J Child Neurol; 2007 Aug; 22(8):995-1003. PubMed ID: 17761655 [TBL] [Abstract][Full Text] [Related]
16. Adolescent spinal muscular atrophy with calf hypertrophy and a deletion in the SMN gene. Yiu EM; Ravat S; Ryan MM; Shield LK; Smith LJ; Kornberg AJ Muscle Nerve; 2008 Jul; 38(1):930-2. PubMed ID: 18508340 [TBL] [Abstract][Full Text] [Related]
17. [Proximal autosomal recessive types of spinal muscular atrophy]. Kolokolov OV; Iudina GK; Solovykh NN; Evgrafov OV Zh Nevrol Psikhiatr Im S S Korsakova; 2003; 103(8):66-8. PubMed ID: 14564781 [TBL] [Abstract][Full Text] [Related]
20. 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; 11(4):235-9. PubMed ID: 17276711 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]