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.
169 related articles for article (PubMed ID: 8795842)
61. [The spectrum of spinal muscular atrophies: a population study]. Rudenskaia GE; Mamedova RA Zh Nevrol Psikhiatr Im S S Korsakova; 1997; 97(8):22-5. PubMed ID: 9343477 [TBL] [Abstract][Full Text] [Related]
62. Brief report: phenotypic rescue of induced pluripotent stem cell-derived motoneurons of a spinal muscular atrophy patient. Chang T; Zheng W; Tsark W; Bates S; Huang H; Lin RJ; Yee JK Stem Cells; 2011 Dec; 29(12):2090-3. PubMed ID: 21956898 [TBL] [Abstract][Full Text] [Related]
63. Deletions in the spinal muscular atrophy gene region in a newborn with neuropathy and extreme generalized muscular weakness. Hergersberg M; Glatzel M; Capone A; Achermann S; Hagmann A; Fischer J; Ersch J; Aguzzi A; Boltshauser E Eur J Paediatr Neurol; 2000; 4(1):35-8. PubMed ID: 10701103 [TBL] [Abstract][Full Text] [Related]
64. Deletions in the SMN and NAIP genes in patients with spinal muscular atrophy in Croatia. Sertić J; Barisić N; Sostarko M; Bosnjak N; Culić V; Cvitanović L; Ferencak G; Brzović Z; Stavljenić-Rukavina A Coll Antropol; 1997 Dec; 21(2):487-92. PubMed ID: 9439064 [TBL] [Abstract][Full Text] [Related]
65. Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration. Rudnik-Schöneborn S; Wirth B; Röhrig D; Saule H; Zerres K Neuromuscul Disord; 1995 Jan; 5(1):19-23. PubMed ID: 7719136 [TBL] [Abstract][Full Text] [Related]
66. Clinical and molecular genetic features of congenital spinal muscular atrophy. Devriendt K; Lammens M; Schollen E; Van Hole C; Dom R; Devlieger H; Cassiman JJ; Fryns JP; Matthijs G Ann Neurol; 1996 Nov; 40(5):731-8. PubMed ID: 8957014 [TBL] [Abstract][Full Text] [Related]
67. Evidence of reduced frequency of spinal muscular atrophy type I in the Cuban population. Zaldívar T; Montejo Y; Acevedo AM; Guerra R; Vargas J; Garofalo N; Alvarez R; Alvarez MA; Hardiman O Neurology; 2005 Aug; 65(4):636-8. PubMed ID: 16116135 [TBL] [Abstract][Full Text] [Related]
68. Augmenting the SMN Protein to Treat Infantile Spinal Muscular Atrophy. Kim JK; Monani UR Neuron; 2018 Mar; 97(5):1001-1003. PubMed ID: 29518354 [TBL] [Abstract][Full Text] [Related]
69. New insights into the pathogenesis of spinal muscular atrophy. Ito Y; Shibata N; Saito K; Kobayashi M; Osawa M Brain Dev; 2011 Apr; 33(4):321-31. PubMed ID: 20605078 [TBL] [Abstract][Full Text] [Related]
70. Refinement of the spinal muscular atrophy locus by genetic and physical mapping. Wang CH; Kleyn PW; Vitale E; Ross BM; Lien L; Xu J; Carter TA; Brzustowicz LM; Obici S; Selig S Am J Hum Genet; 1995 Jan; 56(1):202-9. PubMed ID: 7825579 [TBL] [Abstract][Full Text] [Related]
71. Genotype-phenotype correlation of SMN locus genes in spinal muscular atrophy children from Argentina. Medrano S; Monges S; Gravina LP; Alías L; Mozzoni J; Aráoz HV; Bernal S; Moresco A; Chertkoff L; Tizzano E Eur J Paediatr Neurol; 2016 Nov; 20(6):910-917. PubMed ID: 27510309 [TBL] [Abstract][Full Text] [Related]
72. Spinal muscular atrophy: new thoughts on the pathogenesis and classification schema. Russman BS; Iannacone ST; Buncher CR; Samaha FJ; White M; Perkins B; Zimmerman L; Smith C; Burhans K; Barker L J Child Neurol; 1992 Oct; 7(4):347-53. PubMed ID: 1469240 [TBL] [Abstract][Full Text] [Related]
73. Phenotype and genotype correlation in childhood spinal muscular atrophy. Hausmanowa-Petrusewicz I Neurol Neurochir Pol; 2001; 35 Suppl 3():29-35. PubMed ID: 12001651 [TBL] [Abstract][Full Text] [Related]
74. The gene copy ratios of SMN1/SMN2 in Japanese carriers with type I spinal muscular atrophy. Diep Tran T; Kroepfl T; Saito M; Nagura M; Ichiseki H; Kubota M; Toda T; Sakakihara Y Brain Dev; 2001 Aug; 23(5):321-6. PubMed ID: 11504604 [TBL] [Abstract][Full Text] [Related]
75. A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency. Pronicki M; Kowalski P; Piekutowska-Abramczuk D; Taybert J; Karkucinska-Wieckowska A; Szymanska-Debinska T; Karczmarewicz E; Pajdowska M; Migdal M; Milewska-Bobula B; Sykut-Cegielska J; Popowska E Eur J Paediatr Neurol; 2010 May; 14(3):253-60. PubMed ID: 19879173 [TBL] [Abstract][Full Text] [Related]
76. The ultrastructure of peripheral nerve, motor end-plate and skeletal muscle in patients suffering from spinal muscular atrophy with respiratory distress type 1 (SMARD1). Diers A; Kaczinski M; Grohmann K; Hübner C; Stoltenburg-Didinger G Acta Neuropathol; 2005 Sep; 110(3):289-97. PubMed ID: 16025284 [TBL] [Abstract][Full Text] [Related]
77. Spinal muscular atrophy type I mimicking critical illness neuropathy in a paediatric intensive care neonate: electrophysiological features. Fernández-Torre JL; Teja JL; Castellanos A; Figols J; Obeso T; Arteaga R Brain Dev; 2008 Oct; 30(9):599-602. PubMed ID: 18384992 [TBL] [Abstract][Full Text] [Related]
78. De novo and inherited deletions of the 5q13 region in spinal muscular atrophies. Melki J; Lefebvre S; Burglen L; Burlet P; Clermont O; Millasseau P; Reboullet S; Bénichou B; Zeviani M; Le Paslier D Science; 1994 Jun; 264(5164):1474-7. PubMed ID: 7910982 [TBL] [Abstract][Full Text] [Related]
79. Linkage analysis of spinal muscular atrophy. Daniels RJ; Thomas NH; MacKinnon RN; Lehner T; Ott J; Flint TJ; Dubowitz V; Ignatius J; Donner M; Zerres K Genomics; 1992 Feb; 12(2):335-9. PubMed ID: 1346777 [TBL] [Abstract][Full Text] [Related]