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23. Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy. Bertini E; Gadisseux JL; Palmieri G; Ricci E; Di Capua M; Ferriere G; Lyon G Am J Med Genet; 1989 Jul; 33(3):328-35. PubMed ID: 2801766 [TBL] [Abstract][Full Text] [Related]
25. Case reports of progressive infantile muscular atrophy (Werdnig-Hoffmann) in fraternal twins. LEYRER RH AMA Am J Dis Child; 1954 Nov; 88(5):604-5. PubMed ID: 13206380 [No Abstract] [Full Text] [Related]
26. A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN gene. Lohkamp LN; von Au K; Goebel HH; Kress W; Grieben U; Drossel K; Garbes L; Wirth B; Heppner FL; Stenzel W J Child Neurol; 2014 Feb; 29(2):254-9. PubMed ID: 24334346 [TBL] [Abstract][Full Text] [Related]
27. Therapy for Spinal Muscular Atrophy. Mendell JR N Engl J Med; 2018 Feb; 378(5):487. PubMed ID: 29394473 [No Abstract] [Full Text] [Related]
28. Therapy for Spinal Muscular Atrophy. Whittaker HT; Michell-Robinson MA N Engl J Med; 2018 Feb; 378(5):487. PubMed ID: 29394306 [No Abstract] [Full Text] [Related]
29. Therapy for Spinal Muscular Atrophy. Finkel RS; Farwell W N Engl J Med; 2018 Feb; 378(5):487-488. PubMed ID: 29385371 [No Abstract] [Full Text] [Related]
30. [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]
31. Two early infantile hereditary cases of progressive muscular atrophy simulating dystrophy, but on a neural basis. 1891. Werdnig G Arch Neurol; 1971 Sep; 25(3):276-8. PubMed ID: 4952838 [No Abstract] [Full Text] [Related]
32. Stakeholder collaboration for spinal muscular atrophy therapy development. Aartsma-Rus A; Balabanov P; Binetti L; Haas M; Haberkamp M; Mitchell J; Rosa MM; Muntoni F; Finkel R; Mercuri E Lancet Neurol; 2017 Apr; 16(4):264. PubMed ID: 28327335 [No Abstract] [Full Text] [Related]
33. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)]. HORSTMANN W Z Kinderheilkd; 1959; 82():649-67. PubMed ID: 13848453 [No Abstract] [Full Text] [Related]
34. Genetic therapies for spinal muscular atrophy type 1. Aartsma-Rus A Lancet Neurol; 2018 Feb; 17(2):111-112. PubMed ID: 29229374 [No Abstract] [Full Text] [Related]
35. New Frontiers in the Treatment of Spinal Muscular Atrophy. Power CL; O'Rourke DJ Ir Med J; 2018 Mar; 111(3):705. PubMed ID: 30376223 [No Abstract] [Full Text] [Related]
36. [A CASE OF SPINAL PROGRESSIVE MUSCULAR ATROPHY (PROXIMAL TYPE)]. OKUMURA N; TERAO A; MII T; IKEDA H; AKIYAMA J No To Shinkei; 1963 Oct; 15():923-7. PubMed ID: 14052948 [No Abstract] [Full Text] [Related]
37. Turning the tide in spinal muscular atrophy: A different respiratory course. Mayer OH Pediatr Pulmonol; 2019 Jul; 54(7):935-936. PubMed ID: 30884211 [No Abstract] [Full Text] [Related]
38. Lumbosacral ventral spinal nerve root atrophy identified on MRI in a case of spinal muscular atrophy type II. Smith G; Bell SK; Sladky JT; Kang PB; Albayram MS Clin Imaging; 2019; 53():134-137. PubMed ID: 30340076 [TBL] [Abstract][Full Text] [Related]
39. [Difficulty in surrogate decision making in spinal muscular atrophy type 1]. Laxe S An Pediatr (Barc); 2016 Sep; 85(3):165. PubMed ID: 27198884 [No Abstract] [Full Text] [Related]
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