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.
48. [Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]. Spiegel R; Hagmann A; Boltshauser E; Moser H Schweiz Med Wochenschr; 1996 May; 126(21):907-14. PubMed ID: 8693311 [TBL] [Abstract][Full Text] [Related]
49. A study of infantile motor neuron disease with neurofilament and ubiquitin immunocytochemistry. Lee S; Park YD; Yen SH; Ksiezak-Reding H; Goldman JE; Dickson DW Neuropediatrics; 1989 May; 20(2):107-11. PubMed ID: 2544822 [TBL] [Abstract][Full Text] [Related]
50. Spinal Muscular Atrophy: Past, Present, and Future. Ross LF; Kwon JM Neoreviews; 2019 Aug; 20(8):e437-e451. PubMed ID: 31371553 [TBL] [Abstract][Full Text] [Related]
51. Neuronal death is enhanced and begins during foetal development in type I spinal muscular atrophy spinal cord. Soler-Botija C; Ferrer I; Gich I; Baiget M; Tizzano EF Brain; 2002 Jul; 125(Pt 7):1624-34. PubMed ID: 12077011 [TBL] [Abstract][Full Text] [Related]
55. Cardiac defects contribute to the pathology of spinal muscular atrophy models. Shababi M; Habibi J; Yang HT; Vale SM; Sewell WA; Lorson CL Hum Mol Genet; 2010 Oct; 19(20):4059-71. PubMed ID: 20696672 [TBL] [Abstract][Full Text] [Related]
56. [Nerve growth factors: a hypothesis on their role in the pathogenesis of infantile spinal amyotrophies]. Henderson CE; Fardeau M Rev Neurol (Paris); 1988; 144(11):730-6. PubMed ID: 3231962 [TBL] [Abstract][Full Text] [Related]
57. [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children]. BRANDT S Nord Med; 1950 Sep; 44(37):1499. PubMed ID: 14806955 [No Abstract] [Full Text] [Related]
58. Infantile spinal muscular atrophy (SMA) and multiple congenital bone fractures in sibs: a lethal new syndrome. Borochowitz Z; Glick B; Blazer S J Med Genet; 1991 May; 28(5):345-8. PubMed ID: 1865475 [TBL] [Abstract][Full Text] [Related]
59. Spinal muscular atrophy due to double gene conversion event. Maamouri W; Hammer MB; Bouhlel Y; Souilem S; Khmiri N; Nehdi H; Hentati F; Amouri R Int J Neurosci; 2011 Feb; 121(2):107-11. PubMed ID: 21047176 [TBL] [Abstract][Full Text] [Related]