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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1911 2
1913 1
1917 2
1945 2
1946 8
1947 4
1948 6
1949 4
1950 9
1951 14
1952 19
1953 21
1954 21
1955 14
1956 16
1957 15
1958 29
1959 9
1960 7
1961 11
1962 17
1963 17
1964 9
1965 5
1966 9
1967 7
1968 8
1969 9
1970 11
1971 17
1972 5
1973 15
1974 9
1975 15
1976 20
1977 17
1978 20
1979 17
1980 20
1981 24
1982 19
1983 23
1984 28
1985 24
1986 27
1987 44
1988 82
1989 106
1990 80
1991 76
1992 89
1993 131
1994 106
1995 112
1996 148
1997 132
1998 105
1999 125
2000 131
2001 148
2002 156
2003 154
2004 149
2005 150
2006 142
2007 195
2008 213
2009 236
2010 269
2011 310
2012 340
2013 328
2014 355
2015 359
2016 341
2017 429
2018 474
2019 515
2020 667
2021 662
2022 615
2023 644
2024 250

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9,212 results

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Page 1
Spinal muscular atrophy.
Mercuri E, Sumner CJ, Muntoni F, Darras BT, Finkel RS. Mercuri E, et al. Nat Rev Dis Primers. 2022 Aug 4;8(1):52. doi: 10.1038/s41572-022-00380-8. Nat Rev Dis Primers. 2022. PMID: 35927425 Review.
Spinal muscular atrophy (SMA) is a neurodegenerative disorder caused by mutations in SMN1 (encoding survival motor neuron protein (SMN)). ...
Spinal muscular atrophy (SMA) is a neurodegenerative disorder caused by mutations in SMN1 (encoding survival motor neur …
Spinal Muscular Atrophy.
Kolb SJ, Kissel JT. Kolb SJ, et al. Neurol Clin. 2015 Nov;33(4):831-46. doi: 10.1016/j.ncl.2015.07.004. Neurol Clin. 2015. PMID: 26515624 Free PMC article. Review.
Spinal muscular atrophy is an autosomal-recessive disorder characterized by degeneration of motor neurons in the spinal cord and caused by mutations in the survival motor neuron 1 gene, SMN1. ...
Spinal muscular atrophy is an autosomal-recessive disorder characterized by degeneration of motor neurons in the spinal …
Spinal Muscular Atrophy.
Nicolau S, Waldrop MA, Connolly AM, Mendell JR. Nicolau S, et al. Semin Pediatr Neurol. 2021 Apr;37:100878. doi: 10.1016/j.spen.2021.100878. Epub 2021 Feb 11. Semin Pediatr Neurol. 2021. PMID: 33892848 Review.
Spinal muscular atrophy is one of the most common neuromuscular disorders of childhood and has high morbidity and mortality. ...Newborn screening programs are enabling earlier diagnosis and treatment and better outcomes, but respiratory care and other support …
Spinal muscular atrophy is one of the most common neuromuscular disorders of childhood and has high morbidity and morta …
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care.
Mercuri E, Finkel RS, Muntoni F, Wirth B, Montes J, Main M, Mazzone ES, Vitale M, Snyder B, Quijano-Roy S, Bertini E, Davis RH, Meyer OH, Simonds AK, Schroth MK, Graham RJ, Kirschner J, Iannaccone ST, Crawford TO, Woods S, Qian Y, Sejersen T; SMA Care Group. Mercuri E, et al. Neuromuscul Disord. 2018 Feb;28(2):103-115. doi: 10.1016/j.nmd.2017.11.005. Epub 2017 Nov 23. Neuromuscul Disord. 2018. PMID: 29290580 Free article. Review.
Spinal muscular atrophy (SMA) is a severe neuromuscular disorder due to a defect in the survival motor neuron 1 (SMN1) gene. ...
Spinal muscular atrophy (SMA) is a severe neuromuscular disorder due to a defect in the survival motor neuron 1 (SMN1) …
Spinal Muscular Atrophy.
Oskoui M, Servais L. Oskoui M, et al. Continuum (Minneap Minn). 2023 Oct 1;29(5):1564-1584. doi: 10.1212/CON.0000000000001338. Continuum (Minneap Minn). 2023. PMID: 37851043 Review.
OBJECTIVE: This article provides a comprehensive overview of the diagnostic assessment and treatment of individuals with spinal muscular atrophy (SMA) due to homozygous deletions of SMN1 . ...
OBJECTIVE: This article provides a comprehensive overview of the diagnostic assessment and treatment of individuals with spinal mu …
[Update on spinal muscular atrophy treatment].
Erazo Torricelli R. Erazo Torricelli R. Medicina (B Aires). 2022 Aug 30;82 Suppl 3:76-81. Medicina (B Aires). 2022. PMID: 36054863 Free article. Review. Spanish.
Spinal muscular atrophy (SMA) has been known as a clinical entity for 130 yearsis still recognized today as the most severe autosomal recessive neuromuscular disease (5q,13,2) in pediatrics. ...
Spinal muscular atrophy (SMA) has been known as a clinical entity for 130 yearsis still recognized today as the most se …
Advances in Treatment of Spinal Muscular Atrophy - New Phenotypes, New Challenges, New Implications for Care.
Schorling DC, Pechmann A, Kirschner J. Schorling DC, et al. J Neuromuscul Dis. 2020;7(1):1-13. doi: 10.3233/JND-190424. J Neuromuscul Dis. 2020. PMID: 31707373 Free PMC article. Review.
Spinal Muscular Atrophy (SMA) is caused by autosomal recessive mutations in SMN1 and results in the loss of motor neurons and progressive muscle weakness. ...In this review we provide an overview of available and emerging therapies for spinal muscul …
Spinal Muscular Atrophy (SMA) is caused by autosomal recessive mutations in SMN1 and results in the loss of motor neuro …
Spinal muscular atrophy: diagnosis and management in a new therapeutic era.
Arnold WD, Kassar D, Kissel JT. Arnold WD, et al. Muscle Nerve. 2015 Feb;51(2):157-67. doi: 10.1002/mus.24497. Epub 2014 Dec 16. Muscle Nerve. 2015. PMID: 25346245 Free PMC article. Review.
Spinal muscular atrophy (SMA) describes a group of disorders associated with spinal motor neuron loss. ...
Spinal muscular atrophy (SMA) describes a group of disorders associated with spinal motor neuron loss. ...
Spinal Muscular Atrophy: The Past, Present, and Future of Diagnosis and Treatment.
Nishio H, Niba ETE, Saito T, Okamoto K, Takeshima Y, Awano H. Nishio H, et al. Int J Mol Sci. 2023 Jul 26;24(15):11939. doi: 10.3390/ijms241511939. Int J Mol Sci. 2023. PMID: 37569314 Free PMC article. Review.
Spinal muscular atrophy (SMA) is a lower motor neuron disease with autosomal recessive inheritance. ...
Spinal muscular atrophy (SMA) is a lower motor neuron disease with autosomal recessive inheritance. ...
Management of Spinal Muscular Atrophy in the Adult Population.
Rad N, Cai H, Weiss MD. Rad N, et al. Muscle Nerve. 2022 May;65(5):498-507. doi: 10.1002/mus.27519. Epub 2022 Feb 26. Muscle Nerve. 2022. PMID: 35218574 Review.
Spinal muscular atrophy (SMA) is a group of neurodegenerative disorders resulting from the loss of spinal motor neurons. 95% of patients share a pathogenic mechanism of loss of survival motor neuron (SMN) 1 protein expression due to homozygous deletions or ot …
Spinal muscular atrophy (SMA) is a group of neurodegenerative disorders resulting from the loss of spinal motor neurons …
9,212 results