Talk:Hirayama disease/Archive 1
Appearance
(Redirected from Talk:Monomelic amyotrophy/Archive 1)
This is an archive of past discussions about Hirayama disease. Do not edit the contents of this page. If you wish to start a new discussion or revive an old one, please do so on the current talk page. |
Archive 1 |
GOAL: To maintain the format of Monomelic amyotrophy version as edited by Jytdog at 22:21, 7 May 2018, while replacing all dubious and unverifiable text with accurate well-referenced material.
Additional discussion can be found here:
- Talk:Monomelic amyotrophy
- User talk:GeeBee60#Editing about health and medicine
- Wikipedia talk:No original research#Acceptable sources
Thanks for feedback GeeBee60 (talk) 11:17, 16 May 2018 (UTC)
content examples
(This lifted from a different article, to serve as inspiration / reference while rebuilding MMA article)
- Contents
- 1 Signs and symptoms
- 2 Genetics
- 3 Pathophysiology
- 4 Diagnosis and evaluation
- 4.1 Genetic testing
- 4.2 Clinical
- 4.3 Differential diagnosis
- 5 Management
- 6 Prognosis
- 7 Epidemiology
- 8 History
- 9 Research directions
- 9.1 Gene downregulation and silencing
- 9.2 Reducing toxicity and increasing cell survival
- 9.3 Cell replacement therapies
- 10 References
Further reading
Not appropriate section for the article. If the ref are important, incorporate them. David notMD (talk) 10:38, 25 May 2018 (UTC)
- Di Muzio, A.; Pizzi, C. D.; Lugaresi, A.; Ragno, M.; Uncini, A. (1994). "Benign monomelic amyotrophy of lower limb: A rare entity with a characteristic muscular CT". Journal of the Neurological Sciences. 126 (2): 153–161. doi:10.1016/0022-510X(94)90266-6. PMID 7853021.
- Di Guglielmo, G.; Brahe, C.; Di Muzio, A.; Uncini, A. (1996). "Benign monomelic amyotrophies of upper and lower limb are not associated to deletions of survival motor neuron gene". Journal of the Neurological Sciences. 141 (1–2): 111–113. doi:10.1016/0022-510X(96)00154-2. PMID 8880702.
- Münchau, A.; Rosenkranz, T. (2000). "Benign Monomelic Amyotrophy of the Lower Limb – Case Report and Brief Review of the Literature". European Neurology. 43 (4): 238–240. doi:10.1159/000008183. PMID 10828656.
- Freitas, M. R. G. D.; Nascimento, O. J. M. (2000). "Benign monomelic amyotrophy: A study of twenty-one cases" (PDF). Arquivos de Neuro-Psiquiatria. 58 (3B): 808–813. doi:10.1590/S0004-282X2000000500003. PMID 11018815.
- Gourie-Devi, M.; Nalini, A. (2001). "Sympathetic skin response in monomelic amyotrophy". Acta Neurologica Scandinavica. 104 (3): 162–166. doi:10.1034/j.1600-0404.2001.00016.x. PMID 11551236.
- Nalini, Atchayaram; Gourie-Devi, Mandavilli; Thennarasu, Kandavel; Ramalingaiah, Aravinda Hanumanthapura (22 May 2014). "Monomelic amyotrophy: Clinical profile and natural history of 279 cases seen over 35 years (1976–2010)". Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 15 (5–6): 457–465. doi:10.3109/21678421.2014.903976.
- Neves, M. A. O.; Freitas, M. R. G. D.; Mello, M. P. D.; Dumard, C. H.; Freitas, G. R. D.; Nascimento, O. J. M. (2007). "Benign monomelic amyotrophy with proximal upper limb involvement: Case report". Arquivos de Neuro-Psiquiatria. 65 (2b): 524–527. doi:10.1590/S0004-282X2007000300032. PMID 17665029.
- Zhou, Bo; Chen, Lei; Fan, Dongsheng; Zhou, Dong (26 February 2010). "Clinical features of Hirayama disease in mainland China". Amyotrophic Lateral Sclerosis. 11 (1–2): 133–139. doi:10.3109/17482960902912407.
{{cite journal}}
:|access-date=
requires|url=
(help) Review of 179 cases in mainland China.