References analysis of the Wikipedia article "Degeneratiivinen sairaus" in the Finnish version

doi.org

dx.doi.org

C Soto, N Satani: The intricate mechanisms of neurodegeneration in prion diseases. Trends in molecular medicine, 2011, nro 1, s. 14–24. PubMed:20889378. doi:10.1016/j.molmed.2010.09.001. ISSN 1471-4914. Artikkelin verkkoversio.

Á Patzkó, ME Shy: Update on Charcot-Marie-Tooth Disease. Current neurology and neuroscience reports, 2011, nro 1, s. 78–88. PubMed:21080241. doi:10.1007/s11910-010-0158-7. ISSN 1528-4042. Artikkelin verkkoversio.

M Delatycki, R Williamson, S Forrest: Friedreich ataxia: an overview. Journal of Medical Genetics, 2000, nro 1, s. 1–8. PubMed:10633128. doi:10.1136/jmg.37.1.1. ISSN 0022-2593. Artikkelin verkkoversio.

JD Warren, JD Rohrer, MN Rossor: Frontotemporal dementia. The BMJ, 6.8.2013, nro 347. PubMed:23920254. doi:10.1136/bmj.f4827. ISSN 0959-8138. Artikkelin verkkoversio.

H Li, Y Zou, X Bao, H Wang, J Wang, H Jin: Monozygotic twins with infantile neuroaxonal dystrophy: A case report and literature review. Experimental and Therapeutic Medicine, 2016, nro 5, s. 3387–3389. PubMed:27882168. doi:10.3892/etm.2016.3761. ISSN 1792-0981. Artikkelin verkkoversio.

AE Davidson, S Hayes, AJ Hardcastle, SJ Tuft: The pathogenesis of keratoconus. Eye, 2014, nro 2, s. 189–195. PubMed:24357835. doi:10.1038/eye.2013.278. ISSN 0950-222X. Artikkelin verkkoversio.

IS Bazan, WH Fares: Pulmonary hypertension: diagnostic and therapeutic challenges. Therapeutics and Clinical Risk Management, 17.8.2015, nro 11, s. 1221–1233. PubMed:26316767. doi:10.2147/TCRM.S74881. ISSN 1176-6336. Artikkelin verkkoversio.

JC Maroon et al.: Chronic Traumatic Encephalopathy in Contact Sports: A Systematic Review of All Reported Pathological Cases. PLoS ONE, 11.2.2015, nro 2. PubMed:25671598. doi:10.1371/journal.pone.0117338. ISSN 1932-6203. Artikkelin verkkoversio.

D Fraser-Pitt, D O’Neil: Cystic fibrosis – a multiorgan protein misfolding disease. Future Science OA, 2015, nro 2. PubMed:28031875. doi:10.4155/fso.15.57. ISSN 2056-5623. Artikkelin verkkoversio.

MS van der Knaap, M Bugiani: Leukodystrophies: a proposed classification system based on pathological changes and pathogenetic mechanisms. Acta Neuropathologica, 2017, nro 3, s. 351–382. PubMed:28638987. doi:10.1007/s00401-017-1739-1. ISSN 1432-0533. Artikkelin verkkoversio.

J Shin et al.: Wasting Mechanisms in Muscular Dystrophy. The international journal of biochemistry & cell biology, 2013, nro 10, s. 2266–2279. PubMed:23669245. doi:10.1016/j.biocel.2013.05.001. ISSN 1357-2725. Artikkelin verkkoversio.

L Gao et al.: Recent molecular biological progress in Marfan syndrome and Marfan-associated disorders. Ageing Research Reviews, 2010, nro 3, s. 363–368. doi:10.1016/j.arr.2009.09.001. ISSN 1568-1637. Artikkelin verkkoversio.

AW El-Hattab, F Scaglia: Mitochondrial DNA Depletion Syndromes: Review and Updates of Genetic Basis, Manifestations, and Therapeutic Options. Neurotherapeutics, 2013, nro 2, s. 186–198. PubMed:23385875. doi:10.1007/s13311-013-0177-6. ISSN 1933-7213. Artikkelin verkkoversio.

K Ubhi, P Low, E Masliah: Multiple System Atrophy: A Clinical and Neuropathological Perspective. Trends in neurosciences, 2011, nro 11, s. 581–590. PubMed:21962754. doi:10.1016/j.tins.2011.08.003. ISSN 0166-2236. Artikkelin verkkoversio.

D Fitzner, M Simons: Chronic Progressive Multiple Sclerosis – Pathogenesis of Neurodegeneration and Therapeutic Strategies. Current Neuropharmacology, 1.9.2010, nro 3, s. 305–315. doi:10.2174/157015910792246218. ISSN 1570-159X. Artikkelin verkkoversio.

WRH Evans, CJ Hendriksz: Niemann–Pick type C disease – the tip of the iceberg? A review of neuropsychiatric presentation, diagnosis and treatment. BJPsych Bulletin, 2017, nro 2, s. 109–114. PubMed:28400970. doi:10.1192/pb.bp.116.054072. ISSN 2056-4694. Artikkelin verkkoversio.

P Abdel-Ahad et al.: Les manifestations psychiatriques dans la polyarthrite rhumatoïde. L'Encéphale, 2016, nro 2, s. 172–176. doi:10.1016/j.encep.2015.12.008. ISSN 0013-7006. Artikkelin verkkoversio.

Y Shen, Y Zhang, L Shen: Postmenopausal women with osteoporosis and osteoarthritis show different microstructural characteristics of trabecular bone in proximal tibia using high-resolution magnetic resonance imaging at 3 tesla. BMC Musculoskeletal Disorders, 15.4.2013, nro 14, s. 136. PubMed:23587336. doi:10.1186/1471-2474-14-136. ISSN 1471-2474. Artikkelin verkkoversio.

LF Owolabi: Progressive Supranuclear Palsy Misdiagnosed as Parkinson's Disease: A Case Report and Review of Literature. Annals of Medical and Health Sciences Research, 2013, nro Suppl1, s. S44–S47. PubMed:24349849. doi:10.4103/2141-9248.121221. ISSN 2141-9248. Artikkelin verkkoversio.

JS Walia et al.: Long-Term Correction of Sandhoff Disease Following Intravenous Delivery of rAAV9 to Mouse Neonates. Molecular Therapy, 2015, nro 3, s. 414–422. PubMed:25515709. doi:10.1038/mt.2014.240. ISSN 1525-0016. Artikkelin verkkoversio.

A Anand et al.: Using Current Data to Define New Approach in Age Related Macular Degeneration: Need to Accelerate Translational Research. Current Genomics, 2014, nro 4, s. 266–277. PubMed:25132797. doi:10.2174/1389202915666140516204512. ISSN 1389-2029. Artikkelin verkkoversio.

C Simone et al.: Is Spinal Muscular Atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications? CMLS, 2016, nro 5, s. 1003–1020. PubMed:26681261. doi:10.1007/s00018-015-2106-9. ISSN 1420-682X. Artikkelin verkkoversio.

HL Paulson: The Spinocerebellar Ataxias. Journal of neuro-ophthalmology, 2009, nro 3, s. 227–237. PubMed:19726947. doi:10.1097/WNO0b013e3181b416de. ISSN 1070-8022. Artikkelin verkkoversio.

SK Jafri, R Kumar, SH Ibrahim: Subacute sclerosing panencephalitis – current perspectives. Pediatric Health, Medicine and Therapeutics, 26.6.2018, nro 9, s. 67–71. PubMed:29985487. doi:10.2147/PHMT.S126293. ISSN 1179-9927. Artikkelin verkkoversio.

C Hamel: Retinitis pigmentosa. Orphanet Journal of Rare Diseases, 11.10.2006, nro 1, s. 40. PubMed:17032466. doi:10.1186/1750-1172-1-40. ISSN 1750-1172. Artikkelin verkkoversio.

europepmc.org

nih.gov

ncbi.nlm.nih.gov

PC Nopoulos: Huntington disease: a single-gene degenerative disorder of the striatum. Dialogues in Clinical Neuroscience, 2016, nro 1, s. 91–98. PubMed:27069383. ISSN 1294-8322. Artikkelin verkkoversio.

JD Warren, JD Rohrer, MN Rossor: Frontotemporal dementia. The BMJ, 6.8.2013, nro 347. PubMed:23920254. doi:10.1136/bmj.f4827. ISSN 0959-8138. Artikkelin verkkoversio.

SE Mole, RE Williams: GeneReviews®. Seattle, Washington: University of Washington, 1993. Teoksen verkkoversio (viitattu 17.9.2018).

AE Davidson, S Hayes, AJ Hardcastle, SJ Tuft: The pathogenesis of keratoconus. Eye, 2014, nro 2, s. 189–195. PubMed:24357835. doi:10.1038/eye.2013.278. ISSN 0950-222X. Artikkelin verkkoversio.

HL Paulson: The Spinocerebellar Ataxias. Journal of neuro-ophthalmology, 2009, nro 3, s. 227–237. PubMed:19726947. doi:10.1097/WNO0b013e3181b416de. ISSN 1070-8022. Artikkelin verkkoversio.

C Hamel: Retinitis pigmentosa. Orphanet Journal of Rare Diseases, 11.10.2006, nro 1, s. 40. PubMed:17032466. doi:10.1186/1750-1172-1-40. ISSN 1750-1172. Artikkelin verkkoversio.

pubmed.ncbi.nlm.nih.gov

JD Warren, JD Rohrer, MN Rossor: Frontotemporal dementia. The BMJ, 6.8.2013, nro 347. PubMed:23920254. doi:10.1136/bmj.f4827. ISSN 0959-8138. Artikkelin verkkoversio.

AE Davidson, S Hayes, AJ Hardcastle, SJ Tuft: The pathogenesis of keratoconus. Eye, 2014, nro 2, s. 189–195. PubMed:24357835. doi:10.1038/eye.2013.278. ISSN 0950-222X. Artikkelin verkkoversio.

HL Paulson: The Spinocerebellar Ataxias. Journal of neuro-ophthalmology, 2009, nro 3, s. 227–237. PubMed:19726947. doi:10.1097/WNO0b013e3181b416de. ISSN 1070-8022. Artikkelin verkkoversio.

C Hamel: Retinitis pigmentosa. Orphanet Journal of Rare Diseases, 11.10.2006, nro 1, s. 40. PubMed:17032466. doi:10.1186/1750-1172-1-40. ISSN 1750-1172. Artikkelin verkkoversio.

rarediseases.info.nih.gov

Ehlers-Danlos syndromes rarediseases.info.nih.gov. Arkistoitu 16.6.2018. Viitattu 17.9.2018.

Cytochrome c oxidase deficiency rarediseases.info.nih.gov. Arkistoitu 22.10.2017. Viitattu 17.9.2018.

web.archive.org

What is Degenerative Disease docdoc.com.sg. Arkistoitu 17.9.2018. Viitattu 17.9.2018.

neurodegenerative disorder National Cancer Institute. 2.2.2011. Arkistoitu 23.4.2018. Viitattu 17.9.2018.

Neurodegenerative Diseases medlineplus.gov. Arkistoitu 28.7.2018. Viitattu 17.9.2018.

Ehlers-Danlos syndromes rarediseases.info.nih.gov. Arkistoitu 16.6.2018. Viitattu 17.9.2018.

Cytochrome c oxidase deficiency rarediseases.info.nih.gov. Arkistoitu 22.10.2017. Viitattu 17.9.2018.

worldcat.org

JD Warren, JD Rohrer, MN Rossor: Frontotemporal dementia. The BMJ, 6.8.2013, nro 347. PubMed:23920254. doi:10.1136/bmj.f4827. ISSN 0959-8138. Artikkelin verkkoversio.

AE Davidson, S Hayes, AJ Hardcastle, SJ Tuft: The pathogenesis of keratoconus. Eye, 2014, nro 2, s. 189–195. PubMed:24357835. doi:10.1038/eye.2013.278. ISSN 0950-222X. Artikkelin verkkoversio.

HL Paulson: The Spinocerebellar Ataxias. Journal of neuro-ophthalmology, 2009, nro 3, s. 227–237. PubMed:19726947. doi:10.1097/WNO0b013e3181b416de. ISSN 1070-8022. Artikkelin verkkoversio.

C Hamel: Retinitis pigmentosa. Orphanet Journal of Rare Diseases, 11.10.2006, nro 1, s. 40. PubMed:17032466. doi:10.1186/1750-1172-1-40. ISSN 1750-1172. Artikkelin verkkoversio.

Degeneratiivinen sairaus (Finnish Wikipedia)

cancer.gov

docdoc.com.sg

doi.org

dx.doi.org

europepmc.org

medlineplus.gov

nih.gov

ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov

rarediseases.info.nih.gov

sciencemediacentre.org

web.archive.org

worldcat.org