Distonija (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Distonija" in Serbian language version.

refsWebsite

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14nih.gov

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14doi.org

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3archive.org

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1institutducerveau-icm.org

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1msdmanuals.com

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1web.archive.org

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1dystonia.org.uk

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1passeportsante.net

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archive.org

Hersheson, Joshua; Mencacci, Niccolo E.; Davis, Mary; MacDonald, Nicola; Trabzuni, Daniah; Ryten, Mina; Pittman, Alan; Paudel, Reema; Kara, Eleanna; Fawcett, Katherine; Plagnol, Vincent; Bhatia, Kailash P.; Medlar, Alan J.; Stanescu, Horia C.; Hardy, John; Kleta, Robert; Wood, Nicholas W.; Houlden, Henry (2013). „Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia”. Annals of Neurology. 73 (4): 546—53. PMC 3698699 . PMID 23424103. doi:10.1002/ana.23832.
Valente, Enza Maria; Bentivoglio, Anna Rita; Cassetta, Emanuele; Dixon, Peter H.; Davis, Mary B.; Ferraris, Alessandro; Ialongo, Tamara; Frontali, Marina; Wood, Nicholas W.; Albanese, Alberto (2001). „DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial-cervical or upper limb onset”. Annals of Neurology. 49 (3): 362—6. PMID 11261511. doi:10.1002/ana.73.
Grimes, D. A.; Han, F.; Lang, A. E.; St. George-Hyssop, P.; Racacho, L.; Bulman, D. E. (2002). „A novel locus for inherited myoclonus-dystonia on 18p11”. Neurology. 59 (8): 1183—6. PMID 12391345. doi:10.1212/WNL.59.8.1183.

doi.org

Bertucco, M.; Terence, S. (2015). „Current and emerging strategies for treatment of childhood dystonia”. J Hand Therapy. 28 (2): 185—194. PMC 4424089 . PMID 25835254. doi:10.1016/j.jht.2014.11.002.
Albanese, A.; Lalli, S. (2009). „Is this dystonia?”. Mov Disord. 24 (12): 1725—1731. PMID 19554620. doi:10.1002/mds.22597.
Phukan J, Albanese A, Gasser T, Warner T (2011). „Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis.”. Lancet Neurol. 10 (12): 1074—1085. PMID 22030388. doi:10.1016/S1474-4422(11)70232-0.
Skogseid, I. M. (2014). „Dystonia - new advances in classification, genetics, pathophysiology and treatment”. Acta Neurol Scand Suppl. 129 (198): 13—9. PMID 24588501. doi:10.1111/ane.12231.
Jinnah, H.A.; Albanese, Alberto (2014). „The New Classification System for the Dystonias: Why Was It Needed and How Was It Developed?”. Mov Disord Clin Pract. 1 (4): 280—4. PMID 25485288. doi:10.1002/mdc3.12100.
Albanese A, Bhatia K, Bressman SB, DeLong MR, Fahn S, Fung VSC; et al. (2013). „Concept and classification of dystonia”. Mov Disord [Internet]. 28 (7): 863—73. PMC 3729880 . PMID 23649720. doi:10.1002/mds.25475. .
Mink, J. (2013). „Special concerns in defining, studying, and treating dystonia in children”. Movement Disorders. 28 (7): 921—925. PMC 3806453 . PMID 23893449. doi:10.1002/mds.25548.
Skogseid, I. M. (2014). „Dystonia--new advances in classification, genetics, pathophysiology and treatment”. Acta Neurol Scand Suppl. 129 (198): 13—9. PMID 24588501. doi:10.1111/ane.12231.
Hersheson, Joshua; Mencacci, Niccolo E.; Davis, Mary; MacDonald, Nicola; Trabzuni, Daniah; Ryten, Mina; Pittman, Alan; Paudel, Reema; Kara, Eleanna; Fawcett, Katherine; Plagnol, Vincent; Bhatia, Kailash P.; Medlar, Alan J.; Stanescu, Horia C.; Hardy, John; Kleta, Robert; Wood, Nicholas W.; Houlden, Henry (2013). „Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia”. Annals of Neurology. 73 (4): 546—53. PMC 3698699 . PMID 23424103. doi:10.1002/ana.23832.
Valente, Enza Maria; Bentivoglio, Anna Rita; Cassetta, Emanuele; Dixon, Peter H.; Davis, Mary B.; Ferraris, Alessandro; Ialongo, Tamara; Frontali, Marina; Wood, Nicholas W.; Albanese, Alberto (2001). „DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial-cervical or upper limb onset”. Annals of Neurology. 49 (3): 362—6. PMID 11261511. doi:10.1002/ana.73.
Grimes, D. A.; Han, F.; Lang, A. E.; St. George-Hyssop, P.; Racacho, L.; Bulman, D. E. (2002). „A novel locus for inherited myoclonus-dystonia on 18p11”. Neurology. 59 (8): 1183—6. PMID 12391345. doi:10.1212/WNL.59.8.1183.
Chouery, E.; Kfoury, J.; Delague, V.; Jalkh, N.; Bejjani, P.; Serre, J. L.; Mégarbané, A. (2008). „A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12”. Neurogenetics. 9 (4): 287—93. PMID 18688663. doi:10.1007/s10048-008-0142-4.
Charlesworth, Gavin; Plagnol, Vincent; Holmström, Kira M.; Bras, Jose; Sheerin, Una-Marie; Preza, Elisavet; Rubio-Agusti, Ignacio; Ryten, Mina; Schneider, Susanne A.; Stamelou, Maria; Trabzuni, Daniah; Abramov, Andrey Y.; Bhatia, Kailash P.; Wood, Nicholas W. (2012). „Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis”. The American Journal of Human Genetics. 91 (6): 1041—50. PMC 3516598 . PMID 23200863. doi:10.1016/j.ajhg.2012.10.024.
Roubertie, A.; Echenne, Bernard; Cif, Laura; Vayssiere, Nathalie; Hemm, Simone; Coubes, Philippe (2000). „Treatment of early-onset dystonia: Update and a new perspective”. Child's Nerv Sys. 16 (6): 334—340. PMID 10933228. doi:10.1007/s003810050528.

dystonia.org.uk

MacKinnon, Fiona. „Hemidistonija”. The Dystonia Society, London. Архивирано из оригинала 23. 11. 2019. г. Приступљено 23. 11. 2019.

institutducerveau-icm.org

„La dystonie : Causes, mécanismes biologiques, symptômes, diagnostic et traitements”. Institut du Cerveau (на језику: француски). Приступљено 17. 1. 2022.

msdmanuals.com

„Dystonie - Troubles du cerveau, de la moelle épinière et des nerfs”. Manuels MSD pour le grand public (на језику: француски). Приступљено 17. 1. 2022.

nih.gov

ncbi.nlm.nih.gov

Bertucco, M.; Terence, S. (2015). „Current and emerging strategies for treatment of childhood dystonia”. J Hand Therapy. 28 (2): 185—194. PMC 4424089 . PMID 25835254. doi:10.1016/j.jht.2014.11.002.
Albanese, A.; Lalli, S. (2009). „Is this dystonia?”. Mov Disord. 24 (12): 1725—1731. PMID 19554620. doi:10.1002/mds.22597.
Phukan J, Albanese A, Gasser T, Warner T (2011). „Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis.”. Lancet Neurol. 10 (12): 1074—1085. PMID 22030388. doi:10.1016/S1474-4422(11)70232-0.
Skogseid, I. M. (2014). „Dystonia - new advances in classification, genetics, pathophysiology and treatment”. Acta Neurol Scand Suppl. 129 (198): 13—9. PMID 24588501. doi:10.1111/ane.12231.
Jinnah, H.A.; Albanese, Alberto (2014). „The New Classification System for the Dystonias: Why Was It Needed and How Was It Developed?”. Mov Disord Clin Pract. 1 (4): 280—4. PMID 25485288. doi:10.1002/mdc3.12100.
Albanese A, Bhatia K, Bressman SB, DeLong MR, Fahn S, Fung VSC; et al. (2013). „Concept and classification of dystonia”. Mov Disord [Internet]. 28 (7): 863—73. PMC 3729880 . PMID 23649720. doi:10.1002/mds.25475. .
Mink, J. (2013). „Special concerns in defining, studying, and treating dystonia in children”. Movement Disorders. 28 (7): 921—925. PMC 3806453 . PMID 23893449. doi:10.1002/mds.25548.
Skogseid, I. M. (2014). „Dystonia--new advances in classification, genetics, pathophysiology and treatment”. Acta Neurol Scand Suppl. 129 (198): 13—9. PMID 24588501. doi:10.1111/ane.12231.
Hersheson, Joshua; Mencacci, Niccolo E.; Davis, Mary; MacDonald, Nicola; Trabzuni, Daniah; Ryten, Mina; Pittman, Alan; Paudel, Reema; Kara, Eleanna; Fawcett, Katherine; Plagnol, Vincent; Bhatia, Kailash P.; Medlar, Alan J.; Stanescu, Horia C.; Hardy, John; Kleta, Robert; Wood, Nicholas W.; Houlden, Henry (2013). „Mutations in the autoregulatory domain of β-tubulin 4a cause hereditary dystonia”. Annals of Neurology. 73 (4): 546—53. PMC 3698699 . PMID 23424103. doi:10.1002/ana.23832.
Valente, Enza Maria; Bentivoglio, Anna Rita; Cassetta, Emanuele; Dixon, Peter H.; Davis, Mary B.; Ferraris, Alessandro; Ialongo, Tamara; Frontali, Marina; Wood, Nicholas W.; Albanese, Alberto (2001). „DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial-cervical or upper limb onset”. Annals of Neurology. 49 (3): 362—6. PMID 11261511. doi:10.1002/ana.73.
Grimes, D. A.; Han, F.; Lang, A. E.; St. George-Hyssop, P.; Racacho, L.; Bulman, D. E. (2002). „A novel locus for inherited myoclonus-dystonia on 18p11”. Neurology. 59 (8): 1183—6. PMID 12391345. doi:10.1212/WNL.59.8.1183.
Chouery, E.; Kfoury, J.; Delague, V.; Jalkh, N.; Bejjani, P.; Serre, J. L.; Mégarbané, A. (2008). „A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12”. Neurogenetics. 9 (4): 287—93. PMID 18688663. doi:10.1007/s10048-008-0142-4.
Charlesworth, Gavin; Plagnol, Vincent; Holmström, Kira M.; Bras, Jose; Sheerin, Una-Marie; Preza, Elisavet; Rubio-Agusti, Ignacio; Ryten, Mina; Schneider, Susanne A.; Stamelou, Maria; Trabzuni, Daniah; Abramov, Andrey Y.; Bhatia, Kailash P.; Wood, Nicholas W. (2012). „Mutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis”. The American Journal of Human Genetics. 91 (6): 1041—50. PMC 3516598 . PMID 23200863. doi:10.1016/j.ajhg.2012.10.024.
Roubertie, A.; Echenne, Bernard; Cif, Laura; Vayssiere, Nathalie; Hemm, Simone; Coubes, Philippe (2000). „Treatment of early-onset dystonia: Update and a new perspective”. Child's Nerv Sys. 16 (6): 334—340. PMID 10933228. doi:10.1007/s003810050528.

passeportsante.net

„La Dystonie - Symptômes, Risques, Traitements”. https://www.passeportsante.net/ (на језику: француски). 27. 7. 2016. Приступљено 17. 1. 2022. Спољашња веза у |website= (помоћ)

web.archive.org

MacKinnon, Fiona. „Hemidistonija”. The Dystonia Society, London. Архивирано из оригинала 23. 11. 2019. г. Приступљено 23. 11. 2019.