Distonija (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Distonija" in Serbian language version.
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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
- 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.
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
- 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.
passeportsante.net
- „La Dystonie - Symptômes, Risques, Traitements”. https://www.passeportsante.net/ (на језику: француски). 27. 7. 2016. Приступљено 17. 1. 2022. Спољашња веза у
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web.archive.org
- MacKinnon, Fiona. „Hemidistonija”. The Dystonia Society, London. Архивирано из оригинала 23. 11. 2019. г. Приступљено 23. 11. 2019.