Amiotrofična lateralna skleroza (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Amiotrofična lateralna skleroza" in Serbian language version.

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14nih.gov

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13doi.org

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7semanticscholar.org

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2web.archive.org

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1harvard.edu

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1zenodo.org

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1worldcat.org

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1elsevier.com

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1whonamedit.com

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doi.org

Kwong LK, Uryu K, Trojanowski JQ, Lee VM (2008). „TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis”. Neurosignals. 16 (1): 41—51. PMID 18097159. S2CID 36021142. doi:10.1159/000109758.
Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A (2010). „Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form”. Acta Neuropathol. 119 (3): 335—44. PMID 20111867. S2CID 22951808. doi:10.1007/s00401-010-0646-5.
Reaume A, Elliott J, Hoffman E, Kowall N, Ferrante R, Siwek D, Wilcox H, Flood D, Beal M, Brown R, Scott R, Snider W (1996). „Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury”. Nat Genet. 13 (1): 43—7. PMID 8673102. S2CID 13070253. doi:10.1038/ng0596-43.
Bruijn L, Houseweart M, Kato S, Anderson K, Anderson S, Ohama E, Reaume A, Scott R, Cleveland D (1998). „Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1”. Science. 281 (5384): 1851—4. Bibcode:1998Sci...281.1851B. PMID 9743498. doi:10.1126/science.281.5384.1851.
Conwit, Robin A. (2006). „Preventing familial ALS: A clinical trial may be feasible but is an efficacy trial warranted?”. Journal of the Neurological Sciences. 251 (1–2): 1—2. ISSN 0022-510X. PMID 17070848. S2CID 33105812. doi:10.1016/j.jns.2006.07.009.
Phukan J, Pender NP, Hardiman O (2007). „Cognitive impairment in amyotrophic lateral sclerosis”. Lancet Neurol. 6 (11): 994—1003. PMID 17945153. S2CID 25786746. doi:10.1016/S1474-4422(07)70265-X.
Al-Chalabi, A.; Lewis, C. M. (2011). „Modelling the effects of penetrance and family size on rates of sporadic and familial disease”. Human Heredity. 71 (4): 281—8. PMID 21846995. S2CID 3808240. doi:10.1159/000330167.
Grad, Leslie I.; Rouleau, Guy A.; Ravits, John; Cashman, Neil R. (август 2017). „Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS)”. Cold Spring Harbor Perspectives in Medicine. 7 (8): a024117. PMC 5538408 . PMID 28003278. doi:10.1101/cshperspect.a024117. .
Van Damme, Philip; Robberecht, Wim; Van Den Bosch, Ludo (2017). „Modelling amyotrophic lateral sclerosis: Progress and possibilities”. Disease Models & Mechanisms. 10 (5): 537—549. PMC 5451175 . PMID 28468939. doi:10.1242/dmm.029058.
Bonvicini, F.; Marcello, N.; Mandrioli, J.; Pietrini, V.; Vinceti, M. (2010). „Exposure to pesticides and risk of amyotrophic lateral sclerosis: A population-based case-control study”. Annali dell'istituto Superiore di Sanita. 46 (3): 284—7. PMID 20847462. doi:10.4415/ANN_10_03_10.
Malek, A. M.; Barchowsky, A.; Bowser, R.; Youk, A.; Talbott, E. O. (2012). „Pesticide exposure as a risk factor for amyotrophic lateral sclerosis: A meta-analysis of epidemiological studies: Pesticide exposure as a risk factor for ALS”. Environmental Research. 117: 112—119. PMID 22819005. doi:10.1016/j.envres.2012.06.007. ]
Vinceti, M.; Bottecchi, I.; Fan, A.; Finkelstein, Y.; Mandrioli, J. (2012). „Are environmental exposures to selenium, heavy metals, and pesticides risk factors for amyotrophic lateral sclerosis?”. Reviews on Environmental Health. 27 (1): 19—41. PMID 22755265. S2CID 38486119. doi:10.1515/reveh-2012-0002.
Kamel, F.; Umbach, D. M.; Bedlack, R. S.; Richards, M.; Watson, M.; Alavanja, M. C.; Blair, A.; Hoppin, J. A.; Schmidt, S.; Sandler, D. P. (2012). „Pesticide exposure and amyotrophic lateral sclerosis”. Neurotoxicology. 33 (3): 457—62. PMC 3358481 . PMID 22521219. doi:10.1016/j.neuro.2012.04.001.

elsevier.com

linkinghub.elsevier.com

Phukan J, Pender NP, Hardiman O (2007). „Cognitive impairment in amyotrophic lateral sclerosis”. Lancet Neurol. 6 (11): 994—1003. PMID 17945153. S2CID 25786746. doi:10.1016/S1474-4422(07)70265-X.

harvard.edu

adsabs.harvard.edu

Bruijn L, Houseweart M, Kato S, Anderson K, Anderson S, Ohama E, Reaume A, Scott R, Cleveland D (1998). „Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1”. Science. 281 (5384): 1851—4. Bibcode:1998Sci...281.1851B. PMID 9743498. doi:10.1126/science.281.5384.1851.

nih.gov

ncbi.nlm.nih.gov

Kwong LK, Uryu K, Trojanowski JQ, Lee VM (2008). „TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis”. Neurosignals. 16 (1): 41—51. PMID 18097159. S2CID 36021142. doi:10.1159/000109758.
Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A (2010). „Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form”. Acta Neuropathol. 119 (3): 335—44. PMID 20111867. S2CID 22951808. doi:10.1007/s00401-010-0646-5.
Reaume A, Elliott J, Hoffman E, Kowall N, Ferrante R, Siwek D, Wilcox H, Flood D, Beal M, Brown R, Scott R, Snider W (1996). „Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury”. Nat Genet. 13 (1): 43—7. PMID 8673102. S2CID 13070253. doi:10.1038/ng0596-43.
Bruijn L, Houseweart M, Kato S, Anderson K, Anderson S, Ohama E, Reaume A, Scott R, Cleveland D (1998). „Aggregation and motor neuron toxicity of an ALS-linked SOD1 mutant independent from wild-type SOD1”. Science. 281 (5384): 1851—4. Bibcode:1998Sci...281.1851B. PMID 9743498. doi:10.1126/science.281.5384.1851.
Conwit, Robin A. (2006). „Preventing familial ALS: A clinical trial may be feasible but is an efficacy trial warranted?”. Journal of the Neurological Sciences. 251 (1–2): 1—2. ISSN 0022-510X. PMID 17070848. S2CID 33105812. doi:10.1016/j.jns.2006.07.009.
Phukan J, Pender NP, Hardiman O (2007). „Cognitive impairment in amyotrophic lateral sclerosis”. Lancet Neurol. 6 (11): 994—1003. PMID 17945153. S2CID 25786746. doi:10.1016/S1474-4422(07)70265-X.
Al-Chalabi, A.; Lewis, C. M. (2011). „Modelling the effects of penetrance and family size on rates of sporadic and familial disease”. Human Heredity. 71 (4): 281—8. PMID 21846995. S2CID 3808240. doi:10.1159/000330167.
Grad, Leslie I.; Rouleau, Guy A.; Ravits, John; Cashman, Neil R. (август 2017). „Clinical Spectrum of Amyotrophic Lateral Sclerosis (ALS)”. Cold Spring Harbor Perspectives in Medicine. 7 (8): a024117. PMC 5538408 . PMID 28003278. doi:10.1101/cshperspect.a024117. .
Van Damme, Philip; Robberecht, Wim; Van Den Bosch, Ludo (2017). „Modelling amyotrophic lateral sclerosis: Progress and possibilities”. Disease Models & Mechanisms. 10 (5): 537—549. PMC 5451175 . PMID 28468939. doi:10.1242/dmm.029058.
Bonvicini, F.; Marcello, N.; Mandrioli, J.; Pietrini, V.; Vinceti, M. (2010). „Exposure to pesticides and risk of amyotrophic lateral sclerosis: A population-based case-control study”. Annali dell'istituto Superiore di Sanita. 46 (3): 284—7. PMID 20847462. doi:10.4415/ANN_10_03_10.
Malek, A. M.; Barchowsky, A.; Bowser, R.; Youk, A.; Talbott, E. O. (2012). „Pesticide exposure as a risk factor for amyotrophic lateral sclerosis: A meta-analysis of epidemiological studies: Pesticide exposure as a risk factor for ALS”. Environmental Research. 117: 112—119. PMID 22819005. doi:10.1016/j.envres.2012.06.007. ]
Vinceti, M.; Bottecchi, I.; Fan, A.; Finkelstein, Y.; Mandrioli, J. (2012). „Are environmental exposures to selenium, heavy metals, and pesticides risk factors for amyotrophic lateral sclerosis?”. Reviews on Environmental Health. 27 (1): 19—41. PMID 22755265. S2CID 38486119. doi:10.1515/reveh-2012-0002.
Kamel, F.; Umbach, D. M.; Bedlack, R. S.; Richards, M.; Watson, M.; Alavanja, M. C.; Blair, A.; Hoppin, J. A.; Schmidt, S.; Sandler, D. P. (2012). „Pesticide exposure and amyotrophic lateral sclerosis”. Neurotoxicology. 33 (3): 457—62. PMC 3358481 . PMID 22521219. doi:10.1016/j.neuro.2012.04.001.

ninds.nih.gov

"Amyotrophic Lateral Sclerosis Fact Sheet" Архивирано на сајту Wayback Machine (12. октобар 2010) on National Institute of Neurological Disorders and Stroke

semanticscholar.org

api.semanticscholar.org

Kwong LK, Uryu K, Trojanowski JQ, Lee VM (2008). „TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis”. Neurosignals. 16 (1): 41—51. PMID 18097159. S2CID 36021142. doi:10.1159/000109758.
Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A (2010). „Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form”. Acta Neuropathol. 119 (3): 335—44. PMID 20111867. S2CID 22951808. doi:10.1007/s00401-010-0646-5.
Reaume A, Elliott J, Hoffman E, Kowall N, Ferrante R, Siwek D, Wilcox H, Flood D, Beal M, Brown R, Scott R, Snider W (1996). „Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury”. Nat Genet. 13 (1): 43—7. PMID 8673102. S2CID 13070253. doi:10.1038/ng0596-43.
Conwit, Robin A. (2006). „Preventing familial ALS: A clinical trial may be feasible but is an efficacy trial warranted?”. Journal of the Neurological Sciences. 251 (1–2): 1—2. ISSN 0022-510X. PMID 17070848. S2CID 33105812. doi:10.1016/j.jns.2006.07.009.
Phukan J, Pender NP, Hardiman O (2007). „Cognitive impairment in amyotrophic lateral sclerosis”. Lancet Neurol. 6 (11): 994—1003. PMID 17945153. S2CID 25786746. doi:10.1016/S1474-4422(07)70265-X.
Al-Chalabi, A.; Lewis, C. M. (2011). „Modelling the effects of penetrance and family size on rates of sporadic and familial disease”. Human Heredity. 71 (4): 281—8. PMID 21846995. S2CID 3808240. doi:10.1159/000330167.
Vinceti, M.; Bottecchi, I.; Fan, A.; Finkelstein, Y.; Mandrioli, J. (2012). „Are environmental exposures to selenium, heavy metals, and pesticides risk factors for amyotrophic lateral sclerosis?”. Reviews on Environmental Health. 27 (1): 19—41. PMID 22755265. S2CID 38486119. doi:10.1515/reveh-2012-0002.

web.archive.org

ALS Clinic at the Penn State Milton S. Hershey Medical Center Pristupljeno 1. 6. 2017.
"Amyotrophic Lateral Sclerosis Fact Sheet" Архивирано на сајту Wayback Machine (12. октобар 2010) on National Institute of Neurological Disorders and Stroke

whonamedit.com

Биографија Жан-Мартен Шаркоа (Jean-Martin Charcot) на whonamedit.com, Приступљено 6. јануар 2011.

worldcat.org

Conwit, Robin A. (2006). „Preventing familial ALS: A clinical trial may be feasible but is an efficacy trial warranted?”. Journal of the Neurological Sciences. 251 (1–2): 1—2. ISSN 0022-510X. PMID 17070848. S2CID 33105812. doi:10.1016/j.jns.2006.07.009.

zenodo.org

Conwit, Robin A. (2006). „Preventing familial ALS: A clinical trial may be feasible but is an efficacy trial warranted?”. Journal of the Neurological Sciences. 251 (1–2): 1—2. ISSN 0022-510X. PMID 17070848. S2CID 33105812. doi:10.1016/j.jns.2006.07.009.