Atassia di Friedreich (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Atassia di Friedreich" in Italian language version.

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Montermini L, Rodius F, Pianese L, et al., The Friedreich Ataxia Critical Region Spans A 150-kb Interval on Chromosome 9q13, in Am. J. Hum. Genet., vol. 57, n. 5, 1995, pp. 1061–7, PMC 1801369, PMID 7485155.

doi.org

dx.doi.org

(DE) Friedreich N, Ueber degenerative Atrophie der spinalen Hinterstränge, in Arch Pathol Anat Phys Klin Med, vol. 26, 3–4, 1863, pp. 391–419, DOI:10.1007/BF01930976.
(DE) Friedreich N, Ueber degenerative Atrophie der spinalen Hinterstränge, in Arch Pathol Anat Phys Klin Med, vol. 26, 5–6, 1863, pp. 433–459, DOI:10.1007/BF01878006.
(DE) Friedreich N, Ueber degenerative Atrophie der spinalen Hinterstränge, in Arch Pathol Anat Phys Klin Med, vol. 27, 1–2, 1863, pp. 1–26, DOI:10.1007/BF01938516.
(DE) Friedreich N, Ueber Ataxie mit besonderer Berücksichtigung der hereditären Formen, in Arch Pathol Anat Phys Klin Med, vol. 68, n. 2, 1876, pp. 145–245, DOI:10.1007/BF01879049.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, Bibcode:1996Sci...271.1423C, DOI:10.1126/science.271.5254.1423, PMID 8596916.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, DOI:10.1126/science.271.5254.1423, PMID 8596916.
Luca Leonardi, Maria Gabriella Aceto e Christian Marcotulli, A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study, in Neurological Sciences: Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, vol. 38, n. 3, 2017-3, pp. 459–463, DOI:10.1007/s10072-016-2800-x. URL consultato il 17 settembre 2019.

harvard.edu

adsabs.harvard.edu

Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, Bibcode:1996Sci...271.1423C, DOI:10.1126/science.271.5254.1423, PMID 8596916.

nih.gov

ncbi.nlm.nih.gov

Delatycki M, Williamson R, Forrest S, Friedreich ataxia: an overview, in J Med Genet, vol. 37, n. 1, 2000, pp. 1-8 As, PMID 10633128.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, Bibcode:1996Sci...271.1423C, DOI:10.1126/science.271.5254.1423, PMID 8596916.
Barbeau A, Sadibelouiz M, Roy M, Lemieux B, Bouchard JP, Geoffroy G, Origin of Friedreich's disease in Quebec, in The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, vol. 11, 4 Suppl, 1984, pp. 506-9, PMID 6391645.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, DOI:10.1126/science.271.5254.1423, PMID 8596916.
Montermini L, Rodius F, Pianese L, et al., The Friedreich Ataxia Critical Region Spans A 150-kb Interval on Chromosome 9q13, in Am. J. Hum. Genet., vol. 57, n. 5, 1995, pp. 1061–7, PMC 1801369, PMID 7485155.
(EN) A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study, su ncbi.nlm.nih.gov.
Luca Leonardi, Maria Gabriella Aceto e Christian Marcotulli, A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study, in Neurological Sciences: Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, vol. 38, n. 3, 2017-3, pp. 459–463, DOI:10.1007/s10072-016-2800-x. URL consultato il 17 settembre 2019.

oadoi.org

(DE) Friedreich N, Ueber degenerative Atrophie der spinalen Hinterstränge, in Arch Pathol Anat Phys Klin Med, vol. 26, 3–4, 1863, pp. 391–419, DOI:10.1007/BF01930976.
(DE) Friedreich N, Ueber degenerative Atrophie der spinalen Hinterstränge, in Arch Pathol Anat Phys Klin Med, vol. 26, 5–6, 1863, pp. 433–459, DOI:10.1007/BF01878006.
(DE) Friedreich N, Ueber degenerative Atrophie der spinalen Hinterstränge, in Arch Pathol Anat Phys Klin Med, vol. 27, 1–2, 1863, pp. 1–26, DOI:10.1007/BF01938516.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, Bibcode:1996Sci...271.1423C, DOI:10.1126/science.271.5254.1423, PMID 8596916.
Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Cañizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M, Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion, in Science, vol. 271, n. 5254, marzo 1996, pp. 1423–7, DOI:10.1126/science.271.5254.1423, PMID 8596916.

web.archive.org

Adam Shatz, "Where Life Is Seized", in London Review of Books, 19 gennaio 2017 (archiviato dall'url originale il 12 gennaio 2017).

whonamedit.com

(EN) Ole Daniel Enersen, Atassia di Friedreich, in Who Named It?.

zenodo.org

(DE) Friedreich N, Ueber Ataxie mit besonderer Berücksichtigung der hereditären Formen, in Arch Pathol Anat Phys Klin Med, vol. 68, n. 2, 1876, pp. 145–245, DOI:10.1007/BF01879049.