{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,9]],"date-time":"2026-10-09T15:24:06Z","timestamp":1791559446724,"version":"4.3.4"},"reference-count":74,"publisher":"Elsevier BV","issue":"4","license":[{"start":{"date-parts":[[2020,5,1]],"date-time":"2020-05-01T00:00:00Z","timestamp":1588291200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,5,1]],"date-time":"2020-05-01T00:00:00Z","timestamp":1588291200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Revue Neurologique"],"published-print":{"date-parts":[[2020,5]]},"DOI":"10.1016\/j.neurol.2019.11.003","type":"journal-article","created":{"date-parts":[[2020,1,3]],"date-time":"2020-01-03T12:09:22Z","timestamp":1578053362000},"page":"225-234","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":21,"title":["A historical approach to hereditary spastic paraplegia"],"prefix":"10.1016","volume":"176","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-6927-7946","authenticated-orcid":false,"given":"O.","family":"Walusinski","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.neurol.2019.11.003_bib0375","series-title":"Recherches et observations sur le spinitis ou inflammation de la moelle \u00e9pini\u00e8re","author":"Clot","year":"1820"},{"key":"10.1016\/j.neurol.2019.11.003_bib0380","series-title":"Essai sur l\u2019anatomie et les vices de conformation de la moelle \u00e9pini\u00e8re chez l\u2019Homme","author":"Ollivier\u00a0d\u2019Angers","year":"1823"},{"key":"10.1016\/j.neurol.2019.11.003_bib0385","first-page":"42","article-title":"Observations on Diseases of the Spinal Marrow","volume":"14","author":"Abercrombie","year":"1818","journal-title":"Edinb Med Surg J"},{"key":"10.1016\/j.neurol.2019.11.003_bib0390","doi-asserted-by":"crossref","first-page":"1255","DOI":"10.1007\/s00415-012-6424-7","article-title":"Charles-Prosper Ollivier d\u2019Angers (1796-1845)","volume":"259","author":"Walusinski","year":"2012","journal-title":"J Neurol"},{"key":"10.1016\/j.neurol.2019.11.003_bib0395","first-page":"18","article-title":"History of the emergence and recognition of syringomyelia in the 19th century","volume":"18","author":"Walusinski","year":"2012","journal-title":"Vesalius"},{"key":"10.1016\/j.neurol.2019.11.003_bib0400","series-title":"Trait\u00e9 de la moelle \u00e9pini\u00e8re et de ses maladies: contenant l\u2019histoire anatomique, physiologique et pathologique de ce centre nerveux chez l\u2019homme","author":"Ollivier\u00a0d\u2019Anger","year":"1827"},{"key":"10.1016\/j.neurol.2019.11.003_bib0405","series-title":"Trait\u00e9 des maladies de la moelle \u00e9pini\u00e8re: contenant l\u2019histoire anatomique, physiologique et pathologique de ce centre nerveux chez l\u2019homme","author":"Ollivier\u00a0d\u2019Angers","year":"1837"},{"key":"10.1016\/j.neurol.2019.11.003_bib0410","article-title":"Du tabes dorsal spasmodique","volume":"4","author":"Charcot","year":"1876","journal-title":"Progr Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0415","first-page":"357","article-title":"\u00dcber einen wenig bekannten spinalen Symptomencomplex","volume":"12","author":"Erb","year":"1875","journal-title":"Berlin Klin Woch"},{"key":"10.1016\/j.neurol.2019.11.003_bib0420","first-page":"505","article-title":"De la paralysie spinale spastique (tabes spasmodique)","volume":"48","author":"Ricklin","year":"1877","journal-title":"Gazet Med Paris"},{"key":"10.1016\/j.neurol.2019.11.003_bib0425","series-title":"Scl\u00e9rose lat\u00e9rale protopathique in Douzi\u00e8me Le\u00e7on. \u0152uvres compl\u00e8tes de JM. Charcot. Le\u00e7ons sur les Maladies du Syst\u00e8me nerveux. Tome 2","author":"Charcot","year":"1894"},{"key":"10.1016\/j.neurol.2019.11.003_bib0430","series-title":"Traitement par les eaux de Bar\u00e8ges des my\u00e9lites chroniques, des paralysies qui en sont la suite et en particulier de la paralysie infantile","author":"B\u00e9tous","year":"1887"},{"key":"10.1016\/j.neurol.2019.11.003_bib0435","series-title":"\u00c9tude sur le tabes dorsal spasmodique","author":"B\u00e9tous","year":"1876"},{"key":"10.1016\/j.neurol.2019.11.003_bib0440","article-title":"\u00dcber die spastiche Spinalparalyse spasmodique (tabes dorsal Charcot)","volume":"70","author":"Erb","year":"1877","journal-title":"Virch Arch Pathol Anat Physiol Klinische Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0445","first-page":"823","article-title":"Du lathyrisme m\u00e9dullaire spasmodique","volume":"47","author":"Proust","year":"1883","journal-title":"Bull Acad Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0450","series-title":"\u00c9tude sur le tabes dorsal spasmodique. Scl\u00e9rose primitive des faisceaux lat\u00e9raux","author":"Jubineau","year":"1883"},{"key":"10.1016\/j.neurol.2019.11.003_bib0455","doi-asserted-by":"crossref","first-page":"224","DOI":"10.1007\/BF02054325","article-title":"\u00dcber einen Fall von sogenannter spastischer Spinalparalyse mit anatomischem Befunde, nebst einige Bemerkungen \u00fcber die prim\u00e4re Erkrankung der Pyramidenseitenstrangbahnen","volume":"15","author":"Westphal","year":"1884","journal-title":"Arch Psychiatr Nervenk"},{"key":"10.1016\/j.neurol.2019.11.003_bib0460","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1177\/2514183X19880387","article-title":"Fulgence Raymond (1844-1910), regrettably forgotten successor of Jean-Martin Charcot","volume":"3","author":"Walusinski","year":"2019","journal-title":"Clin Transl Neurosci"},{"key":"10.1016\/j.neurol.2019.11.003_bib0465","series-title":"Dictionnaire encyclop\u00e9dique des Sciences m\u00e9dicales. Tome XV\u2013Sys-Tar","author":"Dechambre","year":"1885"},{"key":"10.1016\/j.neurol.2019.11.003_bib0470","first-page":"213","article-title":"Contribution \u00e0 l\u2019\u00e9tude des contractures hyst\u00e9riques. Int\u00e9grit\u00e9 de la moelle \u00e9pini\u00e8re dans un cas de contracture hyst\u00e9rique permanente g\u00e9n\u00e9ralis\u00e9e ayant dur\u00e9 plusieurs ann\u00e9es","volume":"5","author":"Klumpke","year":"1885","journal-title":"Rev Med (Paris)"},{"key":"10.1016\/j.neurol.2019.11.003_bib0475","doi-asserted-by":"crossref","first-page":"676","DOI":"10.1007\/BF02224539","article-title":"Beitr\u00e4ge zur Pathologie des R\u00fcckenmarks","volume":"10","author":"Str\u00fcmpell","year":"1880","journal-title":"Arch Psychiatr Nervenk"},{"key":"10.1016\/j.neurol.2019.11.003_bib0480","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1007\/BF02172796","article-title":"\u00dcber eine bestimmte Form der prim\u00e4ren kombinierten Systemerkrankung des R\u00fcckenmarks","volume":"17","author":"Str\u00fcmpell","year":"1886","journal-title":"Arch Psychiatr Nervenk"},{"key":"10.1016\/j.neurol.2019.11.003_bib0485","first-page":"457","article-title":"Scl\u00e9rose des cordons post\u00e9rieurs et des cordons lat\u00e9raux, coexistant chez le m\u00eame malade. Pr\u00e9dominance presque exclusive des sympt\u00f4mes sp\u00e9ciaux de la scl\u00e9rose des cordons lat\u00e9raux","volume":"14","author":"Raymond","year":"1882","journal-title":"Arch Physiol Norm Pathol"},{"key":"10.1016\/j.neurol.2019.11.003_bib0490","series-title":"Die spastische Spinalparalyse im Kindesalter. Inaug. Diss","author":"Naef","year":"1885"},{"key":"10.1016\/j.neurol.2019.11.003_bib0495","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1007\/BF01665286","article-title":"\u00dcber die heredit\u00e4re spastische Spinalparalyse","volume":"4","author":"Str\u00fcmpell","year":"1893","journal-title":"Deut Zeitschr Nerv"},{"key":"10.1016\/j.neurol.2019.11.003_bib0500","doi-asserted-by":"crossref","DOI":"10.1055\/s-0029-1193358","article-title":"Einige seltenere Formen von Affectionen des R\u00fcckenmarks; Sklerose der Seintenstr\u00e4nge des R\u00fcckenmarks bei vier Kindern der selben Familie","volume":"2","author":"Seeligmuller","year":"1876","journal-title":"Deutsche Medizinische Wochenschrift"},{"key":"10.1016\/j.neurol.2019.11.003_bib0505","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1007\/BF01937523","article-title":"\u00dcber eine heredit\u00e4re Form der progressiven spinalen, mit Bulb\u00e4rparalyse komplizierter Muskelatrophie","volume":"115","author":"Bernhardt","year":"1889","journal-title":"Arch Pathol Anat Physiol Klin Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0510","first-page":"681","article-title":"\u00dcber famili\u00e4re spastische Spinalparalyse","volume":"2","author":"Krafft-Ebing","year":"1892","journal-title":"Wiener Klin Woch"},{"key":"10.1016\/j.neurol.2019.11.003_bib0515","first-page":"138","article-title":"Spastische Spinalparalyse","volume":"58","author":"Jendrassik","year":"1897","journal-title":"Deutsch Arch Klin Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0520","series-title":"Le syndrome tabes spasmodique, \u00e0 propos de deux cas familiaux de parapl\u00e9gie spasmodique infantile. In Le\u00e7ons sur les maladies du syst\u00e8me nerveux (ann\u00e9e 1894-1895)","author":"Raymond","year":"1896"},{"key":"10.1016\/j.neurol.2019.11.003_bib0525","first-page":"1","article-title":"Contribution \u00e0 l\u2019\u00e9tude de la forme familiale de la parapl\u00e9gie spasmodique spinale","volume":"3","author":"Souques","year":"1895","journal-title":"Rev Neurol (Paris)"},{"issue":"90","key":"10.1016\/j.neurol.2019.11.003_bib0530","first-page":"585","article-title":"Parapl\u00e9gie spasmodique familiale","volume":"4","author":"Raymond","year":"1896","journal-title":"Presse Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0535","first-page":"86","article-title":"Paraplegia spastica familiare","volume":"7","author":"Melotti","year":"1885","journal-title":"Bull Sci Med Publ Soc Medicochir Bologne"},{"key":"10.1016\/j.neurol.2019.11.003_bib0540","first-page":"1225","article-title":"Parapl\u00e9gie spasmodique familiale","volume":"43","author":"Ch. Achard,","year":"1896","journal-title":"Gazette Hebd Med Chir"},{"key":"10.1016\/j.neurol.2019.11.003_bib0545","first-page":"1","article-title":"Zur Kenntniss der cerebralen Diplegen des Kindersalters (im Anschluss an die Little'sche Krankheit)","volume":"3","author":"Freud","year":"1893","journal-title":"Beitr\u00e4ge zur Kinderheilkunde, Neue Folge"},{"key":"10.1016\/j.neurol.2019.11.003_bib0550","first-page":"177","article-title":"Les dipl\u00e9gies c\u00e9r\u00e9brales infantiles","volume":"1","author":"Freud","year":"1893","journal-title":"Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2019.11.003_bib0555","article-title":"\u00dcber famili\u00e4re Formen von cerebralen Diplegien","volume":"12","author":"Freud","year":"1893","journal-title":"Neurol Centralblatt"},{"key":"10.1016\/j.neurol.2019.11.003_bib0560","series-title":"Le\u00e7ons sur les maladies de la moelle \u00e9pini\u00e8re. Le\u00e7ons huit et neuf: tabes dorsal spasmodique","author":"Marie","year":"1892"},{"key":"10.1016\/j.neurol.2019.11.003_bib0565","series-title":"Le\u00e7ons sur les maladies nerveuses (Salp\u00eatri\u00e8re 1893-1894)","author":"Brissaud","year":"1895"},{"key":"10.1016\/j.neurol.2019.11.003_bib0570","series-title":"Contribution \u00e0 l\u2019\u00e9tude de la parapl\u00e9gie spasmodique familiale","author":"Lorrain","year":"1898"},{"key":"10.1016\/j.neurol.2019.11.003_bib0575","first-page":"201","article-title":"Maladie familiale \u00e0 sympt\u00f4mes c\u00e9r\u00e9bello-m\u00e9dullaires","volume":"17","author":"Pauly","year":"1897","journal-title":"Rev Med"},{"key":"10.1016\/j.neurol.2019.11.003_bib0580","first-page":"80","article-title":"La syphilis h\u00e9r\u00e9ditaire de la moelle \u00e9pini\u00e8re","volume":"9","author":"Gilles\u00a0de\u00a0la\u00a0Tourette","year":"1896","journal-title":"Nouv Iconogr Salpet"},{"key":"10.1016\/j.neurol.2019.11.003_bib0585","series-title":"Localisations spinales de la syphilis h\u00e9r\u00e9ditaire","author":"Gasne","year":"1897"},{"key":"10.1016\/j.neurol.2019.11.003_bib0590","doi-asserted-by":"crossref","first-page":"283","DOI":"10.1016\/j.neurol.2018.08.007","article-title":"Jules Sottas (1866\u20131945) forgotten despite the eponym: \u201cDejerine-Sottas syndrome\u201d","volume":"175","author":"Walusinski","year":"2019","journal-title":"Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2019.11.003_bib0595","series-title":"Contribution \u00e0 l\u2019\u00e9tude anatomique et clinique des paralysies spinales syphilitiques","author":"Sottas","year":"1894"},{"key":"10.1016\/j.neurol.2019.11.003_bib0600","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1007\/BF01791344","article-title":"Neuropathische Diathese und Knieph\u00e4nomen","volume":"12","author":"Bloch","year":"1881","journal-title":"Arch Psychiatr Nervenk"},{"key":"10.1016\/j.neurol.2019.11.003_bib0605","first-page":"81","article-title":"Hereditary infantile spastic paraplegia","volume":"25","author":"Gee","year":"1889","journal-title":"Barthol Hosp Rep"},{"key":"10.1016\/j.neurol.2019.11.003_bib0610","first-page":"432","article-title":"A contribution to the study of the Family Form of Spastic Paraplegia","volume":"105","author":"Newmark","year":"1893","journal-title":"Am J Med Sci"},{"key":"10.1016\/j.neurol.2019.11.003_bib0615","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1097\/00005053-189711000-00006","article-title":"Hereditary spastic paraplegia","volume":"24","author":"Bayley","year":"1897","journal-title":"J Nerv Mental Disord"},{"key":"10.1016\/j.neurol.2019.11.003_bib0620","first-page":"404","article-title":"Affection spastique bulbo-spinale familiale","volume":"18","author":"Magnan","year":"1905","journal-title":"Nouv Iconogr Salpet"},{"key":"10.1016\/j.neurol.2019.11.003_bib0625","first-page":"98","article-title":"Eight cases of hereditary spastic paraplegia","volume":"5","author":"Jones","year":"1907","journal-title":"Rev Neurol Psychiatry"},{"key":"10.1016\/j.neurol.2019.11.003_bib0630","first-page":"209","article-title":"Un cas de maladie familiale interm\u00e9diaire \u00e0 la parapl\u00e9gie spasmodique et l\u2019h\u00e9r\u00e9do ataxie c\u00e9r\u00e9belleuse","volume":"4","author":"Raymond","year":"1909","journal-title":"L\u2019Enc\u00e9phale"},{"key":"10.1016\/j.neurol.2019.11.003_bib0635","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1007\/BF01910510","article-title":"Klinischer und erbbiologischer Beitrag zur Lehre von den Heredodegenerationen des Nervensystems","volume":"66","author":"Bremer","year":"1922","journal-title":"Arch Psychiatr Nervenk"},{"key":"10.1016\/j.neurol.2019.11.003_bib0640","doi-asserted-by":"crossref","DOI":"10.1097\/00005053-191609000-00004","article-title":"Family spastic paralysis","volume":"44","author":"Rhein","year":"1916","journal-title":"J Nerv Ment Dis"},{"key":"10.1016\/j.neurol.2019.11.003_bib0645","first-page":"293","article-title":"On the influence of abnormal parturition, difficult labours, premature birth and asphyxia neonatorum, on the mental and physical conditions of the child, especially in relation to deformities","volume":"3","author":"Little","year":"1862","journal-title":"Tr Obst Soc London"},{"key":"10.1016\/j.neurol.2019.11.003_bib0650","doi-asserted-by":"crossref","first-page":"1006","DOI":"10.1007\/s12098-017-2475-1","article-title":"Cerebral palsy: an overview","volume":"85","author":"Gulati","year":"2018","journal-title":"Indian J Pediatr"},{"key":"10.1016\/j.neurol.2019.11.003_bib0655","series-title":"Maladies de la moelle \u00e9pini\u00e8re. Tome XIV du Nouveau trait\u00e9 de M\u00e9decine et de Th\u00e9rapeutique","author":"Dejerine","year":"1909"},{"key":"10.1016\/j.neurol.2019.11.003_bib0660","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1001\/archneurpsyc.1933.02240150011001","article-title":"Familial spastic paralysis. Report of three cases in one family and observation at necropsy","volume":"30","author":"Paskind","year":"1933","journal-title":"Arch Neurol Psych"},{"key":"10.1016\/j.neurol.2019.11.003_bib0665","first-page":"141","article-title":"On hereditary ataxia and spastic paraplegia","volume":"4","author":"Bell","year":"1939","journal-title":"Treas Hum Inherit"},{"key":"10.1016\/j.neurol.2019.11.003_bib0670","doi-asserted-by":"crossref","first-page":"655","DOI":"10.1001\/archneurpsyc.1952.02320230081010","article-title":"Hereditary (familial) spastic paraplegia","volume":"68","author":"Schwartz","year":"1952","journal-title":"Arch Neurol Psychiat (Chic.)"},{"key":"10.1016\/j.neurol.2019.11.003_bib0675","doi-asserted-by":"crossref","first-page":"134","DOI":"10.1136\/jnnp.13.2.134","article-title":"Hereditary spastic paraplegia","volume":"13","author":"Bickerstaff","year":"1950","journal-title":"J Neurol Neurosurg Psychiat"},{"key":"10.1016\/j.neurol.2019.11.003_bib0680","doi-asserted-by":"crossref","first-page":"8","DOI":"10.1136\/jnnp.37.1.8","article-title":"Strumpell familial spastic paraplegia: genetics and neuropathology","volume":"37","author":"Behan","year":"1974","journal-title":"J Neurol Neurosurg Psychiat"},{"key":"10.1016\/j.neurol.2019.11.003_bib0685","doi-asserted-by":"crossref","first-page":"1003","DOI":"10.1136\/jnnp.40.10.1003","article-title":"Strumpell's pure familial spastic paraplegia: case study and review of the literature","volume":"40","author":"Holmes","year":"1977","journal-title":"J Neurol Neurosurg Psychiat"},{"key":"10.1016\/j.neurol.2019.11.003_bib0690","doi-asserted-by":"crossref","first-page":"174","DOI":"10.1159\/000358801","article-title":"The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies","volume":"42","author":"Ruano","year":"2014","journal-title":"Neuroepidemiology"},{"key":"10.1016\/j.neurol.2019.11.003_bib0695","doi-asserted-by":"crossref","first-page":"1274","DOI":"10.1212\/WNL.44.7.1274","article-title":"The phenotype of \u201cpure\u201d autosomal dominant spastic paraplegia","volume":"44","author":"D\u00fcrr","year":"1994","journal-title":"Neurology"},{"key":"10.1016\/j.neurol.2019.11.003_bib0700","doi-asserted-by":"crossref","first-page":"352","DOI":"10.1016\/j.neurol.2017.03.034","article-title":"Hereditary spastic paraplegia: more than an upper motor neuron disease","volume":"173","author":"Parodi","year":"2017","journal-title":"Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2019.11.003_bib0705","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1016\/j.neurol.2016.04.005","article-title":"Classifications of neurogenetic diseases: an increasingly complex problem","volume":"172","author":"Vallat","year":"2016","journal-title":"Rev Neurol (Paris)"},{"key":"10.1016\/j.neurol.2019.11.003_bib0710","doi-asserted-by":"crossref","first-page":"462","DOI":"10.1097\/WCO.0000000000000585","article-title":"Hereditary ataxias and paraparesias: clinical and genetic update","volume":"31","author":"Parodi","year":"2018","journal-title":"Curr Opin Neurol"},{"key":"10.1016\/j.neurol.2019.11.003_bib0715","doi-asserted-by":"crossref","first-page":"525","DOI":"10.1007\/s12311-016-0803-z","article-title":"Hereditary spastic paraplegia: clinical and genetic hallmarks","volume":"16","author":"de Souza","year":"2017","journal-title":"Cerebellum"},{"key":"10.1016\/j.neurol.2019.11.003_bib0720","first-page":"28","article-title":"Famous neurologists: Anita Harding (1952\u20131995)","volume":"9","author":"Compston","year":"2009","journal-title":"Adv Clin Neurosci Rehab"},{"key":"10.1016\/j.neurol.2019.11.003_bib0725","doi-asserted-by":"crossref","first-page":"871","DOI":"10.1136\/jnnp.44.10.871","article-title":"Hereditary \u201cpure\u201d spastic paraplegia: a clinical and genetic study of 22 families","volume":"44","author":"Harding","year":"1981","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"10.1016\/j.neurol.2019.11.003_bib0730","doi-asserted-by":"crossref","first-page":"1151","DOI":"10.1016\/S0140-6736(83)92879-9","article-title":"Classification of the hereditary ataxias and paraplegias","volume":"21","author":"Harding","year":"1983","journal-title":"Lancet"},{"key":"10.1016\/j.neurol.2019.11.003_bib0735","doi-asserted-by":"crossref","first-page":"576","DOI":"10.1111\/j.1365-2990.2004.00587.x","article-title":"The extent of axonal loss in the long tracts in hereditary spastic paraplegia","volume":"30","author":"Deluca","year":"2004","journal-title":"Neuropathol Appl Neurobiol"},{"key":"10.1016\/j.neurol.2019.11.003_bib0740","doi-asserted-by":"crossref","first-page":"1961","DOI":"10.1007\/s00415-015-7791-7","article-title":"Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations","volume":"262","author":"Lindig","year":"2015","journal-title":"J Neurol"}],"container-title":["Revue Neurologique"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0035378719309154?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0035378719309154?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,22]],"date-time":"2025-09-22T05:40:19Z","timestamp":1758519619000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0035378719309154"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,5]]},"references-count":74,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2020,5]]}},"alternative-id":["S0035378719309154"],"URL":"https:\/\/doi.org\/10.1016\/j.neurol.2019.11.003","relation":{},"ISSN":["0035-3787"],"issn-type":[{"value":"0035-3787","type":"print"}],"subject":[],"published":{"date-parts":[[2020,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"A historical approach to hereditary spastic paraplegia","name":"articletitle","label":"Article Title"},{"value":"Revue Neurologique","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.neurol.2019.11.003","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 Elsevier Masson SAS. All rights reserved.","name":"copyright","label":"Copyright"}]}}