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SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum.
Neurology. 2009 Oct 6;73(14):1111-9. doi: 10.1212/WNL.0b013e3181bacf59.
Neurology. 2009.
PMID: 19805727
Plasma NfL levels and longitudinal change rates in C9orf72 and GRN-associated diseases: from tailored references to clinical applications.
Saracino D, Dorgham K, Camuzat A, Rinaldi D, Rametti-Lacroux A, Houot M, Clot F, Martin-Hardy P, Jornea L, Azuar C, Migliaccio R, Pasquier F, Couratier P, Auriacombe S, Sauvée M, Boutoleau-Bretonnière C, Pariente J, Didic M, Hannequin D, Wallon D; French Research Network on FTD/FTD-ALS; PREV-DEMALS and Predict-PGRN study groups; Colliot O, Dubois B, Brice A, Levy R, Forlani S, Le Ber I.
Saracino D, et al. Among authors: martin hardy p.
J Neurol Neurosurg Psychiatry. 2021 Dec;92(12):1278-1288. doi: 10.1136/jnnp-2021-326914. Epub 2021 Aug 4.
J Neurol Neurosurg Psychiatry. 2021.
PMID: 34349004
Free PMC article.
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Atypical White Matter Hyperintensities Markedly Impact Plasma Neurofilament Light Chain Variability in GRN Patients.
Vítor J, Saracino D, Ströer S, Camuzat A, Dorgham K, Clot F, Martin-Hardy P, Pasquier F; French research network on FTLD/FTLD-ALS, Predict-PGRN study group; Le Ber I.
Vítor J, et al. Among authors: martin hardy p.
J Alzheimers Dis. 2023;94(4):1351-1360. doi: 10.3233/JAD-230315.
J Alzheimers Dis. 2023.
PMID: 37393503
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