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102 results

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Illustration of the long-term efficacy of pallidal deep brain stimulation in a patient with PKAN dystonia.
Romito LM, Colucci F, Zorzi G, Garavaglia B, Kaymak A, Mazzoni A, Panteghini C, Golfrè Andreasi N, Rinaldo S, Levi V, Carecchio M, Eleopra R. Romito LM, et al. Among authors: carecchio m. Parkinsonism Relat Disord. 2024 Jun;123:106977. doi: 10.1016/j.parkreldis.2024.106977. Epub 2024 Apr 25. Parkinsonism Relat Disord. 2024. PMID: 38691977 No abstract available.
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease.
Carecchio M, Fenoglio C, De Riz M, Guidi I, Comi C, Cortini F, Venturelli E, Restelli I, Cantoni C, Bresolin N, Monaco F, Scarpini E, Galimberti D. Carecchio M, et al. J Neurol Sci. 2009 Dec 15;287(1-2):291-3. doi: 10.1016/j.jns.2009.07.011. Epub 2009 Aug 14. J Neurol Sci. 2009. PMID: 19683260 Free article.
NKX2.1 run-on mutation associated to familial brain-lung-thyroid syndrome.
Cavaliere E, Gortan AJ, Passon N, Fabbro D, Marin D, Carecchio M, Baldan F, Credendino SC, Gallo R, Cogo P, Damante G, De Vita G. Cavaliere E, et al. Among authors: carecchio m. Clin Genet. 2021 Jul;100(1):114-116. doi: 10.1111/cge.13961. Epub 2021 Mar 29. Clin Genet. 2021. PMID: 33778944 Free PMC article.
Cerebrospinal fluid biomarkers in Progranulin mutations carriers.
Carecchio M, Fenoglio C, Cortini F, Comi C, Benussi L, Ghidoni R, Borroni B, De Riz M, Serpente M, Cantoni C, Franceschi M, Albertini V, Monaco F, Rainero I, Binetti G, Padovani A, Bresolin N, Scarpini E, Galimberti D. Carecchio M, et al. J Alzheimers Dis. 2011;27(4):781-90. doi: 10.3233/JAD-2011-111046. J Alzheimers Dis. 2011. PMID: 21891865
C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.
Alazami AM, Schneider SA, Bonneau D, Pasquier L, Carecchio M, Kojovic M, Steindl K, de Kerdanet M, Nezarati MM, Bhatia KP, Degos B, Goh E, Alkuraya FS. Alazami AM, et al. Among authors: carecchio m. Clin Genet. 2010 Dec;78(6):585-90. doi: 10.1111/j.1399-0004.2010.01441.x. Clin Genet. 2010. PMID: 20507343
Atypical parkinsonism with apraxia and supranuclear gaze abnormalities in type 1 Gaucher disease. Expanding the spectrum: case report and literature review.
Alonso-Canovas A, Katschnig P, Tucci A, Carecchio M, Wood NW, Edwards M, Martínez Castrillo JC, Burke D, Heales S, Bhatia KP. Alonso-Canovas A, et al. Among authors: carecchio m. Mov Disord. 2010 Jul 30;25(10):1506-9. doi: 10.1002/mds.23109. Mov Disord. 2010. PMID: 20629148 Review. No abstract available.
102 results