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Year Number of Results
2014 2
2015 2
2017 2
2018 4
2019 11
2020 3
2021 11
2022 11
2023 15
2024 3

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57 results

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Page 1
Physical activity and exercise for the prevention and management of mild cognitive impairment and dementia: a collaborative international guideline.
Veronese N, Soysal P, Demurtas J, Solmi M, Bruyère O, Christodoulou N, Ramalho R, Fusar-Poli P, Lappas AS, Pinto D, Frederiksen KS, Corbi GM, Karpenko O, Georges J, Durães J, Schlögl M, Yilmaz O, Sieber C, Shenkin SD, Smith L, Reginster JY, Maggi S, Limongi F, Ars J, Barbagallo M, Cherubini A, Quinn T; Alzheimer Europe; European College of Neuropsychopharmacology; European Geriatric Medicine Society (Lead Society); European Interdisciplinary Council on Ageing; European Society of Clinical and Economic Aspects of Osteoporosis and Osteoarthritis; International Association of Gerontology and Geriatrics-European Region; Scottish Brain Health ARC; World Psychiatry Association-Preventive Psychiatry Section; endorsed by the European Academy of Neurology. Veronese N, et al. Among authors: duraes j. Eur Geriatr Med. 2023 Oct;14(5):925-952. doi: 10.1007/s41999-023-00858-y. Epub 2023 Sep 28. Eur Geriatr Med. 2023. PMID: 37768499 Free PMC article.
SERAC1 Deficiency- A New Phenotype.
Martins E, Durães J, Nogueira C, Gomes J, Vilarinho L, Macário C. Martins E, et al. Among authors: duraes j. Endocr Metab Immune Disord Drug Targets. 2023 Sep 14. doi: 10.2174/1871530323666230914114456. Online ahead of print. Endocr Metab Immune Disord Drug Targets. 2023. PMID: 37711114
It's Never Too Late for a Diagnosis.
Coelho M, Durães J, Freixo J, Tomás J, Macário C. Coelho M, et al. Among authors: duraes j. Endocr Metab Immune Disord Drug Targets. 2023 Oct 18. doi: 10.2174/0118715303280103231006102831. Online ahead of print. Endocr Metab Immune Disord Drug Targets. 2023. PMID: 37859411
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patients.
Benzoni C, Moscatelli M, Farina L, Magri S, Ciano C, Scaioli V, Alverà S, Cammarata G, Bianchi-Marzoli S, Castellani M, Zito FM, Marotta G, Piacentini S, Villacara A, Mantegazza R, Gellera C, Durães J, Gouveia A, Matos A, do Carmo Macário M, Pareyson D, Taroni F, Di Bella D, Salsano E. Benzoni C, et al. Among authors: duraes j. J Neurol. 2023 Sep;270(9):4219-4234. doi: 10.1007/s00415-023-11762-7. Epub 2023 May 12. J Neurol. 2023. PMID: 37171481
Two sisters with myoclonus and ataxia.
Pereira M, Durães J, Macário MDC. Pereira M, et al. Among authors: duraes j. Pract Neurol. 2020 May;20(3):249-252. doi: 10.1136/practneurol-2019-002446. Epub 2020 Mar 11. Pract Neurol. 2020. PMID: 32161095 No abstract available.
A systematic review of progranulin concentrations in biofluids in over 7,000 people-assessing the pathogenicity of GRN mutations and other influencing factors.
Swift IJ, Rademakers R, Finch N, Baker M, Ghidoni R, Benussi L, Binetti G, Rossi G, Synofzik M, Wilke C, Mengel D, Graff C, Takada LT, Sánchez-Valle R, Antonell A, Galimberti D, Fenoglio C, Serpente M, Arcaro M, Schreiber S, Vielhaber S, Arndt P, Santana I, Almeida MR, Moreno F, Barandiaran M, Gabilondo A, Stubert J, Gómez-Tortosa E, Agüero P, Sainz MJ, Gohda T, Murakoshi M, Kamei N, Kittel-Schneider S, Reif A, Weigl J, Jian J, Liu C, Serrero G, Greither T, Theil G, Lohmann E, Gazzina S, Bagnoli S, Coppola G, Bruni A, Quante M, Kiess W, Hiemisch A, Jurkutat A, Block MS, Carlson AM, Bråthen G, Sando SB, Grøntvedt GR, Lauridsen C, Heslegrave A, Heller C, Abel E, Gómez-Núñez A, Puey R, Arighi A, Rotondo E, Jiskoot LC, Meeter LHH, Durães J, Lima M, Tábuas-Pereira M, Lemos J, Boeve B, Petersen RC, Dickson DW, Graff-Radford NR, LeBer I, Sellami L, Lamari F, Clot F, Borroni B, Cantoni V, Rivolta J, Lleó A, Fortea J, Alcolea D, Illán-Gala I, Andres-Cerezo L, Van Damme P, Clarimon J, Steinacker P, Feneberg E, Otto M, van der Ende EL, van Swieten JC, Seelaar H, Zetterberg H, Sogorb-Esteve A, Rohrer JD. Swift IJ, et al. Among authors: duraes j. Alzheimers Res Ther. 2024 Mar 28;16(1):66. doi: 10.1186/s13195-024-01420-z. Alzheimers Res Ther. 2024. PMID: 38539243 Free PMC article.
Novel GLA T194A variant causes Fabry disease.
Pestana MN, Gomes da Silva F, Durães J, Silva G. Pestana MN, et al. Among authors: duraes j. BMJ Case Rep. 2021 Mar 1;14(3):e239204. doi: 10.1136/bcr-2020-239204. BMJ Case Rep. 2021. PMID: 33649041 Free PMC article.
57 results