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SARS-COV-2 Infection in People Living with HIV: Experience from a Tertiary Hospital in Madrid.
González Guembe M, Tisner Pensado Y, Tejerina Picado F, Diez C, Pérez Latorre L, Fanciulli C, Parras Vázquez F, López Bernaldo de Quirós JC, Berenguer J, Padilla Ortega B, Machado M, Valerio Minero M, Muñoz Garcia P, Bouza Santiago E, Galar A, Catalan P, Alonso R, Bellón JM, Aldámiz-Echevarría Lois T; Gregorio Marañón Microbiology-ID COVID 19 Study Group. González Guembe M, et al. AIDS Res Hum Retroviruses. 2022 May;38(5):394-398. doi: 10.1089/AID.2021.0159. Epub 2022 Jan 28. AIDS Res Hum Retroviruses. 2022. PMID: 34969259
Impact of COVID-19 on global burn care.
Laura P, José A, Nikki A, Khaled A, Barret J, Jeffery C, Shobha C, Jack CS, Scott C, Nadia D, Moustafa E, Liao J, Josef H, Briana H, Sunil K, Tetsuro K, Jorge LV, Gaoxing L, Hajime M, Ariel MA, Naiem M, Kiran N, Nawar A, Faustin N, Anthony O, Tom P, Liang Q, Man RS, Ingrid S, Ahmed T, Vana Molina PL, Shelley W, Mark F. Laura P, et al. Burns. 2022 Sep;48(6):1301-1310. doi: 10.1016/j.burns.2021.11.010. Epub 2021 Nov 17. Burns. 2022. PMID: 34903416 Free PMC article.
Italian adaptation of the Beaumont Behavioral Inventory (BBI): psychometric properties and clinical usability.
Iazzolino B, Pain D, Laura P, Aiello EN, Gallucci M, Radici A, Palumbo F, Canosa A, Moglia C, Calvo A, Mora G, Chiò A. Iazzolino B, et al. Among authors: laura p. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Feb;23(1-2):81-86. doi: 10.1080/21678421.2021.1946085. Epub 2021 Jul 19. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 34279169
One is the loneliest number: genotypic matchmaking using the electronic health record.
Brokamp E, Koziura ME, Phillips JA 3rd, Tang LA, Cogan JD, Rives LC, Robertson AK, Duncan L, Bican A, Peterson JF, Newman JH, Hamid R, Bastarache L; Undiagnosed Diseases Network. Brokamp E, et al. Genet Med. 2021 Oct;23(10):1830-1832. doi: 10.1038/s41436-021-01179-w. Epub 2021 Jul 6. Genet Med. 2021. PMID: 34230636 Free PMC article. No abstract available.
Restless Legs Syndrome: Challenges to Treatment.
P LMB, E SSA, Castro-Villacañas A, Garcia-Borreguero D. P LMB, et al. Sleep Med Clin. 2021 Jun;16(2):269-277. doi: 10.1016/j.jsmc.2021.02.003. Epub 2021 Apr 15. Sleep Med Clin. 2021. PMID: 33985652 Review.
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA; Inherited Neuropathy Consortium; Isasi R, Khan A, Laurà M, Magri S, Pipis M, Pisciotta C, Powell E, Rossor AM, Saveri P, Sowden JE, Tozza S, Vandrovcova J, Dallman J, Grignani E, Marchioni E, Scherer SS, Tang B, Lin Z, Al-Ajmi A, Schüle R, Synofzik M, Maisonobe T, Stojkovic T, Auer-Grumbach M, Abdelhamed MA, Hamed SA, Zhang R, Manganelli F, Santoro L, Taroni F, Pareyson D, Houlden H, Herrmann DN, Reilly MM, Shy ME, Zhai RG, Zuchner S. Cortese A, et al. Nat Genet. 2020 Jun;52(6):640. doi: 10.1038/s41588-020-0649-7. Nat Genet. 2020. PMID: 32457452
38 results