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Year Number of Results
1972 1
1983 1
1984 1
1985 1
1986 2
1987 2
1988 3
1989 2
1990 1
1992 1
1993 2
1994 1
2003 1
2005 1
2008 1
2012 1
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2020 4
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2022 6
2025 0

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38 results

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Page 1
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 May;52(5):473-481. doi: 10.1038/s41588-020-0615-4. Epub 2020 May 4. Nat Genet. 2020. PMID: 32367058 Free PMC article.
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.
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
miR-1 and miR-133b expression in canine osteosarcoma.
Leonardo L, Laura P, Serena BM. Leonardo L, et al. Among authors: laura p. Res Vet Sci. 2018 Apr;117:133-137. doi: 10.1016/j.rvsc.2017.12.002. Epub 2017 Dec 15. Res Vet Sci. 2018. PMID: 29272721
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.
Design and use of improved walking aids.
Nava LC, Laura PA. Nava LC, et al. Among authors: laura pa. J Biomed Eng. 1985 Oct;7(4):329-33. doi: 10.1016/0141-5425(85)90065-2. J Biomed Eng. 1985. PMID: 4057995
38 results