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Elevated Transaminases with Topical Diclofenac: A Case Report.
Daniels AM, Gibbs LM, Herndon CM. Daniels AM, et al. J Pain Palliat Care Pharmacother. 2018 Jun-Sep;32(2-3):161-164. doi: 10.1080/15360288.2018.1546257. Epub 2019 Jan 15. J Pain Palliat Care Pharmacother. 2018. PMID: 30645151
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.
Zhou X, Feliciano P, Shu C, Wang T, Astrovskaya I, Hall JB, Obiajulu JU, Wright JR, Murali SC, Xu SX, Brueggeman L, Thomas TR, Marchenko O, Fleisch C, Barns SD, Snyder LG, Han B, Chang TS, Turner TN, Harvey WT, Nishida A, O'Roak BJ, Geschwind DH; SPARK Consortium; Michaelson JJ, Volfovsky N, Eichler EE, Shen Y, Chung WK. Zhou X, et al. Nat Genet. 2022 Sep;54(9):1305-1319. doi: 10.1038/s41588-022-01148-2. Epub 2022 Aug 18. Nat Genet. 2022. PMID: 35982159 Free PMC article.
What Is the Diagnostic Performance of Conventional Radiographs and Clinical Reassessment Compared With HR-pQCT Scaphoid Fracture Diagnosis?
Daniels AM, Kranendonk J, Wyers CE, Janzing HMJ, Sassen S, van Rietbergen B, Geusens PPMM, Kaarsemaker S, Hannemann PFW, Poeze M, van den Bergh JP. Daniels AM, et al. Clin Orthop Relat Res. 2023 Jan 1;481(1):97-104. doi: 10.1097/CORR.0000000000002310. Epub 2022 Jul 13. Clin Orthop Relat Res. 2023. PMID: 35833810 Free PMC article.
Association between bone shape and the presence of a fracture in patients with a clinically suspected scaphoid fracture.
Bevers MSAM, Wyers CE, Daniels AM, Audenaert EA, van Kuijk SMJ, van Rietbergen B, Geusens PPMM, Kaarsemaker S, Janzing HMJ, Hannemann PFW, Poeze M, van den Bergh JP. Bevers MSAM, et al. Among authors: daniels am. J Biomech. 2021 Nov 9;128:110726. doi: 10.1016/j.jbiomech.2021.110726. Epub 2021 Aug 30. J Biomech. 2021. PMID: 34534791 Free article.
Assessment of the healing of conservatively-treated scaphoid fractures using HR-pQCT.
Bevers MSAM, Daniels AM, van Rietbergen B, Geusens PPMM, van Kuijk SMJ, Sassen S, Kaarsemaker S, Hannemann PFW, Poeze M, Janzing HMJ, van den Bergh JP, Wyers CE. Bevers MSAM, et al. Among authors: daniels am. Bone. 2021 Dec;153:116161. doi: 10.1016/j.bone.2021.116161. Epub 2021 Aug 27. Bone. 2021. PMID: 34455117 Free article.
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, De Vries BBA, Vissers LELM, Nordenskjold M, Kvarnung M, Lindstrand A, Nordgren A, Gecz J, Iascone M, Cereda A, Scatigno A, Maitz S, Zanni G, Bertini E, Zweier C, Schuhmann S, Wiesener A, Pepper M, Panjwani H, Torti E, Abid F, Anselm I, Srivastava S, Atwal P, Bacino CA, Bhat G, Cobian K, Bird LM, Friedman J, Wright MS, Callewaert B, Petit F, Mathieu S, Afenjar A, Christensen CK, White KM, Elpeleg O, Berger I, Espineli EJ, Fagerberg C, Brasch-Andersen C, Hansen LK, Feyma T, Hughes S, Thiffault I, Sullivan B, Yan S, Keller K, Keren B, Mignot C, Kooy F, Meuwissen M, Basinger A, Kukolich M, Philips M, Ortega L, Drummond-Borg M, Lauridsen M, Sorensen K, Lehman A; CAUSES Study; Lopez-Rangel E, Levy P, Lessel D, Lotze T, Madan-Khetarpal S, Sebastian J, Vento J, Vats D, Benman LM, Mckee S, Mirzaa GM, Muss C, Pappas J, Peeters H, Romano C, Elia M, Galesi O, Simon MEH, van Gassen KLI, Simpson K, Stratton R, Syed S, Thevenon J, Palafoll IV, Vitobello A, Bournez M, Faivre L, Xia K; SPARK Consortium; Earl RK, Nowakowski T, Bernier RA, Eichler EE. Gillentine MA, et al. Genome Med. 2021 Apr 19;13(1):63. doi: 10.1186/s13073-021-00870-6. Genome Med. 2021. PMID: 33874999 Free PMC article.
67 results