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1969 1
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1976 1
1977 1
1978 1
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1987 1
1995 2
1997 1
2001 1
2002 2
2004 2
2006 3
2007 4
2008 2
2010 1
2011 2
2012 1
2013 3
2014 4
2015 5
2016 2
2017 3
2018 5
2019 5
2020 5
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2023 4
2024 1

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67 results

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Page 1
Migraine Aura: Pathophysiology, Mimics, and Treatment Options.
Fraser CL, Hepschke JL, Jenkins B, Prasad S. Fraser CL, et al. Semin Neurol. 2019 Dec;39(6):739-748. doi: 10.1055/s-0039-1700525. Epub 2019 Dec 17. Semin Neurol. 2019. PMID: 31847045 Review.
Calcitonin gene-related peptide (CGRP) plays a key role in many of these steps, and a growing class of CGRP-antagonists have emerged as a novel, efficacious preventative therapy. It is still not fully understood why a preponderance of migraine aura symptoms is visual, and …
Calcitonin gene-related peptide (CGRP) plays a key role in many of these steps, and a growing class of CGRP-antagonists have emerged as a no …
Ethnicity and Metabolic Syndrome: Implications for Assessment, Management and Prevention.
Lear SA, Gasevic D. Lear SA, et al. Nutrients. 2019 Dec 19;12(1):15. doi: 10.3390/nu12010015. Nutrients. 2019. PMID: 31861719 Free PMC article. Review.
The metabolic syndrome (MetS) is a constellation of cardiometabolic risk factors that identifies people at increased risk for type 2 diabetes and cardiovascular disease. ...In these studies, lifestyle management has proven an effective therapy for reversal of MetS, …
The metabolic syndrome (MetS) is a constellation of cardiometabolic risk factors that identifies people at increased risk for type 2 …
Clinical features and orbital anomalies in Fraser syndrome and a review of management options.
Das D, Modaboyina S, Raj S, Agrawal S, Bajaj MS. Das D, et al. Indian J Ophthalmol. 2022 Jul;70(7):2559-2563. doi: 10.4103/ijo.IJO_2627_21. Indian J Ophthalmol. 2022. PMID: 35791156 Free PMC article. Review.
PURPOSE: Fraser syndrome is a rare congenital disorder comprising cryptophthalmos, syndactyly, and many times, urogenital anomalies. Herein, the authors aimed to study and report the clinical features and orbital anomalies in cases diagnosed with Fraser
PURPOSE: Fraser syndrome is a rare congenital disorder comprising cryptophthalmos, syndactyly, and many times, urogenit …
Patient ethnicity and cascade genetic testing: a descriptive study of a publicly funded hereditary cancer program.
Braley EF, Bedard AC, Nuk J, Hong Q, Bedard JEJ, Sun S, Schrader KA. Braley EF, et al. Fam Cancer. 2022 Jul;21(3):369-374. doi: 10.1007/s10689-021-00270-0. Epub 2021 Jul 7. Fam Cancer. 2022. PMID: 34232459
The majority of cascade genetic tests were for BRCA1/BRCA2 (58.8%), followed by 16.9% for Lynch syndrome genes. Most patients were female (70%), and the mean age of patients was 49 years old. ...
The majority of cascade genetic tests were for BRCA1/BRCA2 (58.8%), followed by 16.9% for Lynch syndrome genes. Most patients were fe …
Human papillomavirus (HPV) vaccine and autonomic disorders: a position statement from the American Autonomic Society.
Barboi A, Gibbons CH, Axelrod F, Benarroch EE, Biaggioni I, Chapleau MW, Chelimsky G, Chelimsky T, Cheshire WP, Claydon VE, Freeman R, Goldstein DS, Joyner MJ, Kaufmann H, Low PA, Norcliffe-Kaufmann L, Robertson D, Shibao CA, Singer W, Snapper H, Vernino S, Raj SR; American Autonomic Society. Barboi A, et al. Clin Auton Res. 2020 Feb;30(1):13-18. doi: 10.1007/s10286-019-00608-w. Epub 2019 Sep 2. Clin Auton Res. 2020. PMID: 31475305 Review.
INTRODUCTION: Human papillomavirus (HPV) vaccination has been anecdotally connected to the development of dysautonomia, chronic fatigue, complex regional pain syndrome and postural tachycardia syndrome. OBJECTIVES: To critically evaluate a potential connection betwe …
INTRODUCTION: Human papillomavirus (HPV) vaccination has been anecdotally connected to the development of dysautonomia, chronic fatigue, com …
Fraser syndrome and cryptophthalmos: review of the diagnostic criteria and evidence for phenotypic modules in complex malformation syndromes.
Slavotinek AM, Tifft CJ. Slavotinek AM, et al. J Med Genet. 2002 Sep;39(9):623-33. doi: 10.1136/jmg.39.9.623. J Med Genet. 2002. PMID: 12205104 Free PMC article. Review.
Fraser syndrome is characterised by cryptophthalmos, cutaneous syndactyly, malformations of the larynx and genitourinary tract, craniofacial dysmorphism, orofacial clefting, mental retardation, and musculoskeletal anomalies. ...Use of the published diagnostic
Fraser syndrome is characterised by cryptophthalmos, cutaneous syndactyly, malformations of the larynx and genitourinar
Management of soft-tissue injuries in distal radius fractures.
Leversedge FJ, Srinivasan RC. Leversedge FJ, et al. Hand Clin. 2012 May;28(2):225-33. doi: 10.1016/j.hcl.2012.03.005. Epub 2012 Apr 6. Hand Clin. 2012. PMID: 22554666 Review.
This article describes soft-tissue injuries and considerations for treatment associated with distal radius fractures, including injuries to the skin, tendon and muscle, ligaments, the triangular fibrocartilage complex, neurovascular structures, and related conditions such as comp …
This article describes soft-tissue injuries and considerations for treatment associated with distal radius fractures, including injuries to …
A national consensus management pathway for paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS): results of a national Delphi process.
Harwood R, Allin B, Jones CE, Whittaker E, Ramnarayan P, Ramanan AV, Kaleem M, Tulloh R, Peters MJ, Almond S, Davis PJ, Levin M, Tometzki A, Faust SN, Knight M, Kenny S; PIMS-TS National Consensus Management Study Group. Harwood R, et al. Lancet Child Adolesc Health. 2021 Feb;5(2):133-141. doi: 10.1016/S2352-4642(20)30304-7. Epub 2020 Sep 18. Lancet Child Adolesc Health. 2021. PMID: 32956615 Free PMC article. Review.
Paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS) is a novel condition that was first reported in April, 2020. ...The importance of a multidisciplinary team in decision making for children with PIMS-TS is highlighted throughout the …
Paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS) is a novel condition that was first report …
Incidence of Sinusoidal Obstruction Syndrome/Veno-Occlusive Disease and Treatment with Defibrotide in Allogeneic Transplantation: A Multicenter Australasian Registry Study.
Coutsouvelis J, Kirkpatrick CM, Dooley M, Spencer A, Kennedy G, Chau M, Huang G, Doocey R, Copeland TS, Do L, Bardy P, Kerridge I, Cole T, Fraser C, Perera T, Larsen SR, Mason K, O'Brien TA, Shaw PJ, Teague L, Butler A, Watson AM, Ramachandran S, Marsh J, Khan Z, Hamad N. Coutsouvelis J, et al. Transplant Cell Ther. 2023 Jun;29(6):383.e1-383.e10. doi: 10.1016/j.jtct.2023.03.014. Epub 2023 Mar 18. Transplant Cell Ther. 2023. PMID: 36934993
Sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) is an established complication in patients undergoing allogeneic hemopoietic stem cell transplantation (HSCT). ...
Sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) is an established complication in patients undergoing allogeneic hem …
67 results