PubMed Clinical Queries for "Undiagnosed diseases"

PubMed Clinical Queries



From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Undiagnosed diseases" 

Results: 5 of 1961

• Validation of a genetic risk score for atrial fibrillation: A prospective multicenter cohort study.
  Muse ED, Wineinger NE, Spencer EG, Peters M, Henderson R, Zhang Y, Barrett PM, Rivera SP, Wohlgemuth JG, Devlin JJ, et al.PLoS Med. 2018 Mar; 15(3):e1002525. Epub 2018 Mar 13.
• Prevalence of and characteristics associated with insomnia and obstructive sleep apnea among veterans with knee and hip osteoarthritis.
  Taylor SS, Hughes JM, Coffman CJ, Jeffreys AS, Ulmer CS, Oddone EZ, Bosworth HB, Yancy WS Jr, Allen KD.BMC Musculoskelet Disord. 2018 Mar 9; 19(1):79. Epub 2018 Mar 9.
• Leprosy among schoolchildren in the Amazon region: A cross-sectional study of active search and possible source of infection by contact tracing.
  Pedrosa VL, Dias LC, Galban E, Leturiondo A, Palheta J Jr, Santos M, Moraes MO, Talhari C.PLoS Negl Trop Dis. 2018 Feb 26; 12(2):e0006261. Epub 2018 Feb 26.
• Prevalence and pattern of cardiovascular risk factors in a population in India.
  Khetan A, Zullo M, Hejjaji V, Barbhaya D, Agarwal S, Gupta R, Madan Mohan SK, Josephson R.Heart Asia. 2017; 9(2):e010931. Epub 2017 Sep 14.
• Health Services Burden of Undiagnosed and Overdiagnosed COPD.
  Gershon AS, Thiruchelvam D, Chapman KR, Aaron SD, Stanbrook MB, Bourbeau J, Tan W, To T, Canadian Respiratory Research Network..Chest. 2018 Feb 6; . Epub 2018 Feb 6.

See all (1961)

This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 252

• Characterizing undiagnosed chronic obstructive pulmonary disease: a systematic review and meta-analysis.
  Johnson KM, Bryan S, Ghanbarian S, Sin DD, Sadatsafavi M.Respir Res. 2018 Feb 7; 19(1):26. Epub 2018 Feb 7.
• The prevalence of autosomal dominant polycystic kidney disease (ADPKD): A meta-analysis of European literature and prevalence evaluation in the Italian province of Modena suggest that ADPKD is a rare and underdiagnosed condition.
  Solazzo A, Testa F, Giovanella S, Busutti M, Furci L, Carrera P, Ferrari M, Ligabue G, Mori G, Leonelli M, et al.PLoS One. 2018; 13(1):e0190430. Epub 2018 Jan 16.
• Encephalitis diagnosis using metagenomics: application of next generation sequencing for undiagnosed cases.
  Brown JR, Bharucha T, Breuer J.J Infect. 2018 Mar; 76(3):225-240. Epub 2018 Jan 2.
• Analytic survey of 57 cases of oral metastases.
  Liu Y, Vargo RJ, Bilodeau EA.J Oral Pathol Med. 2018 Mar; 47(3):275-280. Epub 2018 Jan 30.
• Negative surgical exploration in patients with Cushing's disease: benefit of two-thirds gland resection on remission rate and a review of the literature.
  Carr SB, Kleinschmidt-DeMasters BK, Kerr JM, Kiseljak-Vassiliades K, Wierman ME, Lillehei KO.J Neurosurg. 2017 Dec 8; :1-8. Epub 2017 Dec 8.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 1132

• Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta.
  Weerakkody R, Ross D, Parry DA, Ziganshin B, Vandrovcova J, Gampawar P, Abdullah A, Biggs J, Dumfarth J, Ibrahim Y, et al.Genet Med. 2018 Mar 15; . Epub 2018 Mar 15.
• Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network.
  Palmer CGS, McConkie-Rosell A, Holm IA, LeBlanc K, Sinsheimer JS, Briere LC, Dorrani N, Herzog MR, Lincoln S, Schoch K, et al.J Genet Couns. 2018 Mar 1; . Epub 2018 Mar 1.
• Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia Genes.
  Coutelier M, Hammer MB, Stevanin G, Monin ML, Davoine CS, Mochel F, Labauge P, Ewenczyk C, Ding J, Gibbs JR, et al.JAMA Neurol. 2018 Feb 26; . Epub 2018 Feb 26.
• Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
  Oláhová M, Yoon WH, Thompson K, Jangam S, Fernandez L, Davidson JM, Kyle JE, Grove ME, Fisk DG, Kohler JN, et al.Am J Hum Genet. 2018 Mar 1; 102(3):494-504. Epub 2018 Feb 22.
• Metabolic causes of nonimmune hydrops fetalis: A next-generation sequencing panel as a first-line investigation.
  Sudrié-Arnaud B, Marguet F, Patrier S, Martinovic J, Louillet F, Broux F, Charbonnier F, Dranguet H, Coutant S, Vezain M, et al.Clin Chim Acta. 2018 Feb 22; 481:1-8. Epub 2018 Feb 22.

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This column displays citations pertaining to topics in medical genetics. See more filter information.