These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 10881656)

  • 21. [Diagnostic management of patients with rare genetic diseases: example of five pathologies].
    Godet V; Hirtzlin I; Costet N
    Rev Epidemiol Sante Publique; 2001 Sep; 49(4):357-66. PubMed ID: 11567202
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Medical case retrieval from a committee of decision trees.
    Quellec G; Lamard M; Bekri L; Cazuguel G; Roux C; Cochener B
    IEEE Trans Inf Technol Biomed; 2010 Sep; 14(5):1227-35. PubMed ID: 20813626
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?].
    Tankeu AT; Tran C
    Praxis (Bern 1994); 2022 Jan; 110(1):38-43. PubMed ID: 34983209
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Chronic Fatigue: When to Suspect an Inherited Metabolic Disease?].
    Tankeu AT; Tran C
    Praxis (Bern 1994); 2022 Jan; 110(1):1-6. PubMed ID: 34983208
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Strategies and logistical requirements for efficient testing in genetic disease.
    Jackson-Cook C; Pandya A
    Clin Lab Med; 1995 Dec; 15(4):839-57. PubMed ID: 8838226
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A multifunctional system of the national genetic register.
    Kobrinsky B; Tester I; Demikova N; Sedov Yu; Marjanchik B; Taperova L; Glukhovskaya Yu; Podolnaja M
    Stud Health Technol Inform; 1998; 52 Pt 1():121-5. PubMed ID: 10384433
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comparing image search behaviour in the ARRS GoldMiner search engine and a clinical PACS/RIS.
    De-Arteaga M; Eggel I; Do B; Rubin D; Kahn CE; Müller H
    J Biomed Inform; 2015 Aug; 56():57-64. PubMed ID: 26002820
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Context-sensitive medical information retrieval.
    Auerbuch M; Karson TH; Ben-Ami B; Maimon O; Rokach L
    Stud Health Technol Inform; 2004; 107(Pt 1):282-6. PubMed ID: 15360819
    [TBL] [Abstract][Full Text] [Related]  

  • 29. GENFILES: a computerized medical genetics information network. II. MEDGEN: the clinical genetics system.
    Mitchell JA; Loughman WD; Epstein CJ
    Am J Med Genet; 1980; 7(3):251-66. PubMed ID: 7468653
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Use of fine needle aspiration for fibroblast culture.
    Kurtycz DF; Logrono R; Harris C; Asplund S; O'Donnell L
    Pediatr Pathol Lab Med; 1998; 18(1):35-9. PubMed ID: 9566280
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Case retrieval in medical databases by fusing heterogeneous information.
    Quellec G; Lamard M; Cazuguel G; Roux C; Cochener B
    IEEE Trans Med Imaging; 2011 Jan; 30(1):108-18. PubMed ID: 20693107
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Clinical application of mass spectrometry in the pediatric field: current topics].
    Yamaguchi S
    Rinsho Byori; 2013 Sep; 61(9):817-25. PubMed ID: 24369594
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis. Fetoscopy.
    Nicolaides K; Rodeck CH
    Br J Hosp Med; 1984 Jun; 31(6):396-405. PubMed ID: 6430373
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Combination of visual and textual similarity retrieval from medical documents.
    Eggel I; Müller H
    Stud Health Technol Inform; 2009; 150():841-5. PubMed ID: 19745431
    [TBL] [Abstract][Full Text] [Related]  

  • 35. "Hyperstat": an educational and working tool in epidemiology.
    Nicolosi A
    Medinfo; 1995; 8 Pt 2():1697. PubMed ID: 8591554
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Efficacy of virtual and asynchronous teaching of computer-assisted diagnosis of genetic diseases seen in clinics.
    Hash MG; Walker PD; Laferriere HE; Melton L; Heller LS; Phillips JA
    Am J Med Genet A; 2022 Apr; 188(4):1142-1148. PubMed ID: 34967985
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Problems of phenotypic similarity and differential diagnostic of hereditary diseases in children].
    Barashnev IuI
    Vestn Akad Med Nauk SSSR; 1982; (6):47-51. PubMed ID: 7051616
    [No Abstract]   [Full Text] [Related]  

  • 38. [Application of gas chromatography-mass spectrometry analysis on urine filter paper in the high-risk screening and diagnosis of inherited metabolic diseases].
    Luo XP; Wang MT; Wei H; Liang Y; Wang HW; Lin HH; Dong YS; Liu WJ; Fang JM; Ning Q
    Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):245-8. PubMed ID: 14754523
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The prevalence of inherited metabolic disorders in Estonian population over 30 years: A significant increase during study period.
    Tiivoja E; Reinson K; Muru K; Rähn K; Muhu K; Mauring L; Kahre T; Pajusalu S; Õunap K
    JIMD Rep; 2022 Nov; 63(6):604-613. PubMed ID: 36341167
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PhD: a web database application for phenotype data management.
    Li JL; Li MX; Deng HY; Duffy PE; Deng HW
    Bioinformatics; 2005 Aug; 21(16):3443-4. PubMed ID: 15985495
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.