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 *

247 related articles for article (PubMed ID: 34901190)

  • 1. Next-Generation Sequencing-Based Genetic Diagnostic Strategies of Inherited Kidney Diseases.
    Zhang J; Zhang C; Gao E; Zhou Q
    Kidney Dis (Basel); 2021 Nov; 7(6):425-437. PubMed ID: 34901190
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Personalized medicine in chronic kidney disease by detection of monogenic mutations.
    Connaughton DM; Hildebrandt F
    Nephrol Dial Transplant; 2020 Mar; 35(3):390-397. PubMed ID: 30809662
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [THE GENETIC BASIS OF CHRONIC KIDNEY DISEASE IN CHILDREN AND YOUNG ADULTS].
    Kagan M; Eliyahu A; Ben Moshe Y; Vivante A
    Harefuah; 2021 Dec; 160(12):839-846. PubMed ID: 34957723
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular genetics of arrhythmias--a new paradigm.
    Schulze-Bahr E; Haverkamp W; Borggrefe M; Wedekind H; Mönnig G; Mergenthaler J; Assmann G; Funke H; Breithardt G
    Z Kardiol; 2000; 89 Suppl 4():IV12-22. PubMed ID: 10810773
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A practical approach to the genomics of kidney disorders.
    Hay E; Cullup T; Barnicoat A
    Pediatr Nephrol; 2022 Jan; 37(1):21-35. PubMed ID: 33675412
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Renal genetics in Australia: Kidney medicine in the genomic age.
    Jayasinghe K; Quinlan C; Stark Z; Patel C; Mallawaarachchi A; Wardrop L; Kerr PG; Trnka P; Mallett AJ;
    Nephrology (Carlton); 2019 Mar; 24(3):279-286. PubMed ID: 30239064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Practical Guide to Genetic Testing for Kidney Disorders of Unknown Etiology.
    Aron AW; Dahl NK; Besse W
    Kidney360; 2022 Sep; 3(9):1640-1651. PubMed ID: 36245662
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Massively parallel sequencing and targeted exomes in familial kidney disease can diagnose underlying genetic disorders.
    Mallett AJ; McCarthy HJ; Ho G; Holman K; Farnsworth E; Patel C; Fletcher JT; Mallawaarachchi A; Quinlan C; Bennetts B; Alexander SI
    Kidney Int; 2017 Dec; 92(6):1493-1506. PubMed ID: 28844315
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases.
    Bullich G; Domingo-Gallego A; Vargas I; Ruiz P; Lorente-Grandoso L; Furlano M; Fraga G; Madrid Á; Ariceta G; Borregán M; Piñero-Fernández JA; Rodríguez-Peña L; Ballesta-Martínez MJ; Llano-Rivas I; Meñica MA; Ballarín J; Torrents D; Torra R; Ars E
    Kidney Int; 2018 Aug; 94(2):363-371. PubMed ID: 29801666
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Towards precision nephrology: the opportunities and challenges of genomic medicine.
    Nestor JG; Groopman EE; Gharavi AG
    J Nephrol; 2018 Feb; 31(1):47-60. PubMed ID: 29043570
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Next-generation sequencing for research and diagnostics in kidney disease.
    Renkema KY; Stokman MF; Giles RH; Knoers NV
    Nat Rev Nephrol; 2014 Aug; 10(8):433-44. PubMed ID: 24914583
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Multilocus Inherited Neoplasia Alleles Syndrome: A Case Series and Review.
    Whitworth J; Skytte AB; Sunde L; Lim DH; Arends MJ; Happerfield L; Frayling IM; van Minkelen R; Woodward ER; Tischkowitz MD; Maher ER
    JAMA Oncol; 2016 Mar; 2(3):373-9. PubMed ID: 26659639
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare inherited kidney diseases: challenges, opportunities, and perspectives.
    Devuyst O; Knoers NV; Remuzzi G; Schaefer F;
    Lancet; 2014 May; 383(9931):1844-59. PubMed ID: 24856029
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel.
    Mori T; Hosomichi K; Chiga M; Mandai S; Nakaoka H; Sohara E; Okado T; Rai T; Sasaki S; Inoue I; Uchida S
    Clin Exp Nephrol; 2017 Feb; 21(1):63-75. PubMed ID: 26920127
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
    Ashton EJ; Legrand A; Benoit V; Roncelin I; Venisse A; Zennaro MC; Jeunemaitre X; Iancu D; Van't Hoff WG; Walsh SB; Godefroid N; Rotthier A; Del Favero J; Devuyst O; Schaefer F; Jenkins LA; Kleta R; Dahan K; Vargas-Poussou R; Bockenhauer D
    Kidney Int; 2018 Apr; 93(4):961-967. PubMed ID: 29398133
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Learning Physiology From Inherited Kidney Disorders.
    van der Wijst J; Belge H; Bindels RJM; Devuyst O
    Physiol Rev; 2019 Jul; 99(3):1575-1653. PubMed ID: 31215303
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rare diseases, rare presentations: recognizing atypical inherited kidney disease phenotypes in the age of genomics.
    Ars E; Torra R
    Clin Kidney J; 2017 Oct; 10(5):586-593. PubMed ID: 28980669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rare genetic causes of complex kidney and urological diseases.
    Groopman EE; Povysil G; Goldstein DB; Gharavi AG
    Nat Rev Nephrol; 2020 Nov; 16(11):641-656. PubMed ID: 32807983
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The LQT syndromes--current status of molecular mechanisms.
    Schulze-Bahr E; Wedekind H; Haverkamp W; Borggrefe M; Assmann G; Breithardt G; Funke H
    Z Kardiol; 1999 Apr; 88(4):245-54. PubMed ID: 10408028
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genomic medicine and risk prediction across the disease spectrum.
    Kotze MJ; Lückhoff HK; Peeters AV; Baatjes K; Schoeman M; van der Merwe L; Grant KA; Fisher LR; van der Merwe N; Pretorius J; van Velden DP; Myburgh EJ; Pienaar FM; van Rensburg SJ; Yako YY; September AV; Moremi KE; Cronje FJ; Tiffin N; Bouwens CS; Bezuidenhout J; Apffelstaedt JP; Hough FS; Erasmus RT; Schneider JW
    Crit Rev Clin Lab Sci; 2015; 52(3):120-37. PubMed ID: 25597499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.