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 *

305 related articles for article (PubMed ID: 29627839)

  • 1. Genotype-Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis.
    Park E; Cho MH; Hyun HS; Shin JI; Lee JH; Park YS; Choi HJ; Kang HG; Cheong HI
    Kidney Blood Press Res; 2018; 43(2):513-521. PubMed ID: 29627839
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical and molecular aspects of distal renal tubular acidosis in children.
    Besouw MTP; Bienias M; Walsh P; Kleta R; Van't Hoff WG; Ashton E; Jenkins L; Bockenhauer D
    Pediatr Nephrol; 2017 Jun; 32(6):987-996. PubMed ID: 28188436
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.
    Palazzo V; Provenzano A; Becherucci F; Sansavini G; Mazzinghi B; Orlandini V; Giunti L; Roperto RM; Pantaleo M; Artuso R; Andreucci E; Bargiacchi S; Traficante G; Stagi S; Murer L; Benetti E; Emma F; Giordano M; Rivieri F; Colussi G; Penco S; Manfredini E; Caruso MR; Garavelli L; Andrulli S; Vergine G; Miglietti N; Mancini E; Malaventura C; Percesepe A; Grosso E; Materassi M; Romagnani P; Giglio S
    Kidney Int; 2017 May; 91(5):1243-1255. PubMed ID: 28233610
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathophysiology, diagnosis and treatment of inherited distal renal tubular acidosis.
    Mohebbi N; Wagner CA
    J Nephrol; 2018 Aug; 31(4):511-522. PubMed ID: 28994037
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Distal renal tubular acidosis. Clinical manifestations in patients with different underlying gene mutations.
    Alonso-Varela M; Gil-Peña H; Coto E; Gómez J; Rodríguez J; Rodríguez-Rubio E; Santos F;
    Pediatr Nephrol; 2018 Sep; 33(9):1523-1529. PubMed ID: 29725771
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and genetic analysis of distal renal tubular acidosis in three Chinese children.
    Liu J; Shen Q; Li G; Zhai Y; Fang X; Xu H
    Ren Fail; 2018 Nov; 40(1):520-526. PubMed ID: 30230413
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Homozygous and compound heterozygous mutations in the ATP6V1B1 gene in patients with renal tubular acidosis and sensorineural hearing loss.
    Mohebbi N; Vargas-Poussou R; Hegemann SC; Schuknecht B; Kistler AD; Wüthrich RP; Wagner CA
    Clin Genet; 2013 Mar; 83(3):274-8. PubMed ID: 22509993
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1 genes.
    Elhayek D; Perez de Nanclares G; Chouchane S; Hamami S; Mlika A; Troudi M; Leban N; Ben Romdane W; Gueddiche MN; El Amri F; Mrabet S; Ben Chibani J; Castaño L; Haj Khelil A; Ariceta G
    BMC Med Genet; 2013 Nov; 14():119. PubMed ID: 24252324
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis and audiologic assessment in six Chinese children with primary distal renal tubular acidosis.
    Gao Y; Xu Y; Li Q; Lang Y; Dong Q; Shao L
    Ren Fail; 2014 Sep; 36(8):1226-32. PubMed ID: 24975934
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and molecular findings in three Moroccan families with distal renal tubular acidosis and deafness: Report of a novel mutation of ATP6V1B1 gene.
    Boualla L; Jdioui W; Soulami K; Ratbi I; Sefiani A
    Curr Res Transl Med; 2016; 64(1):5-8. PubMed ID: 27140593
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Five Novel Mutations in Chinese Children with Primary Distal Renal Tubular Acidosis.
    Zhang R; Wang C; Lang Y; Gao Y; Chen Z; Lu J; Zhao X; Shao L
    Genet Test Mol Biomarkers; 2018 Oct; 22(10):599-606. PubMed ID: 30256676
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular aspects and long-term outcome of patients with primary distal renal tubular acidosis.
    Gómez-Conde S; García-Castaño A; Aguirre M; Herrero M; Gondra L; García-Pérez N; García-Ledesma P; Martín-Penagos L; Dall'Anese C; Ariceta G; Castaño L; Madariaga L
    Pediatr Nephrol; 2021 Oct; 36(10):3133-3142. PubMed ID: 33881640
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel compound heterozygous ATP6V1B1 mutations in a Chinese child patient with primary distal renal tubular acidosis: a case report.
    Zhao X; Lu J; Gao Y; Wang X; Lang Y; Shao L
    BMC Nephrol; 2018 Dec; 19(1):364. PubMed ID: 30558562
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Genotype-phenotype analysis and prognosis in children with primary distal renal tubular acidosis].
    Jiang YR; Wang M; Wan JL; Zhang GF; Yang HP; Li Q
    Zhonghua Er Ke Za Zhi; 2022 Jul; 60(7):700-705. PubMed ID: 35768359
    [No Abstract]   [Full Text] [Related]  

  • 15. Treatment and long-term outcome in primary distal renal tubular acidosis.
    Lopez-Garcia SC; Emma F; Walsh SB; Fila M; Hooman N; Zaniew M; Bertholet-Thomas A; Colussi G; Burgmaier K; Levtchenko E; Sharma J; Singhal J; Soliman NA; Ariceta G; Basu B; Murer L; Tasic V; Tsygin A; Decramer S; Gil-Peña H; Koster-Kamphuis L; La Scola C; Gellermann J; Konrad M; Lilien M; Francisco T; Tramma D; Trnka P; Yüksel S; Caruso MR; Chromek M; Ekinci Z; Gambaro G; Kari JA; König J; Taroni F; Thumfart J; Trepiccione F; Winding L; Wühl E; Ağbaş A; Belkevich A; Vargas-Poussou R; Blanchard A; Conti G; Boyer O; Dursun I; Pınarbaşı AS; Melek E; Miglinas M; Novo R; Mallett A; Milosevic D; Szczepanska M; Wente S; Cheong HI; Sinha R; Gucev Z; Dufek S; Iancu D; ; Kleta R; Schaefer F; Bockenhauer D
    Nephrol Dial Transplant; 2019 Jun; 34(6):981-991. PubMed ID: 30773598
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia.
    Hammi Y; Charfi H; Ferjani M; Sayari T; Mrad R; Gargah T
    Tunis Med; 2023; 101(8-9):704-708. PubMed ID: 38445406
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of two novel mutations in the SLC4A1 gene in two unrelated Chinese families with distal renal tubular acidosis.
    Zhang Z; Liu KX; He JW; Fu WZ; Yue H; Zhang H; Zhang CQ; Zhang ZL
    Arch Med Res; 2012 May; 43(4):298-304. PubMed ID: 22609520
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis.
    Dahmani M; Talbi S; Ammar-Khodja F; Ouhab S; Boudjenah F; Djebbar M; Bonnet C; Petit C
    Int J Pediatr Otorhinolaryngol; 2020 Feb; 129():109772. PubMed ID: 31733597
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ATP6V1B1 mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families.
    Subasioglu Uzak A; Cakar N; Comak E; Yalcinkaya F; Tekin M
    Ren Fail; 2013 Oct; 35(9):1281-4. PubMed ID: 23923981
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutational analyses of the ATP6V1B1 and ATP6V0A4 genes in patients with primary distal renal tubular acidosis.
    Miura K; Sekine T; Takahashi K; Takita J; Harita Y; Ohki K; Park MJ; Hayashi Y; Tajima A; Ishihara M; Hisano M; Murai M; Igarashi T
    Nephrol Dial Transplant; 2013 Aug; 28(8):2123-30. PubMed ID: 23729491
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.