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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

121 related items for PubMed ID: 38146730

  • 1. Genetic Studies in Infants with Congenital Nephrotic Syndrome: A Case Series.
    Karunakar P, Chidambaram AC, Krishnamurthy S, Sivamurukan P, Deepthi B, Gowda M.
    Saudi J Kidney Dis Transpl; 2023 Mar 01; 34(2):191-195. PubMed ID: 38146730
    [Abstract] [Full Text] [Related]

  • 2. Effectiveness of Supramaximal Angiotensin-converting Enzyme Inhibition in Controlling Proteinuria in Congenital Nephrotic Syndrome with Cytomegalovirus Infection and an NPHS1 Mutation.
    Dange N, Sathe KP, Kondekar A, Sawant V.
    Saudi J Kidney Dis Transpl; 2023 Sep 01; 34(5):462-467. PubMed ID: 38995307
    [Abstract] [Full Text] [Related]

  • 3. Adequate clinical control of congenital nephrotic syndrome by enalapril.
    Guez S, Giani M, Melzi ML, Antignac C, Assael BM.
    Pediatr Nephrol; 1998 Feb 01; 12(2):130-2. PubMed ID: 9543371
    [Abstract] [Full Text] [Related]

  • 4. Neonatal nephrotic presentation of a child with heterozygous NPHS1 mutation.
    Lemley KV.
    Pediatr Nephrol; 2006 Jun 01; 21(6):864-6. PubMed ID: 16703378
    [Abstract] [Full Text] [Related]

  • 5. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).
    Hinkes BG, Mucha B, Vlangos CN, Gbadegesin R, Liu J, Hasselbacher K, Hangan D, Ozaltin F, Zenker M, Hildebrandt F, Arbeitsgemeinschaft für Paediatrische Nephrologie Study Group.
    Pediatrics; 2007 Apr 01; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 6. Cyclosporine A responsive congenital nephrotic syndrome with single heterozygous variants in NPHS1, NPHS2, and PLCE1.
    Eichinger A, Ponsel S, Bergmann C, Günthner R, Hoefele J, Amann K, Lange-Sperandio B.
    Pediatr Nephrol; 2018 Jul 01; 33(7):1269-1272. PubMed ID: 29663071
    [Abstract] [Full Text] [Related]

  • 7. Genetics of congenital and infantile nephrotic syndrome.
    Sharief SN, Hefni NA, Alzahrani WA, Nazer II, Bayazeed MA, Alhasan KA, Safdar OY, El-Desoky SM, Kari JA.
    World J Pediatr; 2019 Apr 01; 15(2):198-203. PubMed ID: 30721404
    [Abstract] [Full Text] [Related]

  • 8. Simultaneous mutations of LAMB2 and NPHP1genes in a Chinese girl with isolated congenital nephrotic syndrome: a case report.
    Qiu L, Zhou J.
    BMC Pediatr; 2016 Mar 22; 16():44. PubMed ID: 27004562
    [Abstract] [Full Text] [Related]

  • 9. [Congenital nephrotic syndrome].
    Hattori M.
    Nihon Rinsho; 2004 Oct 22; 62(10):1861-6. PubMed ID: 15500131
    [Abstract] [Full Text] [Related]

  • 10. NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.
    Guaragna MS, Cleto TL, Souza ML, Lutaif AC, de Castro LC, Penido MG, Maciel-Guerra AT, Belangero VM, Guerra-Junior G, De Mello MP.
    Nephrology (Carlton); 2016 Sep 22; 21(9):753-7. PubMed ID: 26560236
    [Abstract] [Full Text] [Related]

  • 11. A girl with MIRAGE syndrome who developed steroid-resistant nephrotic syndrome: a case report.
    Ishiwa S, Kamei K, Tanase-Nakao K, Shibata S, Matsunami K, Takeuchi I, Sato M, Ishikura K, Narumi S.
    BMC Nephrol; 2020 Aug 12; 21(1):340. PubMed ID: 32787808
    [Abstract] [Full Text] [Related]

  • 12. [NPHS1 mutations in a Chinese family with congenital nephrotic syndrome].
    Shi Y, Ding J, Liu JC, Wang H, Bu DF.
    Zhonghua Er Ke Za Zhi; 2005 Nov 12; 43(11):805-9. PubMed ID: 16316524
    [Abstract] [Full Text] [Related]

  • 13. A case report of congenital nephrotic syndrome caused by new mutations of NPHS1.
    Li Z, Zhuang L, Han M, Li F.
    J Int Med Res; 2021 Aug 12; 49(8):3000605211038133. PubMed ID: 34396835
    [Abstract] [Full Text] [Related]

  • 14. Congenital Nephrotic Syndrome in India in the Current Era: A Multicenter Case Series.
    Sinha R, Vasudevan A, Agarwal I, Sethi SK, Saha A, Pradhan S, Ekambaram S, Thaker N, Matnani M, Banerjee S, Sharma J, Singhal J, Ashraf S, Mandal K.
    Nephron; 2020 Aug 12; 144(1):21-29. PubMed ID: 31655822
    [Abstract] [Full Text] [Related]

  • 15. Congenital nephrotic syndrome.
    AbuMaziad AS, Abusaleh R, Bhati S.
    J Perinatol; 2021 Dec 12; 41(12):2704-2712. PubMed ID: 34983935
    [Abstract] [Full Text] [Related]

  • 16. Novel NPHS1 splice site mutations in a Chinese child with congenital nephrotic syndrome.
    Fu R, Gou MF, Ma WH, He JJ, Luan Y, Liu J.
    Genet Mol Res; 2015 Jan 23; 14(1):433-9. PubMed ID: 25729976
    [Abstract] [Full Text] [Related]

  • 17. Congenital nephrotic syndrome: is early aggressive treatment needed? Yes.
    Hölttä T, Jalanko H.
    Pediatr Nephrol; 2020 Oct 23; 35(10):1985-1990. PubMed ID: 32377865
    [Abstract] [Full Text] [Related]

  • 18. Efficacy of enalapril in the treatment of steroid resistant idiopathic nephrotic syndrome.
    Prasher PK, Varma PP, Baliga KV.
    J Assoc Physicians India; 1999 Feb 23; 47(2):180-2. PubMed ID: 10999084
    [Abstract] [Full Text] [Related]

  • 19. Three Novel Heterozygous Mutations of NPHS1 Gene Causing Infants with Congenital Nephrotic Syndrome: Two Chinese (Han) Cases.
    Lv H, Liu F, Wang Q, Dong Z, Ren P, Zhang H, Yan X, Li L.
    Clin Lab; 2023 Aug 01; 69(8):. PubMed ID: 37560858
    [Abstract] [Full Text] [Related]

  • 20. Congenital nephrotic syndrome with prolonged renal survival without renal replacement therapy.
    Wong W, Morris MC, Kara T.
    Pediatr Nephrol; 2013 Dec 01; 28(12):2313-21. PubMed ID: 23949594
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.