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

180 related items for PubMed ID: 16703378

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

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

  • 3. 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; 33(7):1269-1272. PubMed ID: 29663071
    [Abstract] [Full Text] [Related]

  • 4. 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; 21(9):753-7. PubMed ID: 26560236
    [Abstract] [Full Text] [Related]

  • 5. Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients.
    Patrakka J, Kestilä M, Wartiovaara J, Ruotsalainen V, Tissari P, Lenkkeri U, Männikkö M, Visapää I, Holmberg C, Rapola J, Tryggvason K, Jalanko H.
    Kidney Int; 2000 Sep; 58(3):972-80. PubMed ID: 10972661
    [Abstract] [Full Text] [Related]

  • 6. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan.
    Abid A, Khaliq S, Shahid S, Lanewala A, Mubarak M, Hashmi S, Kazi J, Masood T, Hafeez F, Naqvi SA, Rizvi SA, Mehdi SQ.
    Gene; 2012 Jul 10; 502(2):133-7. PubMed ID: 22565185
    [Abstract] [Full Text] [Related]

  • 7. 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 10; 119(4):e907-19. PubMed ID: 17371932
    [Abstract] [Full Text] [Related]

  • 8. 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 10; 15(2):198-203. PubMed ID: 30721404
    [Abstract] [Full Text] [Related]

  • 9. [A case of severe congenital nephrotic syndrome secondary to NPHS1 mutation].
    Quiros A, Lefèbvre C, Collard L, Rigo V, Lombet J.
    Rev Med Liege; 2020 Jul 10; 75(7-8):544-547. PubMed ID: 32779909
    [Abstract] [Full Text] [Related]

  • 10. Congenital nephrotic syndrome with a novel NPHS1 mutation.
    Yoshizawa C, Kobayashi Y, Ikeuchi Y, Tashiro M, Kakegawa S, Watanabe T, Goto Y, Nakanishi K, Yoshikawa N, Arakawa H.
    Pediatr Int; 2016 Nov 10; 58(11):1211-1215. PubMed ID: 27882743
    [Abstract] [Full Text] [Related]

  • 11. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome.
    Sako M, Nakanishi K, Obana M, Yata N, Hoshii S, Takahashi S, Wada N, Takahashi Y, Kaku Y, Satomura K, Ikeda M, Honda M, Iijima K, Yoshikawa N.
    Kidney Int; 2005 Apr 10; 67(4):1248-55. PubMed ID: 15780077
    [Abstract] [Full Text] [Related]

  • 12. Management of children with congenital nephrotic syndrome: challenging treatment paradigms.
    Dufek S, Holtta T, Trautmann A, Ylinen E, Alpay H, Ariceta G, Aufricht C, Bacchetta J, Bakkaloglu SA, Bayazit A, Cicek RY, Dursun I, Duzova A, Ekim M, Iancu D, Jankauskiene A, Klaus G, Paglialonga F, Pasini A, Printza N, Said Conti V, do Sameiro Faria M, Schmitt CP, Stefanidis CJ, Verrina E, Vidal E, Vondrak K, Webb H, Zampetoglou A, Bockenhauer D, Edefonti A, Shroff R.
    Nephrol Dial Transplant; 2019 Aug 01; 34(8):1369-1377. PubMed ID: 30215773
    [Abstract] [Full Text] [Related]

  • 13. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation.
    Uysal B, Dönmez O, Uysal F, Akacı O, Vuruşkan BA, Berdeli A.
    Pediatr Int; 2015 Aug 01; 57(1):177-9. PubMed ID: 25711261
    [Abstract] [Full Text] [Related]

  • 14. Congenital Nephrotic Syndrome - Finish Type.
    Spahiu L, Merovci B, Jashari H, Këpuska AB, Rugova BE.
    Med Arch; 2016 Jun 01; 70(3):232-4. PubMed ID: 27594755
    [Abstract] [Full Text] [Related]

  • 15. Two Korean infants with genetically confirmed congenital nephrotic syndrome of Finnish type.
    Lee BH, Ahn YH, Choi HJ, Kang HK, Kim SD, Cho BS, Moon KC, Ha IS, Cheong HI, Choi Y.
    J Korean Med Sci; 2009 Jan 01; 24 Suppl(Suppl 1):S210-4. PubMed ID: 19194555
    [Abstract] [Full Text] [Related]

  • 16. Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort.
    Trautmann A, Bodria M, Ozaltin F, Gheisari A, Melk A, Azocar M, Anarat A, Caliskan S, Emma F, Gellermann J, Oh J, Baskin E, Ksiazek J, Remuzzi G, Erdogan O, Akman S, Dusek J, Davitaia T, Özkaya O, Papachristou F, Firszt-Adamczyk A, Urasinski T, Testa S, Krmar RT, Hyla-Klekot L, Pasini A, Özcakar ZB, Sallay P, Cakar N, Galanti M, Terzic J, Aoun B, Caldas Afonso A, Szymanik-Grzelak H, Lipska BS, Schnaidt S, Schaefer F, PodoNet Consortium.
    Clin J Am Soc Nephrol; 2015 Apr 07; 10(4):592-600. PubMed ID: 25635037
    [Abstract] [Full Text] [Related]

  • 17. Congenital nephrotic syndrome responsive to angiotensin-converting enzyme inhibition.
    Sreedharan R, Bockenhauer D.
    Pediatr Nephrol; 2005 Sep 07; 20(9):1340-2. PubMed ID: 15965772
    [Abstract] [Full Text] [Related]

  • 18. [Congenital nephrotic syndrome].
    Stajić N, Putnik J, Paripović A, Djurić S, Bogdanović R.
    Srp Arh Celok Lek; 2008 Dec 07; 136 Suppl 4():307-11. PubMed ID: 20804100
    [Abstract] [Full Text] [Related]

  • 19. NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.
    Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C.
    Kidney Int; 2004 Aug 07; 66(2):571-9. PubMed ID: 15253708
    [Abstract] [Full Text] [Related]

  • 20. [Prenatal diagnosis of a fetus affected with Finnish type congenital nephrotic syndrome].
    Chu Y, Hou Q, Wu D, Lou G, Yang K, Guo L, Qi N, Duan X, Wang W, Qin L, Liao S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct 10; 36(10):1022-1024. PubMed ID: 31598951
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.