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PUBMED FOR HANDHELDS

Journal Abstract Search


129 related items for PubMed ID: 30568185

  • 1.
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  • 2. HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome.
    Gbadegesin RA, Adeyemo A, Webb NJ, Greenbaum LA, Abeyagunawardena A, Thalgahagoda S, Kale A, Gipson D, Srivastava T, Lin JJ, Chand D, Hunley TE, Brophy PD, Bagga A, Sinha A, Rheault MN, Ghali J, Nicholls K, Abraham E, Janjua HS, Omoloja A, Barletta GM, Cai Y, Milford DD, O'Brien C, Awan A, Belostotsky V, Smoyer WE, Homstad A, Hall G, Wu G, Nagaraj S, Wigfall D, Foreman J, Winn MP, Mid-West Pediatric Nephrology Consortium.
    J Am Soc Nephrol; 2015 Jul; 26(7):1701-10. PubMed ID: 25349203
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  • 3. HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
    Adeyemo A, Esezobor C, Solarin A, Abeyagunawardena A, Kari JA, El Desoky S, Greenbaum LA, Kamel M, Kallash M, Silva C, Young A, Hunley TE, de Jesus-Gonzalez N, Srivastava T, Gbadegesin R.
    Am J Kidney Dis; 2018 Mar; 71(3):399-406. PubMed ID: 29277510
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  • 4. Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
    Dorval G, Gribouval O, Martinez-Barquero V, Machuca E, Tête MJ, Baudouin V, Benoit S, Chabchoub I, Champion G, Chauveau D, Chehade H, Chouchane C, Cloarec S, Cochat P, Dahan K, Dantal J, Delmas Y, Deschênes G, Dolhem P, Durand D, Ekinci Z, El Karoui K, Fischbach M, Grunfeld JP, Guigonis V, Hachicha M, Hogan J, Hourmant M, Hummel A, Kamar N, Krummel T, Lacombe D, Llanas B, Mesnard L, Mohsin N, Niaudet P, Nivet H, Parvex P, Pietrement C, de Pontual L, Noble CP, Ribes D, Ronco P, Rondeau E, Sallee M, Tsimaratos M, Ulinski T, Salomon R, Antignac C, Boyer O.
    Pediatr Nephrol; 2018 Mar; 33(3):473-483. PubMed ID: 29058154
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  • 6. Centromere protein I (CENPI) is a candidate gene for X-linked steroid sensitive nephrotic syndrome.
    Basit S, Al-Edressi HM, Sairafi MH, Hashmi JA, Alharby E, Safar R, Ramzan K.
    J Nephrol; 2020 Aug; 33(4):763-769. PubMed ID: 31912435
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  • 8. Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.
    Niitsuma S, Kudo H, Kikuchi A, Hayashi T, Kumakura S, Kobayashi S, Okuyama Y, Kumagai N, Niihori T, Aoki Y, So T, Funayama R, Nakayama K, Shirota M, Kondo S, Kagami S, Tsukaguchi H, Iijima K, Kure S, Ishii N.
    Int Immunol; 2020 Apr 12; 32(4):283-292. PubMed ID: 31954058
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  • 10. Familial steroid-responsive nephrotic syndrome and HLA antigens in Bengali children.
    Kari JA, Sinnott P, Khan H, Trompeter RS, Snodgrass GJ.
    Pediatr Nephrol; 2001 Apr 12; 16(4):346-9. PubMed ID: 11354779
    [Abstract] [Full Text] [Related]

  • 11. Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.
    Jia X, Horinouchi T, Hitomi Y, Shono A, Khor SS, Omae Y, Kojima K, Kawai Y, Nagasaki M, Kaku Y, Okamoto T, Ohwada Y, Ohta K, Okuda Y, Fujimaru R, Hatae K, Kumagai N, Sawanobori E, Nakazato H, Ohtsuka Y, Nakanishi K, Shima Y, Tanaka R, Ashida A, Kamei K, Ishikura K, Nozu K, Tokunaga K, Iijima K, Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan.
    J Am Soc Nephrol; 2018 Aug 12; 29(8):2189-2199. PubMed ID: 30012571
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  • 12. Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.
    Suvanto M, Patrakka J, Jahnukainen T, Sjöström PM, Nuutinen M, Arikoski P, Kataja J, Kestilä M, Jalanko H.
    Clin Exp Nephrol; 2017 Aug 12; 21(4):677-684. PubMed ID: 27573339
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  • 15. Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations.
    Landau D, Oved T, Geiger D, Abizov L, Shalev H, Parvari R.
    Pediatr Nephrol; 2007 May 12; 22(5):661-9. PubMed ID: 17219184
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  • 16. Association of HLA-DR/DQ alleles and haplotypes with nephrotic syndrome.
    Ramanathan AS, Senguttuvan P, Chinniah R, Vijayan M, Thirunavukkarasu M, Raju K, Mani D, Ravi PM, Rajendran P, Krishnan JI, Karuppiah B.
    Nephrology (Carlton); 2016 Sep 12; 21(9):745-52. PubMed ID: 26566811
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  • 17. NPHS1 gene mutations in children with Nephrotic Syndrome in northwest Iran.
    Behbahan AG, Poorshiri B, Mortazavi F, Khaniani MS, Derakhshan SM.
    Pak J Biol Sci; 2013 Sep 01; 16(17):882-6. PubMed ID: 24498843
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  • 18. Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.
    Sanna-Cherchi S, Burgess KE, Nees SN, Caridi G, Weng PL, Dagnino M, Bodria M, Carrea A, Allegretta MA, Kim HR, Perry BJ, Gigante M, Clark LN, Kisselev S, Cusi D, Gesualdo L, Allegri L, Scolari F, D'Agati V, Shapiro LS, Pecoraro C, Palomero T, Ghiggeri GM, Gharavi AG.
    Kidney Int; 2011 Aug 01; 80(4):389-96. PubMed ID: 21697813
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  • 20. Alzheimer's disease phospholipase C-gamma-2 (PLCG2) protective variant is a functional hypermorph.
    Magno L, Lessard CB, Martins M, Lang V, Cruz P, Asi Y, Katan M, Bilsland J, Lashley T, Chakrabarty P, Golde TE, Whiting PJ.
    Alzheimers Res Ther; 2019 Feb 02; 11(1):16. PubMed ID: 30711010
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