132 related articles for article (PubMed ID: 35570599)
1. Clinically Different Presentations of Family Members With the Same Homozygote Diacylglycerol Kinase Epsilon Mutation: Case Report.
Çelikkaya E; Güngör T; Karakaya D; Kargın Çakıcı E; Yazılıtaş F; Özaltın F; Bülbül M
Exp Clin Transplant; 2022 May; 20(Suppl 3):45-48. PubMed ID: 35570599
[TBL] [Abstract][Full Text] [Related]
2. The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase
Azukaitis K; Simkova E; Majid MA; Galiano M; Benz K; Amann K; Bockmeyer C; Gajjar R; Meyers KE; Cheong HI; Lange-Sperandio B; Jungraithmayr T; Frémeaux-Bacchi V; Bergmann C; Bereczki C; Miklaszewska M; Csuka D; Prohászka Z; Killen P; Gipson P; Sampson MG; Lemaire M; Schaefer F
J Am Soc Nephrol; 2017 Oct; 28(10):3066-3075. PubMed ID: 28526779
[TBL] [Abstract][Full Text] [Related]
3. Complement mutations in diacylglycerol kinase-ε-associated atypical hemolytic uremic syndrome.
Sánchez Chinchilla D; Pinto S; Hoppe B; Adragna M; Lopez L; Justa Roldan ML; Peña A; Lopez Trascasa M; Sánchez-Corral P; Rodríguez de Córdoba S
Clin J Am Soc Nephrol; 2014 Sep; 9(9):1611-9. PubMed ID: 25135762
[TBL] [Abstract][Full Text] [Related]
4. Novel compound heterozygous mutation of the
Lau SHY; Chan EYH; Yuen LYP; Ng WF; Ma ALT
Hong Kong Med J; 2023 Aug; 29(4):351-354. PubMed ID: 37433757
[No Abstract] [Full Text] [Related]
5. Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy.
Brocklebank V; Kumar G; Howie AJ; Chandar J; Milford DV; Craze J; Evans J; Finlay E; Freundlich M; Gale DP; Inward C; Mraz M; Jones C; Wong W; Marks SD; Connolly J; Corner BM; Smith-Jackson K; Walsh PR; Marchbank KJ; Harris CL; Wilson V; Wong EKS; Malina M; Johnson S; Sheerin NS; Kavanagh D
Kidney Int; 2020 Jun; 97(6):1260-1274. PubMed ID: 32386968
[TBL] [Abstract][Full Text] [Related]
6. Rare genetic variant in the CFB gene presenting as atypical hemolytic uremic syndrome and immune complex diffuse membranoproliferative glomerulonephritis, with crescents, successfully treated with eculizumab.
Alfakeeh K; Azar M; Alfadhel M; Abdullah AM; Aloudah N; Alsaad KO
Pediatr Nephrol; 2017 May; 32(5):885-891. PubMed ID: 28210841
[TBL] [Abstract][Full Text] [Related]
7. Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic Syndrome.
Mele C; Lemaire M; Iatropoulos P; Piras R; Bresin E; Bettoni S; Bick D; Helbling D; Veith R; Valoti E; Donadelli R; Murer L; Neunhäuserer M; Breno M; Frémeaux-Bacchi V; Lifton R; Remuzzi G; Noris M
Clin J Am Soc Nephrol; 2015 Jun; 10(6):1011-9. PubMed ID: 25854283
[TBL] [Abstract][Full Text] [Related]
8. Membrano-proliferative glomerulonephritis, atypical hemolytic uremic syndrome, and a new complement factor H mutation: report of a case.
Gnappi E; Allinovi M; Vaglio A; Bresin E; Sorosina A; Pilato FP; Allegri L; Manenti L
Pediatr Nephrol; 2012 Oct; 27(10):1995-9. PubMed ID: 22669321
[TBL] [Abstract][Full Text] [Related]
9. Clinical features and outcomes of patients with diacylglycerol kinase epsilon nephropathy: a nationwide experience.
Khandelwal P; Thangaraju S; Krishnamurthy S; Ohri A; Pais P; Mathew G; Sharma J; Sharma A; Hari P; Sinha A; Singh G; Bagga A
Pediatr Nephrol; 2023 Sep; 38(9):3009-3016. PubMed ID: 36988693
[TBL] [Abstract][Full Text] [Related]
10. Secondary membranoproliferative glomerulonephritis due to hemolytic uremic syndrome: an unusual presentation.
Jha V; Murthy MS; Kohli HS; Sud K; Gupta KL; Joshi K; Sakhuja V
Ren Fail; 1998 Nov; 20(6):845-50. PubMed ID: 9834983
[TBL] [Abstract][Full Text] [Related]
11. Outcomes of primary nephrotic syndrome in elderly Japanese: retrospective analysis of the Japan Renal Biopsy Registry (J-RBR).
Yokoyama H; Sugiyama H; Narita I; Saito T; Yamagata K; Nishio S; Fujimoto S; Mori N; Yuzawa Y; Okuda S; Maruyama S; Sato H; Ueda Y; Makino H; Matsuo S
Clin Exp Nephrol; 2015 Jun; 19(3):496-505. PubMed ID: 25230687
[TBL] [Abstract][Full Text] [Related]
12. DGKE variants cause a glomerular microangiopathy that mimics membranoproliferative GN.
Ozaltin F; Li B; Rauhauser A; An SW; Soylemezoglu O; Gonul II; Taskiran EZ; Ibsirlioglu T; Korkmaz E; Bilginer Y; Duzova A; Ozen S; Topaloglu R; Besbas N; Ashraf S; Du Y; Liang C; Chen P; Lu D; Vadnagara K; Arbuckle S; Lewis D; Wakeland B; Quigg RJ; Ransom RF; Wakeland EK; Topham MK; Bazan NG; Mohan C; Hildebrandt F; Bakkaloglu A; Huang CL; Attanasio M
J Am Soc Nephrol; 2013 Feb; 24(3):377-84. PubMed ID: 23274426
[TBL] [Abstract][Full Text] [Related]
13. Clinical features of children with anti-CFH autoantibody-associated hemolytic uremic syndrome: a report of 8 cases.
Li Q; Kong X; Tian M; Wang J; Yang Z; Yu L; Liu S; Wang C; Wang X; Sun S
Ren Fail; 2022 Dec; 44(1):1061-1069. PubMed ID: 35730179
[TBL] [Abstract][Full Text] [Related]
14. [Familial membranoproliferative glomerulonephritis].
Bogdanović RM; Dimitrjević JZ; Nikolić VN; Ognjanović MV; Rodić BD; Slavković BV
Srp Arh Celok Lek; 1999; 127(5-6):163-71. PubMed ID: 10500423
[TBL] [Abstract][Full Text] [Related]
15. Various phenotypes of disease associated with mutated DGKE gene.
Bezdíčka M; Pavlíček P; Bláhová K; Háček J; Zieg J
Eur J Med Genet; 2020 Aug; 63(8):103953. PubMed ID: 32413569
[TBL] [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;
Clin J Am Soc Nephrol; 2015 Apr; 10(4):592-600. PubMed ID: 25635037
[TBL] [Abstract][Full Text] [Related]
17. Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome.
Gholizad-Kolveiri S; Hooman N; Alizadeh R; Hoseini R; Otukesh H; Talebi S; Akouchekian M
BMC Med Genet; 2020 Aug; 21(1):169. PubMed ID: 32838746
[TBL] [Abstract][Full Text] [Related]
18. Postpartum thrombotic microangiopathy revealed as atypical hemolytic uremic syndrome successfully treated with eculizumab: a case report.
Kourouklaris A; Ioannou K; Athanasiou I; Panagidou A; Demetriou K; Zavros M
J Med Case Rep; 2014 Sep; 8():307. PubMed ID: 25219386
[TBL] [Abstract][Full Text] [Related]
19. Atypical Hemolytic Uremic Syndrome Associated with Complement Factor H Mutation and IgA Nephropathy: A Case Report Successfully Treated with Eculizumab.
Nakamura H; Anayama M; Makino M; Makino Y; Tamura K; Nagasawa M
Nephron; 2018; 138(4):324-327. PubMed ID: 29241200
[TBL] [Abstract][Full Text] [Related]
20. Treatment aspects of primary nephrotic syndrome in adults.
Rasić S; Uncanin S; Dzemidzić J; Aganović K; Srna A; Rasić I
Bosn J Basic Med Sci; 2006 May; 6(2):16-20. PubMed ID: 16879107
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]