195 related articles for article (PubMed ID: 26693850)
1. Novel AGXT gene mutation in a Sri Lankan family with primary Hyperoxaluria type 1.
Sirisena ND; Tantrigoda NH; Kariyawasam KJ; Jayasekara RW; Dissanayake VH
Nephrology (Carlton); 2016 Jan; 21(1):75-6. PubMed ID: 26693850
[No Abstract] [Full Text] [Related]
2. Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure.
M'dimegh S; Omezzine A; Hamida-Rebai MB; Aquaviva-Bourdain C; M'barek I; Sahtout W; Zellama D; Souche G; Achour A; Abroug S; Bouslama A
Transpl Immunol; 2016 Nov; 39():60-65. PubMed ID: 27568336
[TBL] [Abstract][Full Text] [Related]
3. Mutational analysis of AGXT gene in Libyan children with primary hyperoxaluria type 1 at Tripoli Children Hospital.
Rhuma NR; Fituri OA; Sabei LT
Saudi J Kidney Dis Transpl; 2018; 29(1):30-38. PubMed ID: 29456205
[TBL] [Abstract][Full Text] [Related]
4. Mutation spectrum of primary hyperoxaluria type 1 in Tunisia: implication for diagnosis in North Africa.
Nagara M; Tiar A; Ben Halim N; Ben Rhouma F; Messaoud O; Bouyacoub Y; Kefi R; Hassayoun S; Zouari N; Ben Ammar MS; Abdelhak S; Chemli J
Gene; 2013 Sep; 527(1):316-20. PubMed ID: 23810941
[TBL] [Abstract][Full Text] [Related]
5. Updated genetic testing of Italian patients referred with a clinical diagnosis of primary hyperoxaluria.
Pelle A; Cuccurullo A; Mancini C; Sebastiano R; Stallone G; Negrisolo S; Benetti E; Peruzzi L; Petrarulo M; De Marchi M; Marangella M; Amoroso A; Giachino D; Mandrile G
J Nephrol; 2017 Apr; 30(2):219-225. PubMed ID: 26946417
[TBL] [Abstract][Full Text] [Related]
6. Presentation and role of transplantation in adult patients with type 1 primary hyperoxaluria and the I244T AGXT mutation: Single-center experience.
Lorenzo V; Alvarez A; Torres A; Torregrosa V; Hernández D; Salido E
Kidney Int; 2006 Sep; 70(6):1115-9. PubMed ID: 16912707
[TBL] [Abstract][Full Text] [Related]
7. Primary hyperoxaluria presenting with early renal allograft dysfunction.
Rathnamalala NK; Lanerolle RD; Hoppe B; Beck B
Nephrology (Carlton); 2012 May; 17(4):431. PubMed ID: 22509767
[No Abstract] [Full Text] [Related]
8. A double mutation in AGXT gene in families with primary hyperoxaluria type 1.
Kanoun H; Jarraya F; Hadj Salem I; Mahfoudh H; Chaabouni Y; Makni F; Hachicha J; Fakhfakh F
Gene; 2013 Dec; 531(2):451-6. PubMed ID: 24012869
[TBL] [Abstract][Full Text] [Related]
9. Genetic analysis--a diagnostic tool for primary hyperoxaluria type I.
Milosevic D; Rinat C; Batinic D; Frishberg Y
Pediatr Nephrol; 2002 Nov; 17(11):896-8. PubMed ID: 12432429
[TBL] [Abstract][Full Text] [Related]
10. Identification of 5 novel mutations in the AGXT gene.
Basmaison O; Rolland MO; Cochat P; Bozon D
Hum Mutat; 2000 Jun; 15(6):577. PubMed ID: 10862087
[TBL] [Abstract][Full Text] [Related]
11. Primary Hyperoxaluria Type 1: A Cause for Infantile Renal Failure and Massive Nephrocalcinosis.
Kurt-Sukur ED; Özçakar ZB; Fitöz S; Yilmaz S; Hoppe B; Yalçinkaya F
Klin Padiatr; 2015 Sep; 227(5):293-5. PubMed ID: 26090995
[TBL] [Abstract][Full Text] [Related]
12. Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.
Soliman NA; Nabhan MM; Abdelrahman SM; Abdelaziz H; Helmy R; Ghanim K; Bazaraa HM; Badr AM; Tolba OA; Kotb MA; Eweeda KM; Fayez A
Nephrol Ther; 2017 May; 13(3):176-182. PubMed ID: 28161266
[TBL] [Abstract][Full Text] [Related]
13. Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.
Williams EL; Acquaviva C; Amoroso A; Chevalier F; Coulter-Mackie M; Monico CG; Giachino D; Owen T; Robbiano A; Salido E; Waterham H; Rumsby G
Hum Mutat; 2009 Jun; 30(6):910-7. PubMed ID: 19479957
[TBL] [Abstract][Full Text] [Related]
14. Molecular analysis of the AGXT gene in patients suspected with hyperoxaluria type 1 and three novel mutations from Turkey.
Isiyel E; Ezgu SA; Caliskan S; Akman S; Akil I; Tabel Y; Akinci N; Ozdogan EB; Ozel A; Eroglu FK; Ezgu FS
Mol Genet Metab; 2016 Dec; 119(4):311-316. PubMed ID: 27915025
[TBL] [Abstract][Full Text] [Related]
15. Identification of new mutations in primary hyperoxaluria type 1 (PH1).
von Schnakenburg C; Rumsby G
J Nephrol; 1998; 11 Suppl 1():15-7. PubMed ID: 9604803
[TBL] [Abstract][Full Text] [Related]
16. Mutational Analysis of Agxt in Tunisian Population with Primary Hyperoxaluria Type 1.
M'dimegh S; Omezzine A; M'barek I; Moussa A; Mabrouk S; Kaarout H; Souche G; Chemli J; Aloui S; Aquaviva-Bourdain C; Achour A; Abroug S; Bouslama A
Ann Hum Genet; 2017 Jan; 81(1):1-10. PubMed ID: 27935012
[TBL] [Abstract][Full Text] [Related]
17. Preserving double equipoise in living donor liver-kidney transplantation for primary hyperoxaluria type 1.
Narasimhan G; Govil S; Rajalingam R; Venkataraman C; Shanmugam NP; Rela M
Liver Transpl; 2015 Oct; 21(10):1324-6. PubMed ID: 25980756
[No Abstract] [Full Text] [Related]
18. A de novo mutation in the AGXT gene causing primary hyperoxaluria type 1.
Williams EL; Kemper MJ; Rumsby G
Am J Kidney Dis; 2006 Sep; 48(3):481-3. PubMed ID: 16931222
[TBL] [Abstract][Full Text] [Related]
19. Two novel AGXT mutations identified in primary hyperoxaluria type-1 and distinct morphological and structural difference in kidney stones.
Wang C; Lu J; Lang Y; Liu T; Wang X; Zhao X; Shao L
Sci Rep; 2016 Sep; 6():33652. PubMed ID: 27644547
[TBL] [Abstract][Full Text] [Related]
20. Mutational analysis of AGXT in two Chinese families with primary hyperoxaluria type 1.
Li GM; Xu H; Shen Q; Gong YN; Fang XY; Sun L; Liu HM; An Y
BMC Nephrol; 2014 Jun; 15():92. PubMed ID: 24934730
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
