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6. Elevated serum 1,25-dihydroxyvitamin D concentrations in siblings with primary Fanconi's syndrome. Tieder M; Arie R; Modai D; Samuel R; Weissgarten J; Liberman UA N Engl J Med; 1988 Sep; 319(13):845-9. PubMed ID: 2842681 [No Abstract] [Full Text] [Related]
7. Cystinosis with Fanconi's syndrome. A case report. Adams BK; Naidoo PM S Afr Med J; 1978 May; 53(18):719-21. PubMed ID: 694607 [TBL] [Abstract][Full Text] [Related]
8. Tubulointerstitial nephritis and uveitis syndrome (TINU) with Fanconi's syndrome. Yao YH; Lin CC; Chung YM; Yang AH; Li SY; Lin CC; Lin YP; Yang WC; Yang CY Clin Nephrol; 2011 Feb; 75 Suppl 1():75-8. PubMed ID: 21269599 [TBL] [Abstract][Full Text] [Related]
9. [Cytogenic and biochemical studies of 8 cases of Fanconi's anemia]. de Grouchy J; de Nava C; Marchand JC; Feingold J; Turleau C Ann Genet; 1972 Mar; 15(1):29-40. PubMed ID: 4537612 [No Abstract] [Full Text] [Related]
11. Fanconi's anaemia. Simultaneous onset in 2 siblings and unusual cytological findings. de Vroede M; Feremans W; de Maertelaere-Laurent E; Mandelbaum I; Toppet M; Vamos E; Fondu P Scand J Haematol; 1982 May; 28(5):431-40. PubMed ID: 6956956 [TBL] [Abstract][Full Text] [Related]
12. An adult case of Fanconi's syndrome associated with membranous nephropathy. Yagame M; Tomino Y; Miura M; Suga T; Nomoto Y; Sakai H Tokai J Exp Clin Med; 1986 May; 11(2):101-6. PubMed ID: 3564076 [TBL] [Abstract][Full Text] [Related]
14. Mitochondrial cytopathy combined with Fanconi's syndrome. Wang LC; Lee WT; Tsai WY; Tsau YK; Shen YZ Pediatr Neurol; 2000 May; 22(5):403-6. PubMed ID: 10913735 [TBL] [Abstract][Full Text] [Related]
15. [Fanconi's panmyelopathy as a form of multiple abnormality]. ALTHOFF H Z Kinderheilkd; 1953; 72(3):267-92. PubMed ID: 13057323 [No Abstract] [Full Text] [Related]
16. [Fanconi's anemia. Value of isotopic exploration and evolutive problem]. Sebahoun G; Perrimond H; Bernard PJ; Orsini A Mars Med; 1971; 108(9):565-70. PubMed ID: 5120428 [No Abstract] [Full Text] [Related]
17. [Congenital heart defect as a dominant symptom of Fanconi's syndrome]. Pytel-Dabrowska T; Smukalska E Pediatr Pol; 1988 Dec; 63(12):801-4. PubMed ID: 3267805 [No Abstract] [Full Text] [Related]
18. [Familial hypoplastic anaemia with congenital abnormalities (Fanconi's syndrome): report of a case]. McALPINE SG Glasgow Med J; 1954 Feb; 35(2):46-50. PubMed ID: 13151451 [No Abstract] [Full Text] [Related]
19. A case of membranous lipodystrophy complicated by Fanconi's syndrome. Hishikawa R; Fukase M; Yoshimoto Y; Imai Y; Okada S; Fujita T Bone Miner; 1988 Oct; 5(1):99-105. PubMed ID: 3214684 [TBL] [Abstract][Full Text] [Related]
20. Familial hypoplastic anemia with multiple congenital anomalies (Fanconi's syndrome)--report of three cases. Cases presented are of two sisters and a female cousin with complete clinical and post mortem findings. Esparza A; Thompson WR R I Med J; 1966 Feb; 49(2):103-10. PubMed ID: 5217141 [No Abstract] [Full Text] [Related] [Next] [New Search]