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22. [Ochronosis: report of two familial cases]. Younes M; Mansour A; Neffati F; Zrour S; Bejia I; Ben Amor A; Touzi M; Najjar MF; Bergaoui N Tunis Med; 2011 Feb; 89(2):188-91. PubMed ID: 21308630 [TBL] [Abstract][Full Text] [Related]
23. [Gene diagnosis of alkaptonuria in an infant]. Hu M; Ma HW; Luo Y; Wang L; Song Y; Li F Zhongguo Dang Dai Er Ke Za Zhi; 2012 Oct; 14(10):796-7. PubMed ID: 23092576 [No Abstract] [Full Text] [Related]
24. Familial IgA nephropathy. Pillers DA; Koler RD N Engl J Med; 1985 Jul; 313(3):186. PubMed ID: 4010714 [No Abstract] [Full Text] [Related]
25. [2 cases of familial alkaptonuria with neurological complications]. Słowik J; Bańdur M; Libuszowska D; Bereza M Neurol Neurochir Pol; 1980; 14(5):559-63. PubMed ID: 7453930 [TBL] [Abstract][Full Text] [Related]
26. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2. Pollak MR; Chou YH; Cerda JJ; Steinmann B; La Du BN; Seidman JG; Seidman CE Nat Genet; 1993 Oct; 5(2):201-4. PubMed ID: 8252048 [TBL] [Abstract][Full Text] [Related]
27. [Alkaptonuria]. Berger R; Broyer M Presse Med (1893); 1968 May; 76(24):1182-3. PubMed ID: 5673387 [No Abstract] [Full Text] [Related]
28. Detection of alkaptonuria and mapping of its occurrence in Slovakia. Srsen S; Koska L; Kaprálik I; Sitaj S; Srsnová K Czech Med; 1979; 2(4):186-97. PubMed ID: 535504 [No Abstract] [Full Text] [Related]
29. [Alkaptonuria: diagnostic difficulties in early infancy]. Díaz Vázquez CA; Rodríguez Fernández LM; Rey Galán C; Santos Rodríguez F; Málaga Guerrero S An Esp Pediatr; 1990 Aug; 33(2):168-9. PubMed ID: 2275501 [No Abstract] [Full Text] [Related]
30. [Alkaptonuria: a family with irregular dominance]. ROMEI L; BRACONI L Acta Genet Med Gemellol (Roma); 1960 Jan; 9():103-7. PubMed ID: 14438604 [No Abstract] [Full Text] [Related]
31. [Alkaptonuria and ochronosis]. CSERMELY F; NAGY I; FABIAN I Z Gesamte Inn Med; 1962 Jan; 17():84-6. PubMed ID: 13882525 [No Abstract] [Full Text] [Related]
32. Alkaptonuria: prevalence among Bedouins related by consanguinity. Modilevsky T; Manor E; Marmor A Monogr Hum Genet; 1978; 9():123-5. PubMed ID: 732828 [No Abstract] [Full Text] [Related]
33. A novel point mutation associated with alkaptonuria. Higashino K; Liu W; Ohkawa T; Yamamoto T; Fukui K; Ohno M; Imanishi H; Iwasaki A; Amuro Y; Hada T Clin Genet; 1998 Mar; 53(3):228-9. PubMed ID: 9630082 [No Abstract] [Full Text] [Related]
36. Alkaptonuria. Sussman T Proc R Soc Med; 1969 May; 62(5):485. PubMed ID: 5770593 [No Abstract] [Full Text] [Related]
37. Simultaneous occurrence of alkaptonuria and of Klinefelter syndrome in one patient. Srsen S Padiatr Padol; 1977; 12(2):174-5. PubMed ID: 859724 [No Abstract] [Full Text] [Related]
38. A family with alkaptonuria showing quasidominant inheritance. de Silva AP; Seneviratne SL; Gunatilake SB; Fonseka M; Jayasekera R; de Silva HJ Ceylon Med J; 1999 Sep; 44(3):130-2. PubMed ID: 10675999 [No Abstract] [Full Text] [Related]
39. Thirteen cases of alkaptonuria from one family tree with special reference to osteo-arthrosis alkaptonurica. ABE Y; OSHIMA N; HATANAKA R; AMAKO T; HIROHATA R J Bone Joint Surg Am; 1960 Jul; 42-A():817-31. PubMed ID: 13848727 [No Abstract] [Full Text] [Related]
40. The incidence of alkaptonuria: a study in chemical individuality. 1902. Garrod AE Mol Med; 1996 May; 2(3):274-82. PubMed ID: 8784780 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]