These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
115 related articles for article (PubMed ID: 4462635)
1. Analysis of alkaptonuria incidence in one region of Northwest Slovakia: a preliminary report. Neuwirth A; Srsen S ; Petrìcek J; Mruskovic Birth Defects Orig Artic Ser; 1974; 10(10):244-9. PubMed ID: 4462635 [No Abstract] [Full Text] [Related]
2. Alkaptonuria. Srsen S Johns Hopkins Med J; 1979 Dec; 145(6):217-26. PubMed ID: 513428 [TBL] [Abstract][Full Text] [Related]
3. [Alkaptonuria in the Upper Hron Region in Slovakia (author's transl)]. Srsen S; Koska L; Kaprálik I Cas Lek Cesk; 1978 Dec; 117(49):1517-22. PubMed ID: 737698 [No Abstract] [Full Text] [Related]
4. Alkaptonuria in the Trencín District of Czechoslovakia. Srsen S; Cisárik F; Pásztor L; Harmecko L Am J Med Genet; 1978; 2(2):159-66. PubMed ID: 263435 [TBL] [Abstract][Full Text] [Related]
5. [Incidence of alkaptonuria in relation to genetic isolation and degree of inbreeding in several selected localities in Slovakia (author's transl)]. Srsen S; Koska L; Kaprálik I Cas Lek Cesk; 1978 Mar; 117(12):353-60. PubMed ID: 657192 [No Abstract] [Full Text] [Related]
7. [Random and non-random component of inbreeding coefficient in localities with high incidence of alkaptonuria in Slovakia (author's transl)]. Srsen S; Ferák V; Koska L; Kaprálik I Bratisl Lek Listy; 1979 Feb; 71(2):144-51. PubMed ID: 427609 [No Abstract] [Full Text] [Related]
8. [Analysis of the causes of the relatively frequent incidence of alkaptonuria in Slovakia]. Srsen S Cas Lek Cesk; 1983 Dec; 122(51):1585-7. PubMed ID: 6652675 [No Abstract] [Full Text] [Related]
9. R58fs mutation in the HGD gene in a family with alkaptonuria in the UAE. Abdulrazzaq YM; Ibrahim A; Al-Khayat AI; Nagelkerke N; Ali BR Ann Hum Genet; 2009 Jan; 73(1):125-30. PubMed ID: 18945288 [TBL] [Abstract][Full Text] [Related]
10. An update on molecular genetics of Alkaptonuria (AKU). Zatkova A J Inherit Metab Dis; 2011 Dec; 34(6):1127-36. PubMed ID: 21720873 [TBL] [Abstract][Full Text] [Related]
11. The incidence of alkaptonuria: a study in chemical individuality. 1902 [classical article]. Garrod AE Yale J Biol Med; 2002; 75(4):221-31. PubMed ID: 12784973 [No Abstract] [Full Text] [Related]
12. The human gene for alkaptonuria (AKU) maps to chromosome 3q. Janocha S; Wolz W; Srsen S; Srsnova K; Montagutelli X; Guénet JL; Grimm T; Kress W; Müller CR Genomics; 1994 Jan; 19(1):5-8. PubMed ID: 8188241 [TBL] [Abstract][Full Text] [Related]
13. Alkaptonuria in a 5-year-old boy in Iraq. Al-Mefraji SH East Mediterr Health J; 2008; 14(3):745-6. PubMed ID: 18720640 [No Abstract] [Full Text] [Related]
14. 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]
15. Alkaptonuria in Slovakia: thirty-two years of research on phenotype and genotype. Srsen S; Müller CR; Fregin A; Srsnova K Mol Genet Metab; 2002 Apr; 75(4):353-9. PubMed ID: 12051967 [TBL] [Abstract][Full Text] [Related]
16. aku, a mutation of the mouse homologous to human alkaptonuria, maps to chromosome 16. Montagutelli X; Lalouette A; Coudé M; Kamoun P; Forest M; Guénet JL Genomics; 1994 Jan; 19(1):9-11. PubMed ID: 8188247 [TBL] [Abstract][Full Text] [Related]
17. A novel therapeutic trial of homogentisic aciduria in a murine model of alkaptonuria. Suzuki Y; Oda K; Yoshikawa Y; Maeda Y; Suzuki T J Hum Genet; 1999; 44(2):79-84. PubMed ID: 10083729 [TBL] [Abstract][Full Text] [Related]