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.
25. Alkaptonuria: A Case Report With Diagnostic Challenge. Gali VL; Kerkvliet AM; Kusmak JM; Elwood JK S D Med; 2017 Aug; 70(8):366-368. PubMed ID: 28813744 [TBL] [Abstract][Full Text] [Related]
26. [A child with dark discoloration of urine]. Jeucken YM; Visser G; Jaarsma AS; van Spronsen FJ Ned Tijdschr Geneeskd; 1999 Aug; 143(32):1641-3. PubMed ID: 10494297 [TBL] [Abstract][Full Text] [Related]
27. [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]
28. [Knee ochronotic arthropathy and arthroscopic findings]. Kural C; Cetinus EM; Kural A; Uğraş AA; Kaya I Acta Orthop Traumatol Turc; 2009; 43(1):67-71. PubMed ID: 19293619 [TBL] [Abstract][Full Text] [Related]
29. Nine cases of Alkaptonuria in one family in southern Jordan. Al-Sbou M; Mwafi N Rheumatol Int; 2012 Mar; 32(3):621-5. PubMed ID: 21127875 [TBL] [Abstract][Full Text] [Related]
30. Alkaptonuria in Italy: polymorphic haplotype background, mutational profile, and description of four novel mutations in the homogentisate 1,2-dioxygenase gene. Porfirio B; Chiarelli I; Graziano C; Mannoni A; Morrone A; Zammarchi E; De Bernabé DB; De Córdoba SR J Med Genet; 2000 Apr; 37(4):309-12. PubMed ID: 10819641 [No Abstract] [Full Text] [Related]
31. Spectrophotometric determination of homogentisate using Aspergillus nidulans homogentisate dioxygenase. Fernández-Cañón JM; Peñalva MA Anal Biochem; 1997 Feb; 245(2):218-21. PubMed ID: 9056215 [TBL] [Abstract][Full Text] [Related]
32. A metabolic cause of spinal deformity. Effelsberg NM; Hügle T; Walker UA Metabolism; 2010 Jan; 59(1):140-3. PubMed ID: 19765774 [TBL] [Abstract][Full Text] [Related]
33. Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India. Danda S; Mohan S; Devaraj P; Dutta AK; Nampoothiri S; Yesodharan D; Phadke SR; Jalan AB; Thangaraj K; Verma IC; Danda D; Jebaraj I Clin Rheumatol; 2020 Sep; 39(9):2743-2749. PubMed ID: 32212000 [TBL] [Abstract][Full Text] [Related]
34. Identification of the mutation in the alkaptonuria mouse model. Mutations in brief no. 216. Online. Manning K; Fernández-Cañón JM; Montagutelli X; Grompe M Hum Mutat; 1999; 13(2):171. PubMed ID: 10094559 [TBL] [Abstract][Full Text] [Related]
35. 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]
36. Novel mutations in the homogentisate-1,2-dioxygenase gene identified in Slovak patients with alkaptonuria. Zatková A; Polaková H; Micutková L; Zvarík M; Bosák V; Feráková E; Matusek J; Ferák V; Kádasi L J Med Genet; 2000 Jul; 37(7):539-42. PubMed ID: 10970188 [No Abstract] [Full Text] [Related]
38. A novel mutation in the homogentisate 1,2 dioxygenase gene identified in Chinese Hani pediatric patients with Alkaptonuria. Tao L; Deng C; Ma M; Zhang Y; Duan J; Li Y; Fang L; Zhou Y; He X; Wang Y; Wang M; Li L Clin Chim Acta; 2022 Jul; 532():164-171. PubMed ID: 35550814 [TBL] [Abstract][Full Text] [Related]
39. Nuclear medicine techniques in the assessment of alkaptonuria. Vinjamuri S; Ramesh CN; Jarvis J; Gallagher JA; Ranganath LL Nucl Med Commun; 2011 Oct; 32(10):880-6. PubMed ID: 21876398 [TBL] [Abstract][Full Text] [Related]
40. Are we ready to try to cure alkaptonuria? La Du BN Am J Hum Genet; 1998 Apr; 62(4):765-7. PubMed ID: 9529368 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]