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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

298 related articles for article (PubMed ID: 12939823)

  • 21. Homogentisic acid oxidase activity in homozygous and heterozygous alkaptonuric mice.
    Coudé M; Montagutelli X; Guenet JL; Kamoun P
    Ann Biol Clin (Paris); 1994; 52(7-8):569-70. PubMed ID: 7840434
    [No Abstract]   [Full Text] [Related]  

  • 22. Early detection of alkaptonuria.
    Verma SB
    Indian J Dermatol Venereol Leprol; 2005; 71(3):189-91. PubMed ID: 16394410
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Alkaptonuria presenting with ochronotic spondyloarthropathy.
    Al-Mahfoudh R; Clark S; Buxton N
    Br J Neurosurg; 2008 Dec; 22(6):805-7. PubMed ID: 19085367
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Ashy ears.
    Rallis E; Kintzoglou S
    ScientificWorldJournal; 2010 Aug; 10():1530-1. PubMed ID: 20694448
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 37. Rapid detection methods for five HGO gene mutations causing alkaptonuria.
    Zatkova A; Chmelikova A; Polakova H; Ferakova E; Kadasi L
    Clin Genet; 2003 Feb; 63(2):145-9. PubMed ID: 12630963
    [TBL] [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]
    of 15.