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 *

113 related articles for article (PubMed ID: 27450766)

  • 1. Hereditary lactate dehydrogenase M-subunit deficiency with late-developing pustular psoriasis-like lesions.
    Takeo N; Fujiwara S; Sakai T; Saito-Shono T; Ishikawa K; Hatano Y
    J Dermatol; 2016 Dec; 43(12):1429-1432. PubMed ID: 27450766
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pustular psoriasis-like lesions associated with hereditary lactate dehydrogenase M subunit deficiency without interleukin-36 receptor antagonist mutation: long-term follow-up of two cases.
    Ito T; Aoshima M; Sugiura K; Fujiyama T; Ito N; Sakabe JI; Akiyama M; Maekawa M; Tokura Y
    Br J Dermatol; 2015 Jun; 172(6):1674-1676. PubMed ID: 25640002
    [No Abstract]   [Full Text] [Related]  

  • 3. Hereditary lactate dehydrogenase M-subunit deficiency: lactate dehydrogenase activity in skin lesions and in hair follicles.
    Takayasu S; Fujiwara S; Waki T
    J Am Acad Dermatol; 1991 Feb; 24(2 Pt 2):339-42. PubMed ID: 1999544
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Lactate Dehydrogenase M subunit deficiency].
    Sudo K
    Rinsho Byori; 2002 Jun; 50(6):571-5. PubMed ID: 12166075
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Diagnostic clue and genomic analysis of LDH-M subunit deficiency].
    Maekawa M; Kanno T
    Rinsho Byori; 1993 May; 41(5):512-8. PubMed ID: 8350514
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Erythematosquamous skin lesions in hereditary lactate dehydrogenase M-subunit deficiency.
    Yoshikuni K; Tagami H; Yamada M; Sudo K; Kanno T
    Arch Dermatol; 1986 Dec; 122(12):1420-4. PubMed ID: 3789777
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular characterization of gene expression in human lactate dehydrogenase-A deficiency.
    Miyajima H; Takahashi Y; Suzuki M; Shimizu T; Kaneko E
    Neurology; 1993 Jul; 43(7):1414-9. PubMed ID: 8327147
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hereditary deficiency of lactate dehydrogenase M-subunit.
    Kanno T; Sudo K; Takeuchi I; Kanda S; Honda N; Nishimura Y; Oyama K
    Clin Chim Acta; 1980 Dec; 108(2):267-76. PubMed ID: 7449146
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Population screening of lactate dehydrogenase deficiencies in Fukuoka Prefecture in Japan and molecular characterization of three independent mutations in the lactate dehydrogenase-B(H) gene.
    Maekawa M; Sudo K; Nagura K; Li SS; Kanno T
    Hum Genet; 1994 Jan; 93(1):74-6. PubMed ID: 8270259
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Myoglobinuria due to enzyme abnormalities in glycolytic pathway--especially lactate dehydrogenase M subunit deficiency].
    Maekawa M; Kanno T; Sudo K
    Rinsho Byori; 1991 Feb; 39(2):124-32. PubMed ID: 1828277
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Estimation of the gene frequency of lactate dehydrogenase subunit deficiencies.
    Maekawa M; Kanda S; Sudo K; Kanno T
    Am J Hum Genet; 1984 Nov; 36(6):1204-14. PubMed ID: 6517049
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel missense mutation in human lactate dehydrogenase B-subunit gene.
    Takatani T; Takaoka N; Tatsumi M; Kawamoto H; Okuno Y; Morita K; Masutani T; Murakawa K; Okamoto Y
    Mol Genet Metab; 2001 Aug; 73(4):344-8. PubMed ID: 11509017
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterization of genetic mutation in human lactate dehydrogenase-A (M) deficiency.
    Maekawa M; Sudo K; Kanno T; Li SS
    Biochem Biophys Res Commun; 1990 Apr; 168(2):677-82. PubMed ID: 2334430
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic analysis of a family of lactate dehydrogenase A subunit deficiency.
    Takahashi Y; Miyajima H; Kaneko E
    Intern Med; 1995 May; 34(5):326-9. PubMed ID: 7647396
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary deficiency of lactate dehydrogenase H-subunit.
    Wakabayashi H; Tsuchiya M; Yoshino K; Kaku K; Shigei H
    Intern Med; 1996 Jul; 35(7):550-4. PubMed ID: 8842761
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Gene expression in lactate dehydrogenase-A subunit deficiency].
    Miyajima H; Shimizu T; Kaneko E
    Rinsho Shinkeigaku; 1992 Oct; 32(10):1087-92. PubMed ID: 1297552
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel in-frame deletion mutation in a case of lactate dehydrogenase (LD) H subunit deficiency showing an atypical LD isoenzyme pattern in serum and erythrocytes.
    Sudo K; Maekawa M; Houki N; Okuda T; Akizuki S; Magara T; Kawano K
    Clin Biochem; 1999 Mar; 32(2):137-41. PubMed ID: 10211631
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel deletion mutation of lactate dehydrogenase A(M) gene in fifth family with the enzyme deficiency.
    Maekawa M; Sudo K; Kanno T; Takayasu S; Li SS; Kitajima M; Matsuura Y
    Hum Mol Genet; 1994 May; 3(5):825-6. PubMed ID: 8081370
    [No Abstract]   [Full Text] [Related]  

  • 19. First case of missense mutation (LDH-H:R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patient.
    Hidaka K; Ueda N; Hirata I; Watanabe Y; Minatogawa Y; Iuchi I
    J Hum Genet; 1999; 44(1):69-72. PubMed ID: 9929983
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [LDH-H subunit deficiency].
    Houki N; Tsukada T
    Rinsho Byori; 1986 Apr; 34(4):393-5. PubMed ID: 3747188
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.