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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]
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]
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]