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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 2 |
1996 | 1 |
2010 | 1 |
2019 | 1 |
2024 | 0 |
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Page 1
Identification of human D lactate dehydrogenase deficiency.
Nat Commun. 2019 Apr 1;10(1):1477. doi: 10.1038/s41467-019-09458-6.
Nat Commun. 2019.
PMID: 30931947
Free PMC article.
Hereditary deficiency of lactate dehydrogenase H-subunit.
Wakabayashi H, Tsuchiya M, Yoshino K, Kaku K, Shigei H.
Wakabayashi H, et al.
Intern Med. 1996 Jul;35(7):550-4. doi: 10.2169/internalmedicine.35.550.
Intern Med. 1996.
PMID: 8842761
Free article.
Item in Clipboard
Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schonberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders.
Whyte MP, Kempa LG, McAlister WH, Zhang F, Mumm S, Wenkert D.
Whyte MP, et al.
J Bone Miner Res. 2010 Nov;25(11):2515-26. doi: 10.1002/jbmr.130.
J Bone Miner Res. 2010.
PMID: 20499337
Free article.
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Characterization of the oxidative metabolism in lactate dehydrogenase A deficiency.
Miyajima H, Takahashi Y, Kaneko E.
Miyajima H, et al.
Intern Med. 1995 Jun;34(6):502-6. doi: 10.2169/internalmedicine.34.502.
Intern Med. 1995.
PMID: 7549132
Free article.
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Genetic analysis of a family of lactate dehydrogenase A subunit deficiency.
Takahashi Y, Miyajima H, Kaneko E.
Takahashi Y, et al.
Intern Med. 1995 May;34(5):326-9. doi: 10.2169/internalmedicine.34.326.
Intern Med. 1995.
PMID: 7647396
Free article.
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