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Origin of the lactate dehydrogenase isoenzyme pattern found in the serum of patients having primary muscular dystrophy.

作者信息

WIEME R J, HERPOL J E

出版信息

Nature. 1962 Apr 21;194:287-8. doi: 10.1038/194287b0.

DOI:10.1038/194287b0

PMID:14006802

Abstract

摘要

相似文献

Origin of the lactate dehydrogenase isoenzyme pattern found in the serum of patients having primary muscular dystrophy.

Nature. 1962 Apr 21;194:287-8. doi: 10.1038/194287b0.

[Progressive muscular dystrophy. I. The heterogenicity of serum lactic dehydrgenase].

Klin Wochenschr. 1961 Apr 1;39:346-52. doi: 10.1007/BF01492249.

[On the relation between the lactic and alpha-hydroxybutyric dehydrogenase activities of the serum in children with progressive muscular dystrophy].

Boll Soc Ital Biol Sper. 1962 Jul 31;38:691-3.

[Aldolase, GOT and LDH activity of the serum in progressive muscular dystrophy and myotonic dystrophy].

Riv Sper Freniatr Med Leg Alien Ment. 1961 Mar 31;85:161-9.

Studies of enzymes in serum in muscular dystrophy. II. Diagnostic and prognostic significance in relatives of dystrophic persons.

Pediatrics. 1961 Dec;28:962-70.

A simplified method of demonstrating lactic dehydrogenase isoenzymes in serum.

Clin Chim Acta. 1962 Jan;7:124-8. doi: 10.1016/0009-8981(62)90129-8.

Lactic dehydrogenase isoenzymes in myocardial infarction.

Clin Chim Acta. 1962 Jul;7:540-4. doi: 10.1016/0009-8981(62)90096-7.

Activity of serum aldolase and lactic dehydrogenase in patients affected with Duchenne muscular dystrophy and in their immediate relatives.

J Pediatr. 1959 Jan;54(1):27-33. doi: 10.1016/s0022-3476(59)80033-0.

LDH isoenzymes: laboratory analysis and clinical significance.

Hartford Hosp Bull. 1962 Sep;17:89-95.

Isoenzymes and myocardial infarction.

N Engl J Med. 1960 Sep 15;263:531-6. doi: 10.1056/NEJM196009152631102.

引用本文的文献

Altered expression of lactate dehydrogenase and monocarboxylate transporter involved in lactate metabolism in broiler wooden breast.

Poult Sci. 2020 Jan;99(1):11-20. doi: 10.3382/ps/pez572. Epub 2019 Dec 30.

[THERMAL INACTIVATION OF SERUM- AND ORGAN-LACTATE DEHYDROGENASES AS A METHOD FOR ISOENZYME SEPARATION].

Klin Wochenschr. 1965 May 1;43:500-4. doi: 10.1007/BF01486090.

MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.

Br Med J. 1964 May 23;1(5394):1344-8 CONCL. doi: 10.1136/bmj.1.5394.1336-a.

Lactic dehydrogenases and muscular dystrophy in the chicken.

Proc Natl Acad Sci U S A. 1962 Dec 15;48(12):2123-30. doi: 10.1073/pnas.48.12.2123.

LDH isozyme pattern in induced muscle disease (Coxsackie Group A virus infection).

Experientia. 1967 Jul 15;23(7):581-2. doi: 10.1007/BF02137985.

[A benign recessiv X-chromosomal hereditary muscular dystrophy. II. Examinations of female carriers].

Humangenetik. 1966;3(1):30-40. doi: 10.1007/BF00273016.

Alpha-hydroxybutyrate dehydrogenase activity in sex-linked muscular dystrophy.

J Clin Pathol. 1966 May;19(3):250-6. doi: 10.1136/jcp.19.3.250.

Serum enzyme changes in lambs with experimentally induced acute muscular dystrophy.

Acta Vet Scand. 1971;12(3):365-74. doi: 10.1186/BF03547736.

Photoreceptor-pigment epithelial cell relationships in rats with inherited retinal degeneration. Radioautographic and electron microscope evidence for a dual source of extra lamellar material.

J Cell Biol. 1972 Apr;53(1):185-209. doi: 10.1083/jcb.53.1.185.

Specificity of serum creatine kinase isoenzymes in diagnosis of acute myocardial infarction.

Br Med J. 1973 Feb 17;1(5850):386-9. doi: 10.1136/bmj.1.5850.386.

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Origin of the lactate dehydrogenase isoenzyme pattern found in the serum of patients having primary muscular dystrophy.

作者信息

WIEME R J, HERPOL J E

出版信息

Nature. 1962 Apr 21;194:287-8. doi: 10.1038/194287b0.

DOI:10.1038/194287b0

PMID:14006802

Abstract

摘要

相似文献

Origin of the lactate dehydrogenase isoenzyme pattern found in the serum of patients having primary muscular dystrophy.

Nature. 1962 Apr 21;194:287-8. doi: 10.1038/194287b0.

[Progressive muscular dystrophy. I. The heterogenicity of serum lactic dehydrgenase].

Klin Wochenschr. 1961 Apr 1;39:346-52. doi: 10.1007/BF01492249.

[On the relation between the lactic and alpha-hydroxybutyric dehydrogenase activities of the serum in children with progressive muscular dystrophy].

Boll Soc Ital Biol Sper. 1962 Jul 31;38:691-3.

[Aldolase, GOT and LDH activity of the serum in progressive muscular dystrophy and myotonic dystrophy].

Riv Sper Freniatr Med Leg Alien Ment. 1961 Mar 31;85:161-9.

Studies of enzymes in serum in muscular dystrophy. II. Diagnostic and prognostic significance in relatives of dystrophic persons.

Pediatrics. 1961 Dec;28:962-70.

A simplified method of demonstrating lactic dehydrogenase isoenzymes in serum.

Clin Chim Acta. 1962 Jan;7:124-8. doi: 10.1016/0009-8981(62)90129-8.

Lactic dehydrogenase isoenzymes in myocardial infarction.

Clin Chim Acta. 1962 Jul;7:540-4. doi: 10.1016/0009-8981(62)90096-7.

Activity of serum aldolase and lactic dehydrogenase in patients affected with Duchenne muscular dystrophy and in their immediate relatives.

J Pediatr. 1959 Jan;54(1):27-33. doi: 10.1016/s0022-3476(59)80033-0.

LDH isoenzymes: laboratory analysis and clinical significance.

Hartford Hosp Bull. 1962 Sep;17:89-95.

Isoenzymes and myocardial infarction.

N Engl J Med. 1960 Sep 15;263:531-6. doi: 10.1056/NEJM196009152631102.

引用本文的文献

Altered expression of lactate dehydrogenase and monocarboxylate transporter involved in lactate metabolism in broiler wooden breast.

Poult Sci. 2020 Jan;99(1):11-20. doi: 10.3382/ps/pez572. Epub 2019 Dec 30.

[THERMAL INACTIVATION OF SERUM- AND ORGAN-LACTATE DEHYDROGENASES AS A METHOD FOR ISOENZYME SEPARATION].

Klin Wochenschr. 1965 May 1;43:500-4. doi: 10.1007/BF01486090.

MUSCULAR DYSTROPHY: SOME RECENT ADVANCES IN KNOWLEDGE.

Br Med J. 1964 May 23;1(5394):1344-8 CONCL. doi: 10.1136/bmj.1.5394.1336-a.

Lactic dehydrogenases and muscular dystrophy in the chicken.

Proc Natl Acad Sci U S A. 1962 Dec 15;48(12):2123-30. doi: 10.1073/pnas.48.12.2123.

LDH isozyme pattern in induced muscle disease (Coxsackie Group A virus infection).

Experientia. 1967 Jul 15;23(7):581-2. doi: 10.1007/BF02137985.

[A benign recessiv X-chromosomal hereditary muscular dystrophy. II. Examinations of female carriers].

Humangenetik. 1966;3(1):30-40. doi: 10.1007/BF00273016.

Alpha-hydroxybutyrate dehydrogenase activity in sex-linked muscular dystrophy.

J Clin Pathol. 1966 May;19(3):250-6. doi: 10.1136/jcp.19.3.250.

Serum enzyme changes in lambs with experimentally induced acute muscular dystrophy.

Acta Vet Scand. 1971;12(3):365-74. doi: 10.1186/BF03547736.

Photoreceptor-pigment epithelial cell relationships in rats with inherited retinal degeneration. Radioautographic and electron microscope evidence for a dual source of extra lamellar material.

J Cell Biol. 1972 Apr;53(1):185-209. doi: 10.1083/jcb.53.1.185.

Specificity of serum creatine kinase isoenzymes in diagnosis of acute myocardial infarction.

Br Med J. 1973 Feb 17;1(5850):386-9. doi: 10.1136/bmj.1.5850.386.