Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Juhani Murros"'
Autor:
Juhani Murros
In the early 1960s, Van Den reached the pinnacle of his career and was regarded as South Vietnam's premier artist. His path to success had been long and tortuous. He was born in 1919 in the French colonial time and left his humble village home in the
Publikováno v:
Clinica Chimica Acta. 41:263-268
A sensitive electrophoretic technique for the detection and quantitation of aspartate aminotransferase isoenzymes is presented. A band corresponding to an enzymic activity of 6 IU/l is still visible. The procedure is sufficiently linear for quantitat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab95980475891dce2e9b794375530e43
https://doi.org/10.1016/0009-8981(72)90520-7
https://doi.org/10.1016/0009-8981(72)90520-7
Publikováno v:
Clinica Chimica Acta. 84:145-147
Two healthy young women had an unexplained persistent elevation of aspartate aminotransferase (ASAT) activity. In both cases electrophoresis of serum ASAT isoenzymes displayed an abnormally moving fraction that comprised the whole serum activity, whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aadb0be2c8cf73acb64980ab7c95055f
https://doi.org/10.1016/0009-8981(78)90487-4
https://doi.org/10.1016/0009-8981(78)90487-4
Autor:
Juhani Murros, Kimmo Luomanmäki
Publikováno v:
Acta medica Scandinavica. 208(1-2)
Little attention has been given to the question whether clinical heart failure can be a manifestation of hypocalcemia. A patient with hypopara-thyroidism and heart failure prompted us to analyse the reports on this subject. The conclusion was that if
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b66afb1468e38609faf54f68e9e6c4ae
https://pubmed.ncbi.nlm.nih.gov/7435243
https://pubmed.ncbi.nlm.nih.gov/7435243
Publikováno v:
Clinical genetics. 11(2)
Two XX males who were second cousins are reported. A genetic mechanism producing maleness is suggested. The putative factor had been transmitted solely through males, which excludes the possibility of a heritable X-Y interchange. Recent reports on fl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e9b2212f96c5a17d574a1d7e42356ac
https://pubmed.ncbi.nlm.nih.gov/837567
https://pubmed.ncbi.nlm.nih.gov/837567
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 48(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9215393648bc03bd608f913aece76716
https://pubmed.ncbi.nlm.nih.gov/4758887
https://pubmed.ncbi.nlm.nih.gov/4758887
Publikováno v:
Archives of Neurology. 29:343
Creatine kinase MB isozyme was found in the serum of 29 (91%) patients with progressive or congenital muscular dystrophy. The magnitude of its elevation exceeded that of other enzymes or isozymes studied. Mitochondrial aspartate aminotransferase (mAS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03629a10f71d4605f5ec9b1d1d68f006
https://doi.org/10.1001/archneur.1973.00490290083012
https://doi.org/10.1001/archneur.1973.00490290083012