Zobrazeno 1 - 10
of 10
pro vyhledávání: '"M. T. O'halloran"'
Publikováno v:
Annals of clinical biochemistry. 31
A simple reverse-phase liquid chromatographic method has been developed for the quantitative measurement of 11 3α-OH bile acids in paediatric serum samples. Bile acids are enzymatically reduced to the corresponding 3-keto compound and then derivatiz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cf22dd006a96eb61468086b7a3f0bdb
https://pubmed.ncbi.nlm.nih.gov/7832575
https://pubmed.ncbi.nlm.nih.gov/7832575
Publikováno v:
Pediatric pulmonology. Supplement. 7
Previously we have reported that 37% of infants with cystic fibrosis diagnosed by neonatal screening with the dried blood spot immunoreactive trypsin assay have pancreatic sufficiency. However, 34 of the 78 infants had pancreatic function tests an av
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cdfb7c1837cc36b3ca2fefc01ffecf0
https://pubmed.ncbi.nlm.nih.gov/1782134
https://pubmed.ncbi.nlm.nih.gov/1782134
Publikováno v:
Journal of Paediatrics and Child Health. 7:187-192
SYNOPSIS The clinical features of 36 infants who presented with hypocalcaemia in the first 2 years of life are reviewed and their subsequent progress studied. Males outnumbered females 28:8. While a low serum calcium level is physiological and common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be4b22aedff8a12af93b0d742455eafa
https://doi.org/10.1111/j.1440-1754.1971.tb01054.x
https://doi.org/10.1111/j.1440-1754.1971.tb01054.x
Autor:
J. S. Yu, M. T. O'Halloran
Publikováno v:
Pediatrics. 46:707-711
A family study demonstrates the current complexity of the phenylketonuria group of diseases. Conventional testing methods are unable to discriminate confidently between the carrier state of atypical and classical phenylketonuria. It is therefore impo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::760a58eafdf411186b05c8dd9b60ed37
https://doi.org/10.1542/peds.46.5.707
https://doi.org/10.1542/peds.46.5.707
Publikováno v:
Archives of Disease in Childhood. 45:561-565
Nine children with atypical phenylketonuria are described from a Phenylketonuric Clinic of 56 children. The diagnostic criteria are (i) raised serum phenylalanine level, 4-20 mg./100 ml.; (ii) phenylalanine intolerance indistinguishable from classica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca016f63adad3e75bb9474c21aa78aa8
https://doi.org/10.1136/adc.45.242.561
https://doi.org/10.1136/adc.45.242.561
Publikováno v:
Medical Journal of Australia. 2:404-406
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a8bc2d3acde91c793729c132fe01de1
https://doi.org/10.5694/j.1326-5377.1970.tb50076.x
https://doi.org/10.5694/j.1326-5377.1970.tb50076.x
Publikováno v:
Journal of Paediatrics and Child Health. 7:179-181
SYNOPSIS The sex ratio in 76 children with an elevated serum phenylalanine level was studied in relation to their mode of ascertainment. The ratio of the sexes in the whole group was equal, but males outnumbered females 9:4 in classical cases of PKU
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0da767c79338c687fc74561aee3965a5
https://doi.org/10.1111/j.1440-1754.1971.tb01052.x
https://doi.org/10.1111/j.1440-1754.1971.tb01052.x
Publikováno v:
Australian paediatric journal. 6(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::364393bdfabc66b4e51dce7f7ed01cdd
https://pubmed.ncbi.nlm.nih.gov/5520429
https://pubmed.ncbi.nlm.nih.gov/5520429
Autor:
J S, Yu, M T, O'Halloran
Publikováno v:
Pediatrics. 46(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::935d246ba81839a59df957e8ea070bbb
https://pubmed.ncbi.nlm.nih.gov/5481071
https://pubmed.ncbi.nlm.nih.gov/5481071
Publikováno v:
Archives of Disease in Childhood. 46:124-125
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eb8cc9242df1751fa41c2833428c3e2
https://doi.org/10.1136/adc.46.245.124
https://doi.org/10.1136/adc.46.245.124