Zobrazeno 1 - 10
of 10
pro vyhledávání: '"H. C. O. Martin"'
Publikováno v:
European Journal of Pediatric Surgery. 16:58-60
Colonic duplication is a rare congenital anomaly which presents as a diagnostic and therapeutic challenge. We report a 5-year-old boy with colonic duplication who required multiple hospital admissions, multiple diagnostic tests, and evaluation by var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a150619747267ad8c320c019beeaf442
https://doi.org/10.1055/s-2006-923794
https://doi.org/10.1055/s-2006-923794
Autor:
J. Motbey, H. C. O. Martin
Publikováno v:
ANZ Journal of Surgery. 63:883-887
The perfect suture has been defined, but in certain circumstances some features are more important than others. In paediatric gastrointestinal surgery lack of tissue drag is of great importance. Because the life expectancy of most paediatric patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91238f1498b5be879f280b748082fa5a
https://doi.org/10.1111/j.1445-2197.1993.tb00364.x
https://doi.org/10.1111/j.1445-2197.1993.tb00364.x
Publikováno v:
Pediatric Surgery International. 7:140-142
A 3-year- 8-month-old girl developed obstructive jaundice associated with stricture of the distal end of the common bile duct 7 months after blunt abdominal trauma. Ultrasonography, computerised tomography, and percutaneous trans-hepatic cholangiogra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12744ed81db74e07b370fd02f3a22d10
https://doi.org/10.1007/bf00183924
https://doi.org/10.1007/bf00183924
Publikováno v:
Australasian radiology. 41(1)
SUMMARY The imaging findings of two children with acinic cell carcinoma of the parotid gland are presented. Ultrasonic features are emphasized. One of these children, a 6-year-old boy, suffers from the oculocerebrorenal syndrome of Lowe, a rare conge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1596a998653a0fe71315222fa59c06
https://pubmed.ncbi.nlm.nih.gov/9125068
https://pubmed.ncbi.nlm.nih.gov/9125068
Autor:
R. Smith, K. J. Gaskin, C. Bambach, D. Stiel, David M. Hunt, I. M. Bruzuszcak, H. C. O. Martin, E. V. O'loughlin
Publikováno v:
The American journal of physiology. 260(5 Pt 1)
Abnormal epithelial electrolyte transport has been identified in a range of cystic fibrosis (CF) organs and appears to account for the various clinical manifestations of the disease. The aim of this study was to further define the Cl- secretion defec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7273742f0b316c8540913b06a47aa135
https://pubmed.ncbi.nlm.nih.gov/1709789
https://pubmed.ncbi.nlm.nih.gov/1709789
Autor:
H. C. O. MARTIN
Publikováno v:
Journal of Paediatrics and Child Health. 30:370-370
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7beb4610a1badb8844c8109ac21fb8eb
https://doi.org/10.1111/j.1440-1754.1994.tb00667.x
https://doi.org/10.1111/j.1440-1754.1994.tb00667.x
Publikováno v:
The Lancet. 335:1098
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59e05df387abcd879497d15fd894036b
https://doi.org/10.1016/0140-6736(90)92672-5
https://doi.org/10.1016/0140-6736(90)92672-5
Publikováno v:
Australian and New Zealand Journal of Medicine. 10:336-339
Summary: A three-year-old boy is described with type I hyperlipoproteinaemia in association with recurrent scrotal pain and hepatosplenomegaly. His parents are consanguinous and it is likely that he is homozygous for an autosomal recessive trait, cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::172716521b071c72a05c7e56ddf9eaf0
https://doi.org/10.1111/j.1445-5994.1980.tb04082.x
https://doi.org/10.1111/j.1445-5994.1980.tb04082.x
Autor:
G. Cummins, Anthony W. Middleton, Kamath Kr, Albert Shun, Kevin J. Gaskin, Stuart Dorney, Edward V. O'Loughlin, H. C. O. Martin
Publikováno v:
The Australian and New Zealand journal of surgery. 59(11)
Forty-seven infants (26 male, 21 female) with biliary atresia underwent hepatic portoenterostomy during the 16-year period 1971–87. Twenty-six patients (55%) are alive 1–17 years after surgery, with 21 (45%) being jaundice-free. For children who
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b8fe354da450fb6a90c9398991a39ac
https://pubmed.ncbi.nlm.nih.gov/2818344
https://pubmed.ncbi.nlm.nih.gov/2818344
Publikováno v:
The Medical journal of Australia. 2(9)
Pyomyositis tropicans is a rare disease in non-tropical climates and thus presents diagnostic difficulties. Two children with single staphylococcal psoas muscle abscesses were recently successfully treated. Computerized axial tomography was found to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b57a982efe81d97ea8780bd49b71fe2
https://pubmed.ncbi.nlm.nih.gov/7207352
https://pubmed.ncbi.nlm.nih.gov/7207352