Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Michael J, Thomsett"'
Autor:
Martin B. Draznin, Michael J. Thomsett, Gail E. Richards, Linda A. DiMeglio, Bruce A. Boston, Dorothy I. Shulman
Publikováno v:
The Journal of Pediatrics. 159:566-570
Objective To determine what percentage of diabetes insipidus (DI) in childhood is idiopathic and to assess the natural history of idiopathic DI. Study design We conducted a retrospective chart review of 105 patients with DI who were born or had DI di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a64f5a8ba6d5299dc144badc9808dc3b
https://doi.org/10.1016/j.jpeds.2011.03.044
https://doi.org/10.1016/j.jpeds.2011.03.044
The spectrum of clinical paediatric endocrinology: 28 years of referrals to an individual consultant
Autor:
Michael J. Thomsett
Publikováno v:
Journal of Paediatrics and Child Health. 46:304-309
Aim: To review referrals throughout the career of an individual paediatric endocrinologist. Methods: A retrospective cohort study in metropolitan clinics in Queensland analysed details of all 9062 patients aged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::301094f3406ef722eb7baeed41303835
https://doi.org/10.1111/j.1440-1754.2010.01713.x
https://doi.org/10.1111/j.1440-1754.2010.01713.x
Autor:
Michael J. Thomsett
Publikováno v:
Journal of Paediatrics and Child Health. 45:58-63
Aim: Extreme tall stature may lead to a variety of concerns in tall children and their parents, leading to requests for treatment to reduce final height in some children. This study reviews referrals for tall stature to a single pediatric endocrinolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b09d455f336e1537500c1e78c2dfa09
https://doi.org/10.1111/j.1440-1754.2008.01428.x
https://doi.org/10.1111/j.1440-1754.2008.01428.x
Autor:
John R. Bell, David Ml Brown, Michael J. Thomsett, Janaki Shah, Andrew Cotterill, David Cowley, Mark Harris, Y. Jeske, Francis Bowling, Daphne Liaskou, Catherine S. Choong, Ristan M. Greer, Rosslyn M. Walker, Michelle M Jack
Publikováno v:
Pediatric and Developmental Pathology. 10:25-34
In hyperinsulinism of infancy (HI), unregulated insulin secretion causes hypoglycemia. Pancreatectomy may be required in severe cases, most of which result from a defect in the β-cell KATP channel, encoded by ABCC8 and KCNJ11. Pancreatic histology m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ac77e2a728fdf57138ae6f7dd1276c
https://doi.org/10.2350/06-04-0083.1
https://doi.org/10.2350/06-04-0083.1
Publikováno v:
Journal of Paediatrics and Child Health. 42:108-111
Objectives: To evaluate the use of small doses of glucagon using an insulin syringe in mild or impending hypoglycaemia in children with type 1 diabetes. Methods: Data were collected from patients attending the Paediatric Diabetes Clinic at the Queens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::700b44d35c60421d448e5e2016b23de1
https://doi.org/10.1111/j.1440-1754.2006.00807.x
https://doi.org/10.1111/j.1440-1754.2006.00807.x
Autor:
James L. Penfold, Michael J. Thomsett, Y. Jeske, Kim McLennan, Catherine S. Choong, Andrew Cotterill, N. J. Howard, Timothy W. Jones, David Cowley
Publikováno v:
Clinical Endocrinology. 58:785-794
Summary objective Mutations in the gene for the POU domain transcription factor POU1F1 (human Pit-1) have been reported in patients with GH, TSH and PRL deficiencies. PROP1 (Prophet of Pit-1) gene mutations also cause gonadotrophin deficiencies and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92dfa4903c75e1650ba05277b9812743
https://doi.org/10.1046/j.1365-2265.2003.01781.x
https://doi.org/10.1046/j.1365-2265.2003.01781.x
Autor:
Adrian C. Herington, John R. Bell, Andrew Cotterill, Michael J. Thomsett, Catherine Choong, Rosslyn M. Walker, David Cowley, Ristan M. Greer, Michelle M. Jack
Publikováno v:
Clinical Endocrinology. 58:355-364
AIMS Hyperinsulinism of infancy (HI) is characterized by unregulated insulin secretion in the presence of hypoglycaemia, often resulting in brain damage. Pancreatic resection for control of hypoglycaemia is frequently resisted because of the risk of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bd4942d88c11f63d69caf491ce02201
https://doi.org/10.1046/j.1365-2265.2003.01725.x
https://doi.org/10.1046/j.1365-2265.2003.01725.x
Publikováno v:
Journal of Paediatrics and Child Health. 37:348-351
Objective: To review the common clinical presentations, investigations and final diagnosis of children presenting with genital ambiguity. Methodology: Retrospective search of the Royal Children's Hospital, Brisbane, Australia, medical records and per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2f0b41e5236859a2f62f5f82695695b
https://doi.org/10.1046/j.1440-1754.2001.00669.x
https://doi.org/10.1046/j.1440-1754.2001.00669.x
Autor:
Catherine S. Choong, Michael J. Thomsett, Andrew Cotterill, Christine Rodda, Christopher Smith, H. David McIntyre
Publikováno v:
Clinical Endocrinology. 54:371-376
OBJECTIVES Graves' disease (GD) complicates 0.1% to 0.2% of pregnancies, but congenital thyrotoxicosis is rare occurring in one in 70 of these pregnancies independent of maternal disease status. Antenatal prediction of affected infants is imprecise;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::824907b22e53eab3f6ce76ac319e5989
https://doi.org/10.1046/j.1365-2265.2001.01173.x
https://doi.org/10.1046/j.1365-2265.2001.01173.x
Publikováno v:
Pediatric and Developmental Pathology. 3:532-547
Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is characterized by hyperinsulinism and profound hypoglycemia, with most children requiring pancreatic resection. The histological classification of PHHI is controversial. Most authors acknow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::279741876195ecd3c8d9236e5a9c1459
https://doi.org/10.1007/s100240010117
https://doi.org/10.1007/s100240010117