Detalhe da pesquisa
1.
Higher frequency of vertebrate-infecting viruses in the gut of infants born to mothers with type 1 diabetes.
Pediatr Diabetes
; 21(2): 271-279, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31800147
2.
The Australasian Diabetes Data Network: first national audit of children and adolescents with type 1 diabetes.
Med J Aust
; 206(3): 121-125, 2017 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-28208043
3.
A novel NR5A1 variant in an infant with elevated testosterone from an Australasian cohort of 46,XY patients with disorders of sex development.
Clin Endocrinol (Oxf)
; 78(4): 545-50, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22909003
4.
Environmental determinants of islet autoimmunity (ENDIA): a pregnancy to early life cohort study in children at-risk of type 1 diabetes.
BMC Pediatr
; 13: 124, 2013 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23941366
5.
Is it time to commence newborn screening for congenital adrenal hyperplasia in Australia?
Med J Aust
; 195(5): 260-2, 2011 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-21895585
6.
The association between ketoacidosis and 25(OH)-vitamin D levels at presentation in children with type 1 diabetes mellitus.
Pediatr Diabetes
; 10(1): 38-43, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-18761649
7.
Distinct Gut Virome Profile of Pregnant Women With Type 1 Diabetes in the ENDIA Study.
Open Forum Infect Dis
; 6(2): ofz025, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30815502
8.
Utility of AVP gene testing in familial neurohypophyseal diabetes insipidus.
Clin Endocrinol (Oxf)
; 69(6): 926-30, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18494865
9.
Xq26.3 Duplication in a Boy With Motor Delay and Low Muscle Tone Refines the X-Linked Acrogigantism Genetic Locus.
J Endocr Soc
; 2(10): 1100-1108, 2018 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30525125
10.
Cardiac autonomic dysfunction is associated with high-risk albumin-to-creatinine ratio in young adolescents with type 1 diabetes in AdDIT (adolescent type 1 diabetes cardio-renal interventional trial).
Diabetes Care
; 38(4): 676-81, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25573882
11.
Sertoli-Leydig cell tumor of the ovary, a rare cause of precocious puberty in a 12-month-old infant.
J Clin Endocrinol Metab
; 87(1): 49-56, 2002 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-11788622
12.
Normal cortisol response on low-dose synacthen (1 microg) test in children with Prader Willi syndrome.
J Clin Endocrinol Metab
; 95(12): E464-7, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20810574
13.
The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency.
Clin Biochem Rev
; 30(2): 75-86, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19565027
14.
Investigating maturity onset diabetes of the young.
Clin Biochem Rev
; 30(2): 67-74, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19565026
15.
Genotype-phenotype associations in patients with severe hyperinsulinism of infancy.
Pediatr Dev Pathol
; 10(1): 25-34, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17378627
16.
Mini-dose glucagon rescue for mild hypoglycaemia in children with type 1 diabetes: the Brisbane experience.
J Paediatr Child Health
; 42(3): 108-11, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16509909
17.
Autopsy diagnosis of 21-hydroxylase deficiency CAH in a case of apparent SIDS.
Pediatr Dev Pathol
; 8(3): 397-401, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-16010485
18.
The relationship between insulin secretion, the insulin-like growth factor axis and growth in children with cystic fibrosis.
Clin Endocrinol (Oxf)
; 56(3): 383-9, 2002 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-11940051
19.
A Novel V185DfsX4 Mutation of the AAAS Gene in a 2-year-old Boy with Triple A Syndrome.
Clin Pediatr Endocrinol
; 18(2): 73-5, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-24790383
20.
A novel bioassay for human somatogenic activity in serum samples supports the clinical reliability of immunoassays.
Clin Endocrinol (Oxf)
; 56(4): 475-85, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11966740