Detalhe da pesquisa
1.
The predictive value of the sFlt-1/PlGF ratio in suspected preeclampsia in a New Zealand population: A prospective cohort study.
Aust N Z J Obstet Gynaecol
; 63(1): 34-41, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35670085
2.
Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations.
Am J Med Genet A
; 185(10): 2941-2950, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34089223
3.
Lipoprotein apheresis and PCSK9 inhibitors for severe familial hypercholesterolaemia: Experience from Australia and New Zealand.
J Clin Apher
; 36(1): 48-58, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32911577
4.
Sudden Cardiac Death Due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2.
Am J Hum Genet
; 99(3): 674-682, 2016 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27523597
5.
Two cases of discordant thyroid function tests: familial dysalbuminaemic hyperthyroxinaemia and dystransthyretinaemic hyperthyroxinaemia.
Intern Med J
; 53(1): 152-154, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36693642
6.
Evaluation of the NZ guidelines for screening for persistent postpartum hyperglycaemia following gestational diabetes.
Aust N Z J Obstet Gynaecol
; 58(4): 432-437, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29148563
7.
Pseudohypoaldosteronism type 2: CUL3 mutation confirmed 15 years following initial diagnosis.
Intern Med J
; 52(4): 691-692, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35419964
8.
Is There a Role for HbA1c in Pregnancy?
Curr Diab Rep
; 16(1): 5, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26739347
9.
Effectiveness of EDACS Versus ADAPT Accelerated Diagnostic Pathways for Chest Pain: A Pragmatic Randomized Controlled Trial Embedded Within Practice.
Ann Emerg Med
; 68(1): 93-102.e1, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26947800
10.
Association of Clinical Characteristics With Familial Hypercholesterolaemia Variants in a Lipid Clinic Setting: A Case-Control Study.
J Lipid Atheroscler
; 13(1): 29-40, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38299170
11.
Artefactually low creatinine by Beckman Coulter enzymatic method due to immunoglobulin M paraprotein interference.
Ann Clin Biochem
; 60(6): 423-427, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37482625
12.
Reference intervals for deconjugated urine metanephrines by Bhattacharya analysis.
Ann Clin Biochem
; : 45632231204505, 2023 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37710976
13.
Verification of point-of-care analysers for C-reactive protein, lipid studies and glycated haemoglobin.
Pathology
; 55(7): 989-999, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37778963
14.
High penetrance, recurrent attacks and thrombus formation in a family with hereditary coproporphyria.
JIMD Rep
; 63(3): 211-215, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35433170
15.
Hb Westport [ß121 (GH4) Glu>Asp; HBB:c.366A>C]: A novel ß-globin variant interfering with HbA1c measurement.
Clin Biochem
; 107: 62-66, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35580651
16.
The performance of high sensitivity troponin for the diagnosis of acute myocardial infarction is underestimated.
Clin Chem Lab Med
; 50(4): 727-9, 2011 Dec 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22505533
17.
An updated diagnostic range for serum free light chain kappa/lambda ratio using Freelite reagents on BN II or Optilite.
Pathology
; 2024 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-38705800
18.
Discordant thyroid function tests-beware of albumin variants.
N Z Med J
; 137(1588): 90-93, 2024 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38261778
19.
Intermittent severe, symptomatic hyponatraemia due to the nephrogenic syndrome of inappropriate antidiuresis.
Ann Clin Biochem
; 45(Pt 5): 520-3, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18753429
20.
A case of hereditary coproporphyria with posterior reversible encephalopathy and novel coproporphyrinogen oxidase gene mutation c.863T>G (p.Leu288Trp).
Ann Clin Biochem
; 55(5): 616-619, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29660996