D A Mackey
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Explore the profile of D A Mackey including associated specialties, affiliations and a list of published articles.
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66
Citations
2284
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Recent Articles
1.
Leedman S, Sheeraz M, Sanfilippo P, Edgar D, DAulerio G, Robb D, et al.
J Laryngol Otol
. 2021 Aug;
135(9):839-843.
PMID: 34348821
Objective: This study aimed to assess olfactory dysfunction in patients at six months after confirmed coronavirus disease 2019 infection. Methods: Coronavirus disease 2019 positive patients were assessed six months following...
2.
Bursle C, Riney K, Stringer J, Moore D, Gole G, Kearns L, et al.
JIMD Rep
. 2017 Dec;
42:53-60.
PMID: 29249004
Leber Hereditary Optic Neuropathy is an inherited optic neuropathy caused by mitochondrial DNA point mutations leading to sudden, painless loss of vision. We report a case of an 8-year-old boy...
3.
Lopez Sanchez M, Crowston J, Mackey D, Trounce I
Pharmacol Ther
. 2016 Jun;
165:132-52.
PMID: 27288727
Optic neuropathies are an important cause of blindness worldwide. The study of the most common inherited mitochondrial optic neuropathies, Leber hereditary optic neuropathy (LHON) and autosomal dominant optic atrophy (ADOA)...
4.
Forward H, Yazar S, Hewitt A, Khan J, Mountain J, Pesudovs K, et al.
Ultrasound Obstet Gynecol
. 2014 May;
44(2):166-70.
PMID: 24789332
Objectives: Through comprehensive ophthalmic examination of adult offspring we sought to determine the impact of multiple prenatal ultrasound scans on ocular development. Methods: 2743 pregnant women recruited to the Western...
5.
Ng W, Pasutto F, Bardakjian T, Wilson M, Watson G, Schneider A, et al.
Clin Genet
. 2012 Jan;
83(2):162-8.
PMID: 22283518
Fraser syndrome (FS) and microphthalmia syndromic 9 (MCOPS9) are autosomal recessive conditions with distinct, and some overlapping features affecting the ocular, respiratory and cardiac systems. Mutations in FRAS1 and FREM2...
6.
Mackey D, Hewitt A, Ruddle J, Vote B, Buttery R, Toomes C, et al.
Mol Vis
. 2011 Aug;
17:2118-28.
PMID: 21850187
Purpose: To describe an Australian pedigree of European descent with a variable autosomal dominant phenotype of: pediatric cortical cataract (CC), asymmetric myopia with astigmatism, familial exudative vitreoretinopathy (FEVR), and primary...
7.
Sherwin J, Hewitt A, Kearns L, Coroneo M, Griffiths L, Mackey D
Eye (Lond)
. 2011 Apr;
25(7):893-900.
PMID: 21494284
Objective: The objective of this study was to describe the distribution of conjunctival ultraviolet autofluorescence (UVAF) in an adult population. Methods: We conducted a cross-sectional, population-based study in the genetic...
8.
Cohn A, Turnbull C, Ruddle J, Guymer R, Kearns L, Staffieri S, et al.
Eye (Lond)
. 2010 Nov;
25(2):208-17.
PMID: 21109774
Purpose: (1) To evaluate the spectrum of BEST1 mutations within Australian Best Disease or vitelliform macular dystrophy (VMD) pedigrees, including any novel mutations; (2) to analyse the range of clinical...
9.
Pavone P, Mackey D, Parano E, Barbagallo M, Pratico A, Trifiletti R
Clin Ter
. 2010 Jul;
161(3):241-3.
PMID: 20589354
Aims: We herein report a 5 years experience of management and care of children presenting blepharoptosis at the light of the literature regarding this uncommon pathology. This report aims to...
10.
Carbonaro F, Andrew T, Mackey D, Spector T, Hammond C
Eye (Lond)
. 2010 Feb;
24(7):1165-70.
PMID: 20150923
Purpose: The purpose of this study was to compare the reliability of the 'gold standard' Goldmann applanation tonometer (GAT), with that of the ocular response analyser (ORA), and the dynamic...