Michael Hisaund
Overview
Explore the profile of Michael Hisaund including associated specialties, affiliations and a list of published articles.
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9
Citations
61
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Recent Articles
1.
Extended optical treatment for children with amblyopia in Europe: the EuPatch trial - Authors' reply
Proudlock F, Hisaund M, Papageorgiou E, Manouchehrinia A, Gottlob I
Lancet
. 2024 Dec;
404(10470):2421-2422.
PMID: 39674673
No abstract available.
2.
Proudlock F, Hisaund M, Maconachie G, Papageorgiou E, Manouchehrinia A, Dahlmann-Noor A, et al.
Lancet
. 2024 May;
403(10438):1766-1778.
PMID: 38704172
Background: Amblyopia, the most common visual impairment of childhood, is a public health concern. An extended period of optical treatment before patching is recommended by the clinical guidelines of several...
3.
Kuht H, Maconachie G, Han J, Kessel L, van Genderen M, McLean R, et al.
Ophthalmology
. 2022 Feb;
129(6):708-718.
PMID: 35157951
Purpose: To characterize the genotypic and phenotypic spectrum of foveal hypoplasia (FH). Design: Multicenter, observational study. Participants: A total of 907 patients with a confirmed molecular diagnosis of albinism, PAX6,...
4.
Kuht H, Thomas K, Hisaund M, Maconachie G, Thomas M
J Neuroophthalmol
. 2021 Aug;
41(3):e293-e296.
PMID: 34415280
No abstract available.
5.
Rufai S, Hisaund M, Jeelani N, McLean R
BMJ Open
. 2021 Aug;
11(8):e046935.
PMID: 34380720
Objectives: To evaluate the diagnostic capability of optical coherence tomography (OCT) in children aged under 18 years old with intracranial hypertension (IH). Design: Systematic review. Methods: We conducted a systematic...
6.
Thomas M, Maconachie G, Kuht H, Chan W, Sheth V, Hisaund M, et al.
Int J Mol Sci
. 2021 Apr;
22(5).
PMID: 33806565
Congenital fibrosis of the extraocular muscles (CFEOM) is a congenital cranial dysinnervation disorder caused by developmental abnormalities affecting cranial nerves/nuclei innervating the extraocular muscles. Autosomal dominant CFEOM arises from heterozygous...
7.
Aamir A, Kuht H, McLean R, Maconachie G, Sheth V, Dawar B, et al.
Sci Rep
. 2021 Feb;
11(1):2826.
PMID: 33531592
Infantile nystagmus (IN) may result from aetiologies including albinism and FRMD7 mutations. IN has low prevalence, and twins with IN are rare. Whilst discordant presentation has been previously reported for...
8.
Kuht H, Han J, Maconachie G, Park S, Lee S, McLean R, et al.
Hum Mol Genet
. 2020 Aug;
29(18):2989-3002.
PMID: 32744312
Foveal hypoplasia, optic nerve decussation defects and anterior segment dysgenesis is an autosomal recessive disorder arising from SLC38A8 mutations. SLC38A8 is a putative glutamine transporter with strong expression within the...
9.
Thomas M, Maconachie G, Constantinescu C, Chan W, Barry B, Hisaund M, et al.
Br J Ophthalmol
. 2019 Jul;
104(4):547-550.
PMID: 31302631
Background: The genetic basis of monocular elevation deficiency (MED) is unclear. It has previously been considered to arise due to a supranuclear abnormality. Methods: Two brothers with MED were referred...