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Abstract 11054: A Novel Method of Conjunctival Vascular Screening to Detect Hemodynamic Alterations in Patients with Coronary Microvascular Disease

Circulation (New York, N.Y.), 2021-11, Vol.144 (Suppl_1)

2021

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Mutations Affecting G-Protein Subunit α11 in Hypercalcemia and Hypocalcemia

The New England journal of medicine, 2013-06, Vol.368 (26), p.2476-2486

2013

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Appraisal of Cardiovascular Risk Factors, Biomarkers, and Ocular Imaging in Cardiovascular Risk Prediction

Current cardiology reviews, 2023-01, Vol.19 (6), p.72-81

2023

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Visual quality and performance comparison between 2 refractive rotationally asymmetric multifocal intraocular lenses

Journal of cataract and refractive surgery, 2017-08, Vol.43 (8), p.1020-1026

2017

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User experience analysis of AbC-19 Rapid Test via lateral flow immunoassays for self-administrated SARS-CoV-2 antibody testing

Scientific reports, 2021-07, Vol.11 (1), p.14026-14026, Article 14026

2021

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A novel algorithm for cardiovascular screening using conjunctival microcirculatory parameters and blood biomarkers

Scientific reports, 2022-04, Vol.12 (1), p.6545-6545, Article 6545

2022

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User experience of home-based AbC-19 SARS-CoV-2 antibody rapid lateral flow immunoassay test

Scientific reports, 2022-01, Vol.12 (1), p.1173-1173, Article 1173

2022

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Assessment of the conjunctival microcirculation for patients presenting with acute myocardial infarction compared to healthy controls

Scientific reports, 2021-04, Vol.11 (1), p.7660-7660, Article 7660

2021

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Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Human molecular genetics, 2012-06, Vol.21 (12), p.2768-2778

2012

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Evaluation of TGFBI corneal dystrophy and molecular diagnostic testing

Eye (London), 2019-06, Vol.33 (6), p.874-881

2019

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Visual outcomes and patient satisfaction 3 and 12 months after implantation of a refractive rotationally asymmetric multifocal intraocular lens

Journal of cataract and refractive surgery, 2017-05, Vol.43 (5), p.633-638

2017

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Comparison of the visual performance and quality of vision with combined symmetrical inferonasal near addition versus inferonasal and superotemporal placement of rotationally asymmetric refractive multifocal intraocular lenses

Journal of cataract and refractive surgery, 2016-12, Vol.42 (12), p.1721-1729

2016

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Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

Nature genetics, 2013-01, Vol.45 (1), p.93-97

2013

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Role of Ca2+ and L-Phe in regulating functional cooperativity of disease-associated "toggle" calcium-sensing receptor mutations

PloS one, 2014-11, Vol.9 (11), p.e113622

2014

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Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations

The New England journal of medicine, 2016-04, Vol.374 (14), p.1396-1398

2016

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Topical siRNA delivery to the cornea and anterior eye by hybrid silicon-lipid nanoparticles

Journal of controlled release, 2020-10, Vol.326, p.192-202

2020

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Personalised genome editing – The future for corneal dystrophies

Progress in retinal and eye research, 2018-07, Vol.65, p.147-165

2018

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Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

The journal of clinical endocrinology and metabolism, 2012-10, Vol.97 (10), p.E1995-E2005

2012

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Pupil influence on the quality of vision in rotationally asymmetric multifocal IOLs with surface-embedded near segment

Journal of cataract and refractive surgery, 2017-11, Vol.43 (11), p.1420-1429

2017

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Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway

PloS one, 2016-12, Vol.11 (12), p.e0167916

2016

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Protein Composition of TGFBI-R124C- and TGFBI-R555W-Associated Aggregates Suggests Multiple Mechanisms Leading to Lattice and Granular Corneal Dystrophy

Investigative ophthalmology & visual science, 2015-07, Vol.56 (8), p.4653-4661

2015

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Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders

Scientific reports, 2017-11, Vol.7 (1), p.16174-11, Article 16174

2017

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Unique role for translation initiation factor 3 in the light color regulation of photosynthetic gene expression

Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (40), p.16253-16258

2013

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An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

The Journal of clinical investigation, 2005-10, Vol.115 (10), p.2822-2831

2005

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SEDLIN forms homodimers: characterisation of SEDLIN mutations and their interactions with transcription factors MBP1, PITX1 and SF1

PloS one, 2010-05, Vol.5 (5), p.e10646-e10646

2010

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Abstract 11054: A Novel Method of Conjunctival Vascular Screening to Detect Hemodynamic Alterations in Patients with Coronary Microvascular Disease

Mutations Affecting G-Protein Subunit α11 in Hypercalcemia and Hypocalcemia

Appraisal of Cardiovascular Risk Factors, Biomarkers, and Ocular Imaging in Cardiovascular Risk Prediction

Visual quality and performance comparison between 2 refractive rotationally asymmetric multifocal intraocular lenses

User experience analysis of AbC-19 Rapid Test via lateral flow immunoassays for self-administrated SARS-CoV-2 antibody testing

A novel algorithm for cardiovascular screening using conjunctival microcirculatory parameters and blood biomarkers

User experience of home-based AbC-19 SARS-CoV-2 antibody rapid lateral flow immunoassay test

Assessment of the conjunctival microcirculation for patients presenting with acute myocardial infarction compared to healthy controls

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Evaluation of TGFBI corneal dystrophy and molecular diagnostic testing

Visual outcomes and patient satisfaction 3 and 12 months after implantation of a refractive rotationally asymmetric multifocal intraocular lens

Comparison of the visual performance and quality of vision with combined symmetrical inferonasal near addition versus inferonasal and superotemporal placement of rotationally asymmetric refractive multifocal intraocular lenses

Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3

Role of Ca2+ and L-Phe in regulating functional cooperativity of disease-associated "toggle" calcium-sensing receptor mutations

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations

Topical siRNA delivery to the cornea and anterior eye by hybrid silicon-lipid nanoparticles

Personalised genome editing – The future for corneal dystrophies

Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas

Pupil influence on the quality of vision in rotationally asymmetric multifocal IOLs with surface-embedded near segment

Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway

Protein Composition of TGFBI-R124C- and TGFBI-R555W-Associated Aggregates Suggests Multiple Mechanisms Leading to Lattice and Granular Corneal Dystrophy

Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disorders

Unique role for translation initiation factor 3 in the light color regulation of photosynthetic gene expression

An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidism

SEDLIN forms homodimers: characterisation of SEDLIN mutations and their interactions with transcription factors MBP1, PITX1 and SF1

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