Search Results - "Knight LSW"

Author Index.

Source: Clinical & Experimental Ophthalmology. Feb2022, Vol. 49 Issue 8, p978-984. 7p.

Psychological distress and psychosocial care in adults with glaucoma in Africa: A systematic review protocol.

Authors: Kosoku, Chelsea Charlyne Andoh, Albert Kwadjo Amoah Akuffo, Constance Kukuaa et al.

Source: PLoS ONE. 7/21/2026, Vol. 21 Issue 7, p1-12. 12p.

"Getting to diagnosis was an absolute nightmare": survey insights about the lived experience of spinal CSF leak in Australia and Aotearoa New Zealand.

Authors: Knight LSW Smith RL Britten-Jones AC et al.

Source: Journal of neurology [J Neurol] 2026 Apr 30; Vol. 273 (5). Date of Electronic Publication: 2026 Apr 30.

Publication Type: Journal Article

Journal Info: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0423161 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-1459 (Electronic) Linking ISSN: 03405354 NLM ISO Abbreviation: J Neurol Subsets: MEDLINE

Emotional and Caregiver Burden in Adults with Glaucoma-Related Blindness at a Chinese Tertiary Center.

Authors: Luo, Zhonghua Konatsu, Kojima Yang, Yu et al.

Source: Clinical Ophthalmology. Apr2026, Vol. 20, p1-13. 13p.

A de novo FBN1 variant likely causes congenital bilateral ectopia lentis in a crossbred horse.

Authors: Esdaile, Elizabeth Houston, Kristopher Till, Bradley J. et al.

Source: Scientific Reports. 10/24/2025, Vol. 15 Issue 1, p1-9. 9p.

Correlation of Scleral Rigidity and Corneal Stress-Strain Measurements with Induced Elevation of Intraocular Pressure in Healthy Eyes.

Authors: Boschetti, Graziela Seki, Valeria Batista Boreck Prata, Tiago Santos et al.

Source: Current Eye Research. Sep2025, Vol. 50 Issue 9, p934-939. 6p.

Genome sequencing reveals novel variants in a diverse population with congenital anterior segment anomalies.

Authors: Hussain, Ashraf Villalba, Maria Fernanda Swols, Dayna Morel et al.

Source: Scientific Reports. 1/4/2025, Vol. 14 Issue 1, p1-8. 8p.

Analysis of early-onset glaucoma genes in primary congenital glaucoma patients residing in North India identifies an additional case with THBS1 Arg1034Cys.

Authors: Somarajan, Bindu I Singh, Renu Panigrahi, Arnav et al.

Source: Ophthalmic Genetics. Jun2025, Vol. 46 Issue 3, p276-280. 5p.

Candidate Genes for Non-Syndromic Pediatric Cataracts.

Authors: Rossen, Jennifer L Drackley, Andy Weisman, Allison Goetsch et al.

Source: Clinical Ophthalmology. Mar2026, Vol. 20, p1-19. 19p.

Ectopia lentis associated with a 20-base deletion in the ADAMTSL4 gene in the Old Order Amish population.

Authors: Kuang, Grace Xin, Baozhong Sency, Valerie et al.

Source: Ophthalmic Genetics. Dec2024, Vol. 45 Issue 6, p602-607. 6p.

Deletion of exon 4 of the PITX2 in a child with Axenfeld–Rieger syndrome.

Authors: Tian, Yu Zhou, Xiao-Xia Zhao, Su-Zhou et al.

Source: Ophthalmic Genetics. Dec2024, Vol. 45 Issue 6, p626-632. 7p.

Coronary artery and retinal vascularization by optical coherence tomography angiography: are eyes the window to the heart?

Authors: Sakuno G Sarraf D Sadda SR et al.

Source: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie [Graefes Arch Clin Exp Ophthalmol] 2025 Jun; Vol. 263 (6), pp. 1503-1513. Date of Electronic Publication: 2025 Feb 15.

Publication Type: Journal Article; Review

Journal Info: Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 8205248 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-702X (Electronic) Linking ISSN: 0721832X NLM ISO Abbreviation: Graefes Arch Clin Exp Ophthalmol Subsets: MEDLINE

Axenfeld–Rieger syndrome: orthopedic and orthodontic management in a pediatric patient: a case report.

Authors: Cazzolla, Angela Pia Testa, Nunzio Francesco Spirito, Francesca et al.

Source: Head & Face Medicine. 7/8/2022, Vol. 18 Issue 1, p1-7. 7p.

Unveiling ocular developmental disorders through short-read whole-genome sequencing.

Corporate Authors: AURAGEN consortium

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 Jul 14. Date of Electronic Publication: 2026 Jul 14.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

Caregiver experience following paediatric globe trauma.

Authors: Chu A Ngo A Kraus CL

Source: Eye (London, England) [Eye (Lond)] 2026 Jul 14. Date of Electronic Publication: 2026 Jul 14.

Publication Type: Journal Article

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 8703986 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5454 (Electronic) Linking ISSN: 0950222X NLM ISO Abbreviation: Eye (Lond) Subsets: MEDLINE

Genetic changes and testing associated with childhood glaucoma: A systematic review.

Authors: Kumar, Anika Han, Ying Oatts, Julius T.

Source: PLoS ONE. 2/22/2024, Vol. 19 Issue 2, p1-23. 23p.

A Study on the Candidate Gene Association and Interaction with Measures of UV Exposure in Pseudoexfoliation Patients from India.

Authors: Kandeeban, Suganya Ishwarya, Sureshkumar Nareshkumar, RN. et al.

Source: Current Eye Research. Dec2023, Vol. 48 Issue 12, p1144-1152. 9p.

No Strong Association between the Apolipoprotein E E4 Allele and Glaucoma: A Multicohort Study.

Authors: Mullany S Diaz-Torres S Schmidt JM et al.

Source: Ophthalmology science [Ophthalmol Sci] 2023 Feb 13; Vol. 3 (3), pp. 100287. Date of Electronic Publication: 2023 Feb 13 (Print Publication: 2023).

Publication Type: Journal Article

Journal Info: Publisher: Elsevier, B.V Country of Publication: Netherlands NLM ID: 9918230896206676 Publication Model: eCollection Cited Medium: Internet ISSN: 2666-9145 (Electronic) Linking ISSN: 26669145 NLM ISO Abbreviation: Ophthalmol Sci Subsets: PubMed not MEDLINE

Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants.

Authors: Prem Senthil M Knight LSW Taranath D et al.

Source: Cornea [Cornea] 2022 Aug 01; Vol. 41 (8), pp. 1009-1015. Date of Electronic Publication: 2022 Mar 30.

Publication Type: Journal Article

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8216186 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1536-4798 (Electronic) Linking ISSN: 02773740 NLM ISO Abbreviation: Cornea Subsets: MEDLINE

Coding or non-coding? The question behind sequencing.

Authors: Zonuzi SS; Division of Neuroscience and Neuroscience Institute, The University of Sheffield, Sheffield, UK. s.s.zonuzi@sheffield.ac.uk.

Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 May; Vol. 34 (5), pp. 581-582.

Publication Type: Editorial

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE; In Process