المؤلفون: Salvatore Michele Carnazzo

المصدر: Euromediterranean Biomedical Journal, Vol 18, Iss 22, Pp 103-107 (2023)

مصطلحات موضوعية: dandy-walker complex, posterior cranial fossa malformation, adie's pupil, ocular malformations, foxc1 gene, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: http://www.embj.org/wp-content/uploads/2023/10/Carnazzo_22.pdf; https://doaj.org/toc/2279-7165

URL الوصول: https://doaj.org/article/2e4defbb814340b8ace93b4c429c3c41

المؤلفون: Pasquale Scoppettuolo, Noémie Ligot, Vanessa Wermenbol, Patrick Van Bogaert, Gilles Naeije

المصدر: Frontiers in Neurology, Vol 11 (2020)

مصطلحات موضوعية: COL4A1, Type IV collagen, familial porencephaly, ocular malformations, variable expressivity, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fneur.2020.00827/full; https://doaj.org/toc/1664-2295

URL الوصول: https://doaj.org/article/8189f02a172d41d9b84459e0af271d51

المؤلفون: Jakkidi Prathibha Reddy, Prabhu M Shanker, Geetha Ganesan, Rajesh Prabu

المصدر: Indian Journal of Ophthalmology, Vol 67, Iss 1, Pp 129-131 (2019)

مصطلحات موضوعية: Central nervous system malformations, no light perception, ocular malformations, Optic nerve aplasia, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.ijo.in/article.asp?issn=0301-4738;year=2019;volume=67;issue=1;spage=129;epage=131;aulast=Reddy; https://doaj.org/toc/0301-4738; https://doaj.org/toc/1998-3689

URL الوصول: https://doaj.org/article/067f9ec5889c4d9e872a5cbd3aae7515

المؤلفون: Scoppettuolo, Pasquale, Ligot, Noemie, Wermenbol, Vanessa, Van Bogaert, Patrick, Naeije, Gilles

المصدر: Frontiers in neurology, 11

مصطلحات موضوعية: Neurologie, COL4A1, familial porencephaly, ocular malformations, Type IV collagen, variable expressivity

وصف الملف: 1 full-text file(s): application/pdf

Relation: uri/info:doi/10.3389/fneur.2020.00827; uri/info:scp/85091519541; https://dipot.ulb.ac.be/dspace/bitstream/2013/313655/4/doi_297299.pdf; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/313655

الاتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/313655
https://dipot.ulb.ac.be/dspace/bitstream/2013/313655/4/doi_297299.pdf

المؤلفون: КУТИМОВА ВЕРА ГАВРИЛОВНА, КУТИМОВА ЕЛЕНА ЮРЬЕВНА

مصطلحات موضوعية: ДЕРМОИД РОГОВИЦЫ И КОНЪЮНКТИВЫ,ВРОЖДЕННЫЕ АНОМАЛИИ РАЗВИТИЯ ГЛАЗА,СИНДРОМ ГОЛЬДЕНХАРА,CORNEAL AND CONJUNCTIVAL DERMOID,CONGENITAL OCULAR MALFORMATIONS,GOLDENHAR SYNDROME

وصف الملف: text/html

الاتاحة: http://cyberleninka.ru/article/n/dermoid-rogovitsy-sindrom-goldenhar-klinicheskiy-sluchay
http://cyberleninka.ru/article_covers/16553077.png

المؤلفون: Rajesh S Joshi

المصدر: Journal of Clinical Ophthalmology and Research, Vol 1, Iss 1, Pp 17-19 (2013)

مصطلحات موضوعية: Congenital ocular malformations, disability evaluation, visual acuity, visual handicap, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.jcor.in/article.asp?issn=2320-3897;year=2013;volume=1;issue=1;spage=17;epage=19;aulast=Joshi; https://doaj.org/toc/2320-3897

URL الوصول: https://doaj.org/article/5adb782283cb4984af77b0a5eed76251

المؤلفون: G.P , Dr. Pavanalakshmi, Naidu, Dr. Jaya, Tambakad, Dr. Pavan B

المصدر: Case Reports in Odontology, 02(01), 01-06, (2015-02-23)

مصطلحات موضوعية: Anterior segment, dysgenesis, ocular malformations, Axenfeld-Reiger syndrome, Peters’ anomaly

Relation: https://doi.org/; https://doi.org/10.5281/zenodo.15652; oai:zenodo.org:15652

الاتاحة: https://doi.org/10.5281/zenodo.15652

المؤلفون: Teär Fahnehjelm, Kristina

المساهمون: Karolinska Institutet, Dept of Clinical Neuroscience, Publisher, Karolinska Institutet, Inst för klinisk neurovetenskap, Publisher

مصطلحات موضوعية: MEDICAL AND HEALTH SCIENCES, MEDICIN OCH HÄLSOVETENSKAP, Teratology, ocular malformations, visual impairment, anti-epileptic drugs, congenital infection, optic nerve hypoplasia, coloboma, magnetic resonance imaging, neonatal cholestasis, dried blood spots

وصف الملف: electronic

URL الوصول: http://hdl.handle.net/10616/43021

المؤلفون: Prabhu M Shanker, Rajesh V Prabu, Geetha Ganesan, Jakkidi Prathibha Reddy

المصدر: Indian Journal of Ophthalmology, Vol 67, Iss 1, Pp 129-131 (2019)
Indian Journal of Ophthalmology

مصطلحات موضوعية: Male, Anterior Visual Pathway, business.industry, Optic nerve aplasia, Visual Acuity, Optic Nerve, Anatomy, Aplasia, Central nervous system malformations, medicine.disease, Magnetic Resonance Imaging, Photo Essay, Ophthalmology, lcsh:Ophthalmology, no light perception, lcsh:RE1-994, Optic Nerve Diseases, medicine, Visual Perception, Humans, Visual Pathways, business, Child, ocular malformations

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba4bb7c7c269c0b3a8924d17eebe3184
http://www.ijo.in/article.asp?issn=0301-4738;year=2019;volume=67;issue=1;spage=129;epage=131;aulast=Reddy

المصدر: Вестник Тамбовского университета. Серия: Естественные и технические науки.

مصطلحات موضوعية: ДЕРМОИД РОГОВИЦЫ И КОНЪЮНКТИВЫ,ВРОЖДЕННЫЕ АНОМАЛИИ РАЗВИТИЯ ГЛАЗА,СИНДРОМ ГОЛЬДЕНХАРА,CORNEAL AND CONJUNCTIVAL DERMOID,CONGENITAL OCULAR MALFORMATIONS,GOLDENHAR SYNDROME

وصف الملف: text/html

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______2806::10ff3c8cd8b6cc7fba35a19dc5a39892
http://cyberleninka.ru/article_covers/16553077.png

المؤلفون: Robert W. Sault, Jeffrey Sheridan

المصدر: Ophthalmology and Eye Diseases, Vol 2013, Iss 5, Pp 1-3 (2013)
Ophthalmology and Eye Diseases, Vol 5 (2013)
Ophthalmology and Eye Diseases

مصطلحات موضوعية: genetic structures, lcsh:Ophthalmology, lcsh:RE1-994, Short Report, eye diseases, genetic disorders, sense organs, Peters’ anomaly, sensory amblyopia, ocular malformations

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9929a09519c2a139e186c0f241fc06a
http://la-press.com/peters-anomaly-article-a3537

المؤلفون: Su, CS, O'Hagen, SB, Sullivan, TJ

مصطلحات موضوعية: branchial cleft, branchio-oculo-facial syndrome, nasolacrimal obstruction, ocular malformations, punctal agenesis, Branchiooculofacial Syndrome, Spectrum

Relation: orcid:0000-0002-7380-4339

الاتاحة: https://espace.library.uq.edu.au/view/UQ:406825

المؤلفون: Robert W. Sault, Jeffrey Sheridan

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.la-press.com/redirect_file.php?fileId%3D4773%26fileType%3Dpdf%26filename%3D3537-OED-Peters%E2%80%99-Anomaly-.pdf.

مصطلحات موضوعية: Peters ’ anomaly, genetic disorders, eye diseases, sensory amblyopia, ocular malformations Sault and Sheridan 2 Ophthalmology and Eye Diseases 2013

Time: 5

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.686.7972; http://www.la-press.com/redirect_file.php?fileId%3D4773%26fileType%3Dpdf%26filename%3D3537-OED-Peters%E2%80%99-Anomaly-.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.686.7972
http://www.la-press.com/redirect_file.php?fileId%3D4773%26fileType%3Dpdf%26filename%3D3537-OED-Peters%E2%80%99-Anomaly-.pdf