نتائج البحث

Aberrant gene expression yet undiminished retinal ganglion cell genesis in iPSC-derived models of optic nerve hypoplasia.

• Authors : Aparicio, Jennifer G.¹ (AUTHOR); Hopp, Hanno¹ (AUTHOR); Harutyunyan, Narine¹ (AUTHOR)

• Source: Ophthalmic Genetics. Feb2024, Vol. 45 Issue 1, p1-15. 15p.

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Optic nerve abnormalities in female-restricted Wieacker-Wolff syndrome by a novel variant in the ZC4H2 gene.

• Authors : Ibarra-Ramírez, Marisol¹ (AUTHOR); Fernandez-de-Luna, Marissa L² (AUTHOR); Campos-Acevedo, Luis D¹ (AUTHOR)

• Source: Ophthalmic Genetics. Oct2023, Vol. 44 Issue 5, p465-468. 4p.

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Hereditary motor and sensory neuropathy type VIA with optic nerve pallor in two sisters with pathologic myopia: a case series and review.

• Authors : Babu, Kevin¹ (AUTHOR); Seamon, Kimberly^1,2 (AUTHOR); Jewell, Ann³ (AUTHOR)

• Source: Ophthalmic Genetics. Aug2023, Vol. 44 Issue 4, p379-384. 6p.

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Optic nerve involvement in CACNA1F-related disease: observations from a multicentric case series.

• Authors : Marziali, Elisa¹ (AUTHOR); Van Den Broeck, Filip² (AUTHOR); Bargiacchi, Sara³ (AUTHOR)

• Source: Ophthalmic Genetics. Apr2023, Vol. 44 Issue 2, p152-162. 11p.

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Retinal and optic nerve relapse in retinoblastoma secondary to epiretinal and epipapillary vitreous seeds implantation documented by optical coherence tomography.

• Authors : Stathopoulos, Christina¹ (AUTHOR) ; Tripathy, Devjyoti^1,2 (AUTHOR); Moulin, Alexandre¹ (AUTHOR)

• Source: Ophthalmic Genetics. Dec2022, Vol. 43 Issue 6, p850-854. 5p.

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Osteopathia striata with cranial sclerosis causing a compressive optic neuropathy.

• Authors : Hu JCW; Harkness Eye Institute, Department of Ophthalmology, Columbia University Irving Medical Center, New York, NY, USA.; Abdelhakim AH

Subjects: Osteosclerosis*/Osteosclerosis*/Osteosclerosis*/complications ; Osteosclerosis*/Osteosclerosis*/Osteosclerosis*/genetics ; Osteochondrodysplasias* Osteopathia striata cranial sclerosis

• Source: Ophthalmic genetics [Ophthalmic Genet] 2023 Oct; Vol. 44 (5), pp. 496-500. Date of Electronic Publication: 2022 Nov 29.Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Full-width postlaminar optic nerve tumor invasion of retinoblastoma as risk-factor for leptomeningeal spread of retinoblastoma. A case report and review of the literature.

• Authors : de Jong, Marcus C.¹ (AUTHOR) ; Van Der Valk, Paul² (AUTHOR); Jansen, Robin W.¹ (AUTHOR)

• Source: Ophthalmic Genetics. Feb2020, Vol. 41 Issue 1, p69-72. 4p.

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Expanding the mutational spectrum of FHONDA syndrome.

• Authors : Shoji, Marissa K.¹ (AUTHOR) ; Khodeiry, Mohamed M.¹ (AUTHOR); Sengillo, Jesse D.¹ (AUTHOR)

• Source: Ophthalmic Genetics. Dec2023, Vol. 44 Issue 6, p602-605. 4p.

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Two missense mutations in SALL4 in a patient with microphthalmia, coloboma, and optic nerve hypoplasia

• Authors : Ullah, E; Wu, D; Madireddy, L

Subjects: Biomedical and Clinical Sciences; Ophthalmology and Optometry; Pediatric

• Source: Ophthalmic Genetics. 38(4)

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The Optic Nerve Head in Congenital Fibrosis of the Extraocular Muscles.

• Authors : Khan, Arif O.^1,2 (AUTHOR) ; Shinwari, Jameela² (AUTHOR); Omar, Aisha² (AUTHOR)

• Source: Ophthalmic Genetics. Sep2011, Vol. 32 Issue 3, p175-180. 6p.

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