Hasil Pencarian - Catherin I. Negron

  • Menampilkan 1 - 7 hasil dari 7
Perbaiki Hasil
  1. 1
    Case report: Vitreous hemorrhage as the presenting sign of retinal cavernous hemangioma in a newborn

    Case report: Vitreous hemorrhage as the presenting sign of retinal cavernous hemangioma in a newborn oleh Benjamin J. Fowler, Lilla Simon, Nathan L. Scott, Catherin I. Negron, Audina M. Berrocal

    Diterbitkan 2021-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    CRVO associated with COVID-19 and MTHFR mutation in a 15-year-old male

    CRVO associated with COVID-19 and MTHFR mutation in a 15-year-old male oleh Patrick C. Staropoli, Alison Payson, Catherin I. Negron, Supalert Prakhunhungsit, Pablo Laufer, Audina M. Berrocal

    Diterbitkan 2022-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Foveal photoreceptor atrophy, persistent fetal vasculature, congenital cataracts, and microphthalmia in a pediatric patient with BCOR-associated oculo-facio-cardio-dental (OFCD) syndrome

    Foveal photoreceptor atrophy, persistent fetal vasculature, congenital cataracts, and microphthalmia in a pediatric patient with BCOR-associated oculo-facio-cardio-dental (OFCD) sy... oleh Jason Fan, Natasha Ferreira Santos da Cruz, Catherin I. Negron, Angela Y. Zhu, Ta C. Chang, Audina M. Berrocal

    Diterbitkan 2024-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Familial exudative vitreoretinopathy associated with retinal astrocytic hamartoma

    Familial exudative vitreoretinopathy associated with retinal astrocytic hamartoma oleh Jason Fan, Nandini Venkateswaran, Kenneth C. Fan, Linda A. Cernichiaro, Catherin I. Negron, Craig A. McKeown, Audina M. Berrocal

    Diterbitkan 2022-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    A patient with concurrent Axenfeld-Rieger and Stickler syndromes verified by molecular genetics

    A patient with concurrent Axenfeld-Rieger and Stickler syndromes verified by molecular genetics oleh Jason Fan, Natasha Ferreira Santos da Cruz, Kenneth C. Fan, Catherin I. Negron, Guillermo Amescua, Alana L. Grajewski, Ta C. Chang, Audina M. Berrocal

    Diterbitkan 2023-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    A unique case of vision loss in a patient with hypotrichosis and juvenile macular dystrophy and primary ciliary dyskinesia

    A unique case of vision loss in a patient with hypotrichosis and juvenile macular dystrophy and primary ciliary dyskinesia oleh Kenneth C. Fan, Nimesh A. Patel, Nicolas A. Yannuzzi, Supalert Prakhunhungsit, Catherin I. Negron, Elisa Basora, Andrew A. Colin, Mustafa Tekin, Audina M. Berrocal

    Diterbitkan 2019-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Peripheral combined hamartoma of the retina and retinal pigment epithelium with remote peripapillary choroidal neovascular membrane

    Peripheral combined hamartoma of the retina and retinal pigment epithelium with remote peripapillary choroidal neovascular membrane oleh Thomas A. Lazzarini, Hasenin Al-khersan, Nimesh A. Patel, Jonathan F. Russell, Kenneth C. Fan, Giselle De Oliveira, Catherin I. Negron, Elias Mavrofrides, Audina M. Berrocal

    Diterbitkan 2020-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: