Search Results - "Naguib, Mina M"

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  1. 1

    Atypical Pituitary Adenoma with Orbital Invasion: Case Report and Review of the Literature by Naguib, Mina M., BS, Mendoza, Pia R., MD, Jariyakosol, Supharat, MD, Grossniklaus, Hans E., MD

    Published in Survey of ophthalmology (01-11-2017)
    “…Abstract Pituitary adenoma invasion into the orbit is a rare phenomenon with only 22 cases, including the present case, in the literature. Our case is a…”
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    Journal Article
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    Locally Invasive Diffuse Iris Ring Melanoma Presenting as Unilateral Severe Glaucoma: Case Report and Review of Molecular Genetics by Naguib, Mina M., Chévez-Barrios, Patricia, Orengo-Nania, Silvia, Schefler, Amy C.

    Published in Case reports in oncology (01-01-2021)
    “…We report the clinical history and histopathological findings in a case of diffuse iris ring melanoma (DIM) and review the most recent literature and modern…”
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    Journal Article
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    ENDOPHTHALMITIS AFTER INTRAVITREAL INJECTIONS DURING THE COVID-19 PANDEMIC WITH IMPLEMENTATION OF UNIVERSAL MASKING by Naguib, Mina M., Ghauri, Sophia, Mukhopadhyay, Anirudh, Schefler, Amy C.

    Published in Retina (Philadelphia, Pa.) (01-11-2021)
    “…To evaluate the rates of post-intravitreal injection related endophthalmitis during the COVID-19 pandemic with institution of both physician and patient face…”
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    Journal Article
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    Characteristic Visual Field Defect From Lateral Geniculate Body Stroke by Naguib, Mina M., Woodland, Matthew B., Foroozan, Rod

    Published in Journal of neuro-ophthalmology (01-12-2021)
    “…A 58-year-old man presented with a complaint of subjective visual field loss on the right side and hypertensive emergency. Examination revealed a right…”
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    Evolution of the ‘omega sign’ on optical coherence tomography by Ramakrishnan, Meera S., Naguib, Mina M., Modi, Yasha S.

    Published in Retinal cases & brief reports (01-03-2024)
    “…To present the early postoperative evolution of retained subretinal perfluoro- n -octane (PFO) as captured on optical coherence tomography. Case report of a…”
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    Modified Rapid AChE Method (MRAM) for Hirschsprung Disease Diagnosis: A Journey from Meier-Ruge Until Now by Naguib, Mina M., Robinson, Haynes, Shoffeitt, Carla, Howe, Helena, Metry, Diana, Shehata, Bahig M.

    Published in Fetal and pediatric pathology (01-11-2016)
    “…Hirschsprung disease (HSCR) can be diagnosed using a variety of histological and immunohistochemical methods and stains. Because of the nature of the condition…”
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    Journal Article
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    Xeroderma Pigmentosa: Three New Cases with an In Depth Review of the Genetic and Clinical Characteristics of the Disease by Karass, Michael, Naguib, Mina M., Elawabdeh, Nancy, Cundiff, Caitlin A., Thomason, Jenna, Steelman, Charlotte Katherine, Cone, Ryan, Schwenkter, Ann, Jordan, Caroline, Shehata, Bahig M.

    Published in Fetal and pediatric pathology (01-04-2015)
    “…Xeroderma pigmentosum (XP) is a rare autosomal recessive disorder characterized by hypersensitivity of the skin and eyes to UV-radiation as a result of a…”
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    Journal Article
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    Neurothekeoma of the Cornea by Naguib, Mina M., Craven, Caroline, Kozarsky, Alan, Grossniklaus, Hans E.

    Published in Ocular oncology and pathology (01-10-2016)
    “…Neurothekeomas (NTKs) are benign cutaneous neoplasms of fibrohistiocytic origin and most commonly occur in the head, neck, and upper extremities…”
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    Spinal Cysticercosis Mimicking a Tumor in a Pediatric Patient by Naguib, Mina M., Abramowsky, Carlos R., Shehata, Bahig M.

    Published in Fetal and pediatric pathology (01-04-2012)
    “…Parasitic infections of the central nervous system (CNS) occur mostly in underdeveloped regions of the world. Neurocysticercosis (NC) occurs when the larval…”
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  13. 13

    The Spectrum of Pulmonary Malformation in Trisomy-21 Patient. A Review with Emphasis on the Molecular-Genetic Basis by Salinas, Mark, Elawabdeh, Nancy, Lin, Jenny, Naguib, Mina M., Hodge, Melissa G., Shehata, Bahig M.

    Published in Fetal and pediatric pathology (01-02-2013)
    “…Gene overexpression has been identified as a primary determining factor for the distinct Down syndrome (DS) phenotypes. Previous genetic research has…”
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    Journal Article
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