Results 11 to 20 of about 137,274 (148)
Enfermedad de Vogt Koyanagi Harada Bilateral: Reporte de un Caso [PDF]
Objetivo: Reportar el caso de una paciente diagnosticada con Enfermedad de Vogt Koyanagi Harada bilateral. Caso Clínico: Paciente femenina de 42 años, sin antecedentes médicos de importancia, quien consulta por visión borrosa en ojo derecho de 2 ...
Flor de María Chew Florián
doaj +3 more sources
Síndrome de Vogt-Koyanagi-Harada [PDF]
El síndrome de Vogt-Koyanagi-Harada es una enfermedad con hallazgos dermatológicos, neurológicos y auditivos, asociada con una panuveítis granulomatosa bilateral.
Juan Carlos Serna-Ojeda +1 more
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Echographic findings in the late stages of Vogt-Koyanagi-Harada disease in mexican population
Purpose: To correlate clinical findings of Vogt-Koyanagi-Harada disease with standardized echography findings in a cross-sectional, descriptive and observational study.
Mariana Mayorquín-Ruiz +4 more
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Vogt‐Koyanagi‐Harada disease‐like uveitis induced by nivolumab in metastatic renal cell carcinoma
Introduction Nivolumab can cause various immune‐related adverse events; it rarely induces Vogt‐Koyanagi‐Harada‐disease‐like uveitis. Vogt‐Koyanagi‐Harada‐disease is reported to be closely associated with human leukocyte antigen‐DR4.
Hitomi Imai +9 more
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Síndrome de Vogt Koyanagi Harada [PDF]
Se presenta el caso de una paciente femenina de 28 años de edad, con síndrome de Vogt Koyanagi Harada (SVKH), con síntomas acompañantes de dolor ocular, cefalea y disminución de la visión en ambos ojos y con signos de hipoacusia e irritación meníngea. Se
Brunilda de los Angeles Aveleira Ortiz +2 more
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Premature Ovarian Insufficiency in a Patient With Vogt-Koyanagi-Harada Syndrome: An Unusual Association-A Case Report. [PDF]
Premature ovarian insufficiency (POI) is a clinical syndrome characterized by ovarian failure in women of reproductive age before the age of 40 years. Its main manifestations include menstrual cycle disturbances, such as oligomenorrhea or amenorrhea. The etiology of POI is highly heterogeneous, with a particular emphasis on genetic and immunological ...
Rocha RB +7 more
europepmc +2 more sources
OBJECTIVES: The objectives of this study are to review our current knowledge of the aetiopathogenesis of Vogt-Koyanagi-Harada syndrome, including viral infection, genetic factors and immunomediated mechanisms, and to discuss pathogenesis and its ...
Pratik K. Shah +3 more
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Vogt-Koyanagi-Harada disease. [PDF]
Vogt-Koyanagi-Harada disease is a rare, multisystem, autoimmune disorder with numerous clinical manifestations, mediated through a T-helper 1 response against melanocytes in the eye, inner ear, central nervous system, hair and skin. We describe a 20-year-
Mollan, Susan P +3 more
core +2 more sources
Single-cell RNA-sequencing and chromatin accessibility analysis reveal transcriptomic and epigenomic changes between healthy patients and those affected by the systemic autoimmune disorder Vogt-Koyanagi-Harada disease.
Wen Shi +9 more
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Key Clinical Message A patient with metastatic cutaneous malignant melanoma developed Vogt‐Koyanagi‐Harada disease‐like posterior uveitis after two nivolumab (anti‐PD‐1 antibody) injections.
Toshihiko Matsuo, Osamu Yamasaki
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