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Indian J Dermatol
April 2024
From the Department of Dermatology, Venereology, and Leprology, Postgraduate Institute of Medical Education and Research, Sector 12, Chandigarh, India.
Background: Congenital ichthyoses are a rare Mendelian group of disorders affecting the integument with a heterogeneous clinical presentation amongst which scaling is a constant feature. There is scanty epidemiologic data regarding the clinical profile and histologic patterns of inherited ichthyosis from resource-poor countries.
Aims And Objectives: The study was aimed at assessing the clinic-epidemiologic characteristics associated with the different forms of non-syndromic congenital ichthyosis.
Am J Trop Med Hyg
March 2023
Internal Medicine, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.
We update results from the Mycotic Infections in COVID-19 (MUNCO) Registry, May-September 2021. Data collection from May to September 2021 yielded 728 cases from India, Nepal, Bangladesh, Thailand, and the United States. The cases consisted of mostly mucormycosis (97.
View Article and Find Full Text PDFCancer Med
March 2023
Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Introduction: Analyzing longitudinal cancer quality-of-life (QoL) measurements and their impact on clinical outcomes may improve our understanding of patient trajectories during systemic therapy. We applied an unsupervised growth mixture modeling (GMM) approach to identify unobserved subpopulations ("patient clusters") in the CO.20 clinical trial longitudinal QoL data.
View Article and Find Full Text PDFProstate Cancer Prostatic Dis
March 2024
Department of Urology, University of Texas Health San Antonio, San Antonio, TX, USA.
Indian J Ophthalmol
February 2022
Department of Radiology, All India Institute of Medical Sciences, Patna, Bihar, India.
Purpose: To elucidate the clinico-epidemiologic characteristics of optic neuritis based on the status of serum aquaporin-4 antibody (AQP4-Ab) in patients with optic neuritis (ON).
Methods: Medical records of 106 patients with ON and a follow-up of 3 years were reviewed. For each patient, the following data were extracted: medical history, findings of the ocular examination, brain, orbital or spinal MRI, and serological tests for AQP4.
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