Results 51 to 60 of about 5,254,199 (223)
Letter from Addison Lyman on lectures [PDF]
Letter from Addison Lyman to his brother, Reverend Horace Lyman, discussing upcoming ...
Lyman, Addison
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Deputy Marshal Addison Beck’s diary from April to August 1881. This journal records Beck’s travels through the Indian Territory and the expenses he incurred along the way.
Beck, Addison, 1845-1883
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Coexistence of Addison′s disease and systemic lupus erythematosus (SLE) is a rare occurrence with only few reported cases in the literature. We describe a 29-year-old woman who presented to us with clinical features of acute Addisonian crisis and SLE ...
Okwuonu Chimezie Godswill +1 more
doaj
Autoimmune oophoritis: A rarely encountered ovarian lesion
Autoimmune oophoritis is a rare disorder causing ovarian failure clinically characterized by amenorrhea and infertility. It often occurs in a setting of autoimmune polyendocrine syndromes.
Sunitha Jacob, Murat Koc
doaj +1 more source
Integrated approach to menopausal hormone therapy in women with cardiovascular risk factors or established ischemic heart disease, from early treatment initiation and risk stratification to individualized therapy, multidisciplinary follow‐up, and health‐system recommendations.
Chiara Benedetto +9 more
wiley +1 more source
Video footage from the WBAP-TV television station in Fort Worth, Texas, to accompany a news story about John Milton Addison and his uranium refining ...
WBAP-TV (Television station : Fort Worth, Tex.)
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Paediatric Melanonychia: Diagnosis and Management
ABSTRACT Longitudinal melanonychia (LM) in children presents unique diagnostic and management challenges that cannot be adequately addressed by applying adult‐based criteria. Unlike in adults, there are no validated clinical, dermoscopic or histopathologic criteria for predicting nail unit melanoma in the paediatric population.
Angela J. Jiang +5 more
wiley +1 more source
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases
X-linked adrenoleukodystrophy (x-ALD) is a rare genetic disorder caused by a mutation in the ABCD1 gene, which encodes for a peroxisomal very long chain fatty acid transporter.
Matteo Foschi +12 more
doaj +1 more source
Abstract Objective To evaluate the effectiveness of objective audiological and vestibular assessments in detecting functional changes associated with vitamin B12 deficiency. Data Sources A comprehensive literature search was conducted in PubMed, Scopus, Web of Science, and EMBASE databases.
Nesmah Zainab +2 more
wiley +1 more source
Deputy Marshal Addison Beck’s diary from 1880-1881. This journal records Beck’s travels through the Indian Territory and the expenses he incurred along the way. Part of the beginning of the book was used by Larkin and Ira Beck to record some information,
Beck, Addison, 1845-1883
core +1 more source

