Results 21 to 30 of about 26,665,333 (179)

Addison’s Disease: Diagnosis and Management Strategies

open access: yesInternational Journal of General Medicine, 2023
Mara Carsote,1,2 Claudiu Nistor3,4 1Department of Endocrinology, Faculty of Medicine, “Carol Davila” University of Medicine and Pharmacy, Bucharest, Romania; 2Department of Gonads and Infertility, “C.I.
Carsote M, Nistor C
doaj  

Cure of Psoriasis and Arthritis when Addison’s Disease Was Detected

open access: yesCase Reports in Dermatology, 2010
Introduction: Corticoid therapy is well-known to improve the symptoms of psoriasis. Addison’s disease is an autoimmune disease which leads to a loss of cortisol production in the adrenal glands.
Marcus Lind
doaj   +1 more source

Extreme Hyponatremia Complicated by Osmotic Demyelination in a Previously Healthy Young Individual

open access: yesCanadian Journal of Kidney Health and Disease, 2022
Rationale: Severe hyponatremia can lead to dramatic complications whether it is treated or not. At times, it may be very severe (serum Na concentration: Na S < 115 mmol/L) or even extreme (Na S < 105 mmol/L) a and its cause difficult to identify ...
Nicholas Quigley   +3 more
doaj   +1 more source

Megaloblastic Anemia in a Patient with Addison’s Disease: A Case Report [PDF]

open access: yesInternational Journal of Hematology-Oncology and Stem Cell Research, 2010
"nAbstract "nPrimary adrenal insufficiency (Addison&rsquo;s disease) is due to adrenocortical disease. This study is about a 40 year old man who had been referred to a hematologist who assessed him for anemia.
Shahrbanou Keyhanian   +3 more
doaj  

Thymic hyperplasia in Graves′ disease

open access: yesIndian Journal of Endocrinology and Metabolism, 2013
Graves′ disease is an autoimmune thyroid condition characterized by the production of autoantibodies against the thyrotropin receptor. It is known to be associated with autoimmune conditions such as myasthenia gravis, Addison′s disease, type 1 diabetes ...
Narendra Kotwal   +3 more
doaj   +1 more source

Achalasia in a Patient with Polyglandular Autoimmune Syndrome Type II

open access: yesCase Reports in Gastroenterology, 2015
Achalasia is a rare disease characterized by aperistalsis of the esophageal body and failure of the lower esophageal sphincter to relax. The etiology of this disease remains unknown.
Bashar S. Amr, Chaitanya Mamillapalli
doaj   +1 more source

Autoimmune oophoritis: A rarely encountered ovarian lesion

open access: yesIndian Journal of Pathology and Microbiology, 2015
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

Acute adrenal insufficiency due to primary antiphospholipid antibody syndrome

open access: yesIndian Journal of Endocrinology and Metabolism, 2013
Introduction: We report a case of acute adrenal insufficiency (AAI) in a patient with antiphospholipid syndrome (APS). Case Report: A 44-year-old female patient presented to us with acute abdominal pain associated with recurrent vomiting and giddiness ...
Kishore Kumar Behera   +3 more
doaj   +1 more source

Long‐Term Efficacy of Immunotherapy in Autoimmune Autonomic Ganglionopathy—A 10‐Year Follow Up Study

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Autoimmune autonomic ganglionopathy (AAG) is a rare but potentially treatable cause of severe autonomic failure. Evidence guiding long‐term immunotherapy, treatment sequencing, and residual autonomic impairment is limited. We evaluated long‐term treatment response, residual autonomic dysfunction, and relapse patterns in patients with
Giacomo Chiaro   +6 more
wiley   +1 more source

Posterior Disconnection Syndrome in Early‐Stage Adult‐Onset Cerebral Adrenoleukodystrophy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adult‐onset cerebral adrenoleukodystrophy is potentially treatable but often difficult to recognize before advanced cerebral involvement. Herein, we describe three men with early‐stage disease who initially presented with subtle visual complaints rather than subcortical dementia. Targeted neuropsychological testing revealed higher‐order visual
Kazuto Katsuse   +13 more
wiley   +1 more source

Home - About - Disclaimer - Privacy