Results 51 to 60 of about 176,111 (167)
A 28-year-old Caucasian male with Hashimoto’s disease and vitiligo presented with two weeks of dizziness on exertion following pharyngitis which was treated with prednisone 40 mg by mouth once a day for five days. Initial workup revealed anemia, elevated
G. F. Cittolin-Santos +3 more
doaj +1 more source
Abstract The aim of this study was to investigate the potential effects of monosodium glutamate (MSG), a known flavour enhancer added to many ready‐to‐eat foods, as a feed additive in rainbow trout (Oncorhynchus mykiss). Evaluating the effects of MSG on aquatic organisms will fill the knowledge gap in this field by monitoring the haematological indices
Gonca Alak +16 more
wiley +1 more source
Relapses, Comorbidities, and Predictors of Outcome in Anti‐GABAA Receptor Encephalitis
Objectives To characterize the magnetic resonance imaging (MRI) lesion dynamics, comorbidities, predictors of relapse, and outcomes in anti‐γ‐aminobutyric acid type A receptor (GABAAR) encephalitis, and assess the utility of LIM‐domain‐only‐protein 5 (LMO5) antibodies as tumor markers.
Claudia Papi +33 more
wiley +1 more source
Multiple Gastric Carcinoids and Pernicious Anemia: Report of a Case
A case of pernicious anemia associated with multiple gastric carcinoids is reported. The neoplastic growth was composed of enterochromaffin-like (ECL) cells, and ECL cell hyperplasia was observed also in hyperplastic polyps, inside the fundic glands and
Alfeo Montesi +3 more
core +1 more source
Well-Differentiated Grade 1 Gastric Neuroendocrine Tumor Occurring 11 Years After Pernicious Anemia [PDF]
Type I gastric neuroendocrine tumors (GNETs) are closely associated with autoimmune atrophic gastritis, particularly pernicious anemia. They arise as a consequence of chronic hypergastrinemia, which induces enterochromaffin- like cell hyperplasia and ...
Aicha CHERIF HOSNI, +5 more
doaj +1 more source
ABSTRACT Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune, demyelinating disorder of the central nervous system. Clinical manifestations include optic neuritis, longitudinally extensive transverse myelitis (LETM) involving three or more vertebral segments, and, in most cases, seropositivity for anti‐aquaporin‐4 antibodies (AQP4‐IgG).
Nikolina Pravdic +7 more
wiley +1 more source
S3 guideline diagnostics and therapy of alopecia areata – Part 1: Diagnostics and epidemiology
Summary In the project funded by the Innovation Committee at the G‐BA, the S3 guideline for the diagnosis and treatment of AA was developed between 2023 and 2025. The interdisciplinary expert panel consisted of representatives from the German Dermatological Society, in particular from the Pediatric Dermatology Working Group, the Professional ...
Ulrike Blume‐Peytavi +13 more
wiley +1 more source
ABSTRACT Background Eating disorders (ED) and psychosis/psychotic‐spectrum disorders (PSD) have overlapping symptoms and may co‐occur in a variety of presentations. Due to its debilitating and life‐threatening risk, it is important for clinicians to be aware of how catatonia may present within these co‐occurrences.
Rosiel Elwyn
wiley +1 more source
A long-standing undiagnosed case of vitamin B12 deficiency: a case report
Background Pernicious anemia, an autoimmune disease, presents with gradual, nonspecific symptoms, often leading to delayed diagnosis owing to its overlap with other conditions and variability in laboratory findings, such as neurological symptoms without ...
Amirhossein Mesgarankarimi +2 more
doaj +1 more source
Case Report: Pernicious anemia-associated pancytopenia responds to immunotherapy
Pancytopenia is a life-threatening condition necessitating a prompt, thorough workup to appropriately treat the underlying pathology. We describe a presentation of pancytopenia attributed to myelodysplastic syndrome (MDS)-associated immune-mediated ...
Alexander Krule +4 more
doaj +1 more source

