Results 51 to 60 of about 12,342 (227)

Addison\u27s Disease in Half-Siblings [PDF]

, 1968
In this only reported incidence of Addison\u27s disease in half-siblings, the adrenal failure is postulated to be a sex-linked recessive character.
Bickham, Richard E., Silvestre, Dora, Mellinger, Raymond C.   +2 more
core  

‘I, Me, Myself’: Selfhood and Melancholy in the Journals of Gertrude Savile (1697–1758)

Journal for Eighteenth-Century Studies, EarlyView.
Abstract This article examines the journals of Gertrude Savile from 1727 in light of recent scholarship on early modern and eighteenth‐century melancholy. The concept had myriad associations with medicine, physiology, the imagination, and feeling, but questions remain about how melancholy during this period was considered by those outside the narrow ...
Daniel Beaumont
wiley   +1 more source

Persistence of histoplasma in adrenals 7 years after antifungal therapy

Indian Journal of Endocrinology and Metabolism, 2013
Adrenal histoplasmosis is an uncommon cause for adrenal insufficiency. The duration of treatment for adrenal histoplasmosis is not clear. Existing treatment regimens advocate antifungals given for periods ranging from 6 months to 2 years.
Deepak Kothari, Shweta Chopra, Minakshi Bhardwaj, Ajay K Ajmani, Bindu Kulshreshtha   +4 more
doaj   +1 more source

Temperature interacts with jack pine host defences to influence the growth of mountain pine beetle‐associated fungi

Agricultural and Forest Entomology, EarlyView.
Optimal growing temperatures varied with mountain pine beetle‐associated fungal species. There was only a marginal impact of temperature on the response of fungi to defensive monoterpenes of novel host pine. Interspecific facilitation occurred for Leptiographuim longiclavatum when grown in Ophiostoma montium‐induced treatments at optimal temperatures ...
Adrienne C. Bailey, Jennifer G. Klutsch, Kaitlyn Carey, Laureen F. I. Echiverri, Leah Flaherty   +4 more
wiley   +1 more source

Addison\u27s Disease with Papilledema as the Presenting Feature

, 2023
Adrenal insufficiency as a cause of elevated intracranial pressure is unusual, and can be overlooked, leading to delayed diagnosis of primary endocrine dysfunction with potentially serious consequences.
Melley Fesseha; Jason Peragallo; Sachin Kedar
core  

Examining the Role of Artificial Intelligence in Assessment: A Comparative Study of ChatGPT and Educator‐Generated Multiple‐Choice Questions in a Dental Exam

European Journal of Dental Education, EarlyView.
ABSTRACT Aim To compare the item difficulty and discriminative index of multiple‐choice questions (MCQs) generated by ChatGPT with those created by dental educators, based on the performance of dental students in a real exam setting. Materials and Methods A total of 40 MCQs—20 generated by ChatGPT 4.0 and 20 by dental educators—were developed based on ...
Nezaket Ezgi Özer, Yusuf Balcı, Gaye Bölükbaşı, Betul İlhan, Pelin Güneri   +4 more
wiley   +1 more source

Functional immune profiling reveals CD4+ T cell dysregulation in coeliac disease

Immunology &Cell Biology, EarlyView.
The T cell momentum assay quantifies division, survival and activation decay to reveal intrinsic CD4+ programming defects marked by prolonged activation and impaired feedback control in coeliac disease. This scalable platform provides a functional screen for early T cell dysregulation across autoimmune and immune‐mediated diseases.
Anthony J Farchione, HoChan Cheon, David Vremec, Julika Neumann, Gwenny M Verstappen, Melinda Y Hardy, Mai B Margetts, Lauren J Howson, Lee M Henneken, Maureen Forde, Jason A Tye‐Din, Susanne Heinzel, Philip D Hodgkin, Vanessa L Bryant   +13 more
wiley   +1 more source

Autoimmune oophoritis: A rarely encountered ovarian lesion

Indian 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

Addison's Disease [PDF]

BMJ, 1934
D C, Hare, S L, Simpson
openaire   +7 more sources

Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1

, 2017
Context: Autoimmune polyendocrine syndrome type 1 (APS1) is a monogenic disorder that features autoimmune Addison disease as a major component. Although APS1 accounts for only a small fraction of all patients with Addison disease, early identification of
Bensing, Sophie, Husebye, Eystein S,, Swedish Addison Registry Study Group, Landegren, Nils, Pielberg, Gerli Rosengren, Alimohammad, Mohammad, Eriksson, Daniel,, Husebye, Eystein S., Ekwall, Olov,, Ekwall, Olov, Rosengren Pielberg, Gerli,, Dalin, Frida, Knappskog, Per Morten, Dahlqvist, Per,, Rönnelid, Johan,, Hulting, Anna-Lena, Eriksson, Gabriel Nordling, Ronnelid, Johan, Kampe, Olle, Kämpe, Olle,, Wahlberg, Jeanette, Catrina, Sergiu-Bogdan, Alimohammadi, Mohammad, The Swedish Addison Registry Study Group, Dahlqvist, Per, Catrina, Sergiu-Bogdan,, Elfving, Maria,, Hallgren, Åsa,, Bianchi, Matteo, Husebye, Eystein S, Landegren, Nils,, Winqvist, Ola,, Rosengren Pielberg, Gerli, Winqvist, Ola, Wahlberg, Jeanette,, Husebye, Eystein S.,, Alimohammadi, Mohammad,, Knappskog, Per Morten,, Eriksson, Gabriel Nordling,, Bianchi, Matteo,, Eriksson, Daniel, Hallgren, Asa, Hulting, Anna-Lena,, Bensing, Sophie,, Lindblad-Toh, Kerstin, Lund University., Dalin, Frida,, Lindblad-Toh, Kerstin,   +47 more
core   +1 more source