Results 21 to 30 of about 9,429,824 (263)

Large mitochondrial DNA deletion in an infant with addison disease. [PDF]

JIMD Rep, 2012
Duran GP, Martinez-Aguayo A, Poggi H, Lagos M, Gutierrez D, Harris PR.   +5 more
europepmc   +2 more sources

Autoimmune addison disease and premature ovarian failure [PDF]

Nature Reviews Endocrinology, 2011
Carol Wilson
openalex   +2 more sources

Mucocutaneous hyperpigmentation as a clue to diagnose Addison disease – Two case reports

Dermatologica Sinica, 2022
Hsuan Chen, Fu-Nien Hsieh, Chao-Chun Yang   +2 more
doaj   +2 more sources

Visceral Fat and Novel Biomarkers of Cardiovascular Disease in Patients With Addison’s Disease: A Case-Control Study

Journal of Clinical Endocrinology and Metabolism, 2017
Ragnhildur Bergthorsdottir, Oskar Ragnarsson, Staffan Nilsson   +2 more
exaly   +2 more sources

Novel Gene Mutation in a Korean Patient with X-Linked Adrenoleukodystrophy Presenting with Addison's Disease [PDF]

Endocrinology and Metabolism, 2020
X-linked adrenoleukodystrophy (X-ALD) occurs due to mutations in the ABCD1 gene that encodes the peroxisomal membrane protein peroxisomal transporter ATP-binding cassette sub-family D member 1 (ABCD1).
Yun Kyung Cho, Seo-Young Lee, Sang-Wook Kim   +2 more
doaj   +1 more source

Conceptualising quality early childhood education: Learning from young children in Brazil and South Africa through creative and play‐based methods

British Educational Research Journal, EarlyView., 2023
Abstract Early childhood has increasingly been acknowledged as a vital time for all children. Inclusive and quality education is part of the United Nations Sustainable Development Goals, with the further specification that all children have access to quality pre‐primary education.
Laura H. V. Wright, Irene Rizzini, Malibongwe Gwele, Lynn McNair, Cristina Laclette Porto, Marsha Orgill, E. Kay M. Tisdall, Malcolm Bush, Linda Biersteker   +8 more
wiley   +1 more source

Sleep, Cognition and Cortisol in Addison’s Disease: A Mechanistic Relationship

Frontiers in Endocrinology, 2021
Sleep is a critical biological process, essential for cognitive well-being. Neuroscientific literature suggests there are mechanistic relations between sleep disruption and memory deficits, and that varying concentrations of cortisol may play an ...
M. Henry, Kevin G F Thomas, I. Ross
semanticscholar   +1 more source

The natural history of 21-hydroxylase autoantibodies in autoimmune Addison’s disease

European Journal of Endocrinology, 2021
Background The most common cause of primary adrenal failure (Addison’s disease) in the Western world is autoimmunity characterized by autoantibodies against the steroidogenic enzyme 21-hydroxylase (CYP21A2, 21OH).
A. Wolff, L. Breivik, K. O. Hufthammer, M. A. Grytaas, E. Bratland, E. Husebye, B. Oftedal   +6 more
semanticscholar   +1 more source

Unmasking of Addison’s disease in COVID-19

SAGE Open Medical Case Reports, 2021
This case report highlights the initial presentation of Addison’s disease in a 19-year-old individual with coronavirus disease. Coronavirus disease is an infectious disease, which often presents with fever and respiratory and gastrointestinal symptoms ...
Pallav Bhattarai, H. Allen, A. Aggarwal, Daniel Madden, K. Dalton   +4 more
semanticscholar   +1 more source

Nicotinamide riboside and pterostilbene reduces markers of hepatic inflammation in NAFLD: A double‐blind, placebo‐controlled clinical trial

Hepatology, EarlyView., 2022
NRPT 1X reduces ALT and ceramide 14:0 in 65% of subjects as compared to only 28% in the placebo group. Abstract Background and Aims The prevalence of NAFLD is increasing globally and on a path to becoming the most frequent cause of chronic liver disease. Strategies for the prevention and treatment of NAFLD are urgently needed.
Ryan W. Dellinger, Holly E. Holmes, Tina Hu‐Seliger, Rodney W. Butt, Stephen A. Harrison, Dariush Mozaffarian, Oliver Chen, Leonard Guarente   +7 more
wiley   +1 more source