Results 61 to 70 of about 6,146 (158)

Renal tubular acidosis: A ‘basic’ disorder

Equine Veterinary Education, Volume 38, Issue 7, Page 365-366, July 2026.
H. J. Mason, L. G. Arroyo
wiley   +1 more source

Corticotherapy for traumatic brain-injured Patients - The Corti-TC trial: study protocol for a randomized controlled trial

Trials, 2011
Background Traumatic brain injury (TBI) is a main cause of severe prolonged disability of young patients. Hospital acquired pneumonia (HAP) add to the morbidity and mortality of traumatic brain-injured patients. In one study, hydrocortisone for treatment
Asehnoune Karim, Roquilly Antoine, Sebille Véronique, group The Corti-TC trial   +3 more
doaj   +1 more source

Aldosterone synthase deficiency associated with a CYP11B2 variant of uncertain significance: Case report and literature review

Journal of Clinical and Translational Endocrinology Case Reports
Congenital aldosterone synthase deficiency (ASD) is a rare autosomal recessive condition that causes isolated primary hypoaldosteronism. It has been associated with different pathogenic mutations of the CYP11B2 gene.
Bayan AlNassir, Hessah AlOtaibi
doaj   +1 more source

Posterior Reversible Encephalopathy Syndrome in a Patient with Multiple System Atrophy and Multiple Myeloma

Movement Disorders Clinical Practice, Volume 13, Issue 5, Page 1326-1330, May 2026.
Jackson Mitzner, Jenny Linnoila, Yanal Shaheen, Abby L. Olsen   +3 more
wiley   +1 more source

A Bulking Agent May Lead to Adrenal Insufficiency Crisis: A Case Report [PDF]

Acta Medica Iranica, 2011
Adrenal insufficiency is a life-threatening disorder which must be treated with glucocorticoid replacement and needs permanent dose adjustment during patient's different somatic situations.
Seyed Hossein Samadanifard, Farbod Sedaghat-Hamedani, Elham Kayvanpour, Majid Esmaeilzadeh, Salma Ahi   +4 more
doaj   +2 more sources

Mineralocorticoid replacement during infancy for salt wasting congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Clinics, 2013
OBJECTIVE: The protocols for glucocorticoid replacement in children with salt wasting 21-hydroxylase deficiency are well established; however, the current recommendation for mineralocorticoid replacement is general and suggests individualized dose ...
Larissa G. Gomes, Guiomar Madureira, Berenice B. Mendonca, Tania A. S. S. Bachega   +3 more
doaj  

Clinical role of CYP2C19 polymorphisms in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Acta Chimica Slovenica, 2016
Extraadrenal enzymes such as CYP2C19 may participate in residual 21-hydroxylation of progesterone leading to milder phenotypes of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD). Among 94 21OHD patients 28 were homozygous or
Urh Grošelj, Mojca Žerjav Tanšek, Katarina Trebušak Podkrajšek, Tinka Hovnik, Tadej Battelino, Vita Dolžan   +5 more
doaj   +1 more source

Hyporeninemic hypoaldosteronism in a patient with diabetes mellitus: an unforgettable case report

International Medical Case Reports Journal, 2018
Naziha Chelaghma, Samson O Oyibo Department of Diabetes & Endocrinology, Peterborough City Hospital, Peterborough, UK Abstract: A 58-year-old man presented with a 3-year history of chronic and intermittent hyperkalemia requiring recurrent ...
Chelaghma N, Oyibo SO
doaj  

Late Breaking Abstracts

European Journal of Neurology, Volume 33, Issue S1, June 2026.
wiley   +1 more source

Case Report: Type II Bartter syndrome with a novel KCNJ1 variant in a premature neonate presenting with features of salt-wasting congenital adrenal crisis and pseudo-hypoaldosteronism

Frontiers in Pediatrics
IntroductionBartter syndrome (BS) is a rare group of inherited renal tubulopathies. Diagnosis of BS type II is challenging in the neonatal period as its clinical findings and biochemical features may mimic that of adrenal crisis and pseudo ...
Heung-Ching Tsui, Hua Tse-Timothy Cheng, Kai-Yee Lam, Lai-Ting Leung, Ka-Nam Au, Wai-Yu Wong, Luen Yee-Sylvia Siu, Lap-Ming Wong   +7 more
doaj   +1 more source