Results 151 to 160 of about 8,621 (184)

Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency. [PDF]

JCEM Case Rep
Yousaf S, Nizar R, Alias G, Taylor D, Fulton P, Antoniadi T.   +5 more
europepmc   +1 more source

Double 'A' phenotypes with mineralocorticoid deficiency: A rare presentation of Allgrove syndrome. [PDF]

Clin Pediatr Endocrinol
Ghosh A, Annigeri S, Singh C, Hemram SK.
europepmc   +1 more source

9296 A Novel LC-MS/MS Salivary Fludrocortisone Method With Potential for Monitoring in Adrenal Insufficiency Patients

Megan Dolan, David Marshall, James Hawley, Nicole Reisch, Brian Keevil   +4 more
openalex   +1 more source

WCN25-3657 TACROLIMUS INDUCED HYPONATREMIA TREATED WITH FLUDROCORTISONE

Kidney International Reports
Shrikant Deshmukh, Vajed Mogal
doaj   +1 more source

Discovery of Personalized Treatment for Immuno-Metabolic Depression-Focus on 11beta Hydroxysteroid Dehydrogenase Type 2 (11betaHSD2) and Toll-like Receptor 4 (TLR4) Inhibition with Enoxolone. [PDF]

Pharmaceuticals (Basel)
Murck H.
europepmc   +1 more source

Pregnancy Outcomes in Women With Primary Adrenal Insufficiency: Data From a Multicentre Cohort Study. [PDF]

BJOG
Cauldwell M, Steer PJ, Ahsan M, Ali A, Ashiq S, Ashworth R, Basha D, Chong H, Corbett GA, Dunne F, Hill A, Gajewska-Knapik K, Jakes A, McLaren D, Kinsella T, Lee T, Levy M, MacKiliop L, McAuliffe FM, Mohan A, Mumby C, Nana M, Napier C, Neuberger F, Newman C, Oosterhouse T, Shard A, Shehata H, Stocker L, Tomlinson JW, Beck A, Vaidya B, Wiles K, Williamson C, Zollner J, Ward E, Turner HE.   +36 more
europepmc   +1 more source

Severe neonatal presentation of Xp21 contiguous gene deletion: adrenal crisis and neuromuscular involvement. [PDF]

Acta Myol
Stanković S, Stanković T, Ignjatović M, Jakovljević M, Andrejević M.   +4 more
europepmc   +1 more source

Multimodal Management of Supine Hypertension With Orthostatic Hypotension in an Elderly Male Patient With Parkinson's Disease. [PDF]

Cureus
Dayal M, Shah MS, Radfar N, Patel S, Thomas R.   +4 more
europepmc   +1 more source

Inherited, Non-CAH Primary Adrenal Insufficiency in Children: A Genetic and Clinical Profile from a Tertiary Care Centre. [PDF]

Indian J Endocrinol Metab
Sheya A, Namratha GS, Mahadevan S, Ashirvatham AR, Ranjan A.   +4 more
europepmc   +1 more source

Orthostatic hypotension in Parkinson's disease: therapeutic considerations. [PDF]

Ther Adv Neurol Disord
Wyant KJ, Kotagal V.
europepmc   +1 more source