Results 61 to 70 of about 454,704 (201)

Ketogenic diet for infantile epileptic spasms

open access: yesEpilepsia Open, EarlyView.
Abstract Approximately half of all cases of Infantile Epileptic Spasms Syndrome (IESS) do not respond to vigabatrin and hormonal therapies. There is no clear consensus as to the second‐line therapy for IESS. Ketogenic diet (KD) has emerged as an effective treatment for certain drug‐resistant epilepsies and in many cases of IESS.
Morris H. Scantlebury   +3 more
wiley   +1 more source

Adrenocortical response in cows after intramuscular injection of long-acting adrenocorticotropic hormone (Tetracosactide acetate zinc suspension). [PDF]

open access: yes, 2011
-Adrenocortical response in cows after intramuscular injection of long-acting adrenocorticotropic hormone (Tetracosactide acetate zinc ...
Muhammad Yusuf, Muhammad Yusuf
core  

Assessment of the Use of Adrenocorticotropic Hormone in Psoriatic Arthritis

open access: yes, 2015
Background A 39-amino-acid peptide of the natural form of adrenocorticotropic hormone (ACTH) was designed to provide a prolonged release after administration by intramuscular or subcutaneous injection.
Ami Saraiya   +3 more
core   +1 more source

New Topics in Vasopressin Receptors and Approach to Novel Drugs: Effects of Vasopressin Receptor on Regulations of Hormone Secretion and Metabolisms of Glucose, Fat, and Protein

open access: yesJournal of Pharmacological Sciences, 2009
The neurohypophyseal peptide [Arg8]-vasopressin (AVP) is involved in diverse functions such as the regulation of body fluid homeostasis, metabolism, and hormone secretion.
Akito Tanoue
doaj   +1 more source

Long‐term developmental outcome in infantile epileptic spasms syndrome after high‐dose prednisolone and vigabatrin treatment

open access: yesEpilepsia Open, EarlyView.
Abstract Objective To evaluate long‐term developmental outcomes and identify independent predictors of favorable developmental outcomes at 3 years of age in children with infantile epileptic spasms syndrome (IESS) treated with a standardized stepwise vigabatrin and high‐dose prednisolone protocol.
Soyoung Jang   +5 more
wiley   +1 more source

Evaluation of a new immunoassay for measuring equine serum insulin and plasma adrenocorticotrophic hormone: A method comparison study

open access: yesEquine Veterinary Journal, EarlyView.
Abstract Background Insulin dysregulation (ID) and pituitary pars intermedia dysfunction (PPID) are common equine endocrinopathies detected by measurement of circulating insulin and adrenocorticotrophic hormone (ACTH) concentrations. Different assays may yield variable results, limiting comparability.
Nicola J. Menzies‐Gow   +2 more
wiley   +1 more source

Activation of melanocortin type 3 receptor as a molecular mechanism for adrenocorticotropic hormone efficacy in gouty arthritis.

open access: yes, 2002
OBJECTIVE: To test the hypothesis that local activation of melanocortin receptor(s) by adrenocorticotropic hormone (ACTH) could be responsible, at least in part, for its efficacy in human gouty arthritis.
Mauro Perretti   +7 more
core   +1 more source

Cascade structure of cortisol secretion in the hypothalamic-pituitary-adrenocortical axis including endocrine feedback mechanisms.

open access: yes, 2023
Adapted from [47]. ACTH: Adrenocorticotropic hormone. CRH: Corticotropin-releasing hormone.
Hannes Ernst (17364695)   +5 more
core   +1 more source

Ectopic Adrenocorticotropic Hormone–Producing Renal Cell Carcinoma Causing Psychosis in a Patient With Birt-Hogg-Dubé Syndrome

open access: yesAnnals of Internal Medicine: Clinical Cases
This is, to our knowledge, the first-ever recorded case of Birt-Hogg-Dubé syndrome associated with an adrenocorticotropic hormone–secreting renal cell carcinoma.
Talal Alomar   +4 more
doaj   +1 more source

Adrenocorticotropic hormone-producing pheochromocytoma: analysis of clinical cases

open access: yesОжирение и метаболизм, 2015
Ectopic secretion of ACTH from non-pituitary tumors, referred to as ectopic ACTH syndrome (EAS), accounts for about 10–20% of Cushing’s syndrome (CS). Ectopic hormone-secreting pheochromocytomas (Pheo) are rare.
Evgeniya Ivanovna Marova   +9 more
doaj   +1 more source

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