Results 61 to 70 of about 17,291 (255)
Multiple endocrine neoplasia type 1 (MEN1) and congenital adrenal hyperplasia (CAH) are rare monogenic hereditary endocrinopathies with a prevalence of 1–9 cases per 100,000 and 9–15 cases per 100,000, respectively.
A. S. Bondarenko +3 more
doaj +1 more source
CAH catalytic reaction and inhibitor structure.
A. CAH conversion of cyanuric acid to carboxybiuret, which spontaneously decarboxylates to produce biuret. B. Structure of the CAH substrate analog and inhibitor, barbituric acid.
Hideki Aihara (277567) +5 more
core +1 more source
Evaluation of Potential Hormonal Activities of Ashwagandha (Withania somnifera)
ABSTRACT Ashwagandha is a widely used herb in traditional medicine systems, particularly Ayurveda. Despite its extensive tradition, growing concerns regarding its potential endocrinological effects have prompted scientific scrutiny. This review systematically evaluates the current preclinical, clinical, and case study evidence concerning AS's effects ...
Günter Vollmer, Thomas Brendler
wiley +1 more source
A corrigendum on "A Rare Case of Co-occurrence of Multiple Endocrine Neoplasia Syndrome and Congenital Adrenal Hyperplasia" by Axenia S. Bondarenko, Elizaveta O. Mamedova, Zhanna E. Belaya, Galina A. Melnichenko (2024). Obesity and metabolism. 2024;21(1)
A. S. Bondarenko +3 more
doaj +1 more source
<p><a href="https://github.com/shamaaligunawardana/Supplementary-table---HRQoL-of-children-with-CAH-SR-and-MA/files/14000223/Supplementary.table.1.docx">Supplementary table 1.docx</a></p ...
shamaaligunawardana
core +1 more source
Accurately estimating forest age is key to understanding how forests recover and evaluating restoration success. We developed a two‐step deep learning approach using historical greyscale aerial photographs to map forest age at fine spatial scales. By combining a pre‐trained model with localized fine‐tuning, our U‐Net + ResNet50 architecture achieved ...
Ying Ki Law +10 more
wiley +1 more source
Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
Objective:Classic congenital adrenal hyperplasia (CAH) secondary to 21-hydroxylase deficiency is characterized by increased prenatal adrenal androgen secretion.
Helmuth G. Dörr +4 more
doaj +1 more source
The Impact of “Mother‐Friendly Care” Accreditations on Patient Choice: Evidence From Brazil
ABSTRACT We examine the impact of Brazil's “Mother‐Friendly Care” accreditation program on hospital choice. Using administrative data on births in the Brazilian public health system from 2008–2019, we estimate a nested logit demand model that allows for differential substitution patterns based on existing Baby‐Friendly Hospital Initiative (IHAC ...
Cici McNamara, Felipe Rocha Campos
wiley +1 more source
Fasting GLP-1 Levels in Women with PCOS and CAH
Polycystic ovarian syndrome (PCOS) is the most prevalent condition associated with increased androgens, but some rare diseases, e.g., congenital adrenal hyperplasia (CAH), should also be considered in the differential diagnosis of hyperandrogenemia.
Robeva R. +3 more
doaj +1 more source
ContextCardiometabolic complications are increasingly recognized in congenital adrenal hyperplasia (CAH) due to 21β-hydroxylase deficiency, but adult data remain limited.ObjectiveTo evaluate cardiovascular and metabolic alterations in adult patients with
Lorenzo Campioni +20 more
doaj +1 more source

