Endocrine disorders with parathyroid hormone-independent hypercalcemia
JK Simonsen, L Rejnmark - Endocrinology and Metabolism …, 2021 - endo.theclinics.com
Discussion Although all the examined endocrinological disorders are in some way
associated with altered bone metabolism, nonparathyroid hypercalcemia is observed in only …
associated with altered bone metabolism, nonparathyroid hypercalcemia is observed in only …
Increased risk of nephrolithiasis: an emerging issue in children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
M Chiarito, C Lattanzio, V D'Ascanio, D Capalbo… - Endocrine, 2024 - Springer
Purpose To investigate the incidence of nephrolithiasis in a cohort of children with
congenital adrenal hyperplasia (CAH), and to study if there is an association with the …
congenital adrenal hyperplasia (CAH), and to study if there is an association with the …
Prevalence of nephrocalcinosis in children with congenital adrenal hyperplasia
Background: We aimed to investigate the prevalence of nephrocalcinosis (NC) among
children with diagnosed congenital adrenal hyperplasia (CAH). Our findings would be …
children with diagnosed congenital adrenal hyperplasia (CAH). Our findings would be …
Diagnostic Approach and Treatment of the Pediatric Patient with Hypercalcemia
Hypercalcemia is less frequent in children than adults. Further, the upper limit of normal for
serum calcium is higher in children than adults. Levels are highest in infancy and decline …
serum calcium is higher in children than adults. Levels are highest in infancy and decline …
[HTML][HTML] Beyond Binary: Gender Reassignment in a Case of 11β-Hydroxylase Deficiency
MA Hithayathulla, HDP Nagarajan, V Gopalakrishnan… - Cureus, 2023 - ncbi.nlm.nih.gov
Congenital adrenal hyperplasia (CAH) encompasses a spectrum of disorders characterized
by enzyme deficiencies in the hormone biosynthesis pathways of the adrenal glands …
by enzyme deficiencies in the hormone biosynthesis pathways of the adrenal glands …
Beyond Binary: Gender Reassignment in a Case of 11β-Hydroxylase Deficiency
HM Afsharhussain, PNH Dakssesh, G Vrijesh… - Cureus, 2023 - search.proquest.com
Congenital adrenal hyperplasia (CAH) encompasses a spectrum of disorders characterized
by enzyme deficiencies in the hormone biosynthesis pathways of the adrenal glands …
by enzyme deficiencies in the hormone biosynthesis pathways of the adrenal glands …
An investigation into increased cases of idiopathic infantile hypercalcaemia
LA Amato - 2019 - unsworks.unsw.edu.au
Following increased presentations for idiopathic infantile hypercalcaemia (IIH) between
2011 and 2014, we hypothesized that antenatal vitamin D supplementation might be …
2011 and 2014, we hypothesized that antenatal vitamin D supplementation might be …
[PDF][PDF] Short QT interval in oligosymptomatic teenager boy
M Heñin - cardiolatina.com
Congenital Short QT syndrome (SQTS) is an hereditary, congenital, familial or sporadic
orphan entity which is part of the so-called ion channel defects or channelopathies with …
orphan entity which is part of the so-called ion channel defects or channelopathies with …
[PDF][PDF] Dossier zur Nutzenbewertung gemäß § 35a SGB V
Z Vergleichstherapie - 2017 - g-ba.de
Die zweckmäßige Vergleichstherapie ist regelhaft zu bestimmen nach Maßstäben, die sich
aus den internationalen Standards der evidenzbasierten Medizin ergeben. Bei mehreren …
aus den internationalen Standards der evidenzbasierten Medizin ergeben. Bei mehreren …