Results 81 to 90 of about 622,771 (208)
Severe combined adrenal and gonadal deficiency caused by novel mutations in the cholesterol side chain cleavage enzyme, P450scc [PDF]
, 2008 Context: Mitochondrial cytochrome P450scc converts cholesterol to pregnenolone in all steroidogenic tissues. Although progesterone production from the fetally-derived placenta is necessary to maintain pregnancy to term, four patients with mutations in ...
Huang, NW +6 more
core
Lack of mutations of exon 2 of the MEN1 gene in endocrine and nonendocrine sporadic tumors
Brazilian Journal of Medical and Biological Research, 2001 In addition to the mutations that underlie most cases of the multiple endocrine neoplasia type 1 (MEN1) syndrome, somatic mutations of the MEN1 gene have also been described in sporadic tumors like gastrinomas, insulinomas and bronchial carcinoid ...
S.C. Costa +5 more
doaj +1 more source
Effects of loperamide on the human hypothalamo-pituitary-adrenal axis in vivo and in vitro. [PDF]
, 1992 Loperamide, an opiate agonist of high specificity for p-receptors, was recently reported to suppress ACTH and cortisol levels in normal subjects, but not in patients with proven ACTH-dependent Cushing’s disease. However, there is little information on
Pfeiffer, M. +4 more
core +2 more sources
Hypokalemia: a clinical update
Endocrine Connections, 2018 Hypokalemia is a common electrolyte disturbance, especially in hospitalized patients. It can have various causes, including endocrine ones. Sometimes, hypokalemia requires urgent medical attention. The aim of this review is to present updated information
Efstratios Kardalas +5 more
doaj +1 more source
Minimal Effects of Rearing Enrichments on Pullet Behaviour and Welfare
Animals, 2020 In Australia, free-range pullets are typically reared indoors, which may hinder later adjustment to outdoor access. Rearing enrichments could optimise pullet development.
Dana L.M. Campbell +3 more
doaj +1 more source
Detección precoz de trastornos endocrinológicos
Revista Médica Clínica Las Condes, 2010 Se revisan los trastornos más comunes del sistema endocrino que se detectan en la consulta no especializada. Se hace énfasis en: a) Trastornos tiroideos tales como hipo o hipertiroidismo, nódulos de la tiroides y la importancia de la enfermedad de la ...
M. Patricio Trincado, Dr. +1 more
doaj +1 more source
Frontiers in EndocrinologyAldosterone-producing adenoma (APA) is one of the main types of primary aldosteronism (PA). APAs are predominantly unilateral, whereas bilateral APAs are rare.
Tingting Zhang +6 more
doaj +1 more source
Journal of Clinical Endocrinology and Metabolism, 2018 Context Primary adrenal insufficiency is an important clinical manifestation of X-linked adrenoleukodystrophy (ALD). Other manifestations include spinal cord disease and/or inflammatory demyelinating cerebral disease.
I. C. Huffnagel +8 more
semanticscholar +1 more source
Spontaneous haemorrhage of an adrenal angiomyolipoma: case report [PDF]
, 2019 Background Angiomyolipomas are rare mesenchymal tumours arising from the perivascular epithelioid cells consisting of variable amounts of adipose, thick-walled blood vessels and smooth muscle cells.
Seshadri Sriprasad +4 more
core +1 more source
Endocrine markers in critical illness
Journal of Pediatric Critical Care, 2017 Pointers of endocrine disease play important role in the management a sick child and high index of suspicion is needed to diagnose an endocrine problem in critical care setting.
Vaman Khadilkar, Sagar Lad
doaj +1 more source