Results 61 to 70 of about 533,017 (267)
Latent Adrenal Insufficiency: From Concept to Diagnosis
Primary adrenal insufficiency (PAI) is a rare disease and potentially fatal if unrecognized. It is characterized by destruction of the adrenal cortex, most frequently of autoimmune origin, resulting in glucocorticoid, mineralocorticoid, and adrenal ...
Nada Younes +2 more
doaj +1 more source
Secretopathies emerge as a new class of neurocristopathies
Abstract Neural crest cells are a transient embryonic population of cells that give rise to a wide range of structures, including craniofacial cartilage and bone, peripheral neurons and glia, as well as components of the cardiac outflow tract, among others.
Amanda Teixeira +3 more
wiley +1 more source
CONGENITAL ADRENAL CORTEX HYPERPLASIA IN A NEWBORN (CLINICAL CASE)
Congenital adrenal cortex hyperplasia combines a group of monogenic diseases with an autosomal recessive fashion based on defects in enzymes or transport proteins involved in adrenal steroidogenesis.
N.M. Kretsu +3 more
doaj +1 more source
NF1 inactivation in the adrenal gland cortex.
Whole mount LacZ staining showing a mosaic Cre-mediated recombination in adrenal cortex (dotted line) of 5-weeks-old Rosa26-lacZ reporter x Prx1-Cre mice.
Denise Emmerich (512090) +14 more
core +1 more source
Abstract Infantile epilepsy spasms syndrome (IESS), formerly known as infantile spasms or West Syndrome, is a severe epilepsy syndrome affecting about 3 in 10,000 newborns in the United States. Characterized by clusters of epileptic spasms, interictal hypsarrhythmia, and developmental delays, IESS has diverse causes, including structural‐metabolic ...
Kayla Vieira +5 more
wiley +1 more source
Metabolism of steroids in the adrenal cortex [PDF]
A. Human Adrenal Gland Studies(i) Homogenates prepared from both fascicular and reticular zones of the adrenal cortex of man showed an equal ability to effect lap-- hydroxylation in vitro.(ii) After in vivo administration of corticotrophin ...
Griffiths, Keith
core +1 more source
Ketogenic diet for infantile epileptic spasms
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
Morpho-functional state of human fetuses’ adrenal cortex during influence of maternal infection
Aim of study. To reveal influence of maternal infection on morpho-functional state of fetuses’ adrenal cortex. Methods. The material was obtained during sectional studies, which were conducted on the basis of the "Kharkiv Regional Clinical Perinatal ...
Vira Tovazhnianska
doaj +3 more sources
Isolation of a multipotent mesenchymal stem cell-like population from human adrenal cortex
Background: The highly plastic nature of adrenal cortex suggests the presence of adrenocortical stem cells (ACSC), but the exact in vivo identity of ACSC remains elusive.
Earn H Gan +5 more
doaj +1 more source

