Results 31 to 40 of about 3,629,719 (185)

Cancer in Ecuadorian subjects with Laron syndrome (ELS)

open access: yesEndocrine-Related Cancer, 2023
Meta-analyses from 2018–2022 have shown that obesity increases the risk of various cancers such as acute myeloid lymphoma, chronic myeloid lymphoma, diffuse beta cell lymphoma, Hodgkin's lymphoma, leukemia, multiple myeloma, non-Hodgkin's lymphoma, bladder, breast, cholangiocarcinoma, colorectal, ovarian, esophageal, kidney, liver, prostate, thyroid ...
Jaime Guevara-Aguirre   +7 more
openaire   +3 more sources

The globe and orbit in Laron syndrome. [PDF]

open access: yesAJNR Am J Neuroradiol, 2011
Patients with LS have an inborn growth hormone resistance, resulting in failure to generate IGF-1. The purpose of this study was to evaluate the size of the eye and orbit in LS.We retrospectively reviewed the MR imaging of the brain in 9 patients with LS for the following parameters: axial diameter of the globe, interzygomatic distance, perpendicular ...
Kornreich L, Konen O, Lilos P, Laron Z.
europepmc   +4 more sources

Transient juvenile hypoglycemia in GH insensitive Laron syndrome pigs is associated with insulin hypersensitivity [PDF]

open access: yesMolecular Metabolism
Background and aims: Fasting hypoglycemia has clinical implications for children with growth hormone (GH)-insensitivity syndrome. This study investigates the pathophysiology of juvenile hypoglycemia in a large animal model for GH receptor (GHR ...
Arne Hinrichs   +21 more
doaj   +2 more sources

High growth hormone serum partially protects mice against Trypanosoma cruzi infection

open access: yesFEBS Open Bio, 2023
Chagas disease (CD) is one of the most devasting parasitic diseases in the Americas, affecting 7–8 million people worldwide. In vitro and in vivo experiments have demonstrated that growth hormone (GH) serum levels decrease as CD progresses. Interestingly,
Patricia Mora‐Criollo   +10 more
doaj   +2 more sources

A CHILD WITH LARON SYNDROME ASSOCIATED WITH VASCULITIS. [PDF]

open access: yesActa Endocrinol (Buchar), 2016
Levels of insulin-like growth factor-I are characteristically low in Laron syndrome which is a factor that has important roles on vascular health and development. Congenital insulin-like growth factor-I deficiency was reported to be associated with some vascular disorders.
Unsal Sac R   +4 more
europepmc   +4 more sources

Mexican case report of a never‐treated Laron syndrome patient evolving to metabolic syndrome, type 2 diabetes, and stroke [PDF]

open access: yesClinical Case Reports, 2017
Key Clinical Message Glucose and lipid profile together with blood pressure should always be considered for low sera‐IGF‐1 patients. Even when adulthood is reached, IGF‐1 therapy in these patients should be pursued as metabolic and protective cellular ...
Inma Castilla‐Cortazar   +7 more
doaj   +2 more sources

GH-resistant (Laron) mice: gene therapy with a liver-specific GH receptor causes unbalanced upregulation of female-biased and growth-related genes [PDF]

open access: yesFrontiers in Endocrinology
Growth hormone (GH) receptor (GHR) mutations give rise to GH-resistance (Laron syndrome). We previously treated GH-resistant Ghr-/- mice (Laron mice) with adeno-associated virus (AAV) delivering mouse (m)Ghr controlled by a constitutively active liver ...
Joshua K. Tay   +10 more
doaj   +2 more sources

Lessons from the Genetics of Laron Syndrome

open access: yesTrends in Endocrinology and Metabolism, 1998
In the decade since the cloning and sequencing of the growth hormone receptor (GHR) and the recognition that the circulating GH-binding protein (GHBP) is structurally identical to the extracellular domain of the GHR, 34 mutations have been described.
Arlan L. Rosenbloom   +1 more
exaly   +4 more sources

Laron syndrome: a case report

open access: yesInternational Journal of Contemporary Pediatrics, 2021
Laron syndrome (LS) is a rare, genetic disorder inherited in an autosomal recessive manner. The disease is caused by mutations of the growth hormone (GH) gene, leading to GH/insulin-like growth factor type 1 (IGF1) signalling pathway defect. A 13-month-old, male child, born of second-degree consanguineous marriage presented with short stature (57 cm ...
Ashok V. Puttappanavar   +4 more
openaire   +3 more sources

Primary growth hormone insensitivity (Laron syndrome) and acquired hypothyroidism: a case report [PDF]

open access: yesJournal of Medical Case Reports, 2011
Introduction Primary growth hormone resistance or growth hormone insensitivity syndrome, also known as Laron syndrome, is a hereditary disease caused by deletions or different types of mutations in the growth hormone receptor gene or by post-receptor ...
Corneli Ginevra   +6 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy