Results 91 to 100 of about 7,233,987 (192)
Pathogenesis of x-linked hypophosphatemia (JPG 44 ...
Johannes Kleinheinz (32184) +4 more
core +1 more source
Many adolescents with X-linked hypophosphatemia (XLH) currently have to stop treatment with burosumab at the end of skeletal growth. We describe the experience of a cohort of adolescents with XLH before, during, and after stopping burosumab (median ...
Charlotte Jarvis +9 more
doaj +1 more source
Prevalence and clinical characteristics of X-linked hypophosphatemia in Paraná, southern Brazil
Objective: The aim of this cross-sectional study was to estimate the prevalence of XLH in Paraná, a state in southern Brazil, and report the clinical features and complications of the disease.
Carolina Aguiar Moreira +6 more
doaj +1 more source
Microstructural Evidence for Early Childhood Stress in a Community in Transition at Hisban, Jordan
ABSTRACT Objectives Identification of stress across infancy and childhood can reflect maternal and environmental influences on early life health. In the 19th century community of Hisban, many infants died before 2 years of age with evidence of metabolic disease, including rickets, that likely ties with maternal health.
Kristina Cockerille +4 more
wiley +1 more source
Vascular Calcification: Mechanisms, Models, and Therapies
ABSTRACT Vascular calcification represents an active multifactorial process that mirrors several key features of skeletal bone mineralization. Clinically, it is characterized by diminished arterial compliance and increased arterial wall stiffness, both of which serve as independent predictors of significant adverse cardiovascular events.
Wenya Zhu +5 more
wiley +1 more source
X-linked familial hypophosphatemia
Abstract: Osteomalacia is a diffuse bone disorder characterized by increased bone fragility, and it represents in adults the equivalent of rickets seen in children, sharing the same causes. This condition mainly results from Vitamin D deficiency, but in some cases, it may be due to renal phosphate wasting, which can be hereditary, acquired ...
Boutaina Zerouali +5 more
openaire +1 more source
FGF23, Hypophosphatemia, and Emerging Treatments
FGF23 is an important hormonal regulator of phosphate homeostasis. Together with its co‐receptor Klotho, it modulates phosphate reabsorption and both 1α‐hydroxylation and 24‐hydroxylation in the renal proximal tubules.
Erik A Imel +3 more
doaj +1 more source
Background. X-linked hypophosphatemia is the most common form of hereditary vitamin D-resistant rickets. Today, there is a late diagnosis, later treatment start and a significant deterioration in the quality of life of patients with X-linked ...
L.I. Vakulenko
core +1 more source
International Journal of Rheumatic Diseases, Volume 29, Issue 7, July 2026.
Jin Bu, Luofeng Shen, Yuhong Liu
wiley +1 more source
The role of epigenetic factors in the pathogenesis of familial X-linked mental retardation (XLMR) [PDF]
Mental retardation (MR) is a handicap with severe implications not only for thosethat suffer from this disability, but also for their families, society and the welfaresystems which support them.
Carvill, Gemma
core +1 more source

