Results 71 to 80 of about 5,184,226 (184)
International Journal of Eating Disorders, Volume 59, Issue 9, Page 2004-2012, September 2026.ABSTRACT Objective Anorexia nervosa (AN) is a serious illness in which more than half of all deaths are due to malnutrition. Critically low energy and protein intake are known causes of massive weight loss, whereas micronutrient deficiencies due to a low‐calorie food pattern remain poorly characterized in children with AN. Micronutrient deficiencies in
Zenaida Iordan +6 more
wiley +1 more source
Inequalities in intraspecific plant–lemur interactions drive seed dispersal patterns
Oikos, Volume 2026, Issue 9, September 2026.Biotic interactions occur between individuals and accumulate to shape species‐level interaction structure across a community. Skewed interaction structures, where a few individuals are highly connected and most have few interactions, are increasingly identified at the individual‐level.
Jadelys Tonos +2 more
wiley +1 more source
Journal of Agronomy and Crop Science, Volume 212, Issue 5, September 2026.ABSTRACT This study was conducted to determine the effects of five irrigation levels, corresponding to 25%, 50%, 75%, 100% and 125% of the weekly irrigation amount required to replenish the effective root zone to field capacity (IT25–IT125), on the herbage yield and quality of forage soybean (Glycine max (L.) Merr.) over two growing seasons (2024 and ...
Emre Akkaya +5 more
wiley +1 more source
Brain and Behavior, Volume 16, Issue 8, August 2026.ABSTRACT Background Wilson's disease (WD) is an autosomal recessive disorder of copper metabolism with heterogeneous hepatic and neurological manifestations. Autonomic nervous system (ANS) involvement in WD is poorly recognized and remains inadequately studied, despite its potential to cause significant morbidity if unrecognized.
Sabyasachi Pattanayak +14 more
wiley +1 more source
Phenotypic convergence of Menkes and Wilson disease. [PDF]
, 2019 Menkes disease is an X-linked multisystem disorder with epilepsy, kinky hair, and neurodegeneration caused by mutations in the copper transporter ATP7A. Other ATP7A mutations have been linked to juvenile occipital horn syndrome and adult-onset hereditary
core +2 more sources
Genomic organization of ATOX1, a human copper chaperone
BMC Genetics, 2003 Background Copper is an essential trace element that plays a critical role in the survival of all living organisms. Menkes disease and occipital horn syndrome (OHS) are allelic disorders of copper transport caused by defects in a X-linked gene (ATP7A ...
Kaler Stephen G +2 more
doaj +1 more source
Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome.
, 2002 INTRODUCTION: Menkes disease is an X-linked inherited disorder of intestinal copper absorption resulting in copper deficiency. Cardinal features include hair abnormalities, facial dysmorphism, severe neurological impairment, hypothermia, arterial ...
Armengaud, Didier +8 more
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A Case of Transverse Colon Volvulus With Hemoperitoneum in Menkes Disease
Annals of Internal Medicine: Clinical CasesMenkes disease is an X-linked recessive disorder of copper metabolism resulting in impaired activity of lysyl oxidase, a cuproenzyme essential for collagen and elastin cross-linking.
Kena J. Lemu, Jinye Liu, Saeed S. Graham
doaj +1 more source
The cell biology of the menkes disease protein
, 1999 The cell biology of the menkes disease ...
J Camakaris (13278537) +2 more
core
Menkes disease: a biochemical abnormality in cultured human fibroblasts
, 1976 Cultured skin fibroblasts from patients with Menkes disease, an X-linked disorder involving a defect in copper metabolism, were analyzed for copper concentration by means of atomic absorption spectrophotometry.
Stevenson, R E +3 more
core +1 more source