نتایج جستجو برای: family history fh

تعداد نتایج: 739379  

2017
Fiona M. Begen Julie Barnett Miriam Barber Ros Payne M. Hazel Gowland Jane S. Lucas

BACKGROUND For parents and caregivers of food hypersensitive (FH) children, accommodating their child's dietary needs when eating out can be a challenging experience. This study explored caregivers' experiences and behaviours when eating out with their FH child in order to gain insights into how they support and prepare their child in negotiating safe eating out experiences. METHODS A cross-s...

Journal: :Journal of epidemiology and community health 2002
P J Marang-van de Mheen M C van Maarle M E A Stouthard

Heterozygous familial hypercholesterolaemia (FH) is a common autosomal dominant inherited metabolic disease with a prevalence of 1 in 500 in most Western countries. People with FH experience an increased risk for coronary artery disease (CAD) and excess mortality especially at a young age. Until recently the diagnosis of FH was based on clinical signs and symptoms alone. These included increase...

2015
Jianping Qiao Zhishun Wang Lupo Geronazzo-Alman Lawrence Amsel Cristiane Duarte Seonjoo Lee George Musa Jun Long Xiaofu He Thao Doan Joy Hirsch Christina W. Hoven

We aimed to uncover differences in brain circuits of adolescents with parental positive or negative histories of substance use disorders (SUD), when performing a task that elicits emotional conflict, testing whether the brain circuits could serve as endophenotype markers to distinguish these adolescents. We acquired functional magnetic resonance imaging data from 11 adolescents with a positive ...

Journal: :Circulation research 2003
Samuel Canizales-Quinteros Carlos A Aguilar-Salinas Eduardo Reyes-Rodríguez Laura Riba Maribel Rodríguez-Torres Salvador Ramírez-Jiménez Adriana Huertas-Vázquez Verónica Fragoso-Ontiveros Alejandro Zentella-Dehesa José L Ventura-Gallegos Gerardo Vega-Hernández Angelina López-Estrada Moisés Aurón-Gómez Francisco Gómez-Pérez Juan Rull Nancy J Cox Graeme I Bell Maria Teresa Tusié-Luna

Heterozygous familial hypercholesterolemia (FH) is a highly atherogenic genetic disorder leading to premature coronary heart disease (CHD), usually before 60 years of age. We studied an extended multigenerational kindred with FH linked to chromosome 1p32 in which atherosclerotic complications were either delayed or prevented in individuals with elevated HDL cholesterol (HDL-C) levels or hyperal...

2011
Paolo Mulatero Tracy Ann Williams Silvia Monticone Franco Veglio

Primary aldosteronism (PA) is the most frequent cause of secondary hypertension in adults, accounting for 5% to 15% of hypertensive patients, depending on the severity of blood pressure levels.1,2 Patients with PA undergo a higher rate of cardiovascular complications compared with essential hypertensives, and, thus, the screening of hypertensive subgroups of patients with higher prevalence of P...

2014
Martín Bedolla-Barajas Tonatiuh Ramses Bedolla-Pulido Alan Salvador Camacho-Peña Estefanía González-García Jaime Morales-Romero

PURPOSE There is limited epidemiological evidence of food hypersensitivity (FH) in the adult population. We aimed to determine the prevalence of FH in Mexican adults, their clinical features and to establish common food involved in its appearance. METHODS We designed a cross-sectional study using a fixed quota sampling; 1,126 subjects answered a structured survey to gather information related...

Journal: :Journal of medical genetics 1998
W K Lee L Haddad M J Macleod A M Dorrance D J Wilson D Gaffney M H Dominiczak C J Packard I N Day S E Humphries A F Dominiczak

Familial hypercholesterolaemia (FH) is an autosomal codominant disorder characterised by high levels of LDL cholesterol and a high incidence of coronary artery disease. Our aims were to track the low density lipoprotein receptor (LDLR) gene in individual families with phenotypic FH and to identify and characterise any mutations of the LDLR gene that may be common in the west of Scotland FH popu...

2017
Giuseppe Migliara Valentina Baccolini Annalisa Rosso Elvira D’Andrea Azzurra Massimi Paolo Villari Corrado De Vito

BACKGROUND Familial hypercholesterolemia (FH) is an autosomal-dominant hereditary disorder of lipid metabolism that causes lifelong exposure to increased LDL levels resulting in premature coronary heart disease and, if untreated, death. Recent studies have shown its prevalence to be higher than previously considered, which has important implications for the mortality and morbidity of associated...

Journal: :Endocrine-related cancer 2012
Valentina Piccini Elena Rapizzi Alessandra Bacca Giuseppe Di Trapani Raffaele Pulli Valentino Giachè Benedetta Zampetti Emanuela Lucci-Cordisco Letizia Canu Elisa Corsini Antongiulio Faggiano Luca Deiana Davide Carrara Valeria Tantardini Stefano Mariotti Maria Rosaria Ambrosio Maria Chiara Zatelli Gabriele Parenti Annamaria Colao Carlo Pratesi Giampaolo Bernini Tonino Ercolino Massimo Mannelli

Head and neck paragangliomas (HNPGLs) are neural crest-derived tumors. In comparison with paragangliomas located in the abdomen and the chest, which are generally catecholamine secreting (sPGLs) and sympathetic in origin, HNPGLs are, in fact, parasympathetic in origin and are generally nonsecreting. Overall, 79 consecutive patients with HNPGL were examined for mutations in SDHA, SDHB, SDHC, SDH...

2017
M.N. Rajah L.M.K. Wallace E. Ankudowich E.H. Yu A. Swierkot R. Patel M.M. Chakravarty D. Naumova J. Pruessner R. Joober S. Gauthier S. Pasvanis

Episodic memory impairment is a consistent, pronounced deficit in pre-clinical stages of late-onset Alzheimer's disease (AD). Individuals with risk factors for AD exhibit altered brain function several decades prior to the onset of AD-related symptoms. In the current event-related fMRI study of spatial context memory we tested the hypothesis that middle-aged adults (MA; 40-58 yrs) with a family...

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