نتایج جستجو برای: family history fh
تعداد نتایج: 739379 فیلتر نتایج به سال:
The present study examined the association of cognitive-executive abilities to two risk factors for alcoholism, i.e., antisocial behaviors and a family history (FH+) of alcohol dependence. A sample of 91 right-handed, non-substance-dependent, young male adults recruited from the community were classified into three groups: (1) a control group of n=32 men with no history of DSM-III-R childhood c...
T wo proprotein convertase subtilisin/kexin type 9 (PCSK9) antibodies have obtained approval by the United States Food and Drug Administration: evolocumab (Amgen) and ali-rocumab (Sanofi/Regeneron). Per their package inserts, both are "indicated as an adjunct to diet and maximally tolerated statin therapy for the treatment of adults with heterozygous familial hypercholesterolemia (FH) or clinic...
BACKGROUND The low level of response (LR) to alcohol is a genetically influenced characteristic related to the development of alcohol use disorders (AUDs). This phenotype is found in men with a family history (FH) of alcoholism, predicts future AUDs, and has heritabilities as high as 60%. However, despite evidence of genetic influences for AUDs in both sexes, the majority of studies evaluating ...
No abstract available. Article truncated after the first page. History of Present Illness A 43-year-old woman complained persistent cough over 1 year with mild increasing dyspnea on exertion. She denied fever, sweats or weight loss. had noted fatigue and dry cough, as well shortness breath, particularly when supine. Past Medical (PMH), Social (SH), Family (FH) • An outside bronchoscopy done in ...
An emerging group of high-grade renal cell carcinomas (RCCs), particularly carcinomas arising in the hereditary leiomyomatosis renal cell carcinoma syndrome (HLRCC), show fumarate hydratase (FH) gene mutation and loss of function. On the basis of similar cytomorphology and clinicopathologic features between these tumors and cases described as tubulocystic carcinomas with poorly differentiated f...
Familial hypercholesterolaemia (FH) is the most common autosomal dominant genetic condition, affecting about 1 in 250 people, caused by a pathogenic variant one of several genes involved lipoprotein cholesterol catabolism. Treatment elevated serum low-density people with FH substantially reduces risk ischaemic heart disease and cardiovascular mortality. Yet, vast majority cases are undiagnosed ...
Abstract Objective: Bipolar and Schizophrenia Network for Intermediate Phenotypes (B-SNIP) researchers have proposed three Biotypes that show advantages of a dimensional approach to classification, revealing different levels dysfunction severity through EEG various forms cognitive testing. Although preliminary work has been done showing neuroanatomical differences among the biotypes patterns he...
Abstract Introduction Familial hypercholesterolemia (FH) is often underdiagnosed, particularly in female patients (P), even during hospital admission for acute coronary syndromes (ACS). The aim of this study was to apply the Dutch Lipid Clinic Network (DLCN) Criteria P admitted ACS and evaluate gender age differences. Methods Prospective evaluation with a tertiary center from 2005 2019. Data in...
Current issues related to prostate cancer (PCa) clinical care (e.g., over-screening, over-diagnosis, and over-treatment of nonaggressive PCa) call for risk assessment tools that can be combined with family history (FH) to stratify disease risk among men in the general population. Since 2007, genome-wide association studies (GWASs) have identified more than 100 SNPs associated with PCa susceptib...
OBJECTIVE To investigate the association between family history (FH) of neoplasia, gyneco-obstetric factors and breast cancer (BC) in a case-control study. In cases, to analyze those variables in relation with early onset of BC, the manner of detection (self-examination, prompted by pain, or casual), the size of tumor, and the elapsed time to seek medical attention. MATERIAL AND METHODS Data ...
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