نتایج جستجو برای: familial history

تعداد نتایج: 402168  

Journal: :BMJ case reports 2014
Andrew Sommerlad James Lee Jason Warren Gary Price

A man presenting in his 50s, following conviction for a non-violent crime, to forensic psychiatric services, and then to a neuropsychiatry service with an unusual presentation of psychosis: second person auditory hallucinations, grandiose delusions and somatic delusions. Detailed collateral and family history revealed a background of progressive cognitive deficit and a family history of motor n...

Journal: :مجله دانشکده پزشکی دانشگاه علوم پزشکی تهران 0
علی اکبر توسلی a tavassoli مرتضی رفیعی m rafieei

hypertension is one of the most important modifiable risk factors of vascular heart disease. control of hypertension in different age groups has a significant effect upon the control and prevention of vascular heart disease. a familial pattern is observed in the distribution of blood pressure in different societies. family history of hypertension has a profound effect on the future risk of deve...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2004
Nilanjan Chatterjee Patricia Hartge James R Cerhan Wendy Cozen Scott Davis Naoko Ishibe Joanne Colt Lynn Goldin Richard K Severson

BACKGROUND An elevated risk of developing non-Hodgkin's lymphoma (NHL) has been associated with a family history of NHL and several other malignancies, but the magnitude of risks and mechanisms are uncertain. METHODS We used self-reported family history data from a recent multicenter U.S.-based case-control studies of NHL to evaluate familial aggregation of NHL with various hematolymphoprolif...

Ghorbani, Mohammad Javad, Goodarzi, Hamid Reza, Razmi, Nematollah, Tabei, Seyed Mohammad Bagher, Zibaeenezhad, Mohammad Javad,

Background and Objectives: Coronary artery diseases (CAD) are the most common cause of death in Iran and worldwide. Myocardial infarction (MI) is a complex multifactorial and the most severe type of CAD. Early onset MI in first degree relatives could be considered as an independent risk factor for CAD. This study was performed to investigate the genetic cause of early onset familial CAD.   Cas...

Journal: :Gut 1997
L M Hunt P S Rooney K Bostock M H Robinson J D Hardcastle N C Armitage

BACKGROUND People with a family history of colorectal cancer have an increased risk of the disease themselves. Many centres are advocating family history screening by endoscopy. AIMS The performance of chemical and immunological faecal occult blood tests (Haemoccult and Hemeselect) in 212 subjects with a family history of colorectal cancer was assessed. RESULTS Both Hemeselect and Haemoccul...

Journal: :Gut 2005
J K Ramage A H G Davies J Ardill N Bax M Caplin A Grossman R Hawkins A M McNicol N Reed R Sutton R Thakker S Aylwin D Breen K Britton K Buchanan P Corrie A Gillams V Lewington D McCance K Meeran A Watkinson

Correspondence to: Dr J Ramage, North Hampshire Hospital, Aldermaston Road, Basingstoke, Hants, UK; johnramage1@ compuserve.com . . . . . . . . . . . . . . . . . . . . . . . 1.0 SUMMARY OF RECOMMENDATIONS 1.1 Genetics N Clinical examination to exclude complex cancer syndromes (for example, multiple endocrine neoplasia 1 (MEN1)) should be performed in all cases of neuroendocrine tumours (NETs), ...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2012
Liyong Wu Pedro Rosa-Neto Ging-Yuek R Hsiung A Dessa Sadovnick Mario Masellis Sandra E Black Jianping Jia Serge Gauthier

Early-onset familial Alzheimer's disease (EOFAD) is a condition characterized by early onset dementia (age at onset < 65 years) and a positive family history for dementia. To date, 230 mutations in presenilin (PS1, PS2) and amyloid precursor protein (APP) genes have been identified in EOFAD. The mutations within these three genes (PS1/PS2/APP) affect a common pathogenic pathway in APP synthesis...

Journal: :Arquivos de neuro-psiquiatria 2014
Carlos Henrique F Camargo Sarah Teixeira Camargos Nilson Becker Renato Puppi Munhoz Salmo Raskin Francisco Eduardo C Cardoso Hélio Afonso G Teive

Cervical dystonia (CD) affects the musculature of the neck in a focal way or associated to other parts of the body. The aim of this study was to identify clinical differences between patients with dystonia patients without family history and with family history (sporadic). Eighty-eight patients with CD were recruited in a Movement Disorders Clinic between June of 2008 and June of 2009. Only pat...

Journal: :Indian pediatrics 2016
Anjali Sharma Ujjal Poddar Shikha Agnihotry Rakesh Aggarwal

BACKGROUND Progressive familial intrahepatic cholestasis has been only infrequently reported from India. CASE CHARACTERISTICS An Indian girl with progressive cholestatic liver disease beginning during infancy, normal gamma-glutamyl transpeptidase levels, parental consanguinity, positive family history and a fatal outcome. OBSERVATION A novel, homozygous mutation (c.[589_592inv;592_593insA])...

2014
Vinod Kumar Khurana Raj Kumar Mehta Kapil Chandra

Familial hypercholesterolemia (FH) is a genetic disease presented by high levels of serum low density lipoprotein (LDL), xanthomas and early coronary artery disease (CAD). The diagnosis of Homozygous Familial Hypercholesterolemia (HoFH) is based on a family history of elevated cholesterol, persistent high LDL levels despite maximum medical treatment and the development of xanthomas and early at...

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