نتایج جستجو برای: familial support

تعداد نتایج: 710137  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم پایه 1391

در بیماری als نیز بیماران مبتلا دارای تجمعات پروتئینی در جسم سلولی و آکسونهای نورونهای حرکتی بافت عصبی خود می باشند که بطور عمده متشکل از آنزیم سوپراکسید دیسموتاز 1 (sod1) است. جهش در ژن sod1 در 20% از موارد familial als (fals) مشاهده می شود و به عنوان یک عامل مهم در ایجاد این بیماری شناخته می شود. مکانیزم بیماری زایی تجمعات sod1در بیماری fals اگر چه هنوز به طور کامل مشخص نیست اما تغییر در خصوص...

Journal: :OBM geriatrics 2023

Social support has been shown to have many positive effects on our lives, health, and ability grow flourish. Lack, or diminished social results in loneliness. This thematic review focuses the elderly, loneliness that is part of life them. The highlights connections expectations elderly may them, how being connected others alleviate, Loneliness known negatively affect one’s life, familial relati...

Journal: :Journal of Family Issues 2021

Building on the Behavioral Process Model of Familism, current study examined longitudinal association between public and private ethnic regard familial support, familism values in a sample 141 Latinx 7th–10th graders living semi-rural, emerging immigrant community. Analyses revealed that changes were positively related to ( p<.001) over time, but there no cross-lagged associations. Additiona...

Journal: :Blood 2005
Andrea Altieri Justo Lorenzo Bermejo Kari Hemminki

Non-Hodgkin lymphoma (NHL) consists of a heterogeneous group of tumors. Population-based data on the familial risk for specific histopathologic subtypes have not been established. Such data are useful for clinical counseling and for searching tumor subtypes sharing common genetic pathways. We used the Swedish Family-Cancer Database to calculate standardized incidence ratios (SIRs) for histopath...

Journal: :Brain : a journal of neurology 2000
G C Ebers W J Koopman W Hader A D Sadovnick M Kremenchutzky P Mandalfino D M Wingerchuk J Baskerville G P Rice

We have examined the demographics and long-term outcome of 1044 patients with sporadic and familial multiple sclerosis in a population-based cohort from London, Ontario. The mean follow-up was 25 years in duration, and by this time most patients had reached the unambiguous endpoint scores of the Kurtzke disability status scale (DSS), DSS 6, 8 or 10. An affected family member was identified in 1...

Abstract Familial hypercholesterolemia (FH) is a hereditary dislipidemia. Patients present with extremely high level of low-density lipoprotein cholesterol (LDL-C), which is due to mutation in the gene of LDL receptor. Homozygous patients (HoFH) whose incidence is 1 in 1.000.000 are at high risk of premature aortic valve stenosis, and coronary artery atherosclerosis. In homozygous individual...

Journal: :گوارش 0
morteza khatibian peyman arab

familialmediterranean fever (fmf) is a hereditary syndrome characterized by recurrent attacks of fever and serositis. liver involvement in fmf has been reported in association with amyloidosis or rarely with vasculitis.in this report, a 32 year-old man with recurrent attacks of fever, abdominal pain and arthralgia is described who had moderate increase in liver transaminases only during disease...

Journal: :iranian journal of psychiatry and behavioral sciences 0
mina zarei tehran university of medical sciences reza bidaki mitra hakim-shooshtari

bipolar disorder is a mental disease that can be presented as irritable mood with affective storms, mixed symptoms of depression and mania, rapid cycles, emotional labiality and irritability during all episodes. â confirmed positive familial history of the disease is the single most robust risk factor for developing the illness. this report presents 5.5 years-old girl with the symptoms of bipol...

Journal: :novelty in biomedicine 0
badiozaman radpay department of anesthesiology critical care and pain management, lung transplantation research center, national research institute of tuberculosis and lung disease, tehran, iran mahtab poor zamany nejat kermany department of anesthesiology, labbafinejad medical center, shahid beheshti university of medical sciences, tehran, iran ali asghar halimi-asl department of pediatrics, shohada tajrish medical center, shahid beheshti university of medical sciences, tehran, iran

background: familial dysautonomia (fd) is a rare hereditary syndrome which is an autosomal recessive trait that typically affects jewish children. important signs and symptoms of the disorder include; diminished pain perception, absence of overflow tears, hypotonia, fainting cardiac arrhythmias and autonomic crisis. cases report : in this article we reported 3 cases of fd syndrome which had pre...

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