نتایج جستجو برای: intra familial transmission

تعداد نتایج: 395580  

Journal: :Information 2017
Qiuming Liu Xuejing Jiang Xiaohong Qiu

In this paper, we jointly consider the inhomogeneity and spatial dimension in large scale wireless networks. We study the effects of topology on the throughput capacity. This problem is inherently difficult since it is complex to handle the interference caused by simultaneous transmission. To solve this problem, we, according to the inhomogeneity of topology, divide the transmission into intra-...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Huibing Tan Nicole M Lauzon Stephanie F Bishop Ning Chi Melanie Bechard Steven R Laviolette

The cannabinoid CB1 receptor system is critically involved in the control of associative fear memory formation within the amygdala-prefrontal cortical pathway. The CB1 receptor is found in high concentrations in brain structures that are critical for emotional processing, including the basolateral amygdala (BLA) and the prelimbic division (PLC) of the medial prefrontal cortex (mPFC). However, t...

Journal: :The American journal of psychiatry 2000
M Strober R Freeman C Lampert J Diamond W Kaye

OBJECTIVE Lifetime rates of full and partial anorexia nervosa and bulimia nervosa were determined in first-degree relatives of diagnostically pure proband groups and relatives of matched, never-ill comparison subjects. METHOD Rates of each eating disorder were obtained for 1,831 relatives of 504 probands on the basis of personal structured clinical interviews and family history. Best-estimate...

Journal: :Croatian medical journal 2010
Khaled AbdulQawi Ahmed Youssef Mohamed A Metwally Ibrahim Ragih Mohamed AbdulHamid AbdulAziz Shaheen

AIM To estimate the hepatitis C virus (HCV) vertical transmission rate, the effect of potential risk factors, and the pattern of HCV antibody response and viremia in HCV-infected infants in Benha, Egypt. METHODS A total of 1224 pregnant women who were treated at Benha University Hospital, Egypt, were included in the study. They completed a questionnaire about risk factors for HCV acquisition ...

Journal: :Genetic epidemiology 1998
J F Aitken J Bailey-Wilson A C Green R MacLennan N G Martin

To investigate whether the familial clustering of cutaneous melanoma is consistent with Mendelian inheritance of a major autosomal gene, maximum likelihood segregation analyses were performed in a population-based sample of 1,912 families ascertained through a proband with melanoma diagnosed in Queensland between 1982 and 1990. Analyses were performed with the S.A.G.E. statistical package, usin...

2016
Chang-Fu Kuo Shue-Fen Luo Kuang-Hui Yu Lai-Chu See Weiya Zhang Michael Doherty

BACKGROUND Systemic sclerosis (SSc) is a rare and devastating disease affecting skin and internal organs. Familial aggregation of SSc and co-aggregation with other autoimmune diseases is rarely reported. METHODS We identified 23,658,577 beneficiaries registered with the National Health Insurance database in 2010, 1891 of whom had SSc. We identified 21,009,551 parent-child relationships and 17...

Journal: :Journal of medical genetics 1986
J Köbberling M G Dunnigan

Familial lipodystrophy (referred to in publications as the Köbberling-Dunnigan syndrome) comprises at least two clinical phenotypes which are consistent within each pedigree. In type 1 familial lipodystrophy, loss of subcutaneous fat is confined to the limbs, sparing the face and trunk. In type 2 familial lipodystrophy, the trunk is also affected with the exception of the vulva, giving an appea...

Journal: :Blood 2002
Lea C Harty Albert Y Lin Alisa M Goldstein Elaine S Jaffe Mary Carrington Margaret A Tucker William S Modi

The HLA region has long been implicated in sporadic and familial Hodgkin disease (HD), with recent case-control studies suggesting that HLA class II loci predispose to sporadic nodular sclerosis HD (NSHD). To determine whether this predisposition extends to familial HD, HLA class II loci (DRB1, DQA1, DQB1, DRB3, DRB4, and DRB5) and transporter associated with antigen processing (TAP) loci (TAP1...

Journal: :Annual review of microbiology 1999
E D Belay

Creutzfeldt-Jakob disease (CJD), the first transmissible spongiform encephalopathy (TSE) to be described in humans, occurs in a sporadic, familial, or iatrogenic form. Other TSEs in humans, shown to be associated with specific prion protein gene mutations, have been reported in different parts of the world. These TSEs compose a heterogeneous group of familial diseases that traditionally have be...

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