نتایج جستجو برای: familial residential pattern

تعداد نتایج: 436138  

2013
Alexandra D. Syphard Avi Bar Massada Van Butsic Jon E. Keeley

Increasing numbers of homes are being destroyed by wildfire in the wildland-urban interface. With projections of climate change and housing growth potentially exacerbating the threat of wildfire to homes and property, effective fire-risk reduction alternatives are needed as part of a comprehensive fire management plan. Land use planning represents a shift in traditional thinking from trying to ...

ژورنال: کومش 2022

Introduction: Type 2 diabetes, as a complex disorder, is one of the most prevalent endocrine disorders.  Importantly, the extent of familial aggregation and heritability in Iran is unknown. The aim of the present study was to determine type 2 diabetes heritability in the Tehran families. Materials and Methods: The current research comprises 1691 diabetic and 12050 non-diabetic individuals over ...

Journal: :world journal of plastic surgery 0
waleed alshehri department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia sara alfadil department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia alhanouf alothri department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia abdulaziz o. alabdulkarim department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia shabeer a. wani department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia sari m. rabah department of plastic and reconstructive surgery, king fahd medical city, riyadh, saudi arabia

aplasia cutis conginita (acc) is a condition characterized by congenital absence of skin, usually on the scalp. acc can occur as an isolated condition or in the presence of other congenital anomalies. here we describe a case of a 16 days old baby girl with an isolated acc of the scalp. her elder two siblings have been diagnosed with acc with concomitant cardiac or limb anomalies. the patient wa...

Journal: :international journal of civil engineering 0
shahriar afandizadeh morteza araghi

0

Journal: :Gut 1995
A M Brind G P Bray B C Portmann R Williams

Susceptibility to primary biliary cirrhosis (PBC) may be partly inherited although instances of PBC within families are only infrequently described. The records of 736 patients with PBC seen over a 25 year period were examined to identify those with a positive family history. Ten patients originating from eight families were identified, giving a frequency of 1.33%. They comprised mother and dau...

Journal: :Journal of lipid research 2013
D Meeike Kusters Hans J Avis Marjet J Braamskamp Roeland Huijgen Frits A Wijburg John J Kastelein Albert Wiegman Barbara A Hutten

Studies in children and adults have resulted in conflicting evidence in the quest for the answer to the hypothesis that offspring from hypercholesterolemic mothers might have an increased cardiovascular risk. Previous studies might have suffered from limitations such as cohort size and clinical sampling bias. We therefore explored this hypothesis in large cohorts of both subjects with familial ...

2014
Christine M Mueller Larissa A Korde Mary L McMaster June A Peters Gennady Bratslavsky Rissah J Watkins Alex Ling Christian P Kratz Eric A Wulfsberg Philip S Rosenberg Mark H Greene

BACKGROUND Testicular germ cell tumor (TGCT) is the most common malignancy in young men. Familial clustering, epidemiologic evidence of increased risk with family or personal history, and the association of TGCT with genitourinary (GU) tract anomalies have suggested an underlying genetic predisposition. Linkage data have not identified a rare, highly-penetrant, single gene in familial TGCT (FTG...

2013
David M. Cash Gerard R. Ridgway Yuying Liang Natalie S. Ryan Kirsi M. Kinnunen Thomas Yeatman Ian B. Malone Tammie L.S. Benzinger Clifford R. Jack Paul M. Thompson Bernardino F. Ghetti Andrew J. Saykin Colin L. Masters John M. Ringman Stephen P. Salloway Peter R. Schofield Reisa A. Sperling Nigel J. Cairns Daniel S. Marcus Chengjie Xiong Randall J. Bateman John C. Morris Martin N. Rossor Sébastien Ourselin Nick C. Fox

OBJECTIVE To assess regional patterns of gray and white matter atrophy in familial Alzheimer disease (FAD) mutation carriers. METHODS A total of 192 participants with volumetric T1-weighted MRI, genotyping, and clinical diagnosis were available from the Dominantly Inherited Alzheimer Network. Of these, 69 were presymptomatic mutation carriers, 50 were symptomatic carriers (31 with Clinical De...

2016
Adélaïde Durand Anu Bashamboo Ken McElreavey Raja Brauner

BACKGROUND The mechanism that initiates the onset of puberty is largely unknown but the age of onset is mainly under genetic control and influenced by environmental factors including nutrition. The coexistence in the same family of central precocious puberty and advanced puberty, both representing early puberty, suggests that they may represent a clinical spectrum of the same trait due to early...

Journal: :J. Inf. Sci. Eng. 2009
Cheng-Liang Lin Pang-Chieh Wang Ting-Wei Hou

If Interactive Digital Television (IDTV) and Residential Service Gateway (RG) converge, i.e. to share services and resources, add-on values or new services could be created. We assume that a user will have an IDTV instance and an RG instance. These two can be implemented on a single machine or each on a separate machine connected by a network. Collaboration architectures of IDTV and RG support ...

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