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Familial resemblance of body composition in prepubertal girls and their biological parents
familial resemblance total body potassium body composition
2016/6/14
We evaluated the familial resemblance of body composition
between prepubertal girls of normal weight and body
fatness and their parents by using state-of-the-art technology.
Like mother, like daughter: familial patterns of overweight are mediated by mothers' dietary disinhibition
dietary restraint dietary disinhibition Children
2016/5/30
Obese parents are more likely to have obese
children. Parents provide both the genes and eating environment
for their children and familial patterns of adiposity are the result
of gene-environment ...
Familial cancer clinics strive to identify at-risk individuals with an inherited predisposition to cancer. Familial predisposition to colorectal cancer includes Familial Adenomatous Polyposis and Lync...
Family history of colorectal cancer is a well-established and consistently strong risk factor for this disease. However, simply counting the number of affected relatives is an imprecise measure of col...
Management of women at high familial risk for breast and ovarian cancer
high familial risk breast and ovarian cancer
2015/3/24
Women with a strong family history of breast and/or ovarian cancer have a greatly increased risk for the development of these diseases. The key question for these women is what they can do to ameliora...
The diagnosis of a familial predisposition to develop cancer carries major implications for both the affected person and their well but worried relatives. But familial cancer can almost never be diagn...
There is now an improved ability to detect people at high-risk of cancer through analysis of their family history and genetic testing. Advances in cancer screening, cancer surveillance and cancer prev...
Genetic testing is a useful means of identifying individuals who
are at an increased risk of developing familial cancer. This
information assists such individuals to make lifestyle alterations
and ...
Intra-familial Transmission of Hepatitis B virus Infection in Zahedan
Carrier States Hepatitis B Transmission Iran Prevention and control HBV Seroprevalence
2015/9/29
Background: The household transmission of hepatitis B virus (HBV) is a major health problem. The prevalence rate of this infection is reported about 11% to 57% among family members of HBsAg carriers.
Early Exposure to Environmental Toxin Contributes to Neuronal Vulnerability and Axonal Pathology in a Model of Familial ALS
SOD1 ALS Neurotoxin Axonopathy NMJ Gliosis Toxicity
2013/1/30
Adult onset amyotrophic lateral sclerosis (ALS) arises due to progressive and irreversible functional deficits to the central nervous system, specifically the loss of motor neurons. Sporadic ALS causa...
The Familial Aggregation of Cigarette Smoking in Kish,Iran
Smoking Familial aggregation Pairwise odds ratio Family-based methods
2015/9/25
Background: Based on WHO reports, smoking is an epidemic in developing countries. One of important issues about this behavior is its distribution pattern in family members. The main purpose of this st...
Familial Amyloidosis Cutis Dyschromica
Cutaneous amyloidosis dyschromic amyloidosis primer amyloidosis
2010/2/24
Primary cutaneous amyloidosis is a rare progressive disease that is characterized with the deposition of amyloid under the skin instead of internal organs. Major types are the macular, papular, nodula...
Familial occurrence of lip pits:A case report
Lip pits deformities autosomal dominant trait
2009/12/24
Lip pits are among the rarest congenital deformities recorded. Initially reported in 1845, it’s familial occurrence has been reported just once. These developmental anomalies occur either as an isolat...
Familial Costs of Chemical Warfare。
Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases
Deafness Connexin 26 GJB2 gene Iran
2009/12/7
Background: Mutations of GJB2 gene encoding connexion 26 are the most common cause of hearing loss in many populations. A very wide spectrum of GJB2 gene mutations associated with hearing loss ha...