نتایج جستجو برای: intrafamilial

تعداد نتایج: 714  

Journal: :Ethnicity & disease 2006
Jelena Brezo Charmaine Royal Franklin Ampy Verle Headings

BACKGROUND Exploring the role of ethnic identity may be a good starting point toward a better understanding of health attitudes in different communities. This knowledge would be most useful in addressing diseases that cause significant burden and for which known prevention and morbidity-reducing strategies are effective. OBJECTIVE The main objective was to investigate possible associations be...

Journal: :Annals of hepatology 2012
Mitra Ranjbar Zahra Golzardi Leila Sedigh Shahbaz Nekoozadeh

OBJECTIVE To determine intrafamilial seropositivity of HBV and HCV and to compare them in families of infected persons with HBV and HCV in Hamadan clinic of hepatitis. MATERIAL AND METHODS In this analytic cross-sectional study, 651 family members of 200 HBV and HCV infection index cases were entered into the study and after signing an informed consent, they were referred to Blood Transfusion...

Journal: :Medical Journal of The Islamic Republic of Iran 2018

Journal: :Journal of the American Society of Nephrology : JASN 2016
Wouter N Leonhard Hester Happe Dorien J M Peters

Patients with autosomal dominant polycystic kidney disease (ADPKD) typically carry a mutation in either the PKD1 or PKD2 gene, which leads to massive cyst formation in both kidneys. However, the large intrafamilial variation in the progression rate of ADPKD suggests involvement of additional factors other than the type of mutation. The identification of these factors will increase our understan...

Journal: :The Laryngoscope 2014
Mee Hyun Song Joong-Wook Shin Hong-Joon Park Kyung-A Lee Yoonjung Kim Un-Kyung Kim Ju Hyun Jeon Jae Young Choi

OBJECTIVES/HYPOTHESIS Enlarged vestibular aqueduct (EVA) and hearing loss are known to be caused by SLC26A4 mutations, but large phenotypic variability exists among patients with biallelic SLC26A4 mutations. Intrafamilial phenotypic variability was analyzed in multiplex EVA families carrying biallelic SLC26A4 mutations to identify the contribution of SLC26A4 mutations and other genetic or envir...

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