نتایج جستجو برای: familial history

تعداد نتایج: 402168  

حسین قلیچ‌نیا عمرانی, , محسن روستایی‌زاده, , مژده قبائی, ,

Background: Multiple sclerosis is the most common demyelinating disease of central nervous system. We prepared this study to find its epidemiologic pattern in the Iranian society.Methods: This case-series study involved 70 patients diagnosed with multiple sclerosis according to the McDonald criteria and admitted to the Iranian Center of Neurological Research at Imam Khomeini Hospital from 2002 ...

توکلی, محمودرضا, حسینی, محمود, شکیبی, زینب, عنانی سراب, غلامرضا, غلامی ملکشاهی, رضا, مصباح‌زاده, بهزاد,

Background and Aim: As more people are at risk of cardiovascular diseases the demand for screening them is increasing. Myocardial perfusion imaging (MPI),due to not being aggressive, is used for the detection of coronary diseases and ,moreover, for the finding of the extent, severity, and location of ischemia. In the present study,myocardial perfusion scans were assessed. Materials and Methods:...

J SHARIATI, M TAVALLAI, Z JAVIDI,

In order to study the prevalence of psoriatic arthritis in Imam Reza Hospital and determine the effects of factors like age, sex, familial history, type of skin involvement, nail involvement and duration of disease on psoriatic arthritis, 300 psoriatic patients over a period of 4 years were admitted and examined in the Department of Dermatology and Rheumatology in Imam Reza Teaching Hospita...

2016
Mitra Karbasi Kheir

Cherubism is a rare familial disease that occurs between the ages two and five years and regresses after puberty. Most of the cherubism cases show familial history, but there are some cases without familial histories of disorder. A two-year-old boy with a painless symmetrical progressive swelling of the jaws had visited maxillofacial radiology department. Panoramic radiograph revealed well-defi...

Journal: :Gut 1960
A M VEALE

The history of a family suffering from familial intestinal polyposis is presented, showing how a delayed onset of symptoms together with a lack of knowledge of affected relatives may obscure the familial nature of the disease. The necessity of examining all accessible relatives, irrespective of their advancing years, is stressed. Further, it is shown that in the absence of any familial incidenc...

Journal: :Haematologica 2006
Francesca R Mauro Elena Giammartini Massimo Gentile Isabella Sperduti Veronica Valle Antonio Pizzuti Anna Guarini Diana Giannarelli Robin Foà

The prognostic impact of the presence of a familial trait was analyzed in 1449 patient with chronic lymphocytic leukemia (CLL). A family history of hematologic malignancy (HM) was identified in 181 cases (12.5%) and recorded more frequently among female than male patients (HM: p < 0.05; CLL: p < 0.05). The relative was affected by CLL in 89 cases (6%). Familial and sporadic cases showed non-sta...

2012
Sivia K Lapidus Puja Chitkara Peter W Kim Ivona Aksentijevich Elaine F Remmers Henry Feder Beverly K Barham Anne Jones Michael M Ward Karyl S Barron Daniel L Kastner Silvia Stojanov

Methods PFAPA patients were prospectively recruited. All patients had genetic testing to exclude mutations in the known fever genes (MVK, MEFV, TNFRSF1A, NLRP3, and ELA2). These PFAPA patients have been classified as sporadic or familial cases based on family history. Familial cases included those with a family member having PFAPA or a family member having a feature of PFAPA (recurrent fever, o...

2012
Mithun Das Susil Pal Arnab Ghosh

BACKGROUND Our objective was to test the association between familial risk of type 2 diabetes mellitus (T2DM) and the prevalence of metabolic syndrome (MS) in adult Asian Indians. MATERIALS AND METHODS A total of 448 adult (>30 years) individuals (257 males and 191 females) participated in the study. Familial risk of T2DM was classified into three groups viz., 1=both parents affected; 2=paren...

Journal: :British journal of neurosurgery 2008
H Lord J Ironside D Summers A Gregor S Erridge L Myles

A father and son presented ten years apart with a fourth ventricle ependymoma. The history, imaging and pathology are presented and the aetiology of familial ependymoma discussed.

Journal: :Inflammatory bowel diseases 2006
Jong Beom Park Suk-Kyun Yang Jeong-Sik Byeon Eui-Ryun Park Gyoo Moon Seung Jae Myung Won Kap Park Seo Gue Yoon Hyun Shig Kim Jong Gyun Lee Jin Ho Kim Young Il Min Kwang Yeon Kim

BACKGROUND Little information is available about the familial aggregation of inflammatory bowel disease (IBD) in Asian populations. We therefore determined the risk of familial aggregation of IBD among first-degree relatives of patients with ulcerative colitis (UC) or Crohn's disease (CD) in an ethnically distinct Korean population. METHODS Familial aggregation of IBD was evaluated in terms o...

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