نتایج جستجو برای: cystic

تعداد نتایج: 47254  

Journal: :journal of comprehensive pediatrics 0
brenda may morrow department of pediatric medicine, university of cape town, cape town, south africa; department of pediatric medicine, university of cape town, cape town, south africa. tel: +27216585074, fax: +27216891287

Journal: :iranian biomedical journal 0
marzieh mohseni mohammad razzaghmanesh elham parsi mehr hanieh zare maryam beheshtian hossein najmabadi

background: cystic fibrosis (cf) is a common autosomal recessive disorder that affects many body systems and is produced by mutations in the cystic fibrosis transmembrane conductance regulator (cftr) gene. cf is also the most frequently inherited disorder in the west. the aim of this study was to detect the mutations in the cftr gene in two iranian families with cf. methods: after dna extractio...

Journal: :iranian journal of public health 0
ar khabiri f bagheri mr siavashi m assmar

background: anaphylactic reactions, such as urticaria, edema, respiratory symptoms, and anaphylactic shock often complicate the course of cystic echinococcosis (ce). methods: to investigate the role of the ige immunoreactive antigen 5 (ag 5) in the sero-positive patients with ce, we determined n-terminal of 57 kda subunit of ag5 responsible for ige and c-terminal of this active antigen related ...

Journal: :middle east journal of digestive diseases 0
gholam reza khatami mohammad mehdi mir-nasseri fariba seyghali bahar allah-verdi fatemeh yourdkhani

â  â  b ackground cystic fibrosis (cf) is an autosomal recessive disease caused by a cf trans-membrane regulator (cftr) defect. its prevalence is 1:2500 in caucasians, 1:15300 among african americans and is rare in southâ­east asia. the present study aims to review demographic data, clinical manifestations and laboratory findings of iranian children diagnosed with cf who referred to a childrenâ...

Journal: :hepatitis monthly 0
giuseppe fabio parisi department of medical and pediatric science, bronchopneumology and cystic fibrosis unit, university of catania, catania, italy giovanna di dio department of medical and pediatric science, bronchopneumology and cystic fibrosis unit, university of catania, catania, italy chiara franzonello department of medical and pediatric science, bronchopneumology and cystic fibrosis unit, university of catania, catania, italy alessia gennaro department of medical and pediatric science, bronchopneumology and cystic fibrosis unit, university of catania, catania, italy novella rotolo department of medical and pediatric science, bronchopneumology and cystic fibrosis unit, university of catania, catania, italy elena lionetti department of medical and pediatric science, bronchopneumology and cystic fibrosis unit, university of catania, catania, italy

context cystic fibrosis (cf) is the most widespread autosomal recessive genetic disorder that limits life expectation amongst the caucasian population. as the median survival has increased related to early multidisciplinary intervention, other manifestations of cf have emergedespecially for the broad spectrum of hepatobiliary involvement. the present study reviews the existing literature on liv...

Journal: :acta medica iranica 0
mazdak momeni department of obstetrics, gynecology and reproductive medicine, loma linda university medical center, loma linda, california, usa. yelena korotkaya department of obstetrics and gynecology, suny downstate medical center, brooklyn, new york, usa. gonzalo carrasco department of pathology, icahn school of medicine at mount sinai, new york, usa. monica prasad-hayes department of obstetrics, gynecology and reproductive medicine, loma linda university medical center, loma linda, california, usa.

abstract: primary adenoid cystic carcinoma (acc) of bartholin’s gland is a rare gynecologic malignancy. we report a case of locally advanced acc of bartholin’s gland. a 62-year-old presented with left bartholin’s gland carcinoma and underwent left radical vulvectomy,left-sided inguinal-femoral lymph node dissection, posterior pelvic exenteration, and pedicle abdominal muscle flap. on her 3 mont...

جواهرزاده, مجتبی, حسن زاد, مریم, خدایاری, امیرعلی, خلیل‌زاده, سهیلا, پارسانژاد, نازنین , پور عبدالله, میهن,

  Introduction: Cystic hygromas (lymphangioma) are benign and common developmental anomalies of vasculolymphatic origin.They can arise anywhere along the lymphatic system. However, they are usually located in the neck region and in most cases (80-90%) appear by the age of 2. Most mediastinal cystic hygromas are extensions of cervical lesions, and cystic hygroma confined solely to the mediastinu...

Gulshan Tasleem Shabbir Hussain

Cystic lymphangioma is a rare benign tumour occurring during childhood. This tumour, caused by lymphatic system malformations, commonly occurs in head and neck regions. Herein, we report the case of a three-month-old male infant, diagnosed with a large cystic mass in the abdominal cavity and groin. The infant presented with low-grade fever and significant abdominal distension. Abdominal CT scan...

حسن‌پور, اکبر, هورمزدی, مهشید,

In this case report we present a 49 year old man with history of a mass in right upper quadrant and microscopic hematuria who referred to the hospital 2 months ago. In sonography, one cystic mass with multiple irregular septa in upper segment of right kidney and in CT scan, a multiloculated cystic mass in anterior of right kidney was reported. Under light microscopic examination the ...

Journal: :journal of research in medical sciences 0
mohammad reza haji esmaeili resident of anesthesiology, yazd university of medical science and health service seyed soheil ben razavi assistant professor of pediatric surgery, yazd university of medical science and health service hamid reza abbasi assistant professor of anesthesiology, yazd university of medical science and health service seyed mahmud tabatabaii anesthesiologist, yazd university of medical science and health service mohammad ali sheikhi resident of anesthesiology

cystic hygroma (ch) in the cervical region presents as a challenge to the anesthetist. the anaesthetic difficulties are usually associated with ch because of tumor extension into the mouth, airway management, thoracic extension, hemorrhage, involvement of pretracheal region, post operative respiratory obstruction and coexisting anomalies (down syndromes, turner syndromes and congenital cardiac ...

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