نتایج جستجو برای: dysplasia epiphysealis hemimelica

تعداد نتایج: 28617  

Journal: :iranian journal of radiology 0
hasan erdinc kocer department of electronics and computer education, technical education faculty, selcuk university, konya, turkey kerim kursat cevik department of computer programming, bor vocational high school, nigde university, nigde, turkey; department of computer programming, bor vocational high school, nigde university, nigde, turkey. tel: +90-3883114527, fax: +90-3883118437 mesut sivri department of radiology, medical faculty, selcuk university, konya, turkey mustafa koplay department of radiology, medical faculty, selcuk university, konya, turkey

conclusion various filters are needed to improve the image quality. in this study, seven different filters were implemented and investigated on both noisy and noise-free images. background developmental dysplasia of the hip (ddh) can be detected with ultrasonography (usg) images. however, the accuracy of this method is dependent on the skill of the radiologist. radiologists measure the hip join...

Journal: :journal of dental school, shahid beheshti university of medical sciences 0
جمیله بیگم طاهری jamile beygom taheri dental school, shahid beheshti university of medical sciences, tehran-iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی سمیه عظیمی somayyeh azimi dental school, shahid beheshti university of medical sciences, tehran-iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی حامد مرتضوی hamed mortazavi dental school, shahid beheshti university of medical sciences, tehran-iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی سمیه بابایی somayyeh babaee dental school, shahid beheshti university of medical sciences, tehran-iran.دانشکده دندانپزشکی، دانشگاه علوم پزشکی شهید بهشتی محمدرضا ترحمی mohammad-reza tarahhomi medical school, hamedan university of medical sciences, hamedan-iran.دانشکده پزشکی، دانشگاه علوم پزشکی همدان.

objectives: ectrodactyly-ectodermal dysplasia-clefting syndrome (eec) is a rare syndrome with features of ectrodactyly, ectodermal dysplasia and cleft lip/palate. this study presents an iranian case with classic features and oral complications.   case: we report a 20-year old female with all manifestations of this syndrome. the simultaneous presence of these three malformations is extremely rar...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006
Joon-Yong Chung Till Braunschweig Nan Hu Mark Roth June L Traicoff Quan-Hong Wang Vladimir Knezevic Philip R Taylor Stephen M Hewitt

Esophageal cancer remains a highly lethal malignancy for which the genetic and proteomic events are poorly understood. Studies have reported dysregulated proteins in esophageal carcinoma; however, the magnitude of these changes remains largely uncharacterized. Little is known about alterations early in the neoplastic pathway. Using multiplex tissue immunoblotting, we quantified the expression o...

2006
Joon-Yong Chung Till Braunschweig Nan Hu Mark Roth June L. Traicoff Quan-Hong Wang Vladimir Knezevic Philip R. Taylor Stephen M. Hewitt

Esophageal cancer remains a highly lethal malignancy for which the genetic and proteomic events are poorly understood. Studies have reported dysregulated proteins in esophageal carcinoma; however, the magnitude of these changes remains largely uncharacterized. Little is known about alterations early in the neoplastic pathway. Using multiplex tissue immunoblotting, we quantified the expression o...

Fatemeh Mohamadian, Soudabeh Sargolzaei,

Objectives: E-cadherin is a transmembrane glycoprotein, which is responsible for cell adhesion and its expression decreases in dysplastic lesions. This study aimed to assess the expression of this marker in oral lichen planus (OLP) with and without dysplasia to assess its potential for use as a predictor of malignant transformation. Methods: This descriptive, cross-sectional study w...

2006
R D Odze

This review focuses on the pathological features of dysplasia in Barrett’s oesophagus. Two categorisation schemes are used for grading dysplasia in the gastrointestinal tract, including Barrett’s oesophagus. The inflammatory bowel disease dysplasia morphology study group system is the one most commonly used in the USA. However, some European and most far Eastern countries use the Vienna classif...

Journal: :Journal of clinical pathology 2006
R D Odze

This review focuses on the pathological features of dysplasia in Barrett's oesophagus. Two categorisation schemes are used for grading dysplasia in the gastrointestinal tract, including Barrett's oesophagus. The inflammatory bowel disease dysplasia morphology study group system is the one most commonly used in the USA. However, some European and most far Eastern countries use the Vienna classif...

Journal: :international journal of pediatrics 0
majid mahallei assistant professor of pediatrics and neonatology, tabriz university of medical sciences, tabriz, iran. manizheh mostafa gharehbaghi professor of pediatrics and neonatology, women’s reproductive health research center, tabriz university of medical sciences, tabriz, iran. leila majidzadeh pediatrician, tabriz university of medical sciences, tabriz, iran. nazanin hazhir general practitioner, tabriz university of medical sciences, tabriz, iran.

background bronchopulmonary dysplasia (bpd) is one of the most common serious squeal of preterm infants. it involves approximately one quarter of infants with birth weight less than 1500 grams and 30% of less than 1000 grams. vitamin a has been shown to reduce bpd rate. we compared efficacy of low and high doses of vitamin a for prevention of bpd in very low birth weight preterm infants. materi...

Journal: :international journal of pediatrics 0
moein mobini department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. rahim vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran. saba vakili department of pediatric endocrinology and metabolism, mashhad university of medical science, mashhad, iran.

mccune-albright syndrome (mas) is a rare, heterogenous, clinical condition caused by a rare genetic mutation. the disorder is more common in females and is characterized by a triad of cutaneous, bone and endocrine abnormalities.  we describe a girl patient with mas having precocious puberty and multiple cafe-au-lait macules and deforming polyostotic fibrous dysplasia of bone. clinical presentat...

Journal: :iranian journal of medical sciences 0
suzanne tanya nethan department of oral medicine and radiology, saraswati dental college, lucknow, uttar pradesh, india shruti sinha department of oral medicine and radiology, saraswati dental college, lucknow, uttar pradesh, india sunira chandra department of oral medicine and radiology, saraswati dental college, lucknow, uttar pradesh, india

the ellis-van creveld (evc) syndrome is a chondroectodermal dysplasia and is characterized by the cardinal features of disproportionate short stature, polydactyly, hidrotic ectodermal dysplasia, and congenital heart malformations, along with other skeletal and dental abnormalities. it is a rare condition, with very few cases reported in the medical literature. it is inherited as an autosomal re...

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