نتایج جستجو برای: regional odonto dysplasia

تعداد نتایج: 234433  

Journal: :مجله دانشکده دندانپزشکی مشهد 0
نوشین نوشین محتشم nooshin mohtasham associate professor, dept of oral and maxillofacial pathology, school of dentistry and dental research center of mashhad university of medical sciences, mashhad, iranدانشیار گروه آسیب شناسی دهان، فک و صورت دانشکده دندانپزشکی و مرکز تحقیقات دندانپزشکی دانشگاه علوم پزشکی مشهد نصرالله نصرالله ساغروانیان nasrollah saghravanian assistant professor, dept of oral and maxillofacial pathology, school of dentistry and dental research center of mashhad university of medical sciences, mashhad, iranاستادیار گروه آسیب شناسی دهان، فک و صورت دانشکده دندانپزشکی و مرکز تحقیقات دندانپزشکی دانشگاه علوم پزشکی مشهدسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) نوریه نوریه شریفی noorieh sharifi associate professor, dept of pathology, ghaem hospital, mashhad university of medical sciences, mashhad, iranدانشیار گروه آسیب شناسی بیمارستان قائم دانشگاه علوم پزشکی مشهدسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) محمد تقی محمد تقی شاکری mohammadtaghi shakeri associate professor, dept of epidemiology, ghaem hospital, mashhad university of medical sciences, mashhad, iranدانشیار گروه اپیدمیولوژی و آمار حیاتی بیمارستان قائم دانشگاه علوم پزشکی مشهدسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) شیما شیما عامل قریب shima amelgarieb dentistدندانپزشکسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) ستاره ستاره شجاعی setareh shojaee postgraduate student, dept of oral and maxillofacial pathology, dental school, mashhad university of medical sciences, mashhad, iranدستیار تخصصی گروه آسیب شناسی دهان و فک و صورت دانشکده دندانپزشکی دانشگاه علوم پزشکی مشهد

introduction: leukoplakia is the most common precancerous lesion of the oral mucosa and may range microscopically form benign hyperkeratosis to invasive squamous cell carcinoma. p53 is a tumor suppressor protein; whereas, proliferative cell nuclear antigen (pcna) is a proliferative marker. the aim of this study was to evaluate the immunohistochemical expressions of p53 and pcna in oral leukopla...

Journal: :iranian journal of medical sciences 0
mitra basiratnia shiraz nephrology-urology research center, shiraz university of medical sciences, shiraz, iran alireza baradaran-heravi child and family research institute, department of medical genetics, university of british columbia, vancouver, canada majid yavarian hematology research center, shiraz university of medical sciences, shiraz, iran bita geramizadeh department of pathology, shiraz university of medical sciences, shiraz, iran mehran karimi hematology research center, shiraz university of medical sciences, shiraz, iran

schimke immuno-osseous dysplasia is a rare autosomal recessive multisystem disorder characterized by steroid-resistant nephrotic syndrome, immunodeficiency, and spondyloepiphy-seal dysplasia. mutations in swi/snf2 related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1 (smarcal1) gene are responsible for the disease. the present report describes, for the first tim...

Journal: :acta medica iranica 0
m. eslami f. baghaee m. alaeddini

it is sometimes difficult to recognize a jaw lesion as osteosarcoma, ossifying fibroma or ‎fibrous dysplasia in routine hematoxylin and ‎eosin staining and a more accurate technique is needed to differentiate these ‎lesions. ‎many studies have shown the potential usefulness of silver-stained nucleolar organizer region (agnor) parameters for the diagnosis of various neoplasms. this study was car...

علایی , عبدالرسول, غفاری ساروی , وجیهه,

Çamptomelic dysplasia is a fatal infantile dysplasia characterized by lower limb bowing and mesomelic dwarfism. Most of this skeletal dysplasia occur through spontaneous mutation, but recessive autosomic recession is also likely. Prenatal diagnosis is considered with ultrasonography and amniocentesis. Postnatal diagnosis is characterized by mesomelic dwarfism with limb bowing, pulmonary h...

Journal: :Hong Kong medical journal = Xianggang yi xue za zhi 2012
C H Yau K Y Choi N S Kwong P C Lau M K Yuen N C Kwok Y Y Chow Sylvia L Y Siu K W Li Diana K Lam

OBJECTIVES. To clarify the use of ultrasonography by determining the frequency of developmental dysplasia of the hip among breech-presented Chinese neonates in Hong Kong. DESIGN. Prospective case series. SETTING. Regional hospital, Hong Kong. PATIENTS. All breech-presented Chinese neonates born during January 2008 to June 2009 were included (except premature neonates). They were examined clinic...

Journal: :Folia morphologica 2004
Mariusz Koda Luiza Kanczuga-Koda Joanna Reszec Mariola Sulkowska Waldemar Famulski Marek Baltaziak Wojciech Kisielewski Stanislaw Sulkowski

Apoptosis and proliferation are processes associated with the development and progression of breast cancer. The sensitivity of tumour cells to the induction of apoptosis depends on the balance between pro- and anti-apoptotic proteins. The expression of Bak and Bcl-2 was examined using an immunohistochemical method in 71 primary breast cancers. Furthermore, Bcl-2 and Bak were assessed in the nor...

2013
Lyn S Chitty Asma Khalil Angela N Barrett Eva Pajkrt David R Griffin Tim J Cole

OBJECTIVE To improve the prenatal diagnosis of thanatophoric dysplasia by defining the change in fetal size across gestation and the frequency of sonographic features, and developing non-invasive molecular genetic diagnosis based on cell-free fetal DNA (cffDNA) in maternal plasma. METHODS Fetuses with a confirmed diagnosis of thanatophoric dysplasia were ascertained, records reviewed, sonogra...

Journal: :iranian journal of allergy, asthma and immunology 0
farzaneh motamed fariborz zieh mostafa sedighi

in this case report we will describe a rare association between anhyrotic ectodermal dysplasia (aed) and immunodeficiency and autoimmunity [in our case: idiopathic thrombocytopenic purpura (itp) and crohn disease]. aed is a rare congenital disorder characterized by sparse hair, abnormal teeth and anhidrosis due to lack of eccrine glands. the survey of 87 cases with (aed) revealed only one irrit...

Journal: :Journal of neuropathology and experimental neurology 2012
Takafumi Sakakibara Sayuri Sukigara Takashi Saito Taisuke Otsuki Akio Takahashi Yuu Kaneko Takanobu Kaido Yuko Saito Noriko Sato Yukio Kimura Eiji Nakagawa Kenji Sugai Masayuki Sasaki Yu-Ichi Goto Masayuki Itoh

Transmantle dysplasia is a rare type of focal cortical dysplasia (FCD) characterized by expansion of the cortex from the deep white matter to the surface and in which there is a FCD IIA or IIB pathologic pattern. To characterize possible mechanisms underlying this regional disorder of radial migrating cells, we studied the expression patterns of neocortical layer-specific markers using immunohi...

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