نتایج جستجو برای: sulzberger disease

تعداد نتایج: 1490508  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه صنعتی اصفهان - دانشکده کشاورزی 1394

بیماری سلیاک (coeliac disease)یک اختلال خودایمنی با زمینه ژنتیکی است. در بیماری سلیاک، سیستم ایمنی ترکیبات موجود در گلوتن را به عنوان تهدیدی برای بدن به حساب آورده و به آن ها حمله می کند. این امر باعث آسیب پرزهای روده باریک شده و توانایی بدن در جذب مواد غذایی را از بین می برد. گلوتن پروتئینی است که در غلاتی نظیر گندم، جو، چاودار و برخی اوقات جو دوسر یافت می شود. درمانی برای بیماری سلیاک وجود ند...

2016

and male alopecia [1–4] . The prerequisite for delivering appropriate patient care is an understanding of the pathologic dynamics of hair loss and a potential multitude of causal relationships. Once the diagnosis is certain, treatment appropriate for that diagnosis is likely to control the problem. Ultimately, the best way to alleviate the emotional distress related to hair loss is to effective...

Journal: :Skin appendage disorders 2016
Alfredo Rebora

and male alopecia [1–4] . The prerequisite for delivering appropriate patient care is an understanding of the pathologic dynamics of hair loss and a potential multitude of causal relationships. Once the diagnosis is certain, treatment appropriate for that diagnosis is likely to control the problem. Ultimately, the best way to alleviate the emotional distress related to hair loss is to effective...

Journal: :International journal of cancer 2007
Angèle L Oei René H Verheijen Michael V Seiden Benedict B Benigno Alberto Lopes John T Soper Agamemnon A Epenetos Leon F Massuger

This study analyzes the site of disease recurrence in ovarian cancer patients to assess the influence of a single intraperitoneal (IP) administration of yttrium-90-labeled murine monoclonal antibody HMFG1 ((90)Y-muHMFG1) on the pattern of disease recurrence. In a large phase III trial ovarian cancer patients in complete clinical remission with FIGO stage Ic-IV were randomized between standard t...

2000
Marcello Ciafaloni Paolo Ciafaloni Denis Comelli

Hard processes at the TeV scale exhibit enhanced (double log) EW corrections even for inclusive observables, leading to violation of the Bloch-Nordsieck theorem. This effect, previously related to the non abelian nature of free EW charges in the initial state (ee, ep, pp ...), is here investigated for fermion initiated hard processes and to all orders in EW couplings. We find that the effect is...

2015
T. A. Ostler M. O. A. Ellis

Using the Landau-Lifshitz-Bloch (LLB) equation for ferromagnetic materials, we derive analytic expressions for temperature-dependent absorption spectra as probed by ferromagnetic resonance. By analyzing the resulting expressions, we can predict the variation of the resonance frequency and damping with temperature and coupling to the thermal bath. We base our calculations on the technologically ...

Journal: :Srpski arhiv za celokupno lekarstvo 2010
Snezana Minić Miljana Obradović Igor Kovacević Dusan Trpinac

INTRODUCTION Incontinentia pigmenti (IP) is an X-linked genodermatosis in which skin changes are combined with dental, eye and central nervous system anomalies. OBJECTIVE The goal of the study was to analyze ocular findings, IP minor criteria in available literature concerning IP cases published until now. METHODS We have done meta-analysis of 1931 IP patients found in 302 references publis...

2007
Nakjung Choi Hyeongu Son Youngseok Lee Yanghee Choi

Though the popular Cisco NetFlow is widely used for flow-level traffic measurement in IPv4 networks, it is not suitable for IPv6 networks because of the fixed flow structure that cannot carry IPv6-related information. Therefore, the IETF IP Flow Information eXport (IPFIX) standard that employs the flexible flow template structure has been recently proposed to support various flow-level traffic ...

Journal: :Annals of dermatology 2008
Ji Young Song Chan Ho Na Byoung Soo Chung Kyu Cherl Choi Bong Seok Shin

Incontinentia pigmenti (Bloch-Sulzberger's disease) is an X-linked dominantly inherited disorder which is usually lethal in hemizygous males, but rarely found in male infants. It can be explained by the presence of an extra X chromosome (Klinefelter's syndrome), hypomorphic mutations, and somatic mosaicism. We herein report a rare case of incontinentia pigmenti with typical course of skin manif...

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