نتایج جستجو برای: hereditary stability

تعداد نتایج: 382625  

Journal: :iranian journal of blood and cancer 0
nazemi a molavi ma raeisi e

background: neonates affected by hereditary spherocytosis may suffer from significant jaundice. this study was conducted on neonates with jaundice hospitalized at the children’s hospital in bandar abbas, south iran, to determine the frequency of hereditary spherocytosis among them. patients and methods: in this cross-sectional study, 814 neonates with jaundice hospitalized at the children’s hos...

محمدی, شباهنگ, امام جمعه, حسام‌الدین, حسین‌نژاد یزدی, مریم, دانشی, احمد, فرهادی, محمد, یداله زاده, مهدی,

    Background & Aim: When inner ear is disturbed, both hearing sensitivity and selective property decrease. Early rehabilitation for proper progression of speech and language appropriate to age is mandatory. Several studies were performed to compare factors that affect the results of cochlear implantations to select the best candidates on the basis of different criteria. This study was underta...

Journal: :Journal of Graph Theory 2013
Mirka Miller Joseph F. Ryan Zdenek Ryjácek Jakub Teska Petr Vrána

If C is a subclass of the class of claw-free graphs, then C is said to be stable if, for any G ∈ C, the local completion of G at any vertex is also in C. If cl is a closure operation that turns a claw-free graph into a line graph by a series of local completions and C is stable, then cl(G) ∈ C for any G ∈ C. In the talk we consider stability of hereditary classes of claw-free graphs defined in ...

Journal: :Evolution & development 1999
D S Thaler

Evolution and development are both lineage processes but are often conceptualized as occurring by different and mutually exclusive mechanisms. It is conventionally asserted that evolution occurs via the random generation of diversity and the subsequent survival of those that pass selection. On the other hand, development is too often presented as proceeding via the unfolding of a deterministic ...

In this paper‎, ‎we study the class of rings in which every $P$-flat‎ ‎ideal is flat and which will be called $PFF$-rings‎. ‎In particular‎, ‎Von Neumann regular rings‎, ‎hereditary rings‎, ‎semi-hereditary ring‎, ‎PID and arithmetical rings are examples of $PFF$-rings‎. ‎In the context domain‎, ‎this notion coincide with‎ ‎Pr"{u}fer domain‎. ‎We provide necessary and sufficient conditions for‎...

Journal: :iranian red crescent medical journal 0
heidar sharafi baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran seyed moayed alavian baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran; middle east liver diseases (meld) center, p.o. box 14155/3651, tehran, ir iran. tel: +98-2188945186, fax: +98-2188945188

Journal: :Journal of Mathematical Analysis and Applications 1968

Journal: :Journal of Neuropathology and Experimental Neurology 2005

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه صنعتی اصفهان - دانشکده شیمی 1389

in this project, some new polyaspartimides, (pas)s, have been synthesized form michael addition reaction between new synthetic bismaleimide (bmi) and some aromatic diamines. a characteristic property of this polyaspartimides is a pendent carboxylic group, which introduced to these polymers from new bismaleimide. bismaleimides (bmi) is one of the interesting compounds, which can be self-polymeri...

Journal: :genetics in the 3rd millennium 0
غلام علی شهیدی gholam ali shahidi assist prof of neurology, rasul akram hospital, iran university of medical sciences, tehran, iran محمد روحانی mohammad rohani

the hereditary ataxias comprise a wide spectrum of heterogeneous disorders that share three features: ataxia, involvement of cerebellum or its connections, and heritability. in many hereditary ataxias, the underlying gene mutations have been identified. knowledge of the causative mutations allows a rational classification of hereditary ataxias as autosomal recessive, autosomal dominant or mater...

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