نتایج جستجو برای: hereditary non

تعداد نتایج: 1390343  

Journal: :The Journal of the Association of Physicians of India 2014
Prachee Deshpande Shreepad Bhat Anup Karmarkar

Hereditary Haemorrhagic Telangiectasia also known as Osler-Rendu-Weber disease is a rare autosomal dominant disorder affecting small vessels of skin and mucosa, usually misdiagnosed because of its non specific symptomatology. This disease usually presents as epistaxis, gastrointestinal bleeding and visceral arteriovenous malformations. Although the epistaxis and gastrointestinal blood loss can ...

2011
Ralph H Hruban Scott E Kern

Alias: Familial pancreatic cancer Inheritance It has been estimated that as many as 10% of pancreatic cancers have a hereditary basis; five genetic syndromes have been identified that are associated with the familial aggregation of pancreatic cancer; these include: The second breast cancer syndrome (BRCA2), the familial atypical multiple mole melanoma (FAMMM), the Peutz-Jeghers Syndrome, the he...

Journal: :iranian journal of public health 0
d.d. farhud; t.rezaie jami; m.r. khosh-sorour; m. islami; b.broumand

alport syndrome is a progressive hereditary nephritis leading to renal failure. nearly all of the documents declare that alport syndrome is inherited as x-linked dominant trait and reports of autosomal inheritance form is very rare. this paper presents an iranian large alport family with autosomal recessive inheritance. in our patients alport disease was confirmed with electron microscopic stud...

Journal: :journal of algebraic systems 2014
tayyebeh amouzegar

let $m$ be a right module over a ring $r$, $tau_m$ a preradical on $sigma[m]$, and$ninsigma[m]$. in this note we show that if $n_1, n_2in sigma[m]$ are two$tau_m$-lifting modules such that $n_i$ is $n_j$-projective ($i,j=1,2$), then $n=n_1oplusn_2$ is $tau_m$-lifting. we investigate when homomorphic image of a $tau_m$-lifting moduleis $tau_m$-lifting.

Journal: :Haematologica 2013
Sabina Swierczek Archana M Agarwal Kubendran Naidoo Felipe R Lorenzo Jonathan Whisenant Roberto H Nussenzveig Neeraj Agarwal Theresa L Coetzer Josef T Prchal

Hereditary pyropoikilocytosis is a severe hemolytic anemia caused by spectrin deficiency and defective spectrin dimer self-association, typically found in African populations. We describe two Utah families of northern European ancestry including 2 propositi with atypical non-microcytic hereditary pyropoikilocytosis, 7 hereditary elliptocytosis members and one asymptomatic carrier. The underlyin...

Journal: :Discussiones Mathematicae Graph Theory 2013
Izak Broere Johannes Heidema

The well-known Rado graph R is universal in the set of all countable graphs I, since every countable graph is an induced subgraph of R. We study universality in I and, using R, show the existence of 20 pairwise non-isomorphic graphs which are universal in I and denumerably many other universal graphs in I with prescribed attributes. Then we contrast universality for and universality in induced-...

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