Results 81 to 90 of about 1,044,930 (284)
Concrete Solution to the Nonsingular Quartic Binary Moment Problem [PDF]
, 2014 Given real numbers $\beta \equiv \beta ^{\left( 4\right) }\colon \beta_{00}$, $\beta _{10}$, $\beta _{01}$, $\beta _{20}$, $\beta _{11}$, $ \beta _{02}$, $\beta _{30}$, $\beta _{21}$, $\beta _{12}$, $\beta _{03}$, $\beta _{40}$, $\beta _{31}$, $\beta _{22}$, $\beta _{13}$, $\beta _{04}$, with $\beta _{00} >0$, the quartic real moment problem for $\beta
arxiv +1 more source
Pathophysiology and treatment of patients with beta-thalassemia – an update
F1000Research, 2017 Thalassemia (thal) is an autosomal recessive, hereditary, chronic hemolytic anemia due to a partial or complete deficiency in the synthesis of α-globin chains (α-thal) or β-globin chains (β-thal) that compose the major adult hemoglobin (α 2β 2).
E. Fibach, E. Rachmilewitz
semanticscholar +1 more source
Genomic technologies and the diagnosis of 46, XY differences of sex development
Andrology, EarlyView.Abstract Differences/disorders of sex development can be caused by disruptions to the molecular and cellular mechanisms that control development and sex determination of the reproductive organs with 1:100 live births affected. Multiple genes are associated with 46, XY differences/disorders of sex development that can cause varying clinical phenotypes ...
Firman Idris +2 more
wiley +1 more source
Chronic hyperplastic anemia as an independent risk factor for atherosclerotic lesions: a lesson from thalassemia intermedia [PDF]
, 2010 Introduction. Cardiovascular involvement represents a well-known complication and the primary cause of mortality, both in transfusion-dependent beta thalassemia major (β-TM) and in transfusion-independent beta thalassemia intermedia (β-TI ...
Alessandra Spiga +7 more
core +1 more source
Revista Brasileira de Hematologia e Hemoterapia, 2010 Variations in the phenotypic expression of heterozygous beta thalassemia reflect the formation of different populations. To better understand the profile of heterozygous beta-thalassemia of the Brazilian population, we aimed at establishing parameters to
Ana L. B. Domingos +5 more
doaj +1 more source
A Child Lost to Follow Up Carrying Beta Thalassemia Major: A Case Report
Journal of Nepal Medical Association, 2020 Thalassemia is inherited autosomal recessive disorders characterized by reduced rate of hemoglobin synthesis due to a defect in alpha or beta globin chain synthesis. Maldives has a beta thalassemia prevalence rate of 16–18%.
Prakash Banjade, Jeetendra Bhandari
doaj +1 more source
Neutrinoless double beta decay experiment [PDF]
arXiv, 2020 The search for neutrinoless double beta decay ($0\nu\beta\beta$) is one of the key experiments for determining unresolved properties of neutrinos. Experimental observation of $0\nu\beta\beta$ would provide a clear demonstration of the Majorana nature of neutrinos and a lepton number violating process in particle physics.
arxiv
Acta Paediatrica, EarlyView.ABSTRACT Aim This study tested the relationship between the hospitalisation experience and distress among Jewish and Bedouin parents of hospitalised children in the south of Israel. Methods An anonymous self‐reported questionnaire containing the Distress Thermometer for Parents and the Parental Perceptions of Hospital Care in Children was completed by ...
Elena Gelman +2 more
wiley +1 more source
Study of Pregnancy Outcome in E-Beta Thalassaemia Mothers [PDF]
, 2009 Forty eight E-Beta thalassaemia patients were studied in NRS Medical College, Kolkata, West Bengal during the period from 2000-2006. In all patients Hb% ranged from 5.2g% - 9.6g%.
Bhattacharyaya, Maitryaee +1 more
core +1 more source
BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCT. [PDF]
, 2014 The genetic background of donor and recipient is an important factor determining the outcome of allogeneic hematopoietic SCT (allo-HSCT). We applied whole-genome analysis to investigate genetic variants - other than HLA class I and II - associated with ...
Andreani M +13 more
core +1 more source