نتایج جستجو برای: deficiency zero

تعداد نتایج: 285480  

Journal: :Journal of Physics: Conference Series 2019

وحیدی نیا , علی اصغر ,

Iron deficiency and iron deficiency anaemia are the most common nutrient deficiency especially in reproductive – aged women. This study carried out to determine prevalence of iron deficiency and iron deficiency anaemia in rural women of Ilam , in 1995. Thus result showed that 23.8% of all women had iron deficiency and, in pregnant, lactating, and non-pregnant , non-lactating, women it ...

Reducing iron solubility in calcareous soils causes iron chlorosis symptoms in the plant. In order to investigate the response of M. scutellata to direct and indirect iron deficiency, a factorial experiment was conducted in a completely randomized design with three replications. The experimental factors included three levels of lime (0, 4 and 8%) and five levels of Fe (0, 5 and 10 mg Fe Kg soil...

Abstract Background: Iron deficiency is the most common nutritional deficiencies in the world. So that 15% of the total world population is involved.  The present study examined the association between iron deficiency anemia and primary hypothyroidism and the prevalence of iron deficiency anemia and primary hypothyroidism, respectively, in patients with iron deficiency anemia and primar...

Background and Aim: Phenylketonuria (PKU., OMIM261600) is the most common genetic disorder autosomal recessive mode of inheritance and the metabolism of amino-acids, which is due to deficiency of the liver enzyme phenylalanine - hydroxylase as a result of mutations in the gene encoding it is achieved. The present study aimed at investigating the incidence of PKU n  the South Khorasan province b...

Journal: :International Journal of Computer Applications 2010

Journal: :Progress of Theoretical Physics 1951

Journal: :Journal of immunology 2004
Lucian Visan Ioana A Visan Andreas Weishaupt Harald H Hofstetter Klaus V Toyka Thomas Hünig Ralf Gold

Genetic deficiency or instability of myelin protein zero (P0) results in hereditary motor sensory neuropathy. In view of recent advances in gene therapy, substitution of the molecular defect may become realistic in the near future. Here we investigate the impact of genetic deficiency of P0 on selection of the autoreactive T cell repertoire in the corresponding mouse model. We show that P0 mRNA ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید