... Abstract The role of early infant nutrition in the development of allergic symptoms and allergicsensitization has been disputed for 70 years. Interaction between genetic factorsand infant feeding has been limited to studies on parental heredity of allergy andlength of breastfeeding, as well...

... Abstract The study of 500 families has permitted to confirm without exceptions the heredity of the subgroups A1 and A2. ...

... Abstract The importance of an empirically adequate basis for the use of new blood group systems as evidence in paternity cases is stressed. However, in spite of an established mechanism of heredity within a blood group system certain mother-child-putative-father combinations may represent...

... once weaning has commenced, irrespective of atopic heredity. However, intervention studies are currently conducted to prove this hypothesis generated by observational studies. Introduction The pooled lifetime prevalence of self-reported food allergy is 17% in Europe [ 1 ]. There is some...

... microsomia, or Goldenhar syndrome (which is accompanied by epibulbar dermoid), complicated by anomalies of the upper limbs and kidney, presents sporadic cases in monozygotic twins, it is argued to be induced by environmental factors or multifactorial heredity rather than monogenic heredity [ 3 ]. Vascular...

... characteristics, both hysteria and neurasthenia were thought to be ‘functional diseases'. Moreover, it was suggested that heredity and the presence in both of the predisposing condition called ‘nervous weakness' were other shared factors. Nervous weakness was considered essential for the definition...

..., and induction of apoptosis. Mitochondria also contain their own DNA, known as mitochondrial DNA (mtDNA). Through these varied roles, mitochondria are important in heredity, growth, metabolism, and the occurrence and progression of diseases. Podocytes are highly specialized epithelial cells of the kidney...

... susceptibility are related to heredity. Todate, 3 cases of radio-associated glioblastoma and 5 casesof transformed vestibular schwannoma related to radiosurgerywere reported in the literature. They do not present allthe traditional criteria. Thus, we reported through our experience2 cases illustrating...

... the accumulation of bone mineral during childhood and adolescence, including heredity, gender, diet, physical activity, endocrine status, and sporadic risk factors such as cigarette smoking. In addition to these modifiable factors during childhood, evidence has also accrued that fracture risk might be programmed...

...References References 1. Schäfer L: On the history of the concept neurasthenia and its modern variants chronic-fatigue-syndrome, fibromyalgia and multiple chemical sensitivities (in German). Fortschr Neurol Psychiatr 2002;70:570-582. 2. Turnbull P: Psychiatry and heredity degeneration...

... TR: Five generations of angioneurotic edema. Arch Intern Med 1917;20:840-852. 19. Osler W: Hereditary angio-neurotic oedema. Am J Med Sci 1888;95:362-367. 20. Donaldson VH, Evans RR: A biochemical abnormality in heredity angioneurotic edema: absence of serum inhibition of C1-esterase. Am J...