Analyses and exposure assessment of bacterial endotoxin in agricultural environments

مرکز و کتابخانه مطالعات اسلامی به زبان های اروپایی

منو

" Analyses and exposure assessment of bacterial endotoxin in agricultural environments "
Rena Saito

Document Type	:	BL
Record Number	:	775949
Doc. No	:	b595945
Main Entry	:	H Bickel
Title & Author	:	Inborn Errors of Calcium and Bone Metabolism : : Monograph based upon Proceedings of the Twelfth Symposium of the Society for the Study of Inborn Errors of Metabolism.\ H Bickel
Publication Statement	:	Dordrecht : Springer Netherlands, 1984
Page. NO	:	(388 pages)
ISBN	:	9401161593
	:	: 9789401161596
Contents	:	Front ; Contents; Preface; Contributors and Active Participants; Hormones derived from vitamin D : Their regulation and function; Intestinal absorption of calcium and phosphorus in adult man in health and disease; Human parathyroid hormone: Immunochemical studies and determination of circulating hormone in patients with primary hyperparathyroidism and renal insufficiency; Parathyroid hormone in hereditary diseases of mineral metabolism; 5 Parathyroid function in infants and children. Use of I,25-dihydroxycholecalciferol (I,25(OH)2D3) in the treatment of hypoparathyroidism and pseudoƯhypoparathyroidism7 Calcitonin: Recent advances in genetic and physiological aspects; Aspects of growth and bone structure in hypophosphataemic rickets; Pseudovitamin D deficiency (vitamin D dependency); Metabolic forms of rickets (and osteomalacia); X-linked hypophosphataemia and autosomal recessive vitamin D dependency: Models for the resolution of vitamin D refractory rickets; IGC-hydroxyvitamin D : A comparative study in children; 13 Tubular Fanconi Syndromes with bone involvement. Diseases of bone in search of an inborn error15 Idiopathic juvenile osteoporosis; Metabolic effects of a diphosphonate in the treatment of ectopic calcification in children; Cartilage chemistry in bone dysplasias with neonatal presentation; Calcium and vitamin D metabolism during anticonvulsant therapy; a-Aminoadipic aciduria, a new inborn error of lysine metabolism; a-Ketoadipic aciduria --; a new inborn defect of lysine degradation; Phenylketonuria variants; Phenylalanine hydroxylase determinations in patients with phenylketonuria and hyperphenylalaninaemia. A patient with a permanent chemical phenylketonuria and a normal phenylalanine toleranceUse of a semi-synthetic amino acid, 3-methoxyphenyl-L-alanine to measure amino acid absorption; 25 Animal models for histidinaemia; Galactokinase deficiency in an Italian infant; 27 Homocystinuria : Cyst(e)ine levels in the plasma; Index.
LC Classification	:	‭RC930‬‭.H353 1984‬
Added Entry	:	H Bickel
	:	J Stern