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Your search keyword '"Mogoş I"' showing total 18 results

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18 results on '"Mogoş I"'

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1. [Biochemistry of the blood and urine in members of families suspected of having hereditary metabolic defects].

3. [Urine biochemistry in children with supposed metabolic diseases].

4. [Common biochemical facts of certain inborn errors of metabolism and in cancer observed in children and in adults].

8. [Comparative biochemical studies of certain urinary metabolites in patients with the nephrotic syndrome, eye diseases, alkaptonuria, obstructive myocardiopathy, and cancer and in newborn infants].

9. [Metabolic errors of the cystinuria-lysinuria, cystinosis type detected in the newborn infant and child with renal and ocular diseases].

10. [Combined and isolated forms of metabolic errors detected in children].

11. [New types of congenital metabolic errors detected in newborn infants].

12. [Aspects of plasma and lung biochemistry in experimental pneumoconiosis].

13. [Studies of a case of aminoacidopathy due to isolated hypervalinemia].

14. [Combined forms of galactosemias, mucopolysaccharidoses and pentosurias diagnosed in children].

15. [Correlations between biochemical data and clinical course of newborn infants].

17. [Combined forms of metabolic errors detected in newborn infants].

18. [In vivo and in vitro cytostatic effects of potassium sulfocyanate].

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