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A new polygenic disturbance: cystinuria, leucinuria and spinal muscular atrophy

Journal of neurology, 1974-01, Vol.207 (1), p.73-83

1974

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Study of the amino acid metabolism in a case of hereditary intolerance to fructose

Revue roumaine de medecine interne (1964), 1974, Vol.11 (3), p.279

1974

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Cerebrospinal fluid, blood and urine amino acid dynamics in atherosclerosis

Physiologie (Bucarest), 1982-04, Vol.19 (2), p.111

1982

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

Physiologie (Bucarest), 1981-10, Vol.18 (4), p.251

1981

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

Physiologie (Bucarest), 1981, Vol.18 (3), p.187

1981

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Pattern of the cerebrospinal fluid (CSF) and blood biogenic amines and of the CSF, blood and urine amino acids as pathogenetic ground of the senile depressive illness

Physiologie (Bucarest), 1980-07, Vol.17 (3), p.183

1980

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Aspects of the biochemistry of the urine in a newborn infant with "typical" valinuria and the effect of ingestion of valine on amino acid transport at the level of the brain in animals

Physiologie (Bucarest), 1978-04, Vol.15 (2), p.85

1978

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A study of aminoacidemia and aminoaciduria in epileptic children

Neurologie et psychiatrie, 1976-10, Vol.14 (4), p.277

1976

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Variations of serum concentration of 4-hydroxyproline during treatment of liver cirrhosis with colchicine (preliminary data)

Physiologie (Bucarest), 1983-01, Vol.20 (1), p.11

1983

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Effects of ingestion of sodium metabisulfite on vitamin C in the rat organism

Physiologie (Bucarest), 1978-01, Vol.15 (1), p.61

1978

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New types of congenital metabolic errors detected in newborn infants

Physiologie (Bucarest), 1975, Vol.12 (4), p.27k

1975

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A case of mucopolysaccharidosis associated with phenylalaninemia

Revista de pediatrie, obstetrica si ginecologie. Pediatria, 1981-04, Vol.30 (2), p.173

1981

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Aspects of plasma and lung biochemistry in experimental pneumoconiosis

Physiologie (Bucarest), 1976-04, Vol.13 (2), p.141

1976

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Certain aspects of the biochemistry of urine in families with handicapped children

Physiologie (Bucarest), 1982-04, Vol.19 (2), p.133

1982

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Urine biochemistry in children with supposed metabolic diseases

Physiologie (Bucarest), 1982-01, Vol.19 (1), p.25

1982

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Atypical forms of phenylketonuria (PKU), cause of mental deficiency

Neurologia, psihiatria, neurochirurgia, 1965-09, Vol.10 (5), p.453

1965

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Various organic acids in the saliva of periodontopathies and gingivopathies in humans

Revista de chirurgie, oncologie, radiologie, o. r. l., oftalmologie, stomatologie. Seria: Stomatologie, 1986-04, Vol.33 (2), p.109

1986

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Lysozyme and carboxypeptidase in the saliva of patients with periodontopathies

Revista de chirurgie, oncologie, radiologie, o. r. l., oftalmologie, stomatologie. Seria: Stomatologie, 1986-04, Vol.33 (2), p.99

1986

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Correlations between biochemical data and clinical course of newborn infants

Physiologie (Bucarest), 1982-04, Vol.19 (2), p.123

1982

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Common biochemical facts of certain inborn errors of metabolism and in cancer observed in children and in adults

Physiologie (Bucarest), 1980-10, Vol.17 (4), p.303

1980

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Biochemistry of the blood and urine in members of families suspected of having hereditary metabolic defects

Physiologie (Bucarest), 1980-04, Vol.17 (2), p.101

1980

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Combined and isolated forms of metabolic errors detected in children

Physiologie (Bucarest), 1980-01, Vol.17 (1), p.57

1980

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Studies of a case of aminoacidopathy due to isolated hypervalinemia

Physiologie (Bucarest), 1979-04, Vol.16 (2), p.123

1979

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Combined forms of galactosemias, mucopolysaccharidoses and pentosurias diagnosed in children

Physiologie (Bucarest), 1979-10, Vol.16 (4), p.293

1979

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Further types of alkaptonuria, cystinuria and histidinemia detected in children

Physiologie (Bucarest), 1979-01, Vol.16 (1), p.41

1979

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A new polygenic disturbance: cystinuria, leucinuria and spinal muscular atrophy

Study of the amino acid metabolism in a case of hereditary intolerance to fructose

Cerebrospinal fluid, blood and urine amino acid dynamics in atherosclerosis

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

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

Pattern of the cerebrospinal fluid (CSF) and blood biogenic amines and of the CSF, blood and urine amino acids as pathogenetic ground of the senile depressive illness

Aspects of the biochemistry of the urine in a newborn infant with "typical" valinuria and the effect of ingestion of valine on amino acid transport at the level of the brain in animals

A study of aminoacidemia and aminoaciduria in epileptic children

Variations of serum concentration of 4-hydroxyproline during treatment of liver cirrhosis with colchicine (preliminary data)

Effects of ingestion of sodium metabisulfite on vitamin C in the rat organism

New types of congenital metabolic errors detected in newborn infants

A case of mucopolysaccharidosis associated with phenylalaninemia

Aspects of plasma and lung biochemistry in experimental pneumoconiosis

Certain aspects of the biochemistry of urine in families with handicapped children

Urine biochemistry in children with supposed metabolic diseases

Atypical forms of phenylketonuria (PKU), cause of mental deficiency

Various organic acids in the saliva of periodontopathies and gingivopathies in humans

Lysozyme and carboxypeptidase in the saliva of patients with periodontopathies

Correlations between biochemical data and clinical course of newborn infants

Common biochemical facts of certain inborn errors of metabolism and in cancer observed in children and in adults

Biochemistry of the blood and urine in members of families suspected of having hereditary metabolic defects

Combined and isolated forms of metabolic errors detected in children

Studies of a case of aminoacidopathy due to isolated hypervalinemia

Combined forms of galactosemias, mucopolysaccharidoses and pentosurias diagnosed in children

Further types of alkaptonuria, cystinuria and histidinemia detected in children

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