(Q68890171)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

review article

1 reference

title

Profiling of amino acids in body fluids and tissues by means of liquid chromatography (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

author name string

Z Deyl

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

J Hyanek

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

M Horakova

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

publication date

1 June 1986

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

volume

379

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

page(s)

177-250

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

The enantiomeric analysis of a mixture of all common protein amino acids by high-performance liquid chromatography using a new chiral mobile phase

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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The determination of β-aminoisobutyric acid in human serum by ion-exchange chromatography

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7 January 2021

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Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 Patients

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7 January 2021

Cystinuria: Genetic Heterogeneity and Allelism

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7 January 2021

Argininosuccinic aciduria: identification and reactions of the abnormal metabolite in a newly described form of mental disease, with some preliminary metabolic studies

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7 January 2021

Separation and Properties of Argininosuccinate and Its Two Anhydrides and Their Detection in Biological Materials*

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7 January 2021

A spectrophotometric method for the simultaneous measurement of L-glutamine and L-asparagine in biological materials

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7 January 2021

Spectrum of catechol amine biochemistry in patients with neuroblastoma

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7 January 2021

Dicarboxylic aminoaciduria: an inborn error of glutamate and aspartate transport with metabolic implications, in combination with a hyperprolinemia.

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7 January 2021

Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.

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7 January 2021

Gamma-carboxyglutamic acid in urine of newborn infants

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7 January 2021

Determination of anserine, carnosine, and other histidine compounds in muscle extractives

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7 January 2021

Serum Carnosinase Deficiency Concomitant with Mental Retardation

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7 January 2021

Citrullinemia: enzymatic evidence for genetic heterogeneity

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7 January 2021

Enzymologic and metabolic studies in two families affected by argininosuccinic aciduria

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7 January 2021

Enzyme studies in a patient with saccharopinuria: a defect of lysine metabolism.

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Familial hyperargininaemia

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7 January 2021

Excretion of cis- and trans-4-hydroxycyclohexylacetic acid in addition to hawkinsin in a family with a postulated defect of 4-hydroxyphenylpyruvate dioxygenase

1 reference

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7 January 2021

Ontogeny of Amino Acid Reabsorption in Human Kidney. Evidence from the Homozygous Infant with Familial Renal Iminoglycinuria for Multiple Proline and Glycine Systems

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7 January 2021

Intestinal transport of cystine and cysteine in man: evidence for separate mechanisms

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7 January 2021

Precursors of melanin in the blood and urine in malignant melanoma

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7 January 2021

Urinary excretion of 3,4-dihydroxyphenylalanine (DOPA) in two children of short stature with malnutrition

1 reference

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7 January 2021

HYPERPIGMENTATION OF THE SKIN WITH DOPA-URIA OF A NEWBORN. (A PECULIAR SIGN OF AN INFANT BORN OF A THYROTOXIC MOTHER TREATED WITH METHIMAZOL)

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7 January 2021

Sulfur-containing amino acids in the plasma and urine of homocystinurics

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7 January 2021

β-mercaptolactate cysteine disulfiduria in two normal sisters. Isolation and characterization of β-mercaptolactate cysteine disulfide

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7 January 2021

Homocystinuria due to cystathionine synthase deficiency: the effect of pyridoxine

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7 January 2021

Hyperlysinaemia. Harmless inborn error of metabolism?

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7 January 2021

Folic acid non-dependent formiminoglutamic aciduria in two siblings

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7 January 2021

Formiminotransferase Deficiency Syndrome Associated with Megaloblastic Anemia Responsive to Pyridoxine or Folic Acid

1 reference

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7 January 2021

Dicarboxylic aminoaciduria: an inborn error of amino acid conservation.

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7 January 2021

Familial spinocerebellar degeneration, hemolytic anemia, and glutathione deficiency

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7 January 2021

Spectrophotometric determination of carnosine, anserine, and taurine in skeletal muscle

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7 January 2021

Pyroglutamic aciduria--a new inborn error of metabolism

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7 January 2021

Serum gamma-glutamyl transpeptidase deficiency

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7 January 2021

New defect in fatty-acid metabolism with hypoglycemia and organic aciduria

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7 January 2021

Screening for organic acidurias and amino acidopathies in newborns and children

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7 January 2021

Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids

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7 January 2021

Results of screening for phenylalanine and other amino acid disturbances among pregnant women

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7 January 2021

Histidinuria: A renal and intestinal histidine transport deficiency found in two mentally retarded children

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7 January 2021

Histidinaemia: Study of Relation Between Clinical and Biological Findings in 7 Subjects

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7 January 2021

Potential use of 3-methylhistidine excretion as an index of progressive reduction in muscle protein catabolism during starvation

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7 January 2021

Quantitative changes in plasma amino acids in patients with renal disease

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7 January 2021

Studies on 3-methylhistidine metabolism in children with protein-energy malnutrition

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7 January 2021

Letter: Lysine metabolism in Reye's syndrome

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7 January 2021

The distribution of homocarnosine in mammals

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7 January 2021

Clinical and biochemical studies on periodic hyperammonemia with hyperlysinemia and homocitrullinuria

1 reference

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7 January 2021

Excretion of S-Adenosylmethionine and S-Adenosylhomocysteine in Homocystinuria

1 reference

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7 January 2021

Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts

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7 January 2021

Homocystinuria with methylmalonic aciduria: Two cases in a sibship

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7 January 2021

Effect of Vitamin B6 Depletion in Adult Man on the Excretion of Cystathionine and Other Methionine Metabolites

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7 January 2021

On a new, hereditary disorder in tryptophan metabolism dependent on vitamin B6

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7 January 2021

Familial hydroxykynureninuria

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7 January 2021

Variations in human urinary O-hydroxylysyl glycoside levels and their relationship to collagen metabolism

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7 January 2021

A Heritable Disorder of Connective Tissue

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7 January 2021

Inherited human collagen lysyl hydroxylase deficiency: Ascorbic acid response

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7 January 2021

3-Hydroxyproline content of normal urine

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7 January 2021

Amino acid excretion of premature infants receiving different amounts of protein

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7 January 2021

Differential diagnosis of tetrahydrobiopterin deficiency

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7 January 2021

Enzyme activity in classical and variant forms of maple syrup urine disease

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7 January 2021

A new sulfur-containing amino acid

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7 January 2021

Metabolic Studies of a Family with Massive Formiminoglutamic Aciduria

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7 January 2021

Abnormal methionine adenosyltransferase in hypermethioninemia

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7 January 2021

Further studies on a patient with iminodipeptiduria: A probable case of prolidase deficiency

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7 January 2021

Letter: Metabolic defect in hyperornithinaemia

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7 January 2021

Nutritional management of the female with phenylketonuria during pregnancy

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7 January 2021

Hyperpipecolic acidemia associated with hepatomegaly, mental retardation, optic nerve dysplasia and progressive neurological disease

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7 January 2021

Defective hydroxyproline metabolism in type II hyperprolinemia

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7 January 2021

Prolidase deficiency: report of a second case with quantitation of the excessively excreted amino acids

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7 January 2021

Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism

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7 January 2021

Plasma tryptophan and other amino acids in pellagra.

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7 January 2021

Idiopathic hypervalinemia: valine and alpha keto-acids in blood following an oral dose of valine

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7 January 2021

Profiling of human body fluids in healthy and diseased states using gas chromatography and mass spectrometry, with special reference to organic acids

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7 January 2021

A versatile lithium buffer elution system for single column automatic amino acid chromatography

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7 January 2021

Column chromatographic separations of amino acids, peptides, and protein in normal human urine

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7 January 2021

Methods for the quantitative analysis or sulphur-containing compounds in physiological fluids

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7 January 2021

Rapid short-column chromatography of amino acids. A method for blood and urine specimens in the diagnosis and treatment of metabolic disease

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7 January 2021

N-EPSILON-(CARBOXYMETHYL)LYSINE, A CONSTITUENT OF HUMAN URINE

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7 January 2021

Urinary formiminoglutamate in man. Normal values related to sex and age. Effects of low calorie intake and alcohol consumption

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7 January 2021

Increased urinary imidazolepropionic acid, N-acetylhistamine and other imidazole compounds in patients with intestinal disorders

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7 January 2021

Trimethylsilylation of Amino Acids. II. Gas Chromatographic and Structural Studies on Trimethylsilyl Derivatives of Straight Chain Amino Acids

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7 January 2021

Elution and thin layer chromatographic separation of plasma amino acids from blood absorbed on filter paper

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7 January 2021

Atypical phenylketonuria caused by 7, 8-dihydrobiopterin synthetase deficiency

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7 January 2021

Gas chromatographic analysis of amino acids in physiological fluids: a critique

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7 January 2021

Diagnosis of disorders in amino acid methabolism by chemical ionization mass spectrometry

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7 January 2021

Bonded peptide stationary phases for the separation of amino acids and peptides using liquid chromatography

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7 January 2021

10.1016/S0378-4347(00)80685-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3525589%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

1 reference