[Renal function disorders in inborn errors of metabolism. 3. Renal function disorders in renal diabetes, Hartnup disease and rickets due to hypophosphatemia].
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Amino Acids↗
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Results for “HARTNUP DISEASE”
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Hartnup disease (a case report).
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Child↗
Hartnup disease in two Colombian siblings.
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Adolescent↗
[Hartnup disease (author's transl)].
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Adolescent↗
Absorption of amino acids and the dipeptide, carnosine, from the gut in normal subjects and a case of Hartnup disease.
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Alanine↗
Hartnup disease--a case report.
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Diagnosis, Differential↗
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. II. SOME OBSERVATIONS ON RATS ABOUT TRYPTOPHAN METABOLISM.
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Child↗
Hartnup disease in three siblings.
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Adolescent↗
BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS.
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Amino Acid Metabolism, Inborn Errors↗
HARTNUP DISEASE IN TWO SIBLINGS. CLINICAL OBSERVATIONS AND BIOCHEMICAL STUDIES.
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Adolescent↗
[Hartnup disease (apropos of 2 initial cases in African Negroes)].
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Adolescent↗
Studies of intestinal transport defect in Hartnup disease.
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Adolescent↗
Intestinal absorption of dipeptides and corresponding free amino acids in Hartnup disease.
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Amino Acids↗
Proceedings: Absorption of amino acids and peptides in Hartnup disease.
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Adult↗
[Hartnup disease is related to a mutation in the SL C6A19 gene coding for the B degrees AT1 aminoacid transporter].
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Amino Acid Transport System A↗
Tryptophan metabolism in nervous disease.
The paper describes effects of tryptophan loading on tryptophan metabolism in healthy persons as well as alterations of tryptophan metabolism observed in varians diseases associated with nervous symptoms, i.e. Wilson's disease, Hartnup disease, phenylketonuria and acute intermittent porphyria. The results are discussed.
Acute Disease↗