(Q55244157)

28 June 2018

title

Neopterin in AIDs, other immunodeficiencies, and bacterial and viral infections. (English)

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author

Nenad Blau

4

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author name string

A Niederwieser

1

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P Joller

2

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R Seger

3

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A Prader

5

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J D Bettex

6

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R Lüthy

7

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B Hirschel

8

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J Schaedelin

9

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U Vetter

10

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publication date

1 April 1986

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28 June 2018

published in

Klinische Wochenschrift

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28 June 2018

volume

64

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issue

7

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page(s)

333-337

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Malignant hyperphenylalaninaemia—Current status (June 1977)

cites work

1 reference

12 December 2020

Immune response-associated production of neopterin. Release from macrophages primarily under control of interferon-gamma

1 reference

12 December 2020

Familial hemophagocytic lymphohistiocytosis

1 reference

12 December 2020

Identification of a pterin as the acrasin of the cellular slime mold Dictyostelium lacteum

1 reference

12 December 2020

Atypical phenylketonuria caused by 7, 8-dihydrobiopterin synthetase deficiency

1 reference

12 December 2020

Primary immunodeficiency diseases. Report prepared for the WHO by a scientific group on immunodeficiency

1 reference

12 December 2020

Hyperphenylalaninaemia with normal phenylalanine-hydroxylase activity and a deficiency of tetrahydrobiopterin and dihydropteridine reductase

1 reference

12 December 2020

Phenylketonuria due to a deficiency of dihydropteridine reductase

1 reference

12 December 2020

High-performance liquid chromatography with column switching for the analysis of biogenic amine metabolites and pterins

1 reference

12 December 2020

Urinary neopterin in the diagnosis of acquired immune deficiency syndrome

1 reference

12 December 2020

Neopterin as a new biochemical marker for diagnosis of allograft rejection. Experience based upon evaluation of 100 consecutive cases

1 reference

12 December 2020

Structural and metabolic relationship between the molybdenum cofactor and urothione

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12 December 2020

Increased urinary excretion of neopterin in patients with malignant tumors and with virus diseases (author's transl)

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12 December 2020

GTP cyclohydrolase I deficiency, a new enzyme defect causing hyperphenylalaninemia with neopterin, biopterin, dopamine, and serotonin deficiencies and muscular hypotonia.

1 reference

12 December 2020

Excretion of pterins in phenylketonuria and phenylketonuria variants

1 reference

12 December 2020

Increase of GTP cyclohydrolase I activity in mononuclear blood cells by stimulation: detection of heterozygotes of GTP cyclohydrolase I deficiency

1 reference

12 December 2020

Interferon-gamma enhances biosynthesis of pterins in peripheral blood mononuclear cells by induction of GTP-cyclohydrolase I activity

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12 December 2020

Identifiers

DOI

10.1007/BF01711954

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28 June 2018

PubMed ID

3012191

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28 June 2018