Literature DB >> 14237738

[METABOLIC DISORDERS IN POLYMORPHIC LIGHT DERMATOSES AND RECENT RESULTS OF INVESTIGATIONS IN CONNECTION WITH THE HARTNUP SYNDROME].

J KIMMIG.   

Abstract

Keywords:  HARTNUP DISEASE; INDOLES; PHENOTHIAZINES; PHOTOSENSITIZATION; TOXICOLOGIC REPORT; TRYPTOPHAN; URINE

Mesh：

Substances：

Year:  1964        PMID： 14237738

Source DB:  PubMed          Journal:  Arch Klin Exp Dermatol        ISSN： 0300-8614


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  4 in total

1.  [N-[beta-(indolyl-(3)-acryloyl] glycine isolation from urine and synthesis].

Authors:  J KIMMIG; W STICHERLING; R TSCHESCHE; H G URBACH
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1958

2.  [Photodermatosis with aminoaciduria, indolaceturia & cerebral manifestations (Hartnup syndrome)].

Authors:  H WEYERS; H BICKEL
Journal:  Klin Wochenschr       Date:  1958-10-01

3.  Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features.

Authors:  D N BARON; C E DENT; H HARRIS; E W HART; J B JEPSON
Journal:  Lancet       Date:  1956-09-01       Impact factor: 79.321

4.  [Photodermatoses and protection from light].

Authors:  I KIMMIG
Journal:  Arch Klin Exp Dermatol       Date:  1955
  4 in total
  2 in total

1.  [Tryptophan metabolism in patients with pellagra].

Authors:  G G Brune; R M Brune; A Wiskemann
Journal:  Arch Dermatol Forsch       Date:  1970

2.  Identification of an error in the tryptophan--niacin pathway in carriers of some dermatoses conditioned or aggravated by sunlight.

Authors:  M Binazzi; P Calandra
Journal:  Arch Klin Exp Dermatol       Date:  1971
  2 in total

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