Hartnup Disease Pages on BioPortfolio:

BioPortfolio.com - BioWeb DIPYRIDAMOLE DIPYRIDAMOLE alaninyl ...
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Vitus' dance (Sydenham's disease) Chorea and Athetosis in rheumatic fever Rheumatic ... hallpik mdashdrug dirithromycin diethyltoluamid hartnup diverticulum ...
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Vitus' dance (Sydenham's disease) Chorea and Athetosis in rheumatic fever ... hallpik mdashdrug dirithromycin diethyltoluamid hartnup herb nutraceut dietari ...
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Results from other life science and pharmaceutical sites:

Hartnup Disease: Tubular and Cystic Kidney Disorders: Merck Manual ...
Hartnup disease is a rare hereditary disorder that results in a skin rash and brain abnormalities because tryptophan and certain other amino acids are not ...
http://www.merck.com/mmhe/sec11/ch146/ch146h.html...

OMIM - HARTNUP DISORDER
MIM #234500 · Text · Clinical Features · Biochemical Features · Population Genetics · Inheritance · Heterogeneity · Mapping · Molecular Genetics ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=234500...

Hartnup Disease: Renal Transport Abnormalities: Merck Manual ...
Hartnup disease is a rare disease due to abnormal absorption and excretion of tryptophan and other amino acids. Symptoms are rash, CNS abnormalities, ...
http://www.merck.com/mmpe/sec19/ch291/ch291d.html...

Hartnup disease.
Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease. Arch Dis Child. 1967 Dec;42(226):682–688. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=11...

Natural history of Hartnup disease. [Arch Dis Child. 1977 ...
Hartnup disease was diagnosed in 12 children and 3 of their 15 sibs in the course of routine urine screening of 6-week-old infants in New South Wales. ...
http://www.ncbi.nlm.nih.gov/pubmed/836052...

Cellular transport of l-histidine in Hartnup disease
The urinary excretion, the intestinal absorption, and the elimination of histidine from blood were studied in two patients with Hartnup disease. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=32...

Hartnup disease. [Tohoku J Exp Med. 1967] - PubMed Result
1970]; A clinicobiochemical study of tryptophan and other plasma and urinary amino acids in the family with Hartnup disease. [Adv Exp Med Biol. ...
http://www.ncbi.nlm.nih.gov/pubmed/4228120...

Clinical and Biochemical Observations in Two Cases of Hartnup Disease
The metabolic disorder in Hartnup disease. Q J Med. 1960 Jul;29:407–421. ... Clinical and Biochemical Features of a Case of Hartnup Disease. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=20...

Persistence of the common Hartnup disease D173N al...[Ann Hum ...
Hartnup disorder is an aminoaciduria that results from mutations in the recently described gene SLC6A19 on chromosome 5p15.33. The disease is inherited in a ...
http://www.ncbi.nlm.nih.gov/pubmed/17555458...

Circumvention of defective neutral amino acid transport in Hartnup ...
Observations on nicotinic acid therapy in Hartnup disease. Arch Dis Child. ... Intestinal absorption of two dipeptides in Hartnup disease . Gut. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=30...

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