ornithine transcarbamylase deficiency Pages on BioPortfolio:

BioPortfolio - Ornithine Carbamoyltransferase Deficiency Disease ...
Ornithine transcarbamylase (OTC) deficiency is the most common inborn...14th August, ... n of 1 trial for an ornithine transcarbamylase deficiency carrier.
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http://www.bioportfolio.com/indepth/Ornithine_Carbamoyltrans...

BioPortfolio Biotechnology BioNews : live article
Mian and colleagues published the results of their research in Molecular Therapy (Long-term correction of ornithine Transcarbamylase deficiency by ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=h...

BioPortfolio - Ornithine Carbamoyltransferase Deficiency Disease
Phase I Study of Adenoviral Vector Mediated Gene Transfer for Ornithine Transcarbamylase in Adults With Partial Ornithine Transcarbamylase Deficiency
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http://www.bioportfolio.com/indepth/Ornithine_Carbamoyltrans...

BioPortfolio.com - BioWeb DEPAKENE VALPROIC ACID Search
Those who had IQ tests administered had an incidence of mental retardation as follows: ornithine transcarbamylase deficiency, 100% (14/ 14 patients tested);
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http://www.bioportfolio.co.uk/DEPAKENE+VALPROIC+ACID-bioweb....

BioPortfolio - Ornithine Carbamoyltransferase - InDepth
Phenotypic correction of ornithine transcarbamylase deficiency using low dose ... BACKGROUND: Ornithine transcarbamylase (OTC) deficiency is the most ...
http://www.bioportfolio.com/indepth/Ornithine_Carbamoyltrans...

BioPortfolio - Carbamoyl-Phosphate Synthase I Deficiency Disease
Urea Cycle Disorders; Carbamoylphosphate Synthetase I Deficiency Disease; Ornithine Transcarbamylase Deficiency Disease; Citrullinemia ...
http://www.bioportfolio.com/indepth/Carbamoyl-Phosphate_Synt...

BioPortfolio - Carbamoyl-Phosphate Synthase I Deficiency Disease ...
cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency. Urea cycle defects (UCDs) typically present with hyperammonemia, ...
http://www.bioportfolio.com/indepth/Carbamoyl-Phosphate_Synt...

BioPortfolio - Idaho Technology
Ornithine transcarbamylase (OTC) deficiency is an X-linked, semidominant... 14th November, 2007, Idaho Technology, Salt Lake City, Utah 84108, USA. ...
http://www.bioportfolio.com/biocorporate/5184-Idaho_Technolo...

BioPortfolio - Idaho Technology - Profile
transcarbamylase gene as a model system. Ornithine transcarbamylase (OTC) deficiency is an X-linked, semidominant...14th November, 2007 ...
http://www.bioportfolio.com/biocorporate/5184-Idaho+Technolo...

Results from other life science and pharmaceutical sites:

Ornithine transcarbamylase deficiency - Genetics Home Reference
Ornithine transcarbamylase deficiency is an inherited disorder that causes ammonia to accumulate in the blood. Ammonia, which is formed when proteins are
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http://ghr.nlm.nih.gov/condition=ornithinetranscarbamylasede...

OMIM - ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO
MIM #311250 · Text · Description · Clinical Features · Inheritance · Mapping · Diagnosis · Clinical Management · Molecular Genetics ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311250...

Improved molecular diagnostics for ornithine transcarbamylase ...
Lethal ornithine transcarbamylase deficiency in a female neonate. J Inherit Metab Dis. .... Family studies in ornithine transcarbamylase deficiency. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

(Ornithine Carbamoyltransferase Deficiency Disease[MAJR]) AND ...
1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency. Mol Genet Metab. 2008 Sep-Oct;95(1-2):21-30. ...
http://ghr.nlm.nih.gov/exit?to=www.ncbi.nlm.nih.gov&uid=7bH4...

Site specific screening for point mutations in ornithine ...
Ornithine transcarbamylase (OTC) deficiency is a frequent X linked disorder of the ... Late-onset ornithine transcarbamylase deficiency in male patients. ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=10...

[Patients with ornithine transcarbamylase deficien...[Anaesthesist ...
Ornithine transcarbamylase deficiency (OTCD) is the most common inborn urea cycle disorder. Patients with OTCD are at risk of acute metabolic decompensation
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http://www.ncbi.nlm.nih.gov/pubmed/16136341...

New mutation and prenatal diagnosis in ornithine transcarbamylase ...
Carrier detection in ornithine transcarbamylase deficiency. ... Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.
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http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

OMIM - ORNITHINE CARBAMOYLTRANSFERASE; OTC
MIM *300461 · Description · Cloning · Gene Structure · Mapping · Molecular Genetics · Animal Model · Allelic Variants ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300461...

Prenatal diagnosis of ornithine transcarbamylase deficiency ...
The prenatal diagnosis of ornithine transcarbamylase deficiency (OTCD) was made by using radioactive microassays for ornithine transcarbamylase (OTC) ...
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16...

Molecular Therapy - Long-Term Correction of Ornithine ...
Long-Term Correction of Ornithine Transcarbamylase Deficiency by WPRE-Mediated Overexpression Using a Helper-Dependent Adenovirus ...
http://www.nature.com/mt/journal/v10/n3/full/mt20041250a.htm...

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