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MIC - Metabolic Information Centre

183;··. 183;··. 183;··. 183;··. 183;··. 183;··. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria. Inborn errors of metabolism causing epilepsy. Ammonium Accumulation and Cell Death in a Rat 3D Brain Cell Model of Glutaric Aciduria Type I. Liver transplantation and cell therapies for inborn errors of metabolism. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. Juvenile glaucoma in propionic acidemia.

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MIC - Metabolic Information Centre | metagene.de Reviews

<META> DESCRIPTION

183;··. 183;··. 183;··. 183;··. 183;··. 183;··. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria. Inborn errors of metabolism causing epilepsy. Ammonium Accumulation and Cell Death in a Rat 3D Brain Cell Model of Glutaric Aciduria Type I. Liver transplantation and cell therapies for inborn errors of metabolism. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. Juvenile glaucoma in propionic acidemia.

<META> KEYWORDS

1 introduction

2 pocket metab

3 impressum

4 diseases

5 symptoms

6 lab parameters

7 authors

8 ramedis

9 bh4 patient

10 title

CONTENT

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introduction,pocket metab,impressum,diseases,symptoms,lab parameters,authors,ramedis,bh4 patient,title,author,year,eggermann t,rahman s,jafari p,mckiernan p,wortmann sb,pena l,propionic acidemia,carrillo carrasco n,rosentreter a,coelho d,gungor o,sass jo

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MIC - Metabolic Information Centre | metagene.de Reviews

https://metagene.de

183;··. 183;··. 183;··. 183;··. 183;··. 183;··. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria. Inborn errors of metabolism causing epilepsy. Ammonium Accumulation and Cell Death in a Rat 3D Brain Cell Model of Glutaric Aciduria Type I. Liver transplantation and cell therapies for inborn errors of metabolism. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. Juvenile glaucoma in propionic acidemia.

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metagene.de

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MIC - Metabolic Information Centre

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MIC - Metabolic Information Centre

http://www.metagene.de/program/s.prg

3

MIC - Metabolic Information Centre

http://www.metagene.de/program/r.prg

183;··. 183;··. 183;··. 183;··. 183;··. 183;··. Search by Ramedis data. METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE (MIM 277400). ISOVALERIC ACIDEMIA (MIM 243500). ACYL-CoA DEHYDROGENASE, VERY LONG-CHAIN, DEFICIENCY OF (MIM 201475). S-ADENOSYLHOMOCYSTEINE HYDROLASE (MIM 180960). ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF (MIM 201450). ISOVALERIC ACIDEMIA (MIM 243500). ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN, DEFICIENCY OF (MIM 201450). L-2-HYDROXYGLUTARIC ACIDURIA (MIM 236792). ARGININOSUC...

4

MIC - Metabolic Information Centre

http://www.metagene.de/program/l.prg

183;··. 183;··. 183;··. 183;··. 183;··. 183;··. Search by Laboratory FInding. Select first character in order to reduce the option list. Autoren: Prof. Dr. Friedrich Trefz, Dr. Frauendienst und Hermann Götz. E-Mail: trefz_f@kreiskliniken-reutlingen.de . Last update 29.12.2009 07:05:52. Click zum Schliessen des Fensters.

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MIC - Metabolic Information Centre

http://www.metagene.de/program/pocket.prg

183;··. 183;··. 183;··. 183;··. PocketMetab is freeware for your PDA: database for SprintDB Pro* with detailed information on 424 inborn errors of metabolism. PocketMetab is designed to support the diagnosis of inborn errors of metabolism. The database gives rapid access to comprehensive information about 424 metabolic diseases, important differential diagnoses, associated clinical and laboratory findings. The trial version of PocketMetab is free to distribute. Hardware and SprintDB Pro not included!

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endogenet.org

Endogenet - Links

http://www.endogenet.org/links.html

Referring a case for diagnosis. Http:/ www.ensembl.org/. Http:/ www.ncbi.nlm.nih.gov/entrez/query.fcgi? OMIM - Online Mendelian Inheritance in Man. Http:/ www.ncbi.nlm.nih.gov/entrez/query.fcgi? Http:/ www.expasy.org/. Http:/ www.ncbi.nlm.nih.gov/gquery/gquery.fcgi. Http:/ www.metagene.de/. Knowledge base for inborn errors of metabolism. Offers an analysis of thyrotoxicosis, hypothyroidism, thyroid nodules and cancer, thyroiditis, and other aspects of human thyroid disease and thyroid physiology.

zfs-reutlingen.de

Zfs - Zentrum für Stoffwechseldiagnostik Reutlingen GmbH

http://www.zfs-reutlingen.de/klinische_symptomatik.htm

Wir über uns. Laborjournale / Vorträge. Denn nicht immer ist die Analyse so einfach wie die Blick-Diagnose eines. Syndaktylie der 2./3. Zehe. Zur Stoffwechseldatenbank www.metagene.de. Coma, Reye-Syndr., SIDS oder Near-SIDS, Cardiomyopathie, Hypotonie, Hypoglykämie, Hyperammonämie, CK-Erhöhung, Hepatopathie, Leberversagen, Muskelschmerzen, Myoglobinurie. Carnitin (S, TB, L). Smith-Lemli-Opitz S.: Syndactylie 2./3. Zehen plus: Hypotonie, Entw. Retardierung, Dysmorphien. Guanidinoacetat, Creatin (U). M Fab...

zfs-reutlingen.de

Zfs - Zentrum für Stoffwechseldiagnostik Reutlingen GmbH

http://www.zfs-reutlingen.de/analytisches_angebot.htm

Wir über uns. Laborjournale / Vorträge. Im aktuellen Neugeborenen-Screening werden bis zu 20 von 350 angeborenen Stoffwechselerkrankungen untersucht. Unser analytisches Angebot geht weit darüber hinaus (80). Chten Sie bitte die klinischen Hinweise auf der Rückseite der Anforderungsbögen. Eine entsprechende Vorselektion über die entsprechende Symptomatik erleichtert die gezielte und damit kostengünstige Analytik. Ungeklärter Grand Mal Epilepsie. Motorischer und/oder mentaler Entwicklungsretardierung.

hmdb.ca

Human Metabolome Database: Documentation and Sources

http://www.hmdb.ca/sources

About the Human Metabolome Database. Quantitative metabolomics services for biomarker discovery and validation. Specializing in ready to use metabolomics kits. Your source for quantitative metabolomics technologies and bioinformatics. HMDB is a detailed database on small molecule from. A naturally occurring molecule typically under 1000 MW. Any protein which catalyzes chemical reactions involving the small molecule. Field Documentation and Sources. Date/time the entry was created. First level of hierarch...

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The owners of the domain name metagene.com are accepting offers from interested parties willing to obtain ownership rights over the domain name. You can place your offer by filling out the form below. This is a good faith offer. If you believe that your rights are violated please read the disclaimer. How to make offer. Fill out the form below. Receive an e-mail with a unique web link. Click on the link and confirm your bid. You will be also asked about the executional details of the transaction. Before p...

metagene.de

MIC - Metabolic Information Centre

183;··. 183;··. 183;··. 183;··. 183;··. 183;··. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria. Inborn errors of metabolism causing epilepsy. Ammonium Accumulation and Cell Death in a Rat 3D Brain Cell Model of Glutaric Aciduria Type I. Liver transplantation and cell therapies for inborn errors of metabolism. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature. Juvenile glaucoma in propionic acidemia.

metagene.eu

Home

METAGENE is designed to support the diagnosis of inborn errors of metabolism in a practical approach. Together with our patient database RAMEDIS ( www.ramedis.de. It is the basis of an expert system. METAGENE gives rapid access to comprehensive information about 428. In the most recent new development we improved the “expert” search function, where clinical, general and special laboratory findings can easy be combined. We appreciate any comments or contribution. Click here to start METAGENE online!

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MetaGeneAnnotator

MetaGeneAnnotator is a gene-finding program for prokaryote and phage. Anonymous and fragmented genomic sequences (longer than 60 bp) can be accepted. The software is freely available for academic use. Previous version of MetaGene is here.). All sequences are individually treated in this server. Total sequence length should be less than 10Mbp. Ambiguous codons are ignored (score = 0). Don't join your sequences with 'N'. Paste your sequence(s) in fasta format:.

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metagene.org -&nbspmetagene Resources and Information.