Hallervorden-Spatz Syndrome Pages on BioPortfolio:

BioPortfolio.com - BioWeb Hiatal Hernia Gastroesophageal Search
Synonyms Galloway Syndrome Hiatal Hernia-Microcephaly-Nephrosis, Galloway Type ... Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Inguinal Hernia Hernia Search
Gottron's Syndrome - HA - Haddad syndrome - HAE - HAF Deficiency - Hageman Factor ... Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome.
...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Hemangioma Search
Hemangioma Thrombocytopenia Syndrome - Quest Diagnostics Patient Health Library .... Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Hemorrhagic Search
Synonyms HHT Osler-Weber Rendu Syndrome Rendu-Osler-Weber Syndrome Disorder ... Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Hemoglobinuria Paroxysmal Search
Synonyms Donath-Landsteiner Hemolytic Anemia Donath-Landsteiner Syndrome Dressler ... Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome.
...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio.com - BioWeb Hemoglobinuria Search
Synonyms Marchiafava-Micheli Syndrome PNH Disorder Subdivisions None General .... Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

BioPortfolio PANK2 Antibody
... GO:0005524 GO:0005739 GO:0015937 GO:0016740 - Gene Description： pantothenate kinase 2 (Hallervorden-Spatz syndrome) - - Gene Alias： C20orf48,
HARP, ...
http://www.bioportfolio.co.uk/antibody/anti-PANK2.htm...

BioPortfolio.com - BioWeb Hiatal Hernia Gastroesophageal/ Search
Galloway Mowat Syndrome - Quest Diagnostics Patient Health Library ... syndrome - Hallermann-Streiff-Francois syndrome - Hallervorden-Spatz Syndrome. ...
http://www.bioportfolio.co.uk/cgi-bin/dialogserver.exe?CMD=s...

Results from other life science and pharmaceutical sites:

Open Directory - Health: Conditions and Diseases: Neurological ...
MCW HealthLink - An article about Hallervorden-Spatz disease, with an explanation, the symptoms and prognosis. ... "Hallervorden-Spatz Syndrome"
search on: ...
http://www.dmoz.org/Health/Conditions_and_Diseases/Neurologi...

Hallervorden-Spatz Syndrome Gene Discovery [NEI News and Events]
The gene that causes Hallervorden-Spatz syndrome has been identified by National ... Hallervorden-Spatz syndrome is a rare, inherited, neurological disorder ...
http://www.nei.nih.gov/news/statements/hallervorden-spatz.as...

The First Scientific Workshop of Hallervorden-Spatz Syndrome ...
The First Scientific Workshop of Hallervorden-Spatz Syndrome. ... Organization Conducting Meeting: Hallervorden-Spatz Syndrome Association and Oregon Health
...
http://www.ninds.nih.gov/news_and_events/proceedings/Hallerv...

PANK2 - pantothenate kinase 2 (Hallervorden-Spatz syndrome ...
The official name of this gene is “pantothenate kinase 2 (Hallervorden-Spatz syndrome).” PANK2 is the gene's official symbol. The PANK2 gene is also known
...
http://ghr.nlm.nih.gov/gene=pank2...

Hallervorden-Spatz syndrome. [Arch Neurol. 1977] - PubMed Result
Two siblings with Hallervorden-Spatz syndrome showed striking homotypism and homochronism. Neuropathologic examination and electron microscopic studies were
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http://www.ncbi.nlm.nih.gov/pubmed/201232...

Defining Mutation Found in Hallervorden-Spatz Syndrome
Because all classic and many atypical cases tested had the PANK2 gene mutation, the syndrome should be termed pantothenate kinase-associated ...
http://www.medscape.com/viewarticle/447306...

Hallervorden-Spatz syndrome: clinical and magnetic...[Ann Neurol ...
Two women with a presumptive diagnosis of Hallervorden-Spatz syndrome had a combination of dystonia and parkinsonism. One had retinitis pigmentosa. ...
http://www.ncbi.nlm.nih.gov/pubmed/3202617...

OMIM - NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1
MIM #234200 · Text · Description · Clinical Features · Diagnosis · Mapping · Molecular Genetics · Genotype/Phenotype Correlations · Population Genetics ...
http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=234200...

A novel pantothenate kinase gene (PANK2) is defective in ...
Hallervorden-Spatz syndrome (HSS) is an autosomal recessive neurodegenerative disorder associated with iron accumulation in the brain. ...
http://www.nature.com/ng/journal/v28/n4/full/ng572.html...

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