Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Ardalan–Shoja–Kiuru_syndrome> ?p ?o }
Showing triples 1 to 37 of
37
with 100 triples per page.
- Ardalan–Shoja–Kiuru_syndrome abstract "Ardalan–Shoja–Kiuru syndrome is a clinical syndrome featuring hereditary gelsolin amyloidosis and retinitis pigmentosa. This syndrome was first recognized by two Iranian physicians, Mohammad Ardalan and Mohammadali Shoja and Finnish neurologist Sari Kiuru-Enari in an Iranian family. Hereditary gelsolin amyloidosis has originally been reported by Finnish ophthalmologist Jouko Meretoja and is known as Meretoja syndrome or Familial Amyloidosis, Finnish type. In addition to the classic manifestations of Finnish type Familial Amyloidosis, cutis laxa, progressive peripheral neuropathy and corneal lattice dystrophy, some of the afflicted members of the Iranian family have retinitis pigmentosa. This feature had not been previously reported with this type of amyloidosis. Ardalan–Shoja–Kiuru syndrome or hereditary gelsolin amyloidosis plus retintis pigmentosa has not been found outside this single Iranian family.".
- Ardalan–Shoja–Kiuru_syndrome wikiPageID "20584334".
- Ardalan–Shoja–Kiuru_syndrome wikiPageLength "2103".
- Ardalan–Shoja–Kiuru_syndrome wikiPageOutDegree "14".
- Ardalan–Shoja–Kiuru_syndrome wikiPageRevisionID "691072183".
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Amyloidosis.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Category:Amyloidosis.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Category:Syndromes.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Corneal_dystrophy.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Cutis_laxa.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Finland.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Gelsolin.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Hereditary_gelsolin_amyloidosis.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Iran.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Neurology.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Ophthalmology.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Peripheral_neuropathy.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Retinitis_pigmentosa.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLink Syndrome.
- Ardalan–Shoja–Kiuru_syndrome wikiPageWikiLinkText "Ardalan–Shoja–Kiuru syndrome".
- Ardalan–Shoja–Kiuru_syndrome wikiPageUsesTemplate Template:Reflist.
- Ardalan–Shoja–Kiuru_syndrome subject Category:Amyloidosis.
- Ardalan–Shoja–Kiuru_syndrome subject Category:Syndromes.
- Ardalan–Shoja–Kiuru_syndrome hypernym Syndrome.
- Ardalan–Shoja–Kiuru_syndrome type Disease.
- Ardalan–Shoja–Kiuru_syndrome type Disorder.
- Ardalan–Shoja–Kiuru_syndrome type Redirect.
- Ardalan–Shoja–Kiuru_syndrome type Syndrome.
- Ardalan–Shoja–Kiuru_syndrome comment "Ardalan–Shoja–Kiuru syndrome is a clinical syndrome featuring hereditary gelsolin amyloidosis and retinitis pigmentosa. This syndrome was first recognized by two Iranian physicians, Mohammad Ardalan and Mohammadali Shoja and Finnish neurologist Sari Kiuru-Enari in an Iranian family. Hereditary gelsolin amyloidosis has originally been reported by Finnish ophthalmologist Jouko Meretoja and is known as Meretoja syndrome or Familial Amyloidosis, Finnish type.".
- Ardalan–Shoja–Kiuru_syndrome label "Ardalan–Shoja–Kiuru syndrome".
- Ardalan–Shoja–Kiuru_syndrome sameAs Q4787807.
- Ardalan–Shoja–Kiuru_syndrome sameAs Síndrome_de_Meretoja.
- Ardalan–Shoja–Kiuru_syndrome sameAs Meretojan_tauti.
- Ardalan–Shoja–Kiuru_syndrome sameAs m.0524cd8.
- Ardalan–Shoja–Kiuru_syndrome sameAs Q4787807.
- Ardalan–Shoja–Kiuru_syndrome wasDerivedFrom Ardalan–Shoja–Kiuru_syndrome?oldid=691072183.
- Ardalan–Shoja–Kiuru_syndrome isPrimaryTopicOf Ardalan–Shoja–Kiuru_syndrome.