Angiokeratoma: decision-making aid for the diagnosis of Fabry disease. - Wikidata - awgldk - TriplyDB

Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

http://www.wikidata.org/entity/Q37997470

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The alpha-galactosidase A p.Arg118Cys variant does not cause a Fabry disease phenotype: data from individual patients and family studies.Uncertain diagnosis of fabry disease in patients with neuropathic pain, angiokeratoma or cornea verticillata: consensus on the approach to diagnosis and follow-up Life-threatening bleeding from gastric mucosal angiokeratomas during anticoagulation: A case report of Fabry disease.Capillary malformations: a classification using specific names for specific skin disorders.Recommendations for the inclusion of Fabry disease as a rare febrile condition in existing algorithms for fever of unknown origin.Angiokeratoma corporis diffusum in a patient with Hodgkin lymphoma: a new paraneoplastic skin manifestation?Mutation identification of Fabry disease in families with other lysosomal storage disorders.Genital angiokeratoma in a woman with Fabry disease: the dermatologist's role.Multicentric study on the diagnosis of Fabry's disease using angiokeratoma biopsy registries

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

http://www.wikidata.org/entity/Q37997470

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease.

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J.1365-2133.2012.10742.X

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British Journal of Dermatology

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Angiokeratoma: decision-making aid for the diagnosis of Fabry disease

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C H Orteu

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D Antuzzi

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D Linder

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Interdisciplinary Study Group on Fabry Disease (ISGF)

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N Aspite

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R Parini

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S Manco

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P2860

The 1.9 a structure of human alpha-N-acetylgalactosaminidase: The molecular basis of Schindler and Kanzaki diseases

Hereditary haemorrhagic telangiectasia: a clinical and scientific review

Angiokeratoma of the scrotum: a case of scrotal bleeding

A new case of alpha-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum, with Ménière's syndrome and without mental retardation

Life expectancy and cause of death in males and females with Fabry disease: findings from the Fabry Registry

Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey.

Fabry disease and the skin: data from FOS, the Fabry outcome survey.

Ear symptoms in children with Fabry disease: data from the Fabry Outcome Survey.

Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartylglucosaminuria, Hurler, Maroteaux-Lamy, and S

The pharmacological chaperone 1-deoxygalactonojirimycin reduces tissue globotriaosylceramide levels in a mouse model of Fabry disease.

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Maria Rita Bongiorno

Giorgia Cardinali

Claudio Feliciani

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2012-04-01T00:00:00Z

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