Farber disease in infancy resembling juvenile idiopathic arthritis: identification of two new mutations and a good early response to allogeneic haematopoietic stem cell transplantation-Reference-Cited by-同舟云学术

Farber disease in infancy resembling juvenile idiopathic arthritis: identification of two new mutations and a good early response to allogeneic haematopoietic stem cell transplantation

Published:2014-03-10 Issue:8 Volume:53 Page:1533-1534
ISSN:1462-0324
Container-title:Rheumatology
language:en
Short-container-title:Rheumatology

Author:

Torcoletti M.,Petaccia A.,Pinto R. M.,Hladnik U.,Locatelli F.,Agostoni C.,Corona F.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Link

http://academic.oup.com/rheumatology/article-pdf/53/8/1533/5026410/keu010.pdf

Reference7 articles.

1. Ceramidase Deficiency in Farber's Disease (Lipogranulomatosis)

2. Farber disease: clinical presentation, pathogenesis and a new approach to treatment

3. Molecular analysis of acid ceramidase deficiency in patients with Farber disease

4. In vivo delivery of human acid ceramidase via cord blood transplantation and direct injection of lentivirus as novel treatment approaches for Farber disease

5. Bone marrow transplantation for infantile ceramidase deficiency (Farber disease)

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