Pages that link to "Q43765904"
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The following pages link to Farber lipogranulomatosis with predominant joint involvement mimicking juvenile idiopathic arthritis (Q43765904):
Displayed 7 items.
- Acid Ceramidase Deficiency is characterized by a unique plasma cytokine and ceramide profile that is altered by therapy. (Q38787556) (← links)
- Brief Report: Peripheral Osteolysis in Adults Linked to ASAH1 (Acid Ceramidase) Mutations: A New Presentation of Farber's Disease (Q40115169) (← links)
- C26-Ceramide as highly sensitive biomarker for the diagnosis of Farber Disease (Q41094126) (← links)
- Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: identification of the first large deletion in ASAH1 gene (Q44533383) (← links)
- Acid ceramidase deficiency: Farber disease and SMA-PME (Q90370648) (← links)
- Acid Sphingomyelinase Deficiency Ameliorates Farber Disease (Q91966157) (← links)
- Hematopoietic stem cell transplant does not prevent neurological deterioration in infants with Farber disease: Case report and literature review (Q93029687) (← links)