Familial Lipogranulomatosis (Farber's disease)
- 1 June 1976
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 9 (6) , 625-630
- https://doi.org/10.1111/j.1399-0004.1976.tb01624.x
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Ceramidase Deficiency in Farber's Disease (Lipogranulomatosis)Science, 1972
- Ceramides in a Patient with Lipogranulomatosis (Farber's Disease) with Chronic CourseScandinavian Journal of Clinical and Laboratory Investigation, 1971
- CHEMICAL STUDIES OF FARBER'S DISEASEActa Neurologica Scandinavica, 1970
- Farber's lipogranulomatosisThe American Journal of Medicine, 1969
- Ceramide and Ganglioside Accumulation in Farber's Lipogranulomatosis.Experimental Biology and Medicine, 1967
- THE “LIPOGRANULOMATOSIS” SYNDROME; REVIEW, WITH REPORT OF PATIENT SHOWING MILDER INVOLVEMENTPublished by Elsevier ,1967
- A disorder of mucopolysaccharide metabolism with articular, respiratory, and neurologic manifestationsArthritis & Rheumatism, 1966
- Retinopathy in a Case of Farber's LipogranulomatosisArchives of Ophthalmology (1950), 1966
- Farber's disease: Report of a case with observations on its histogenesis and notes on the nature of the stored materialThe Journal of Pediatrics, 1962
- Disseminated Lipogranulomatosis (Farber's Disease)Acta Paediatrica, 1958