The biochemical defect in Farber's disease.
暂无分享,去创建一个
[1] H. Moser,et al. Diagnosis of lipogranulomatosis (Farber disease) by use of cultured fibroblasts. , 1976, The Journal of pediatrics.
[2] H. Moser,et al. Ceramidase and ceramide synthesis in human kidney and cerebellum. Description of a new alkaline ceramidase. , 1975, Biochimica et biophysica acta.
[3] H. Moser,et al. Above-normal urinary excretion of urinary ceramides in Farber's disease, and characterization of their components by high-performance liquid chromatography. , 1975, Clinical chemistry.
[4] H. Hers,et al. Lysosomes and storage diseases , 1973 .
[5] P. Dustin,et al. LA MALADIE DE FARBER. ETUDE ANATOMO CLINIQUE ET ULTRASTRUCTURALE , 1973 .
[6] H. Moser,et al. Ceramidase Deficiency in Farber's Disease (Lipogranulomatosis) , 1972, Science.
[7] R. Zetterström,et al. Ceramides in a patient with lipogranulomatosis (Farber's disease) with chronic course. , 1971, Scandinavian journal of clinical and laboratory investigation.
[8] J. Clausen,et al. CHEMICAL STUDIES OF FARBER'S DISEASE , 1970, Acta neurologica Scandinavica.
[9] H. Moser,et al. Farber's lipogranulomatosis. Report of a case and demonstration of an excess of free ceramide and ganglioside. , 1969, The American journal of medicine.
[10] S. Gatt,et al. Enzymatic hydrolysis of sphingolipids. 8. Further purification and properties of rat brain ceramidase. , 1969, Biochemistry.
[11] A. Nilsson,et al. The presence of spingomyelin- and ceramide-cleaving enzymes in the small intestinal tract. , 1969, Biochimica et biophysica acta.
[12] S. Gatt. [24] Enzymatic hydrolysis of sphingolipids , 1969 .
[13] H. Moser,et al. Ceramide and Ganglioside Accumulation in Farber's Lipogranulomatosis.∗ , 1967 .
[14] J. Clausen,et al. [Farber's disease (disseminated lipogranulomatosis). Clinical picture and summary of the chemical findings]. , 1967, Helvetica paediatrica acta.
[15] A. E. Claireaux,et al. THE PATHOLOGY OF LIMB ISCHAEMIA , 1967, The Ulster Medical Journal.
[16] S. Farber,et al. THE “LIPOGRANULOMATOSIS” SYNDROME; REVIEW, WITH REPORT OF PATIENT SHOWING MILDER INVOLVEMENT* , 1967 .
[17] M. Sribney. Enzymatic synthesis of ceramide. , 1966, Biochimica et biophysica acta.
[18] S. Gatt. Enzymatic hydrolysis of sphingolipids. I. Hydrolysis and synthesis of ceramides by an enzyme from rat brain. , 1966, The Journal of biological chemistry.
[19] C. Pearson,et al. A disorder of mucopolysaccharide metabolism with articular, respiratory, and neurologic manifestations , 1966 .
[20] D. Cogan,et al. Retinopathy in a case of Farber's lipogranulomatosis. , 1966, Archives of ophthalmology.
[21] S. Abul-Haj,et al. Farber's disease , 1962 .
[22] R. Zetterström. Disseminated Lipogranulomatosis (Farber's Disease) , 1958 .
[23] S. Farber,et al. Lipogranulomatosis; a new lipo-glycoprotein storage disease. , 1957, Journal of the Mount Sinai Hospital, New York.