These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. Diagnosis of glycosphingolipidoses by urinary-sediment analysis. Desnick RJ; Dawson G; Desnick SJ; Sweeley CC; Krivit W N Engl J Med; 1971 Apr; 284(14):739-44. PubMed ID: 5548035 [No Abstract] [Full Text] [Related]
5. Prenatal diagnosis of disorders of fatty acid transport and mitochondrial oxidation. Rinaldo P; Studinski AL; Matern D Prenat Diagn; 2001 Jan; 21(1):52-4. PubMed ID: 11180241 [No Abstract] [Full Text] [Related]
6. [Clinical and pathobiochemical findings in genetic diseases of carbohydrate and lipid metabolism]. Beyreiss K Zentralbl Pathol; 1992 Jun; 138(3):154-67. PubMed ID: 1525131 [No Abstract] [Full Text] [Related]
7. Fatty acid oxidation disorders: a new class of metabolic diseases. Hale DE; Bennett MJ J Pediatr; 1992 Jul; 121(1):1-11. PubMed ID: 1625065 [No Abstract] [Full Text] [Related]
8. [Physiopathology and clinical aspects of lipid metabolism disorders. Clinical aspects and therapy of primary hyperlipoproteinemias]. Haller H; Hanefeld M; Leonhardt W Dtsch Gesundheitsw; 1971 Sep; 26(37):1721-6. PubMed ID: 5122707 [No Abstract] [Full Text] [Related]
9. Possible role for protein kinase C in the pathogenesis of inborn errors of metabolism. Boneh A J Cell Biochem; 1995 Sep; 59(1):27-32. PubMed ID: 8530533 [TBL] [Abstract][Full Text] [Related]
10. The degradation of tritiated dihydrosphingosine in the intact rat. Keenan RW; Okabe K Biochemistry; 1968 Jul; 7(7):2696-701. PubMed ID: 5660083 [No Abstract] [Full Text] [Related]
12. Enzyme defects in the sphingolipidoses and their application to diagnosis. Brady RO Ann Clin Lab Sci (1971); 1972; 2(4):285-94. PubMed ID: 4342099 [No Abstract] [Full Text] [Related]