182 related articles for article (PubMed ID: 117977)
1. Inherited lipid storage diseases of the central nervous system.
Percy AK; Shapiro LJ; Kaback MM
Curr Probl Pediatr; 1979 Sep; 9(11):1-51. PubMed ID: 117977
[No Abstract] [Full Text] [Related]
2. [Lipid histochemical studies of lysosomal lipid metabolism diseases].
Dietzmann K; Mohnike D
Acta Histochem Suppl; 1984; 30():211-3. PubMed ID: 6201955
[No Abstract] [Full Text] [Related]
3. Enzymatic abnormalities in diseases of sphingolipid metabolism.
Brady RO
Clin Chem; 1967 Jul; 13(7):565-77. PubMed ID: 5006481
[No Abstract] [Full Text] [Related]
4. [Procedure for the diagnosis of sphingolipidoses or allied diseases in adult patients with neurological or psychiatric symptoms (author's transl)].
Pilz H; Heipertz R; Seidel D
Nervenarzt; 1979 Dec; 50(12):749-61. PubMed ID: 94938
[No Abstract] [Full Text] [Related]
5. Heritable catabolic and anabolic disorders of lipid metabolism.
Brady RO
Metabolism; 1977 Mar; 26(3):329-45. PubMed ID: 13262
[TBL] [Abstract][Full Text] [Related]
6. Neurolipidoses: examples of lysosomal storage diseases.
Blakemore WF
Vet Clin North Am Small Anim Pract; 1980 Feb; 10(1):81-90. PubMed ID: 6773205
[No Abstract] [Full Text] [Related]
7. Enzymatic diagnosis of sphingolipidoses.
Suzuki K
Methods Enzymol; 1987; 138():727-62. PubMed ID: 2885713
[No Abstract] [Full Text] [Related]
8. The liver in lipid storage disease: biochemical basis of pathogenesis and clinical features.
Brady RO; James SP; Barranger JA
Prog Liver Dis; 1982; 7():331-46. PubMed ID: 6810410
[No Abstract] [Full Text] [Related]
9. Enzymic diagnosis of sphingolipidoses.
Suzuki K
Methods Enzymol; 1978; 50():456-88. PubMed ID: 26837
[No Abstract] [Full Text] [Related]
10. Inborn errors of lipid metabolism: early identification.
Crocker AC
Clin Perinatol; 1976 Mar; 3(1):99-113. PubMed ID: 821692
[No Abstract] [Full Text] [Related]
11. [Prenatal diagnosis of incurable familial metabolic diseases. Prenatal diagnosis of disorders of lipid metabolism].
Harzer K
Med Welt; 1979; 30(48):1810-6. PubMed ID: 42836
[No Abstract] [Full Text] [Related]
12. [Diagnosis of lysosomal storage diseases using ultrastructural studies and biopsies of the conjunctiva].
Libert J; Danis P
Bull Mem Soc Fr Ophtalmol; 1981; 93():144-50. PubMed ID: 6809088
[No Abstract] [Full Text] [Related]
13. Basic findings and current developments in sphingolipidoses.
Pilz H; Heipertz R; Seidel D
Hum Genet; 1979 Mar; 47(2):113-34. PubMed ID: 108196
[TBL] [Abstract][Full Text] [Related]
14. Concentrations of an activator protein for sphingolipid hydrolysis in liver and brain samples from patients with lysosomal storage diseases.
Inui K; Wenger DA
J Clin Invest; 1983 Nov; 72(5):1622-8. PubMed ID: 6415115
[TBL] [Abstract][Full Text] [Related]
15. [Recent advances in sphingolipidosis research].
Tamai Y; Kojima H
Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1291-303. PubMed ID: 1972585
[No Abstract] [Full Text] [Related]
16. [Phenotypes in heteroglycanoses and sphingolipidoses (author's transl)].
Gehler J
Monatsschr Kinderheilkd; 1981 Nov; 129(11):610-20. PubMed ID: 6798422
[TBL] [Abstract][Full Text] [Related]
17. Diagnostic and therapeutic applications of sphingolipid hydrolyzing enzymes.
Brady RO
Curr Top Cell Regul; 1985; 26():39-50. PubMed ID: 3935381
[No Abstract] [Full Text] [Related]
18. [Lysosomal storage diseases].
Schulze M; Groeschel S; Gburek-Augustat J; Nägele T; Horger M
Rofo; 2015 Dec; 187(12):1057-60. PubMed ID: 26609772
[No Abstract] [Full Text] [Related]
19. Progress in investigations of sphingolipidoses.
Adachi M; Schneck L; Volk BW
Acta Neuropathol; 1978 Aug; 43(1-2):1-18. PubMed ID: 97916
[No Abstract] [Full Text] [Related]
20. The biochemistry of sphingolipid storage diseases.
Sandhoff K
Angew Chem Int Ed Engl; 1977 May; 16(5):273-85. PubMed ID: 406814
[No Abstract] [Full Text] [Related]
[Next] [New Search]