197 related articles for article (PubMed ID: 26609772)
1. [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]
2. 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]
3. 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]
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. Cerebral degenerative disorders of infancy and childhood.
Noronha MJ
Dev Med Child Neurol; 1974 Apr; 16(2):228-41. PubMed ID: 4209600
[No Abstract] [Full Text] [Related]
6. [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]
7. Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseases.
Kopitz J; Harzer K; Kohlschütter A; Zöller B; Blenck N; Cantz M
Am J Med Genet; 1996 May; 63(1):198-202. PubMed ID: 8723110
[TBL] [Abstract][Full Text] [Related]
8. Magnetic resonance techniques in neuronal ceroid lipofuscinoses and some other lysosomal diseases affecting the brain.
Autti T; Raininko R; Vanhanen SL; Santavuori P
Curr Opin Neurol; 1997 Dec; 10(6):519-24. PubMed ID: 9425568
[No Abstract] [Full Text] [Related]
9. Lysosomal disorders associated with leukoencephalopathy.
Renaud DL
Semin Neurol; 2012 Feb; 32(1):51-4. PubMed ID: 22422206
[TBL] [Abstract][Full Text] [Related]
10. [Sweat gland pathology in neurodegenerative disorders].
Kimura S
No To Hattatsu; 1991 Jan; 23(1):20-5. PubMed ID: 1847293
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Clinical aspects of globoid cell and metachromatic leukodystrophies.
Hagberg B
Birth Defects Orig Artic Ser; 1971 Feb; 7(1):103-12. PubMed ID: 5173355
[TBL] [Abstract][Full Text] [Related]
13. Lysosomal leukodystrophies: Krabbe disease and metachromatic leukodystrophy.
Kohlschütter A
Handb Clin Neurol; 2013; 113():1611-8. PubMed ID: 23622382
[TBL] [Abstract][Full Text] [Related]
14. Enzymatic diagnosis of sphingolipidoses.
Suzuki K
Methods Enzymol; 1987; 138():727-62. PubMed ID: 2885713
[No Abstract] [Full Text] [Related]
15. Newborn screening for lysosomal storage disorders.
Nakamura K; Hattori K; Endo F
Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):63-71. PubMed ID: 21312327
[TBL] [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. Genetic disorders of lysosomes.
Hirschhorn R; Weissmann G
Prog Med Genet; 1976; 1():49-101. PubMed ID: 180565
[No Abstract] [Full Text] [Related]
18. 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]
19. [Diagnostic procedure in neurodegenerative diseases with a chronic course].
Boltshauser E; Spycher MA
Klin Padiatr; 1986; 198(2):79-83. PubMed ID: 3702276
[TBL] [Abstract][Full Text] [Related]
20. [Recent advances in the diagnosis and treatment of lysosomal storage diseases].
Wu XR; Bao XH
Beijing Da Xue Xue Bao Yi Xue Ban; 2005 Aug; 37(4):440-4. PubMed ID: 16086072
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]