350 related articles for article (PubMed ID: 2960768)
1. Glycogen storage disease type II (Pompe's disease): the first biochemical evidence in Thailand.
Rangdaeng S; Scollard DM; Srichairatanakol S; Sutthachit M; Phornphutkul C
J Med Assoc Thai; 1987 Sep; 70(9):536-42. PubMed ID: 2960768
[No Abstract] [Full Text] [Related]
2. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
Pilz H; Goebel HH; Stefan H; Seidel D; Kohlschütter A
J Clin Chem Clin Biochem; 1977 Dec; 15(12):705-8. PubMed ID: 342670
[No Abstract] [Full Text] [Related]
3. [Pompe's disease or glycogen storage disease].
Vanto T; Salmi TT; Kalimo H; Lang H; Näntö V; Berlin M; Penttinen R
Duodecim; 1982; 98(9):709-16. PubMed ID: 7049663
[No Abstract] [Full Text] [Related]
4. [Acid alpha-glucosidase deficiency: Pompe's disease].
Iwamasa T
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):686-92. PubMed ID: 3152090
[No Abstract] [Full Text] [Related]
5. Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures.
Meola G; Scarpini E; Manfredi L; Velicogna M; Pellegrini G; Redi CA; Scarlato G
Basic Appl Histochem; 1984; 28(3):245-55. PubMed ID: 6440527
[TBL] [Abstract][Full Text] [Related]
6. Bone marrow transplantation for Pompé's disease.
Hoogerbrugge PM; Wagemaker G; van Bekkum DW; Reuser AJ; vd Ploeg AT
N Engl J Med; 1986 Jul; 315(1):65-6. PubMed ID: 3086726
[No Abstract] [Full Text] [Related]
7. Comparative investigation of alpha-glucosidase activity in leucocytes and skeletal muscle of patients with Morbus Pompe.
Didt L; Winkler M; Bührdel P; Bormann M; Böhme HJ; Hofmann E
Z Med Lab Diagn; 1988; 29(1):7-11. PubMed ID: 3129881
[No Abstract] [Full Text] [Related]
8. Receptor-mediated uptake of acid alpha-glucosidase corrects lysosomal glycogen storage in cultured skeletal muscle.
Van der Ploeg AT; Loonen MC; Bolhuis PA; Busch HM; Reuser AJ; Galjaard H
Pediatr Res; 1988 Jul; 24(1):90-4. PubMed ID: 2970619
[TBL] [Abstract][Full Text] [Related]
9. Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods.
Ninomiya N; Iwamasa T; Matsuda I; Nonaka I
J Inherit Metab Dis; 1983; 6(3):131-2. PubMed ID: 6422147
[No Abstract] [Full Text] [Related]
10. [Immunochemical study of acid alpha-1,4-glucosidase in 7 patients with type II glycogenosis].
Bienvenu J; Mathieu M; Collombel C; Baltassat P; Divry P; Dorche C; Cotte J
Pediatrie; 1979 Sep; 34(6):659-76. PubMed ID: 388338
[No Abstract] [Full Text] [Related]
11. Tissue alpha-glucosidase activity and glycogen content in patients with generalized glycogenosis.
Steinitz K; Rutenberg A
Isr J Med Sci; 1967; 3(3):411-21. PubMed ID: 4951241
[No Abstract] [Full Text] [Related]
12. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
Braulke T; Sandig KR
Kinderarztl Prax; 1984 Aug; 52(8):377-82. PubMed ID: 6384623
[No Abstract] [Full Text] [Related]
13. [Acid maltase deficiency in 2 adolescent siblings].
Gracia P; Benlloch T; de la Fuente G; Durántez A; Espanña P; Cánovas A; Illera ER
Med Clin (Barc); 1982 Sep; 79(5):227-31. PubMed ID: 6755088
[No Abstract] [Full Text] [Related]
14. Clinical diversity in glycogenosis type II. Biosynthesis and in situ localization of acid alpha-glucosidase in mutant fibroblasts.
Reuser AJ; Kroos M; Willemsen R; Swallow D; Tager JM; Galjaard H
J Clin Invest; 1987 Jun; 79(6):1689-99. PubMed ID: 3108320
[TBL] [Abstract][Full Text] [Related]
15. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency.
Matsuishi T; Terasawa K; Yoshida I; Yano E; Yamashita F; Hidaka T; Ishihara O; Yoshino M; Nonaka I; Kurokawa T; Nakamura Y
Neuropediatrics; 1982 Nov; 13(4):173-6. PubMed ID: 6818487
[TBL] [Abstract][Full Text] [Related]
16. Study of alpha-D-glucosidase activity in patients with Pompe's disease.
Lin CY; Hwang B; Hsiao KJ; Jin YR
Taiwan Yi Xue Hui Za Zhi; 1986 Aug; 85(8):766-70. PubMed ID: 3540186
[No Abstract] [Full Text] [Related]
17. [Mitigated adult forms of acid maltase deficiency (Pompe's disease). Morphologic and pathobiochemical studies].
Pongratz D; Hübner G; Deufel T; Wieland OH
Klin Wochenschr; 1983 Aug; 61(15):743-50. PubMed ID: 6413751
[No Abstract] [Full Text] [Related]
18. [Late infantile form of Pompe's disease. Deficiency of alpha-1,4-glucosidase (acid maltase)].
Colomer J; Roig M; Campistol J; Rullan G; Fernández-Alvarez E
An Esp Pediatr; 1984 Sep; 21(3):250-9. PubMed ID: 6391315
[TBL] [Abstract][Full Text] [Related]
19. [Ichthyosiform scaling in alpha-1,4-glucosidase deficiency].
Gebhart W; Mainitz M; Jurecka W; Niebauer G; Paschke E; Stöckler S; Sluga E
Hautarzt; 1988 Apr; 39(4):228-32. PubMed ID: 3290163
[TBL] [Abstract][Full Text] [Related]
20. Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia.
Ullrich K; Gröbe H; Korinthenberg R; von Bassewitz DB
Pathol Res Pract; 1986 Oct; 181(5):627-32. PubMed ID: 2947052
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]