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.
173 related articles for article (PubMed ID: 7009171)
1. [Glycogenosis II in Japanese quails]. Murakami H; Takagi A; Nanaka S; Ishiura S; Sugita H Jikken Dobutsu; 1980 Oct; 29(4):475-8. PubMed ID: 7009171 [No Abstract] [Full Text] [Related]
2. Generalized glycogen storage disease in Japanese quail (Coturnix coturnix japonica). Matsui T; Kuroda S; Mizutani M; Kiuchi Y; Suzuki K; Ono T Vet Pathol; 1983 May; 20(3):312-21. PubMed ID: 6576505 [TBL] [Abstract][Full Text] [Related]
3. Infantile and late onset form of generalised glycogenosis type II in cattle. Howell JM; Dorling PR; Cook RD; Robinson WF; Bradley S; Gawthorne JM J Pathol; 1981 Aug; 134(4):267-77. PubMed ID: 7033492 [TBL] [Abstract][Full Text] [Related]
4. Clinical and metabolic correction of pompe disease by enzyme therapy in acid maltase-deficient quail. Kikuchi T; Yang HW; Pennybacker M; Ichihara N; Mizutani M; Van Hove JL; Chen YT J Clin Invest; 1998 Feb; 101(4):827-33. PubMed ID: 9466978 [TBL] [Abstract][Full Text] [Related]
5. Mature 98,000-dalton acid alpha-glucosidase is deficient in Japanese quails with acid maltase deficiency. Suhara Y; Ishiura S; Tsukahara T; Sugita H Muscle Nerve; 1989 Aug; 12(8):670-8. PubMed ID: 2506448 [TBL] [Abstract][Full Text] [Related]
6. Bovine generalised glycogenosis type II. Uptake of lysosomal alpha-glucosidase by cultured skeletal muscle and reversal of glycogen accumulation. Di Marco PN; Howell JM; Dorling PR FEBS Lett; 1985 Oct; 190(2):301-4. PubMed ID: 3899727 [TBL] [Abstract][Full Text] [Related]
7. Skeletal-muscle alpha-glucosidases in bovine generalized glycogenosis type II. Dorling PR; Howell JM; Gawthorne JM Biochem J; 1981 Aug; 198(2):409-12. PubMed ID: 7034730 [TBL] [Abstract][Full Text] [Related]
8. Adeno-associated virus-mediated transfer of human acid maltase gene results in a transient reduction of glycogen accumulation in muscle of Japanese quail with acid maltase deficiency. Lin CY; Ho CH; Hsieh YH; Kikuchi T Gene Ther; 2002 May; 9(9):554-63. PubMed ID: 11973631 [TBL] [Abstract][Full Text] [Related]
9. A new mutant of Japanese quail (Coturnix coturnix japonica) characterized by generalized glycogenosis. Nunoya T; Tajima M; Mizutani M Lab Anim; 1983 Apr; 17(2):138-42. PubMed ID: 6575219 [TBL] [Abstract][Full Text] [Related]
10. Bone marrow transplantation in type IIa glycogen storage disease. Harris RE; Hannon D; Vogler C; Hug G Birth Defects Orig Artic Ser; 1986; 22(1):119-32. PubMed ID: 3516240 [No Abstract] [Full Text] [Related]
14. [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]
15. [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]
16. [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]
17. Bovine generalized glycogenosis type II: a clinico-pathological study. Edwards JR; Richards RB Br Vet J; 1979; 135(4):338-48. PubMed ID: 294950 [No Abstract] [Full Text] [Related]
18. Heterozygote detection in a family of Lapland dogs with a recessively inherited metabolic disease: canine glycogen storage disease type II. Walvoort HC; Koster JF; Reuser AJ Res Vet Sci; 1985 Mar; 38(2):174-8. PubMed ID: 3923581 [TBL] [Abstract][Full Text] [Related]
19. [Clinical and biochemical correlations in certain metabolic myopathies]. de Barsy T Bull Mem Acad R Med Belg; 1992; 147(10):385-92; discussion 392-3. PubMed ID: 1303789 [TBL] [Abstract][Full Text] [Related]
20. Detection of a homozygous D645E mutation of the acid alpha-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II. Chen CP; Lin SP; Tzen CY; Tsai FJ; Hwu WL; Wang W Prenat Diagn; 2004 Mar; 24(3):231-2. PubMed ID: 15057961 [No Abstract] [Full Text] [Related] [Next] [New Search]