186 related articles for article (PubMed ID: 370427)
1. [Tests for the detection of inborn errors of metabolism--urinary alpha-glucosidase analysis for the detection of glycogen storage disease type II (author's transl)].
Soyama K; Ono E
Rinsho Byori; 1978 Dec; 26(12):1022-6. PubMed ID: 370427
[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. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
Farmer PM
Ann Clin Lab Sci; 1982; 12(6):431-8. PubMed ID: 6817693
[TBL] [Abstract][Full Text] [Related]
4. Glycogen storage disease type II: enzymatic screening in dried blood spots on filter paper.
Chamoles NA; Niizawa G; Blanco M; Gaggioli D; Casentini C
Clin Chim Acta; 2004 Sep; 347(1-2):97-102. PubMed ID: 15313146
[TBL] [Abstract][Full Text] [Related]
5. [The automatic screening test for glycogen storage disease type II (Pompoe's disease) (author's transl)].
Soyama K; Ono E; Fukui I; Shimada N; Kusunoki T; Tanaka K; Hashimoto K; Sudo K; Minegishi H
Rinsho Byori; 1978; 26(3):245-8. PubMed ID: 349205
[No Abstract] [Full Text] [Related]
6. [Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)].
Shi HP; Zhang GX; Guo YF; Fang BL; Zhang WM; Chen F; Luo HY
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1985 Dec; 7(6):475-7. PubMed ID: 2940012
[No Abstract] [Full Text] [Related]
7. The first trimester prenatal diagnosis of Pompe's disease at risk.
Ezaki M; Sugiyama K; Wada Y; Suzumori K
Jinrui Idengaku Zasshi; 1987 Sep; 32(3):267-9. PubMed ID: 3329254
[No Abstract] [Full Text] [Related]
8. Urinary alpha-glucosidase analysis for the detection of the adult form of Pompe's disease.
Soyama K; Ono E; Shimada N; Tanaka K; Kusunoki T
Clin Chim Acta; 1977 May; 77(1):61-7. PubMed ID: 17490
[TBL] [Abstract][Full Text] [Related]
9. [The use of antibodies for differential determination of neutral and acid alpha-glucosidases in human urine in normal and pathological states].
Ushakova NA; Kazlas EV; Belen'kiĭ DM; Lukomskaia IS
Vopr Med Khim; 1988; 34(1):68-71. PubMed ID: 3130725
[TBL] [Abstract][Full Text] [Related]
10. [Clinical, biochemical, morphological and electrophysiological studies of glycogenosis Type II in childhood with double deficiency of enzymes (author's transl)].
Lück R; Platt D; Lange RH; Kunze K
Z Kinderheilkd; 1975 Jul; 120(1):19-28. PubMed ID: 125955
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. [Acid maltase deficiency myopathy infantile and adult forms (author's transl)].
Saenz Lope E; Cocero Oviedo E; Ricoy Campo JR; Benlloch T
Arch Neurobiol (Madr); 1981; 44(1):49-62. PubMed ID: 6784694
[No Abstract] [Full Text] [Related]
13. Angiocardiographic and enzyme studies in a patient with type II glycogenosis (Pompe's disease). A case report.
Bonnici F; Shapiro R; Joffe HS; Petersen EM
S Afr Med J; 1980 Nov; 58(21):860-2. PubMed ID: 6777881
[TBL] [Abstract][Full Text] [Related]
14. A simple differential immunoprecipitation assay of urinary acid and neutral alpha-glucosidases for glycogenosis II.
Tsuji A; Yang RC; Omura K; Imabayashi T; Suzuki Y
Clin Chim Acta; 1987 Aug; 167(3):313-20. PubMed ID: 3304722
[TBL] [Abstract][Full Text] [Related]
15. [Prenatal diagnosis of glycogenosis type II (Pompe) and subsequent therapeutic abortion (author's transl)].
Schaub J; Osang M; von Bassewitz DB; Grote W; Terinde R; Lombeck I; Bremer HJ
Dtsch Med Wochenschr; 1974 Nov; 99(44):2219-22, 27. PubMed ID: 4529697
[No Abstract] [Full Text] [Related]
16. Muscular form of glycogenosis type II (Pompe's disease).
Tanaka K; Shimazu S; Oya N; Tomisawa M; Kusunoki T; Soyama K; Ono E
Pediatrics; 1979 Jan; 63(1):124-9. PubMed ID: 375166
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. [EMG-findings in typ-II-glycogenosis (Pompe's disease, acid maltase deficiency) (author's transl)].
Gehlen W; Stefan H
EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1978 Mar; 9(1):24-9. PubMed ID: 416945
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Acid maltase deficiency in adolescence: report of an unusual case.
Olguntürk R; Bilgiç A; Cağlar M; Sinangil F
Turk J Pediatr; 1982; 24(2):115-9. PubMed ID: 6214067
[No Abstract] [Full Text] [Related]
[Next] [New Search]