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.
162 related articles for article (PubMed ID: 416945)
1. [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]
2. [Glycogen storage disease (Pompe's disease) presenting as myopathy in the adult (author's transl)]. Stefan H; Böker DK; Müller J; Gullotta F Dtsch Med Wochenschr; 1977 Oct; 102(42):1512-4. PubMed ID: 269788 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. [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]
5. [Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)]. Gullotta F; Stefan H; Mattern H J Neurol; 1976; 213(3):199-216. PubMed ID: 61260 [TBL] [Abstract][Full Text] [Related]
6. [Myopathy in the adult form of glycogenosis II. Two case reports and review of the literature]. Horstmann S; Meier C; Mumenthaler M; Gitzelmann R Fortschr Neurol Psychiatr; 1990 Sep; 58(9):343-50. PubMed ID: 2175729 [TBL] [Abstract][Full Text] [Related]
7. [High frequency discharges as a non-specific EMG activity in adult acid maltase deficiency (author's transl)]. Manz F Arch Psychiatr Nervenkr (1970); 1980; 228(1):45-51. PubMed ID: 6930199 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. [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]
10. [A retrospective study of six patients with late-onset Pompe disease]. Saux A; Laforet P; Pagès AM; Figarella-Branger D; Pellissier JF; Pagès M; Labauge P Rev Neurol (Paris); 2008 Apr; 164(4):336-42. PubMed ID: 18439925 [TBL] [Abstract][Full Text] [Related]
11. [WPW syndrome combined with AV block 2 in an adult with glycogenosis (Type II)]. Francesconi M; Auff E; Ursin C; Sluga E Wien Klin Wochenschr; 1982 Aug; 94(15):401-4. PubMed ID: 6959422 [TBL] [Abstract][Full Text] [Related]
13. Acid maltase deficiency in childhood. Early diagnosis and clinical follow-up of late-onset glycogen storage disease type II. di Fiore MT; Manfredi R; Marri L; Zucchini A; Azzaroli L; Manfredi G Acta Neurol (Napoli); 1993 Aug; 15(4):258-67. PubMed ID: 8249669 [TBL] [Abstract][Full Text] [Related]
14. [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]
15. [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]
16. [Adult form of acid maltase deficiency presenting as progressive spinal muscular atrophy]. Pongratz D; Kötzner H; Hübner G; Deufel T; Wieland OH Dtsch Med Wochenschr; 1984 Apr; 109(14):537-41. PubMed ID: 6368168 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. [26-year-old female patient with elevated liver enzymes]. Martin K; Schlotter B; Müller-Höcker J; Loeschke K; Pongratz D; Folwaczny C Z Gastroenterol; 2002 Oct; 40(10):885-90. PubMed ID: 12436356 [TBL] [Abstract][Full Text] [Related]
19. [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]
20. [Hemodynamic findings in the adult form of type II glycogenosis]. Wiegand V; Rumpf K; Bardosi A; Meinck H; Kreuzer H Z Kardiol; 1986 Jan; 75(1):44-6. PubMed ID: 3457496 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]