160 related articles for article (PubMed ID: 4239581)
21. Glycogen storage diseases of muscle problems in biochemical genetics.
Rowland LP; Dimauro S; Bank WJ
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):43-51. PubMed ID: 4281320
[TBL] [Abstract][Full Text] [Related]
22. [Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
Schaub J; Osang M
MMW Munch Med Wochenschr; 1976 May; 118(19):609-14. PubMed ID: 180406
[TBL] [Abstract][Full Text] [Related]
23. [Congenital diseases of the glycide metabolism].
Santi ML
Minerva Med; 1972 Dec; 63(86):4708-14. PubMed ID: 4509141
[No Abstract] [Full Text] [Related]
24. [Difficulties in determination of the type of glycogenosis].
Minculescu M; Onofrei T; Rusu M; Septilici N; Minculescu I; Popa V; Serbănescu C; Pena J; Wolcz G; Ionuş D; Galaczi A
Pediatria (Bucur); 1974 Jan; 23(1):19-34. PubMed ID: 4526155
[No Abstract] [Full Text] [Related]
25. Studies in glycogen storage disease. IV. Leukocyte phosphorylase in a family with type VI GSD.
Schwartz D; Savin M; Drash A; Field J
Metabolism; 1970 Mar; 19(3):238-45. PubMed ID: 4313495
[No Abstract] [Full Text] [Related]
26. The floppy infant syndrome in muscular glycogenosis.
Zellweger H
Padiatr Padol; 1972; 7(4):365-71. PubMed ID: 4263587
[No Abstract] [Full Text] [Related]
27. The role of lysosomes in the pathogeny of storage diseases.
Hers HG
Arch Belg Dermatol Syphiligr; 1972; 28(1):51-7. PubMed ID: 4266285
[No Abstract] [Full Text] [Related]
28. [Hepatic surcharges. I. Carbohydrate surcharges].
Chevrel B
Rev Med Chir Mal Foie; 1970; 45(4):231-6. PubMed ID: 5270902
[No Abstract] [Full Text] [Related]
29. Heterogenous glycogen storage disease in one family.
Domaniç N; Akman N; Ozand P; Müftüoglu AU
Hum Hered; 1976; 26(3):217-25. PubMed ID: 1066318
[TBL] [Abstract][Full Text] [Related]
30. The glycogen storage diseases.
Drash A; Field J
Dis Mon; 1971 Oct; ():3-40. PubMed ID: 4255992
[No Abstract] [Full Text] [Related]
31. Impaired platelet function in glucose-6-phosphatase deficiency.
Corby DG; Putnam CW; Greene HL
J Pediatr; 1974 Jul; 85(1):71-6. PubMed ID: 4212074
[No Abstract] [Full Text] [Related]
32. [SOME NOTIONS ON INBORN ERRORS OF CARBOHYDRATE METABOLISM].
LUST M
Scalpel (Brux); 1963 Oct; 116():835-45. PubMed ID: 14096212
[No Abstract] [Full Text] [Related]
33. [On 2 uncommon cases of cardio-muscular glycogenosis (with enzyme study)].
Berio A; Marchi AG; Bertolotti E; Nordio S
Minerva Pediatr; 1967 Apr; 19(14):688-92. PubMed ID: 5247206
[No Abstract] [Full Text] [Related]
34. [Liver glycogenosis: first 2 Brazilian cases with double enzyme defect].
Seibt FL; Mello de Oliveira JA; Santoro JR; Alcantara A; Dora GL; Pena GA
Ann Histochim; 1973; 18(3):253-65. PubMed ID: 4526225
[No Abstract] [Full Text] [Related]
35. [Chromatographic analysis in the differential diagnosis of mucopolysaccharidosis].
Sietti C
Minerva Pediatr; 1971 Jun; 23(23):1047-8. PubMed ID: 4255651
[No Abstract] [Full Text] [Related]
36. A histochemical and electron microscopic study of skeletal muscle in a case of Pompe's disease (glycogenosis II).
Cardiff RD
Pediatrics; 1966 Feb; 37(2):249-59. PubMed ID: 4221626
[No Abstract] [Full Text] [Related]
37. Glycogen storage disease.
Br Med J; 1969 Apr; 2(5649):68. PubMed ID: 5251661
[No Abstract] [Full Text] [Related]
38. A technique for the enzymatic diagnosis of glycogen storage disease on very small tissue specimens.
Ockerman PA
Acta Paediatr Scand; 1968 Mar; 57(2):105-9. PubMed ID: 4303026
[No Abstract] [Full Text] [Related]
39. Nutrition in children affected by inherited metabolic diseases.
Giovannini M; Biasucci G; Luotti D; Fiori L; Riva E
Ann Ist Super Sanita; 1995; 31(4):489-502. PubMed ID: 8851705
[TBL] [Abstract][Full Text] [Related]
40. [Glycogen storage diseases].
Field JB
Acta Diabetol Lat; 1969; 6(1):1-19. PubMed ID: 5256103
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
