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2. X-chromosomal inheritance of liver glycogenosis with phosphorylase kinase deficiency. Huijing F; Fernandes J Am J Hum Genet; 1969 May; 21(3):275-84. PubMed ID: 5306139 [No Abstract] [Full Text] [Related]
3. Hepatic phosphorylase b kinase deficiency with normal enzyme activity in leukocytes. Alvarado LJ; Gasca-Centeno E; Grier RE J Pediatr; 1988 Nov; 113(5):865-7. PubMed ID: 3183845 [No Abstract] [Full Text] [Related]
4. Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle. Hug G; Schubert WK; Chuck G Biochem Biophys Res Commun; 1970 Aug; 40(4):982-8. PubMed ID: 4322108 [No Abstract] [Full Text] [Related]
5. Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation. Migeon BR; Huijing F Am J Hum Genet; 1974 May; 26(3):360-8. PubMed ID: 4524311 [No Abstract] [Full Text] [Related]
7. Adenine phosphoribosyltransferase deficiency in man. Report of a second family. Fox IH; Meade JC; Kelley WN Am J Med; 1973 Nov; 55(5):614-20. PubMed ID: 4749203 [No Abstract] [Full Text] [Related]
8. The X-chromosome and the enzymes controlling muscle glycogen: phosphorylase kinase. Lyon JB Biochem Genet; 1970 Feb; 4(1):169-85. PubMed ID: 5444100 [No Abstract] [Full Text] [Related]
9. Phosphorylase b kinase inheritance in mice. Lyon JB; Porter J; Robertson M Science; 1967 Mar; 155(3769):1550-1. PubMed ID: 6020474 [TBL] [Abstract][Full Text] [Related]
10. 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]
12. Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency. Lederer B; Van Hoof F; Van den Berghe G; Hers H Biochem J; 1975 Apr; 147(1):23-35. PubMed ID: 168880 [TBL] [Abstract][Full Text] [Related]
14. Autosomal recessive phosphorylase kinase deficiency in liver, caused by mutations in the gene encoding the beta subunit (PHKB). van den Berg IE; van Beurden EA; de Klerk JB; van Diggelen OP; Malingré HE; Boer MM; Berger R Am J Hum Genet; 1997 Sep; 61(3):539-46. PubMed ID: 9326319 [TBL] [Abstract][Full Text] [Related]
15. Hepatic glycogenosis due to phosphorylase deficiency. Limitations of enzyme studies on liver biopsy specimens. Wagner R; Huijing F; Porter E Am J Med; 1971 Nov; 51(5):685-91. PubMed ID: 5287080 [No Abstract] [Full Text] [Related]
16. [Glycogen metabolism in animal tissues--its regulation and disorders]. Tarui S; Ikura Y Tanpakushitsu Kakusan Koso; 1967 Dec; 12(14):1388-405. PubMed ID: 4299659 [No Abstract] [Full Text] [Related]
17. Glycogen storage disease type IX: benign glycogenosis of liver and hepatic phosphorylase kinase deficiency. Schimke RN; Zakheim RM; Corder RC; Hug G J Pediatr; 1973 Dec; 83(6):1031-4. PubMed ID: 4518931 [No Abstract] [Full Text] [Related]
18. Erythrocyte and leukocyte phosphoglycerate kinase deficiency with neurologic disease. Konrad PN; McCarthy DJ; Mauer AM; Valentine WN; Paglia DE J Pediatr; 1973 Mar; 82(3):456-60. PubMed ID: 4698932 [No Abstract] [Full Text] [Related]
19. X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice. Varsányi M; Vrbica A; Heilmeyer LM Biochem Genet; 1980 Apr; 18(3-4):247-61. PubMed ID: 7447922 [TBL] [Abstract][Full Text] [Related]
20. In vivo response of skeletal muscle glycogen phosphorylase, phosphorylase b kinase and cyclic AMP to epinephrine administration. POSNER JB; STERN R; KREBS EG Biochem Biophys Res Commun; 1962 Oct; 9():293-6. PubMed ID: 13985662 [No Abstract] [Full Text] [Related] [Next] [New Search]