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.
22. Liver glycogenosis caused by a defective phosphorylase system: hemolysate analysis. Baussan C; Moatti N; Odievre M; Lemonnier A Pediatrics; 1981 Jan; 67(1):107-12. PubMed ID: 6787554 [TBL] [Abstract][Full Text] [Related]
23. Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscle. Madlom M; Besley GT; Cohen PT; Marrian VJ Eur J Pediatr; 1989 Oct; 149(1):52-3. PubMed ID: 2606129 [TBL] [Abstract][Full Text] [Related]
24. Fueling around with glycogen: the implications of muscle phosphorylase b kinase deficiency. Haller RG Neurology; 2008 May; 70(20):1872-3. PubMed ID: 18474841 [No Abstract] [Full Text] [Related]
25. MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. ROWLAND LP; FAHN S; SCHOTLAND DL Arch Neurol; 1963 Oct; 9():325-42. PubMed ID: 14055781 [No Abstract] [Full Text] [Related]
26. Glycogen storage disease confined to the heart with deficient activity of cardiac phosphorylase kinase: a new type of glycogen storage disease. Eishi Y; Takemura T; Sone R; Yamamura H; Narisawa K; Ichinohasama R; Tanaka M; Hatakeyama S Hum Pathol; 1985 Feb; 16(2):193-7. PubMed ID: 3918928 [TBL] [Abstract][Full Text] [Related]
28. Clinical and biochemical features of 10 adult patients with muscle phosphorylase kinase deficiency. Wilkinson DA; Tonin P; Shanske S; Lombes A; Carlson GM; DiMauro S Neurology; 1994 Mar; 44(3 Pt 1):461-6. PubMed ID: 8145916 [TBL] [Abstract][Full Text] [Related]
29. A splice junction mutation in the alpha(M) gene of phosphorylase kinase in a patient with myopathy. Bruno C; Manfredi G; Andreu AL; Shanske S; Krishna S; Ilse WK; DiMauro S Biochem Biophys Res Commun; 1998 Aug; 249(3):648-51. PubMed ID: 9731190 [TBL] [Abstract][Full Text] [Related]
31. Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunit. Wehner M; Clemens PR; Engel AG; Kilimann MW Hum Mol Genet; 1994 Nov; 3(11):1983-7. PubMed ID: 7874115 [TBL] [Abstract][Full Text] [Related]
32. Biochemical determinations in a recently investigated case of McArdle's disease. Luca N; Bănileanu S Eur Neurol; 1974; 11(1):58-68. PubMed ID: 4524323 [No Abstract] [Full Text] [Related]
33. Adult-onset exercise intolerance due to phosphorylase b kinase deficiency. Bak H; Cordato D; Carey WF; Milder D J Clin Neurosci; 2001 May; 8(3):286-7. PubMed ID: 11386811 [TBL] [Abstract][Full Text] [Related]
34. Immunological studies on glycogen storage diseases type 3 and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency. Dreyfus JC; Alexandre Y Biochem Biophys Res Commun; 1971 Sep; 44(6):1364-70. PubMed ID: 5003690 [No Abstract] [Full Text] [Related]
35. MCARDLE'S DISEASE: HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE. FAHN S; SCHOTLAND DL; ROWLAND LP Trans Am Neurol Assoc; 1963; 88():145-7. PubMed ID: 14272202 [No Abstract] [Full Text] [Related]