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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 143654)

  • 1. [Muscular glycogenesis and haemolytic anaemia due to enzyme deficiency in two siblings. Familial form of Tarui's disease due to a deficiency in muscular and erythrocytic phosphofructokinase (author's transl)].
    Dupond JL; Robert M; Carbillet JP; Leconte des Floris R
    Nouv Presse Med; 1977 Sep; 6(30):2665-8. PubMed ID: 143654
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Familial congenital muscular dystrophy caused by phosphofructokinase deficiency].
    Guibaud P; Carrier H; Mathieu M; Dorche C; Parchoux B; Béthenod M; Larbre F
    Arch Fr Pediatr; 1978 Dec; 35(10):1105-15. PubMed ID: 155429
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Muscle phosphofructokinase deficiency (Tarui's disease).
    Tarlow MJ; Ellis DA; Pearce GW; Anderson M
    Proc Nutr Soc; 1979 Dec; 38(3):110A. PubMed ID: 161022
    [No Abstract]   [Full Text] [Related]  

  • 4. [Glycogen storage disease, type VII. Muscular phosphofructokinase deficiency].
    Tarui S
    Saishin Igaku; 1969 Jun; 24(6):1235-46. PubMed ID: 4241020
    [No Abstract]   [Full Text] [Related]  

  • 5. Familial phosphofructokinase deficiency is associated with a disturbed calcium homeostasis in erythrocytes.
    Ronquist G; Rudolphi O; Engström I; Waldenström A
    J Intern Med; 2001 Jan; 249(1):85-95. PubMed ID: 11168788
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Myopathic form of phosphofructokinase deficiency].
    Serratrice G; Monges A; Roux H; Aquaron R; Gambarelli D
    Rev Neurol (Paris); 1969 Apr; 120(4):271-7. PubMed ID: 4241954
    [No Abstract]   [Full Text] [Related]  

  • 7. [Exercise-induced muscle pain due to phosphofrutokinase deficiency: Diagnostic contribution of metabolic explorations (exercise tests, 31P-nuclear magnetic resonance spectroscopy)].
    Drouet A; Zagnoli F; Fassier T; Rannou F; Baverel F; Piraud M; Bahuau M; Petit F; Streichenberger N; Marcorelles P; Vital Durand D
    Rev Neurol (Paris); 2013; 169(8-9):613-24. PubMed ID: 24011984
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Muscle phosphofructokinase deficiency in two generations.
    Vorgerd M; Karitzky J; Ristow M; Van Schaftingen E; Tegenthoff M; Jerusalem F; Malin JP
    J Neurol Sci; 1996 Sep; 141(1-2):95-9. PubMed ID: 8880699
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Muscle phosphofructokinase deficiency (Tarui's disease): report of a case.
    Lin HC; Young C; Wang PJ; Shen YZ
    J Formos Med Assoc; 1999 Mar; 98(3):205-8. PubMed ID: 10365541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Muscle phosphofructokinase deficiency: two cases with unusual polysaccharide accumulation and immunologically active enzyme protein.
    Agamanolis DP; Askari AD; Di Mauro S; Hays A; Kumar K; Lipton M; Raynor A
    Muscle Nerve; 1980; 3(6):456-67. PubMed ID: 6450324
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Iodoacetate inhibition of glyceraldehyde-3-phosphate dehydrogenase as a model of human myophosphorylase deficiency (McArdle's disease) and phosphofructokinase deficiency (Tarui's disease).
    Brumback RA
    J Neurol Sci; 1980 Dec; 48(3):383-98. PubMed ID: 6449564
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Haemolytic anaemia with acanthocytosis and erythrocytic glutathione peroxidase deficiency in severe hepatic diseases. 5 cases (author's transl)].
    Najman A; Fraitag B; Puget K; Lichtenstein H; Bodin P; Gorin NC; Michelson AM; Conte M; Duhamel G
    Nouv Presse Med; 1980 Jan; 9(3):161-5. PubMed ID: 7355098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inherited phosphofructokinase deficiency in an American cocker spaniel.
    Giger U; Smith BF; Woods CB; Patterson DF; Stedman H
    J Am Vet Med Assoc; 1992 Nov; 201(10):1569-71. PubMed ID: 1289336
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Various classes of mutations in patients with phosphofructokinase deficiency (Tarui's disease).
    Raben N; Sherman JB; Adams E; Nakajima H; Argov Z; Plotz P
    Muscle Nerve Suppl; 1995; 3():S35-8. PubMed ID: 7603525
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phosphofructokinase deficiency (Tarui disease) associated with hepatic glucuronyltransferase deficiency (Gilbert's syndrome): a case and family study.
    Fogelfeld L; Sarova-Pinchas I; Meytes D; Barash V; Brok-Simoni F; Feigl D
    Isr J Med Sci; 1990 Jun; 26(6):328-33. PubMed ID: 2380035
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Glycogenosis type VII (glycogen storage disease type VII, human muscle-phosphofructokinase deficiency, Tarui's disease)].
    Yamasaki T; Nakajima H
    Ryoikibetsu Shokogun Shirizu; 2001; (36):28-34. PubMed ID: 11596390
    [No Abstract]   [Full Text] [Related]  

  • 17. Characterization of the enzymatic lesion in inherited phosphofructokinase deficiency in the dog: an animal analogue of human glycogen storage disease type VII.
    Vora S; Giger U; Turchen S; Harvey JW
    Proc Natl Acad Sci U S A; 1985 Dec; 82(23):8109-13. PubMed ID: 2933748
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of cases.
    Burwinkel B; Hu B; Schroers A; Clemens PR; Moses SW; Shin YS; Pongratz D; Vorgerd M; Kilimann MW
    Eur J Hum Genet; 2003 Jul; 11(7):516-26. PubMed ID: 12825073
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Metabolic myopathies.
    DiMauro S; Miranda AF; Sakoda S; Schon EA; Servidei S; Shanske S; Zeviani M
    Am J Med Genet; 1986 Dec; 25(4):635-51. PubMed ID: 2878616
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Disorders of glycogen metabolism of muscle.
    DiMauro S; Bresolin N; Hays AP
    CRC Crit Rev Clin Neurobiol; 1984; 1(2):83-116. PubMed ID: 6242726
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.