145 related articles for article (PubMed ID: 11440399)
1. Haemolytic anaemia and exercise intolerance due to phosphofructokinase deficiency in related springer spaniels.
Skibild E; Dahlgaard K; Rajpurohit Y; Smith BF; Giger U
J Small Anim Pract; 2001 Jun; 42(6):298-300. PubMed ID: 11440399
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive inherited phosphofructokinase deficiency in English springer spaniel dogs.
Giger U; Reilly MP; Asakura T; Baldwin CJ; Harvey JW
Anim Genet; 1986; 17(1):15-23. PubMed ID: 2940948
[TBL] [Abstract][Full Text] [Related]
3. Hemolysis caused by phosphofructokinase deficiency in English springer spaniels: seven cases (1983-1986).
Giger U; Harvey JW
J Am Vet Med Assoc; 1987 Aug; 191(4):453-9. PubMed ID: 2958437
[TBL] [Abstract][Full Text] [Related]
4. Missense mutation in PFKM associated with muscle-type phosphofructokinase deficiency in the Wachtelhund dog.
Inal Gultekin G; Raj K; Lehman S; Hillström A; Giger U
Mol Cell Probes; 2012 Dec; 26(6):243-7. PubMed ID: 22446493
[TBL] [Abstract][Full Text] [Related]
5. Hereditary phosphofructokinase deficiency in wachtelhunds.
Hillström A; Tvedten H; Rowe A; Giger U
J Am Anim Hosp Assoc; 2011; 47(2):145-50. PubMed ID: 21311071
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
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. Molecular basis of canine muscle type phosphofructokinase deficiency.
Smith BF; Stedman H; Rajpurohit Y; Henthorn PS; Wolfe JH; Patterson DF; Giger U
J Biol Chem; 1996 Aug; 271(33):20070-4. PubMed ID: 8702726
[TBL] [Abstract][Full Text] [Related]
10. Hemolytic anemia in dogs and cats due to erythrocyte enzyme deficiencies.
Owen JL; Harvey JW
Vet Clin North Am Small Anim Pract; 2012 Jan; 42(1):73-84. PubMed ID: 22285158
[TBL] [Abstract][Full Text] [Related]
11. Other erythrocyte enzyme deficiencies associated with non-haematological symptoms: phosphoglycerate kinase and phosphofructokinase deficiency.
Fujii H; Miwa S
Baillieres Best Pract Res Clin Haematol; 2000 Mar; 13(1):141-8. PubMed ID: 10916683
[TBL] [Abstract][Full Text] [Related]
12. Polysaccharide storage myopathy in canine phosphofructokinase deficiency (type VII glycogen storage disease).
Harvey JW; Calderwood Mays MB; Gropp KE; Denaro FJ
Vet Pathol; 1990 Jan; 27(1):1-8. PubMed ID: 2137952
[TBL] [Abstract][Full Text] [Related]
13. Hemolysis, myopathy, and cardiac disease associated with hereditary phosphofructokinase deficiency in two Whippets.
Gerber K; Harvey JW; D'Agorne S; Wood J; Giger U
Vet Clin Pathol; 2009 Mar; 38(1):46-51. PubMed ID: 19228357
[TBL] [Abstract][Full Text] [Related]
14. Mutations in muscle phosphofructokinase gene.
Raben N; Sherman JB
Hum Mutat; 1995; 6(1):1-6. PubMed ID: 7550225
[TBL] [Abstract][Full Text] [Related]
15. Postnatal hematologic development in phosphofructokinase-deficient dogs.
Harvey JW; Reddy GR
Blood; 1989 Nov; 74(7):2556-61. PubMed ID: 2529931
[TBL] [Abstract][Full Text] [Related]
16. Glycogenosis type VII (Tarui disease) in a Swedish family: two novel mutations in muscle phosphofructokinase gene (PFK-M) resulting in intron retentions.
Nichols RC; Rudolphi O; Ek B; Exelbert R; Plotz PH; Raben N
Am J Hum Genet; 1996 Jul; 59(1):59-65. PubMed ID: 8659544
[TBL] [Abstract][Full Text] [Related]
17. Inherited phosphofructokinase deficiency in dogs with hyperventilation-induced hemolysis: increased in vitro and in vivo alkaline fragility of erythrocytes.
Giger U; Harvey JW; Yamaguchi RA; McNulty PK; Chiapella A; Beutler E
Blood; 1985 Feb; 65(2):345-51. PubMed ID: 3155631
[TBL] [Abstract][Full Text] [Related]
18. Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.
Sherman JB; Raben N; Nicastri C; Argov Z; Nakajima H; Adams EM; Eng CM; Cowan TM; Plotz PH
Am J Hum Genet; 1994 Aug; 55(2):305-13. PubMed ID: 8037209
[TBL] [Abstract][Full Text] [Related]
19. Late-onset muscle weakness in partial phosphofructokinase deficiency: a unique myopathy with vacuoles, abnormal mitochondria, and absence of the common exon 5/intron 5 junction point mutation.
Sivakumar K; Vasconcelos O; Goldfarb L; Dalakas MC
Neurology; 1996 May; 46(5):1337-42. PubMed ID: 8628478
[TBL] [Abstract][Full Text] [Related]
20. Heterogeneity of the molecular lesions in inherited phosphofructokinase deficiency.
Vora S; Davidson M; Seaman C; Miranda AF; Noble NA; Tanaka KR; Frenkel EP; Dimauro S
J Clin Invest; 1983 Dec; 72(6):1995-2006. PubMed ID: 6227635
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
