Similar articles for PMID: 8598869

Year	Number of Results
1966	2
1968	1
1970	1
1977	1
1982	1
1994	2
1995	2
1996	5
1997	2
1998	2
1999	2
2000	2
2001	2
2003	1
2004	5
2005	5
2006	3
2007	2
2009	2
2010	3
2014	1
2018	1
2019	1
2024	0

1

Brief report: inherited metabolic myopathy and hemolysis due to a mutation in aldolase A.

Kreuder J, Borkhardt A, Repp R, Pekrun A, Göttsche B, Gottschalk U, Reichmann H, Schachenmayr W, Schlegel K, Lampert F. Kreuder J, et al. N Engl J Med. 1996 Apr 25;334(17):1100-4. doi: 10.1056/NEJM199604253341705. N Engl J Med. 1996. PMID: 8598869 Free article. No abstract available.

2

Inherited metabolic myopathy and hemolysis due to a mutation in aldolase A.

Kopp A, Bistrian BR. Kopp A, et al. N Engl J Med. 1996 Oct 17;335(16):1242-3. doi: 10.1056/NEJM199610173351618. N Engl J Med. 1996. PMID: 8999331 No abstract available.

3

Human aldolase A natural mutants: relationship between flexibility of the C-terminal region and enzyme function.

Esposito G, Vitagliano L, Costanzo P, Borrelli L, Barone R, Pavone L, Izzo P, Zagari A, Salvatore F. Esposito G, et al. Biochem J. 2004 May 15;380(Pt 1):51-6. doi: 10.1042/BJ20031941. Biochem J. 2004. PMID: 14766013 Free PMC article.

4

Identification of a novel mutation (Leu256-->Pro) in the human aldolase B gene associated with hereditary fructose intolerance.

Ali M, Sebastio G, Cox TM. Ali M, et al. Hum Mol Genet. 1994 Apr;3(4):684. Hum Mol Genet. 1994. PMID: 8069328 No abstract available.

5

The lethal hemolytic mutation in beta I sigma 2 spectrin Providence yields a null phenotype in neonatal skeletal muscle.

Weed SA, Stabach PR, Oyer CE, Gallagher PG, Morrow JS. Weed SA, et al. Lab Invest. 1996 Jun;74(6):1117-29. Lab Invest. 1996. PMID: 8667615

6

Tropomyosin in the groove? Molecular insights into an inherited myopathy.

Chase PB. Chase PB. J Physiol. 2007 Jun 15;581(Pt 3):889. doi: 10.1113/jphysiol.2007.135517. Epub 2007 May 24. J Physiol. 2007. PMID: 17525111 Free PMC article. No abstract available.

7

Mode of interactions of human aldolase isozymes with cytoskeletons.

Kusakabe T, Motoki K, Hori K. Kusakabe T, et al. Arch Biochem Biophys. 1997 Aug 1;344(1):184-93. doi: 10.1006/abbi.1997.0204. Arch Biochem Biophys. 1997. PMID: 9244396

8

Hemolytic anemia and severe rhabdomyolysis caused by compound heterozygous mutations of the gene for erythrocyte/muscle isozyme of aldolase, ALDOA(Arg303X/Cys338Tyr).

Yao DC, Tolan DR, Murray MF, Harris DJ, Darras BT, Geva A, Neufeld EJ. Yao DC, et al. Blood. 2004 Mar 15;103(6):2401-3. doi: 10.1182/blood-2003-09-3160. Epub 2003 Nov 13. Blood. 2004. PMID: 14615364 Free article.

9

Molecular evolution of amphioxus fructose-1,6-bisphosphate aldolase.

Kuba M, Yatsuki H, Kusakabe T, Takasaki Y, Nikoh N, Miyata T, Yamaguchi T, Hori K. Kuba M, et al. Arch Biochem Biophys. 1997 Dec 15;348(2):329-36. doi: 10.1006/abbi.1997.0384. Arch Biochem Biophys. 1997. PMID: 9434745

10

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.

Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG. Nowak KJ, et al. Nat Genet. 1999 Oct;23(2):208-12. doi: 10.1038/13837. Nat Genet. 1999. PMID: 10508519

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