"glycogen storage disease type v"[mh] - Search Results

Year	Number of Results
1960	1
1961	2
1962	2
1963	2
1964	1
1965	2
1966	2
1973	1
1975	4
1976	6
1977	15
1978	10
1979	8
1980	7
1981	14
1982	9
1983	13
1984	17
1985	14
1986	15
1987	13
1988	13
1989	11
1990	23
1991	15
1992	12
1993	11
1994	8
1995	12
1996	15
1997	8
1998	16
1999	11
2000	18
2001	15
2002	16
2003	21
2004	13
2005	10
2006	16
2007	30
2008	34
2009	27
2010	11
2011	11
2012	10
2013	17
2014	17
2015	25
2016	16
2017	17
2018	19
2019	17
2020	21
2021	16
2022	18
2023	17
2024	4

1

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V).

Quinlivan R, Beynon RJ, Martinuzzi A. Quinlivan R, et al. Cochrane Database Syst Rev. 2008 Apr 16;(2):CD003458. doi: 10.1002/14651858.CD003458.pub3. Cochrane Database Syst Rev. 2008. PMID: 18425888 Updated. Review.

2

Pharmacological and nutritional treatment for McArdle's disease (Glycogen Storage Disease type V).

Quinlivan R, Beynon RJ. Quinlivan R, et al. Cochrane Database Syst Rev. 2004;(3):CD003458. doi: 10.1002/14651858.CD003458.pub2. Cochrane Database Syst Rev. 2004. PMID: 15266486 Updated. Review.

3

Diagnosis and genetic analysis of a case with glycogen storage disease type V caused by compound heterozygous mutations in the PYGM gene.

Jiang WZ, Xu YW, Wang YW, Zhu XC, Gong YY, Zhou HW, Fu ZZ. Jiang WZ, et al. Yi Chuan. 2022 Nov 20;44(11):1063-1071. doi: 10.16288/j.yczz.22-223. Yi Chuan. 2022. PMID: 36384998

4

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V).

Quinlivan R, Martinuzzi A, Schoser B. Quinlivan R, et al. Cochrane Database Syst Rev. 2010 Dec 8;(12):CD003458. doi: 10.1002/14651858.CD003458.pub4. Cochrane Database Syst Rev. 2010. PMID: 21154353 Updated. Review.

5

Pharmacological and nutritional treatment for McArdle disease (Glycogen Storage Disease type V).

Quinlivan R, Martinuzzi A, Schoser B. Quinlivan R, et al. Cochrane Database Syst Rev. 2014 Nov 12;2014(11):CD003458. doi: 10.1002/14651858.CD003458.pub5. Cochrane Database Syst Rev. 2014. PMID: 25391139 Free PMC article. Review.

6

Repeatedly in Rhabdomyolysis.

Gooch C, Dean SJ, Marzullo L. Gooch C, et al. Pediatr Emerg Care. 2021 Dec 1;37(12):e1759-e1760. doi: 10.1097/PEC.0000000000002079. Pediatr Emerg Care. 2021. PMID: 32205805

7

McArdle's disease (glycogen storage disease type V) and anesthesia--a case report and review of the literature.

Bollig G. Bollig G. Paediatr Anaesth. 2013 Sep;23(9):817-23. doi: 10.1111/pan.12164. Epub 2013 Apr 9. Paediatr Anaesth. 2013. PMID: 23565573 Review.

8

Can hyperuricemia predict glycogen storage disease (McArdle's disease) in rheumatology practice? (Myogenic hyperuricemia).

Üsküdar Cansu D, Erdoğan B, Korkmaz C. Üsküdar Cansu D, et al. Clin Rheumatol. 2019 Oct;38(10):2941-2948. doi: 10.1007/s10067-019-04572-8. Epub 2019 May 1. Clin Rheumatol. 2019. PMID: 31044384 Review.

9

Metabolic Myopathies.

Tarnopolsky MA. Tarnopolsky MA. Continuum (Minneap Minn). 2016 Dec;22(6, Muscle and Neuromuscular Junction Disorders):1829-1851. doi: 10.1212/CON.0000000000000403. Continuum (Minneap Minn). 2016. PMID: 27922496 Review.

10

Muscle diffusion tensor imaging in glycogen storage disease V (McArdle disease).

Rehmann R, Schlaffke L, Froeling M, Kley RA, Kühnle E, De Marées M, Forsting J, Rohm M, Tegenthoff M, Schmidt-Wilcke T, Vorgerd M. Rehmann R, et al. Eur Radiol. 2019 Jun;29(6):3224-3232. doi: 10.1007/s00330-018-5885-1. Epub 2018 Dec 17. Eur Radiol. 2019. PMID: 30560358

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