PubMed for Bookshelf ID: 1499022

Year	Number of Results
2006	1
2008	1
2009	1
2011	1
2012	1
2013	2
2014	5
2015	8
2016	3
2017	6
2018	7
2022	1
2024	0

1

Variation among DNA banking consent forms: points for clinicians to bank on.

Huang SJ, Amendola LM, Sternen DL. Huang SJ, et al. J Community Genet. 2022 Aug;13(4):389-397. doi: 10.1007/s12687-022-00601-3. Epub 2022 Jul 14. J Community Genet. 2022. PMID: 35834113 Free PMC article.

2

Resistance Exercise Training in McArdle Disease: Myth or Reality?

Pietrusz A, Scalco RS, Quinlivan R. Pietrusz A, et al. Case Rep Neurol Med. 2018 Sep 30;2018:9658251. doi: 10.1155/2018/9658251. eCollection 2018. Case Rep Neurol Med. 2018. PMID: 30363996 Free PMC article.

3

Mastication and Oral Motor Function in McArdle Disease: Patient Reported Complaints.

Kouwenberg CV, Voermans NC, Quinlivan R, van den Engel-Hoek L. Kouwenberg CV, et al. J Neuromuscul Dis. 2018;5(3):353-357. doi: 10.3233/JND-180320. J Neuromuscul Dis. 2018. PMID: 30103350 Free article.

4

McArdle Disease Presenting With Muscle Pain in a Teenage Girl: The Role of Whole-Exome Sequencing in Neurogenetic Disorders.

Walters WD, Garnica AD, Schaefer GB. Walters WD, et al. Semin Pediatr Neurol. 2018 Jul;26:50-51. doi: 10.1016/j.spen.2017.03.004. Epub 2017 Apr 1. Semin Pediatr Neurol. 2018. PMID: 29961518

5

Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins.

Núñez-Manchón J, Ballester-Lopez A, Koehorst E, Linares-Pardo I, Coenen D, Ara I, Rodriguez-Lopez C, Ramos-Fransi A, Martínez-Piñeiro A, Lucente G, Almendrote M, Coll-Cantí J, Pintos-Morell G, Santos-Lozano A, Arenas J, Martín MA, de Castro M, Lucia A, Santalla A, Nogales-Gadea G. Núñez-Manchón J, et al. J Inherit Metab Dis. 2018 Nov;41(6):1027-1035. doi: 10.1007/s10545-018-0203-2. Epub 2018 Jun 20. J Inherit Metab Dis. 2018. PMID: 29926259

6

Pre- and peripartal management of a woman with McArdle disease: a case report.

Stopp T, Feichtinger M, Eppel W, Stulnig TM, Husslein P, Göbl C. Stopp T, et al. Gynecol Endocrinol. 2018 Sep;34(9):736-739. doi: 10.1080/09513590.2018.1451507. Epub 2018 Mar 21. Gynecol Endocrinol. 2018. PMID: 29560763

7

Clinical utility gene card for McArdle disease.

Taylor RL, Davis M, Turner E, Brull A, Pinos T, Cabrera M, Nowak KJ. Taylor RL, et al. Eur J Hum Genet. 2018 May;26(5):758-764. doi: 10.1038/s41431-017-0070-6. Epub 2018 Jan 25. Eur J Hum Genet. 2018. PMID: 29371640 Free PMC article.

8

Spontaneous Compartment Syndrome in a Patient with McArdle Disease: A Case Report and Review of the Literature.

Triplet JJ, Goss DA Jr, Taylor B. Triplet JJ, et al. JBJS Case Connect. 2017 Jul-Sep;7(3):e49. doi: 10.2106/JBJS.CC.16.00196. JBJS Case Connect. 2017. PMID: 29252879 Review.

9

Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update.

Santalla A, Nogales-Gadea G, Encinar AB, Vieitez I, González-Quintana A, Serrano-Lorenzo P, Consuegra IG, Asensio S, Ballester-Lopez A, Pintos-Morell G, Coll-Cantí J, Pareja-Galeano H, Díez-Bermejo J, Pérez M, Andreu AL, Pinós T, Arenas J, Martín MA, Lucia A. Santalla A, et al. BMC Genomics. 2017 Nov 14;18(Suppl 8):819. doi: 10.1186/s12864-017-4188-2. BMC Genomics. 2017. PMID: 29143597 Free PMC article.

10

PRES leading to the diagnosis of McArdle disease.

Martinez-Thompson JM, Pittock SJ, Milone M. Martinez-Thompson JM, et al. J Clin Neurosci. 2017 Dec;46:62-64. doi: 10.1016/j.jocn.2017.08.013. Epub 2017 Sep 5. J Clin Neurosci. 2017. PMID: 28887083

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

34 results

Results by year