PubMed for id: 868172

Year	Number of Results
1996	1
1997	1
2004	1
2008	1
2010	1
2014	1
2015	1
2016	1
2019	2
2020	2
2024	0

1

Disruption of Acetyl-Lysine Turnover in Muscle Mitochondria Promotes Insulin Resistance and Redox Stress without Overt Respiratory Dysfunction.

Williams AS, Koves TR, Davidson MT, Crown SB, Fisher-Wellman KH, Torres MJ, Draper JA, Narowski TM, Slentz DH, Lantier L, Wasserman DH, Grimsrud PA, Muoio DM. Williams AS, et al. Cell Metab. 2020 Jan 7;31(1):131-147.e11. doi: 10.1016/j.cmet.2019.11.003. Epub 2019 Dec 5. Cell Metab. 2020. PMID: 31813822 Free PMC article.

2

Gold nanoparticles synthesized from Euphorbia fischeriana root by green route method alleviates the isoprenaline hydrochloride induced myocardial infarction in rats.

Zhang T, Dang M, Zhang W, Lin X. Zhang T, et al. J Photochem Photobiol B. 2020 Jan;202:111705. doi: 10.1016/j.jphotobiol.2019.111705. Epub 2019 Nov 13. J Photochem Photobiol B. 2020. PMID: 31812087

3

A case report: Becker muscular dystrophy presenting with epilepsy and dysgnosia induced by duplication mutation of Dystrophin gene.

Miao J, Feng JC, Zhu D, Yu XF. Miao J, et al. BMC Neurol. 2016 Dec 12;16(1):255. doi: 10.1186/s12883-016-0777-y. BMC Neurol. 2016. PMID: 27955624 Free PMC article.

4

Acute Myocardial Infarction during Induction Chemotherapy for Acute MLL t(4;11) Leukemia with Lineage Switch and Extreme Leukocytosis.

Colović N, Bogdanović A, Virijević M, Vidović A, Tomin D. Colović N, et al. Srp Arh Celok Lek. 2015 Nov-Dec;143(11-12):734-8. doi: 10.2298/sarh1512734c. Srp Arh Celok Lek. 2015. PMID: 26946771

5

Screening for late-onset Pompe disease in Finland.

Palmio J, Auranen M, Kiuru-Enari S, Löfberg M, Bodamer O, Udd B. Palmio J, et al. Neuromuscul Disord. 2014 Nov;24(11):982-5. doi: 10.1016/j.nmd.2014.06.438. Epub 2014 Jun 28. Neuromuscul Disord. 2014. PMID: 25047669

6

Possible contribution of XYY syndrome to neuroleptic malignant syndrome in a child receiving quetiapine.

Randolph TC. Randolph TC. Am J Health Syst Pharm. 2010 Mar 15;67(6):459-61. doi: 10.2146/ajhp090091. Am J Health Syst Pharm. 2010. PMID: 20208052

7

Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family.

Eeg-Olofsson O, Kalimo H, Eeg-Olofsson KE, Jagell S, Marklund L, Simonsson L, Dahl N. Eeg-Olofsson O, et al. Eur J Paediatr Neurol. 2008 Sep;12(5):404-7. doi: 10.1016/j.ejpn.2007.10.014. Eur J Paediatr Neurol. 2008. PMID: 18833644

8

Carnitine-acylcarnitine translocase deficiency, clinical, biochemical and genetic aspects.

Rubio-Gozalbo ME, Bakker JA, Waterham HR, Wanders RJ. Rubio-Gozalbo ME, et al. Mol Aspects Med. 2004 Oct-Dec;25(5-6):521-32. doi: 10.1016/j.mam.2004.06.007. Mol Aspects Med. 2004. PMID: 15363639 Review.

9

The seventh form of autosomal recessive limb-girdle muscular dystrophy is mapped to 17q11-12.

Moreira ES, Vainzof M, Marie SK, Sertié AL, Zatz M, Passos-Bueno MR. Moreira ES, et al. Am J Hum Genet. 1997 Jul;61(1):151-9. doi: 10.1086/513889. Am J Hum Genet. 1997. PMID: 9245996 Free PMC article.

10

[A case of Kennedy-Alter-Sung (KAS) syndrome presenting as hypersexuality and elevated serum CK: usefulness of genetic analysis].

Hokezu Y, Yanai S, Nagai M, Nagamatsu K, Yamamoto Y. Hokezu Y, et al. Rinsho Shinkeigaku. 1996 Mar;36(3):471-4. Rinsho Shinkeigaku. 1996. PMID: 8741352 Japanese.

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