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For: Meijer IA, Sasarman F, Maftei C, Rossignol E, Vanasse M, Major P, Mitchell GA, Brunel-Guitton C. LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy. Mol Genet Metab Rep 2015;5:85-8. [PMID: 28649549 DOI: 10.1016/j.ymgmr.2015.10.010] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 2.1] [Reference Citation Analysis]
Number Citing Articles
1 Stepien KM, Schmidt WM, Bittner RE, O'Toole O, McNamara B, Treacy EP. Long-term outcomes in a 25-year-old female affected with lipin-1 deficiency. JIMD Rep 2019;46:4-10. [PMID: 31240148 DOI: 10.1002/jmd2.12016] [Cited by in F6Publishing: 6] [Reference Citation Analysis]
2 Nunes D, Nogueira C, Lopes A, Chaves P, Rodrigues E, Cardoso T, Leão Teles E, Vilarinho L. LPIN1 deficiency: A novel mutation associated with different phenotypes in the same family. Mol Genet Metab Rep 2016;9:29-30. [PMID: 27722093 DOI: 10.1016/j.ymgmr.2016.09.004] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
3 Summerlin ML, Regier DS, Fraser JL, Chapman KA, Kafashzadeh D, Billington C Jr, Kisling M, Grochowsky A, Ah Mew N, Shur N. Use of dexamethasone in idiopathic, acute pediatric rhabdomyolysis. Am J Med Genet A 2021;185:500-7. [PMID: 33300687 DOI: 10.1002/ajmg.a.62000] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Pons L, Acquaviva-bourdain C, Teyssedre S, Didier C, Veauville A, Steffann J, Gobin S, de Lonlay P, Guffon N, Fouilhoux A. Intrafamilial Variability in <b><i>LPIN1</i></b>-Related Rhabdomyolysis. Mol Syndromol 2020;11:153-6. [DOI: 10.1159/000507719] [Reference Citation Analysis]
5 Wang H, Chan TW, Vashisht AA, Drew BG, Calkin AC, Harris TE, Wohlschlegel JA, Xiao X, Reue K. Lipin 1 modulates mRNA splicing during fasting adaptation in liver. JCI Insight 2021;6:150114. [PMID: 34494556 DOI: 10.1172/jci.insight.150114] [Reference Citation Analysis]
6 Pizzamiglio C, Lahiri N, Nirmalananthan N, Sood B, Somalanka S, Ostrowski P, Phadke R, O'Donovan DG, Muntoni F, Quinlivan R. First presentation of LPIN1 acute rhabdomyolysis in adolescence and adulthood. Neuromuscul Disord 2020;30:566-71. [PMID: 32522502 DOI: 10.1016/j.nmd.2020.05.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Ilboudo Y, Garrett ME, Bartolucci P, Brugnara C, Clish CB, Hirschhorn JN, Galactéros F, Ashley-Koch AE, Telen MJ, Lettre G. Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis. Blood Cells Mol Dis 2021;86:102504. [PMID: 32949984 DOI: 10.1016/j.bcmd.2020.102504] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Indika NLR, Vidanapathirana DM, Jasinge E, Waduge R, Shyamali NLA, Perera PPR. Lipin-1 Deficiency-Associated Recurrent Rhabdomyolysis and Exercise-Induced Myalgia Persisting into Adulthood: A Case Report and Review of Literature. Case Rep Med 2020;2020:7904190. [PMID: 32549891 DOI: 10.1155/2020/7904190] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
9 Kanderi N, Kirmse B, Regier DS, Chapman KA. LPIN1 rhabdomyolysis: A single site cohort description and treatment recommendations. Molecular Genetics and Metabolism Reports 2022;30:100844. [DOI: 10.1016/j.ymgmr.2022.100844] [Reference Citation Analysis]
10 Minton T, Forrester N, Baba SA, Urankar K, Brady S. A rare case of adult onset LPIN1 associated rhabdomyolysis. Neuromuscul Disord 2020;30:241-5. [PMID: 32115342 DOI: 10.1016/j.nmd.2020.01.004] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
11 Schweitzer GG, Collier SL, Chen Z, McCommis KS, Pittman SK, Yoshino J, Matkovich SJ, Hsu FF, Chrast R, Eaton JM, Harris TE, Weihl CC, Finck BN. Loss of lipin 1-mediated phosphatidic acid phosphohydrolase activity in muscle leads to skeletal myopathy in mice. FASEB J 2019;33:652-67. [PMID: 30028636 DOI: 10.1096/fj.201800361R] [Cited by in Crossref: 19] [Cited by in F6Publishing: 13] [Article Influence: 4.8] [Reference Citation Analysis]
12 Burstal RJ. Volatile anesthesia for a child with LPIN1 gene mutation and recurrent rhabdomyolysis. Paediatr Anaesth 2018;28:813-4. [PMID: 30035342 DOI: 10.1111/pan.13445] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
13 Che R, Wang C, Zheng B, Zhang X, Ding G, Zhao F, Jia Z, Zhang A, Huang S, Feng Q. A rare case of pediatric recurrent rhabdomyolysis with compound heterogenous variants in the LPIN1. BMC Pediatr 2020;20:218. [PMID: 32410653 DOI: 10.1186/s12887-020-02134-5] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
14 Lu S, Lyu Z, Wang Z, Kou Y, Liu C, Li S, Hu M, Zhu H, Wang W, Zhang C, Kuan YS, Liu YW, Chen J, Tian J. Lipin 1 deficiency causes adult-onset myasthenia with motor neuron dysfunction in humans and neuromuscular junction defects in zebrafish. Theranostics 2021;11:2788-805. [PMID: 33456573 DOI: 10.7150/thno.53330] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
15 Finsterer J, Aliyev R. Detection of compound heterozygous variants in LPIN1 does not necessarily imply pathogenicity in a patient with rhabdomyolysis. F1000Res 2020;9:15. [PMID: 32913636 DOI: 10.12688/f1000research.21589.1] [Reference Citation Analysis]
16 Kaur B, Rattalino M. Target‐controlled infusion of Propofol and Remifentanil in a child with recurrent rhabdomyolysis secondary to LPIN1 deficiency. Pediatr Anaesth 2020;30:725-6. [DOI: 10.1111/pan.13887] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
17 Tong K, Yu GS. Acute recurrent rhabdomyolysis in a Chinese boy associated with a novel compound heterozygous LPIN1 variant: a case report. BMC Neurol 2021;21:42. [PMID: 33514355 DOI: 10.1186/s12883-021-02050-w] [Reference Citation Analysis]