| For: | Alaygut D, Torun Bayram M, Kasap B, Soylu A, Türkmen M, Kavukcu S. Rhabdomyolysis with different etiologies in childhood. World J Clin Pediatr 2017; 6(4): 161-168 [PMID: 29184760 DOI: 10.5409/wjcp.v6.i4.161] |
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| URL: | https://www.wjgnet.com/2219-2808/full/v6/i4/161.htm |
| Number | Citing Articles |
| 1 |
Guillermo Navarro-Blackaller, Jonathan Samuel Chávez-Iñiguez, Pablo Maggiani-Aguilera, Gema Lizeth Gómez-Hernández, Elsa Edith Carreón-Bautista, Rodolfo Alejandro Moreno-Alvarado, Guillermo Garcia-Garcia. Rhabdomyolysis and acute kidney injury associated with Clostridium difficile infection, case report. Nefrología (English Edition) 2019; 39(2) doi: 10.1016/j.nefroe.2018.07.009
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| 2 |
Hortense de Calbiac, Apolline Imbard, Pascale de Lonlay. Cellular mechanisms of acute rhabdomyolysis in inherited metabolic diseases. Journal of Inherited Metabolic Disease 2025; 48(1) doi: 10.1002/jimd.12781
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| 3 |
Guillermo Navarro-Blackaller, Jonathan Samuel Chávez-Iñiguez, Pablo Maggiani-Aguilera, Gema Lizeth Gómez-Hernández, Elsa Edith Carreón-Bautista, Rodolfo Alejandro Moreno-Alvarado, Guillermo Garcia-Garcia. Rabdomiólisis y daño renal agudo asociado a infección por Clostridium difficile, reporte de caso. Nefrología 2019; 39(2) doi: 10.1016/j.nefro.2018.07.007
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| 4 |
Zhengxiong Yao, Ping Yuan, Siqi Hong, Mei Li, Li Jiang. Clinical Features of Acute Rhabdomyolysis in 55 Pediatric Patients. Frontiers in Pediatrics 2020; 8 doi: 10.3389/fped.2020.00539
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| 5 |
Ke Tong, Geng-Sheng Yu. Acute recurrent rhabdomyolysis in a Chinese boy associated with a novel compound heterozygous LPIN1 variant: a case report. BMC Neurology 2021; 21(1) doi: 10.1186/s12883-021-02050-w
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| 6 |
Chiara Simoni, Pietro Camozzi, Pietro B. Faré, Mario G. Bianchetti, Lisa Kottanattu, Sebastiano A.G. Lava, Gregorio P. Milani. Myositis and acute kidney injury in bacterial atypical pneumonia: Systematic literature review. Journal of Infection and Public Health 2020; 13(12) doi: 10.1016/j.jiph.2020.10.007
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| 7 |
Huseyin Bilgin, Ayse Ergul Bozaci. The evaluation of inherited metabolic diseases presenting with rhabdomyolysis from Turkey: Single center experience. Molecular Genetics and Metabolism Reports 2024; 39 doi: 10.1016/j.ymgmr.2024.101070
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| 8 |
Liljana Malinovska Nikolovska, Vladimir Chadikovski, Maja Manoleva, Vedran Stojanovik, Mirjana Krmzova Gorgioska, Ljupco Stojkovski. RHABDOMYOLYSIS AND MULTIORGAN FAILURE CAUSED BY CARNITINE PALMITOYL TRANSFERASE TYPE 2 DEFICIENCY. Macedonian Journal of Anaesthesia 2025; 9(3) doi: 10.55302/MJA259366mn
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| 9 |
Aurora Grandioso, Paola Tirelli, Gianmario Forcina, Vittoria Frattolillo, Delia De Biasio, Francesco Giustino Cesaro, Pierluigi Marzuillo, Emanuele Miraglia del Giudice, Anna Di Sessa. Paliperidone-Induced Massive Asymptomatic Creatine Kinase Elevation in Youth: From a Case Report to Literature Review. Pediatric Reports 2025; 17(1) doi: 10.3390/pediatric17010018
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| 10 |
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| 11 |
Changchao Huan, Yao Xu, Wei Zhang, Tingting Guo, Haochun Pan, Song Gao. Research Progress on the Antiviral Activity of Glycyrrhizin and its Derivatives in Liquorice. Frontiers in Pharmacology 2021; 12 doi: 10.3389/fphar.2021.680674
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| 12 |
Michael Gulenay, V. Andres Sasson, Kevin Taylor. Rhabdomyolysis: A Case Report of an Extrapulmonary Presentation of Mycoplasma pneumoniae. Clinical Practice and Cases in Emergency Medicine 2021; 2(5) doi: 10.5811/cpcem.2020.9.46024
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| 13 |
Tarek M. A. Abdallah, Said S. El-Feky, Nourhan A. A. Salem, Ghada M. Mashaal, Zaghloul E. Gouda. LPIN-1 gene variant in Egyptian children: acute recurrent myoglobinuria. Journal of Rare Diseases 2025; 4(1) doi: 10.1007/s44162-025-00106-w
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| 14 |
Teresa B Gibson, Michael D Nguyen, Timothy Burrell, Frank Yoon, Jenna Wong, Sai Dharmarajan, Rita Ouellet-Hellstrom, Wei Hua, Yong Ma, Elande Baro, Sarah Bloemers, Cory Pack, Adee Kennedy, Sengwee Toh, Robert Ball. Electronic phenotyping of health outcomes of interest using a linked claims-electronic health record database: Findings from a machine learning pilot project. Journal of the American Medical Informatics Association 2021; 28(7) doi: 10.1093/jamia/ocab036
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| 15 |
宇 陈. Becker Muscular Dystrophy Caused by an Intron Mutation in the DMD Gene: A Case Report and Literature Review. Advances in Clinical Medicine 2023; 13(08) doi: 10.12677/ACM.2023.1381799
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| 16 |
Nicholas Ivin, Valentina Della Torre, Francis Sanders, Matthew Youngman. Rhabdomyolysis caused by carnitine palmitoyltransferase 2 deficiency: A case report and systematic review of the literature. Journal of the Intensive Care Society 2020; 21(2) doi: 10.1177/1751143719889766
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| 17 |
Megan B Coriell, Andrew T Van Hersh, Siddharth Shah. Prolonged Seizure Activity Followed by Severe Hyperphosphatemia and Hypocalcemia in a Pediatric Patient. Cureus 2021; doi: 10.7759/cureus.14338
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| 18 |
Ojbindra KC, Punya H Dahal, Manisha Koirala, Afua D NtemMensah. Rhabdomyolysis and Neurological Manifestation With Progressive Weakness in a Young Adult: A Rare Extrapulmonary Presentation of Mycoplasma Pneumoniae. Cureus 2021; doi: 10.7759/cureus.20552
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| 19 |
Eun-Woo Park, Ye-Jee Shim, Jung-Sook Ha, Jin-Hong Shin, Soyoung Lee, Jang-Hyuk Cho. Diagnosis of Duchenne Muscular Dystrophy in a Presymptomatic Infant Using Next-Generation Sequencing and Chromosomal Microarray Analysis: A Case Report. Children 2021; 8(5) doi: 10.3390/children8050377
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