Cargando…

Muscle Magnetic Resonance Imaging for the Differentiation of Multiple Acyl-CoA Dehydrogenase Deficiency and Immune-mediated Necrotizing Myopathy

BACKGROUND: Clinically, it is difficult to differentiate multiple acyl-CoA dehydrogenase deficiency (MADD) from immune-mediated necrotizing myopathy (IMNM) because they display similar symptoms. This study aimed to determine whether muscle magnetic resonance imaging (MRI) could be used for different...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zhao, Ya-Wen, Liu, Xiu-Juan, Zhang, Wei, Wang, Zhao-Xia, Yuan, Yun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2018
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776843/ https://www.ncbi.nlm.nih.gov/pubmed/29336361 http://dx.doi.org/10.4103/0366-6999.222323

Ejemplares similares

Clinical and muscle magnetic resonance image findings in patients with late-onset multiple acyl-CoA dehydrogenase deficiency
por: Hong, Dao-Jun, et al.
Publicado: (2019)

Exacerbation of myopathy triggered by antiobesity drugs in a patient with multiple acyl-CoA dehydrogenase deficiency
por: Lin, Po-Yu, et al.
Publicado: (2021)

Pancreatitis in multiple acyl CoA dehydrogenase deficiency: An underdiagnosed complication
por: Elkhateeb, Nour, et al.
Publicado: (2020)

Lipid Storage Myopathy with Ketonuria: A Case of Fatty Acid Oxidation–Related Myopathy and Encephalopathy due to Multiple Acyl-CoA Dehydrogenase Deficiency
por: Chandra, Sadanandavalli R., et al.
Publicado: (2018)

Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Cause of Hepatomegaly
por: Nana Sede Mbakop, Raissa, et al.
Publicado: (2023)

Maternal vitamin deficiency mimicking multiple acyl-CoA dehydrogenase deficiency on newborn screening
por: Gramer, Gwendolyn, et al.
Publicado: (2021)

Lipid storage myopathy due to late-onset multiple Acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH: A case report
por: Tian, Huihong, et al.
Publicado: (2022)

P-14 Multiple acyl-coa dehydrogenase deficiency: a possibly treatable condition
por: Todeschini, A., et al.
Publicado: (2011)

Impaired fat oxidation during exercise in multiple acyl‐CoA dehydrogenase deficiency
por: Madsen, Karen L., et al.
Publicado: (2019)

Characterization of 31 Patients with Riboflavin-Responsive Multiple acyl-CoA Dehydrogenase Deficiency
por: Zhang, Jinru, et al.
Publicado: (2022)

Multiple Acyl-CoA Dehydrogenase Deficiency Presenting as Rhabdomyolysis After Gastrointestinal Endoscopy
por: Liu, Rong-Rong, et al.
Publicado: (2023)

Late-onset multiple acyl-CoA dehydrogenase deficiency mimicking myositis in an elderly patient: a case report
por: Zheng, Yiming, et al.
Publicado: (2020)

Cardiac Hypertrophy in Mice with Long-Chain Acyl-CoA Dehydrogenase (LCAD) or Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
por: Cox, Keith B., et al.
Publicado: (2009)

Combined isobutyryl‐CoA and multiple acyl‐CoA dehydrogenase deficiency in a boy with altered riboflavin homeostasis
por: Tummolo, Albina, et al.
Publicado: (2022)

Clinical aspects of short-chain acyl-CoA dehydrogenase deficiency
por: van Maldegem, Bianca T., et al.
Publicado: (2010)

Medium‐chain Acyl‐COA dehydrogenase deficiency: Pathogenesis, diagnosis, and treatment
por: Mason, Emily, et al.
Publicado: (2022)

FLAD1‐associated multiple acyl‐CoA dehydrogenase deficiency identified by newborn screening
por: Muru, Kai, et al.
Publicado: (2019)

Multiple acyl-CoA dehydrogenase deficiency kills Mycobacterium tuberculosis in vitro and during infection
por: Beites, Tiago, et al.
Publicado: (2021)

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Gene-Targeted Mice
por: Tolwani, Ravi J, et al.
Publicado: (2005)

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in an Infant with Dilated Cardiomyopathy
por: Marcì, Marcello, et al.
Publicado: (2009)

Medium chain acyl-CoA dehydrogenase deficiency in a premature infant
por: Dobrowolski, Steven F., et al.
Publicado: (2017)

Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency
por: Takken, T, et al.
Publicado: (2005)

Novel ETFDH mutations in four cases of riboflavin responsive multiple acyl-CoA dehydrogenase deficiency
por: Fan, Xin, et al.
Publicado: (2018)

Clinical Features of Multiple Acyl-CoA Dehydrogenase Deficiency With ETFDH Variants in the First Korean Cases
por: Kim, Yoo Jinie, et al.
Publicado: (2018)

Beneficial Effect of N-Carbamylglutamate in a Neonatal Form of Multiple Acyl-CoA Dehydrogenase Deficiency
por: Stanescu, Sinziana, et al.
Publicado: (2020)

Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic Disorder
por: Korula, Sophy, et al.
Publicado: (2022)

Clinical characteristics and gene mutation analysis of an adult patient with ETFDH-related multiple acyl-CoA dehydrogenase deficiency
por: Wang, Chenyi, et al.
Publicado: (2020)

First case report of short-chain acyl-CoA dehydrogenase deficiency in China
por: Jiang, MinYan, et al.
Publicado: (2013)

A case report of short-chain acyl-CoA dehydrogenase deficiency (SCADD)
por: Lampret, Barbka Repic, et al.
Publicado: (2015)

Medium-chain Acyl-CoA dehydrogenase deficiency presenting with neonatal pulmonary haemorrhage
por: Staels, Willem, et al.
Publicado: (2015)

Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives
por: Crawford, Sarah, et al.
Publicado: (2023)

Mechanisms Underlying Metabolic and Neural Defects in Zebrafish and Human Multiple Acyl-CoA Dehydrogenase Deficiency (MADD)
por: Song, Yuanquan, et al.
Publicado: (2009)

Diagnostic Challenges in Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: Clinical, Morphological, and Genetic Aspects
por: Lupica, Antonino, et al.
Publicado: (2022)

Multi-organ Abnormalities and mTORC1 Activation in Zebrafish Model of Multiple Acyl-CoA Dehydrogenase Deficiency
por: Kim, Seok-Hyung, et al.
Publicado: (2013)

Acute-onset multiple acyl-CoA dehydrogenase deficiency mimicking Guillain-Barré syndrome: two cases report
por: Hong, Daojun, et al.
Publicado: (2018)

Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency
por: Missaglia, Sara, et al.
Publicado: (2018)

Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin Tribe
por: Staretz-Chacham, Orna, et al.
Publicado: (2021)

Enantiomer‐specific pharmacokinetics of D,L‐3‐hydroxybutyrate: Implications for the treatment of multiple acyl‐CoA dehydrogenase deficiency
por: van Rijt, Willemijn J., et al.
Publicado: (2021)

Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review
por: Siano, Maria Anna, et al.
Publicado: (2021)

Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency
por: Scott Schwoerer, Jessica, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_993gjgovl7v83ktu7s19l59foi