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May 26, 2016 (publication date) through Apr 28, 2024
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Publication Name
World Journal of Cardiology
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1949-8462
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Finsterer J, Zarrouk-Mahjoub S. Mitochondrial vasculopathy. World J Cardiol 2016; 8(5): 333-339 [PMID: 27231520 DOI: 10.4330/wjc.v8.i5.333] |
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| URL: | https://www.wjgnet.com/1949-8462/full/v8/i5/333.htm |
| Number | Citing Articles |
| 1 |
Chrisandra L. Shufelt, Christine Pacheco, Marysia S. Tweet, Virginia M. Miller. Sex-Specific Analysis of Cardiovascular Function. Advances in Experimental Medicine and Biology 2018; 1065: 433 doi: 10.1007/978-3-319-77932-4_27
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| 2 |
Laura Ludovica Gramegna, Irene Cortesi, Micaela Mitolo, Stefania Evangelisti, Lia Talozzi, Luigi Cirillo, Caterina Tonon, Raffaele Lodi. Major cerebral vessels involvement in patients with MELAS syndrome: Worth a scan? A systematic review. Journal of Neuroradiology 2021; 48(5): 359 doi: 10.1016/j.neurad.2021.02.002
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| 3 |
Josef Finsterer. Secondary manifestations of mitochondrial disorders. Journal of Zhejiang University-SCIENCE B 2020; 21(7): 590 doi: 10.1631/jzus.B2000010
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| 4 |
Spoorthi Jagadish, Amy R.U.L. Calhoun, Sreenath Thati Ganganna. Recurrent super-refractory status epilepticus and stroke like episode in a patient with Behr syndrome secondary to biallelic variants in OPA1 gene. Epilepsy & Behavior Reports 2024; 25: 100652 doi: 10.1016/j.ebr.2024.100652
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L. A. Kalashnikova, L. A. Dobrynina, M. V. Dreval, M. V. Gubanova, M. V. Krotenkova, R. N. Konovalov, M. S. Legenko. Intracerebral hemorrhage in the late period of internal carotid artery dissection. Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova 2019; 119(8): 28 doi: 10.17116/jnevro201911908228
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| 6 |
Mohaddeseh Behjati, Mohammad Reza Sabri, Masood Etemadi Far, Majid Nejati. Cardiac complications in inherited mitochondrial diseases. Heart Failure Reviews 2021; 26(2): 391 doi: 10.1007/s10741-020-10009-1
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| 7 |
Ruth Ellen Jones, Jessica Lee, Mujtaba M. Ali. Renal artery aneurysm associated with Leber hereditary optic neuropathy. Journal of Vascular Surgery Cases, Innovations and Techniques 2018; 4(1): 5 doi: 10.1016/j.jvscit.2017.10.001
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| 8 |
Yuxin Li, Weixingzi Xu, Chong Sun, Jie Lin, Jianxun Qu, Jiawen Cao, Haiqing Li, Liqin Yang. Reversible Dilation of Cerebral Macrovascular Changes in MELAS Episodes. Clinical Neuroradiology 2019; 29(2): 321 doi: 10.1007/s00062-018-0662-8
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| 9 |
Rahel Stefanie Wiehe, Boris Gole, Laurent Chatre, Paul Walther, Enrico Calzia, Miria Ricchetti, Lisa Wiesmüller. Endonuclease G promotes mitochondrial genome cleavage and replication. Oncotarget 2018; 9(26): 18309 doi: 10.18632/oncotarget.24822
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| 10 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Cerebral involvement in mitochondrial disorders on imaging. Child's Nervous System 2016; 32(11): 2059 doi: 10.1007/s00381-016-3241-9
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| 11 |
Josef Finsterer. Cerebellar stroke-like lesions in Leigh syndrome may mimic cerebellar cortical bleeding. eNeurologicalSci 2020; 19: 100234 doi: 10.1016/j.ensci.2020.100234
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| 12 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. MELAS reflects a clinical concept with heterogeneous genetic background. Arquivos de Neuro-Psiquiatria 2019; 77(2): 142 doi: 10.1590/0004-282x20190003
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| 13 |
Josef Finsterer, Sinda Zarrouk‐Mahjoub. Regional cerebral hyperperfusion: A biomarker of upcoming stroke‐like episodes?. Journal of Magnetic Resonance Imaging 2018; 47(2): 582 doi: 10.1002/jmri.25735
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| 14 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Macroangiopathy is a typical phenotypic manifestation of MELAS. Metabolic Brain Disease 2017; 32(4): 977 doi: 10.1007/s11011-017-0020-6
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| 15 |
Josef Finsterer, Elmano Henrique Torres de Carvalho. Cerebral Manifestations of Mitochondrial Disorders. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2017; 44(6): 654 doi: 10.1017/cjn.2017.211
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| 16 |
A.J. Brownstein, B.A. Ziganshin, J.A. Elefteriades. Encyclopedia of Cardiovascular Research and Medicine. 2018; : 327 doi: 10.1016/B978-0-12-809657-4.99692-3
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| 17 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Comment on “Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis”. Oxidative Medicine and Cellular Longevity 2018; 2018: 1 doi: 10.1155/2018/4575821
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| 18 |
Josef Finsterer, Rahim Aliyev. Metabolic stroke or stroke-like lesion: Peculiarities of a phenomenon. Journal of the Neurological Sciences 2020; 412: 116726 doi: 10.1016/j.jns.2020.116726
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| 19 |
Patries M. Herst, Matthew R. Rowe, Georgia M. Carson, Michael V. Berridge. Functional Mitochondria in Health and Disease. Frontiers in Endocrinology 2017; 8 doi: 10.3389/fendo.2017.00296
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| 20 |
Josef Finsterer. Cerebral imaging in adult mitochondrial disorders. Journal of the Neurological Sciences 2019; 404: 29 doi: 10.1016/j.jns.2019.07.013
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| 21 |
Josef Finsterer. Cerebellar stroke-like lesions in Leigh syndrome due to the variant m.8993T>C in MT-ATP6. eNeurologicalSci 2020; 18: 100203 doi: 10.1016/j.ensci.2019.100203
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| 22 |
T. Abruzzo, R. van den Berg, S. Vadivelu, S.W. Hetts, M. Dishop, P. Cornejo, V. Narayanan, K.E. Ramsey, C. Coopwood, E.G. Medici-van den Herik, S.D. Roosendaal, M. Lawton, S. Bernes. Arterioectatic Spinal Angiopathy of Childhood: Clinical, Imaging, Laboratory, Histologic, and Genetic Description of a Novel CNS Vascular Pathology. American Journal of Neuroradiology 2022; 43(7): 1060 doi: 10.3174/ajnr.A7551
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| 23 |
Josef Finsterer. Aortic root ectasia as a phenotypic feature of a mitochondrial disorder. Clinical Case Reports 2018; 6(8): 1501 doi: 10.1002/ccr3.1652
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| 24 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Headache in mitochondrial disorders. Clinical Neurology and Neurosurgery 2018; 166: 44 doi: 10.1016/j.clineuro.2018.01.020
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| 25 |
Torsten Kraya, Stephan Zierz. Frequency of Headache in Mitochondrial Disorders: A Response. Headache: The Journal of Head and Face Pain 2018; 58(2): 315 doi: 10.1111/head.13253
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| 26 |
Josef Finsterer. Peculiarities of stroke-like lesions on MRI. European Journal of Radiology Open 2019; 6: 60 doi: 10.1016/j.ejro.2019.01.001
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| 27 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype. Documenta Ophthalmologica 2019; 138(3): 255 doi: 10.1007/s10633-019-09690-x
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| 28 |
Michael V. Berridge, Patries M. Herst, Carole Grasso. The Human Mitochondrial Genome. 2020; : 515 doi: 10.1016/B978-0-12-819656-4.00020-6
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| 29 |
J.A. Elefteriades. Reference Module in Biomedical Sciences. 2018; doi: 10.1016/B978-0-12-801238-3.99692-2
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| 30 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Mitochondrial vasculopathy due to the m.3243A>G mutation is not restricted to the carotid artery. Molecular Genetics and Metabolism Reports 2016; 9: 34 doi: 10.1016/j.ymgmr.2016.10.002
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| 31 |
Kun Zhu, Shuang Li, Huan Chen, Yao Wang, Miao Yu, Hongyan Wang, Weijie Zhao, Yunpeng Cao. Late onset MELAS with m.3243A > G mutation and its association with aneurysm formation. Metabolic Brain Disease 2017; 32(4): 1069 doi: 10.1007/s11011-017-9989-0
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| 32 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Correspondence. Retina 2017; 37(6): e88 doi: 10.1097/IAE.0000000000001722
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| 33 |
Youjie Wang, Enhui Zhang, Chen Ye, Bo Wu. Refractory Hypotension in a Late-Onset Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Male with m.3243 A>G Mutation: A Case Report. Brain Sciences 2023; 13(7): 1080 doi: 10.3390/brainsci13071080
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| 34 |
Josef Finsterer, Michelangelo Mancuso, Davide Pareyson, Jean-Marc Burgunder, Thomas Klopstock. Mitochondrial disorders of the retinal ganglion cells and the optic nerve. Mitochondrion 2018; 42: 1 doi: 10.1016/j.mito.2017.10.003
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| 35 |
Lata Singh, Mithalesh Kumar Singh. Mutagenesis and Mitochondrial-Associated Pathologies. 2022; doi: 10.5772/intechopen.96368
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| 36 |
Josef Finsterer, Sinda Zarrouk‐Mahjoub. Frequency of Headache in Mitochondrial Disorders. Headache: The Journal of Head and Face Pain 2018; 58(2): 313 doi: 10.1111/head.13243
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| 37 |
Josef Finsterer. Blood pressure regulation is multifactorial in mitochondrial disorders. Journal of Hypertension 2022; 40(10): 2081 doi: 10.1097/HJH.0000000000003187
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| 38 |
Josef Finsterer. Mitochondrial metabolic stroke: Phenotype and genetics of stroke-like episodes. Journal of the Neurological Sciences 2019; 400: 135 doi: 10.1016/j.jns.2019.03.021
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| 39 |
Josef Finsterer. Features on cerebral imaging suggesting mitochondrial disorder. Neurodegenerative Disease Management 2018; 8(4): 215 doi: 10.2217/nmt-2018-0015
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| 40 |
Daniel Davila-Williams, Megan Barry, Carolina Vargas, Arastoo Vossough, Timothy J. Bernard, Mubeen F. Rafay. Cerebral Arteriopathies of Childhood – Current Approaches. Seminars in Pediatric Neurology 2022; 43: 101004 doi: 10.1016/j.spen.2022.101004
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| 41 |
Rahul Phadke. Myopathology of Adult and Paediatric Mitochondrial Diseases. Journal of Clinical Medicine 2017; 6(7): 64 doi: 10.3390/jcm6070064
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| 42 |
Laura Doblado, Claudia Lueck, Claudia Rey, Alejandro K. Samhan-Arias, Ignacio Prieto, Alessandra Stacchiotti, Maria Monsalve. Mitophagy in Human Diseases. International Journal of Molecular Sciences 2021; 22(8): 3903 doi: 10.3390/ijms22083903
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| 43 |
Natalia Będkowska, Aneta Zontek, Justyna Paprocka. Stroke-like Episodes in Inherited Neurometabolic Disorders. Metabolites 2022; 12(10): 929 doi: 10.3390/metabo12100929
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| 44 |
Marcos Gil Alberto da Veiga, Clara Marecos, José Pedro Vieira, Carla Conceição. Leigh Syndrome with atypical cerebellum imaging features. eNeurologicalSci 2020; 18: 100214 doi: 10.1016/j.ensci.2019.100214
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| 45 |
Anca R. Florian, Ali Yilmaz. Diagnosis and Management of Mitochondrial Disorders. 2019; : 257 doi: 10.1007/978-3-030-05517-2_16
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| 46 |
A. Benyamine, S. Coze, F. Riccardi, A. Lachaud, P. Belenotti, J. Serratrice. Cuándo pensar en una enfermedad mitocondrial. EMC - Tratado de Medicina 2018; 22(3): 1 doi: 10.1016/S1636-5410(18)91428-5
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Steffen Naegel, Philipp Burow, Dagny Holle, Dietrich Stoevesandt, Simon Heintz, Annemarie Thaele, Stephan Zierz, Torsten Kraya. Erenumab for migraine prevention in a patient with mitochondrial encephalopathy, lactate acidosis, and stroke‐like episodes syndrome: A case report. Headache: The Journal of Head and Face Pain 2021; 61(4): 694 doi: 10.1111/head.14101
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