| 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 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) 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) 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 doi: 10.1016/j.ebr.2024.100652
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| 5 |
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) doi: 10.18632/oncotarget.24822
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| 6 |
Josef Finsterer, Sinda Zarrouk‐Mahjoub. Regional cerebral hyperperfusion: A biomarker of upcoming stroke‐like episodes?. Journal of Magnetic Resonance Imaging 2018; 47(2) doi: 10.1002/jmri.25735
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| 7 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Macroangiopathy is a typical phenotypic manifestation of MELAS. Metabolic Brain Disease 2017; 32(4) doi: 10.1007/s11011-017-0020-6
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| 8 |
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) doi: 10.1017/cjn.2017.211
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| 9 |
Josef Finsterer, Sinda Zarrouk-Mahjoub, Giuseppe Cirillo. 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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| 10 |
Laith R. Sultan, Trudy A. Morgan, Daniel E. McGinn, Kassa Darge, Liya Gendler, Jie Nguyen, Elizabeth Brennan, Julie A. Brother, Rui Xiao, Marni J. Falk, Vinay Nadkarni, Harry Ischiropoulos, Jose A. Adams, Zarazuela Zolkipli Cunningham. Evaluation of muscle microvascular perfusion in primary mitochondrial disease by contrast-enhanced ultrasound: Feasibility study. Therapeutic Advances in Rare Disease 2026; 7 doi: 10.1177/26330040261486870
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| 11 |
Josef Finsterer. Aortic root ectasia as a phenotypic feature of a mitochondrial disorder. Clinical Case Reports 2018; 6(8) doi: 10.1002/ccr3.1652
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| 12 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Headache in mitochondrial disorders. Clinical Neurology and Neurosurgery 2018; 166 doi: 10.1016/j.clineuro.2018.01.020
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| 13 |
Torsten Kraya, Stephan Zierz. Frequency of Headache in Mitochondrial Disorders: A Response. Headache: The Journal of Head and Face Pain 2018; 58(2) doi: 10.1111/head.13253
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| 14 |
Josef Finsterer. Peculiarities of stroke-like lesions on MRI. European Journal of Radiology Open 2019; 6 doi: 10.1016/j.ejro.2019.01.001
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| 15 |
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 doi: 10.1016/j.ymgmr.2016.10.002
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| 16 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Correspondence. Retina 2017; 37(6) doi: 10.1097/IAE.0000000000001722
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| 17 |
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 doi: 10.1016/j.mito.2017.10.003
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| 18 |
Ritika Mishra, Thakur Gurjeet Singh, Rohit Bhatia, Ankit Awasthi. Unveiling the therapeutic journey of snail mucus in diabetic wound care. Naunyn-Schmiedeberg's Archives of Pharmacology 2025; 398(6) doi: 10.1007/s00210-024-03657-9
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| 19 |
Josef Finsterer, Sinda Zarrouk‐Mahjoub. Frequency of Headache in Mitochondrial Disorders. Headache: The Journal of Head and Face Pain 2018; 58(2) doi: 10.1111/head.13243
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| 20 |
Josef Finsterer. Mitochondrial metabolic stroke: Phenotype and genetics of stroke-like episodes. Journal of the Neurological Sciences 2019; 400 doi: 10.1016/j.jns.2019.03.021
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| 21 |
Civan Islak, Ömer Bağcılar, Hakan Hatem Selçuk, Sema Saltık, Bora Korkmazer, Tanyel Zubarioğlu, Serdar Arslan, Ahmet Üstündag, Osman Kızılkılıç. A New Perspective On Arterioectatic Spinal Angiopathy with a Reversible Pattern: Cause or Consequence?. Clinical Neuroradiology 2025; 35(1) doi: 10.1007/s00062-024-01451-x
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| 22 |
Rahul Phadke. Myopathology of Adult and Paediatric Mitochondrial Diseases. Journal of Clinical Medicine 2017; 6(7) doi: 10.3390/jcm6070064
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| 23 |
Natalia Będkowska, Aneta Zontek, Justyna Paprocka. Stroke-like Episodes in Inherited Neurometabolic Disorders. Metabolites 2022; 12(10) doi: 10.3390/metabo12100929
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| 24 |
Marcos Gil Alberto da Veiga, Clara Marecos, José Pedro Vieira, Carla Conceição. Leigh Syndrome with atypical cerebellum imaging features. eNeurologicalSci 2020; 18 doi: 10.1016/j.ensci.2019.100214
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| 25 |
Sounira Mehri, Josef Finsterer. Based on a Single Case, Cardiopulmonary Training Cannot Be Recommended as Therapy for Hemiparesis in MELAS With Ischemic Stroke. The Kaohsiung Journal of Medical Sciences 2026; doi: 10.1002/kjm2.70294
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| 26 |
Anca R. Florian, Ali Yilmaz. Diagnosis and Management of Mitochondrial Disorders. 2019; doi: 10.1007/978-3-030-05517-2_16
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| 27 |
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) doi: 10.1016/S1636-5410(18)91428-5
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| 28 |
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) doi: 10.17116/jnevro201911908228
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| 29 |
Mohaddeseh Behjati, Mohammad Reza Sabri, Masood Etemadi Far, Majid Nejati. Cardiac complications in inherited mitochondrial diseases. Heart Failure Reviews 2021; 26(2) doi: 10.1007/s10741-020-10009-1
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| 30 |
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) doi: 10.1016/j.jvscit.2017.10.001
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| 31 |
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) doi: 10.1007/s00062-018-0662-8
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| 32 |
Paulina Felczak, Iwona Stępniak, Paweł Kowalski, Tomasz Stępień, Teresa Wierzba-Bobrowicz. Pathology of skeletal muscle fibers and small blood vessels in MERRF syndrome: an ultrastructural study. Polish Journal of Pathology 2019; 69(4) doi: 10.5114/pjp.2018.80904
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| 33 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Cerebral involvement in mitochondrial disorders on imaging. Child's Nervous System 2016; 32(11) doi: 10.1007/s00381-016-3241-9
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| 34 |
Josef Finsterer. Cerebellar stroke-like lesions in Leigh syndrome may mimic cerebellar cortical bleeding. eNeurologicalSci 2020; 19 doi: 10.1016/j.ensci.2020.100234
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| 35 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. MELAS reflects a clinical concept with heterogeneous genetic background. Arquivos de Neuro-Psiquiatria 2019; 77(2) doi: 10.1590/0004-282x20190003
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| 36 |
A.J. Brownstein, B.A. Ziganshin, J.A. Elefteriades. Encyclopedia of Cardiovascular Research and Medicine. 2018; doi: 10.1016/B978-0-12-809657-4.99692-3
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| 37 |
Josef Finsterer, Rahim Aliyev. Metabolic stroke or stroke-like lesion: Peculiarities of a phenomenon. Journal of the Neurological Sciences 2020; 412 doi: 10.1016/j.jns.2020.116726
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| 38 |
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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| 39 |
Josef Finsterer. Cerebral imaging in adult mitochondrial disorders. Journal of the Neurological Sciences 2019; 404 doi: 10.1016/j.jns.2019.07.013
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| 40 |
Josef Finsterer. Cerebellar stroke-like lesions in Leigh syndrome due to the variant m.8993T>C in MT-ATP6. eNeurologicalSci 2020; 18 doi: 10.1016/j.ensci.2019.100203
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| 41 |
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) doi: 10.3174/ajnr.A7551
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| 42 |
Josef Finsterer, Sinda Zarrouk-Mahjoub. Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype. Documenta Ophthalmologica 2019; 138(3) doi: 10.1007/s10633-019-09690-x
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| 43 |
Michael V. Berridge, Patries M. Herst, Carole Grasso. The Human Mitochondrial Genome. 2020; doi: 10.1016/B978-0-12-819656-4.00020-6
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| 44 |
J.A. Elefteriades. Reference Module in Biomedical Sciences. 2018; doi: 10.1016/B978-0-12-801238-3.99692-2
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| 45 |
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) doi: 10.1007/s11011-017-9989-0
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| 46 |
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) doi: 10.3390/brainsci13071080
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| 47 |
Lata Singh, Mithalesh Kumar Singh. Mutagenesis and Mitochondrial-Associated Pathologies. 2022; doi: 10.5772/intechopen.96368
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| 48 |
Josef Finsterer. Blood pressure regulation is multifactorial in mitochondrial disorders. Journal of Hypertension 2022; 40(10) doi: 10.1097/HJH.0000000000003187
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| 49 |
Josef Finsterer. Features on Cerebral Imaging Suggesting Mitochondrial Disorder. Neurodegenerative Disease Management 2018; 8(4) doi: 10.2217/nmt-2018-0015
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| 50 |
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 doi: 10.1016/j.spen.2022.101004
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| 51 |
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) doi: 10.3390/ijms22083903
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| 52 |
Yuhao Zhao, Dianxuan Chen, Hailing Chen, Rui Fan, Wenyue Xu, Haishan Jiang. A review of the link between the lactate-GPR81 axis and mitochondrial angiopathy in MELAS based on imaging characteristics. Journal of Neurology 2025; 272(9) doi: 10.1007/s00415-025-13318-3
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| 53 |
A J Brownstein, B A Ziganshin, J A Elefteriades. Encyclopedia of Cardiovascular Research and Medicine(2e). 2026; doi: 10.1016/B978-0-443-15734-9.00153-9
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| 54 |
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) doi: 10.1111/head.14101
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| 55 |
Daehoon Kim, Jieun Shin, Yeon-Kyung Choi, You Mie Lee, Keun-Gyu Park, Hyang Sook Kim, Jun-Kyu Byun. Targeting SLC25A33 Suppresses Vascular Smooth Muscle Cell Proliferation and Migration by Reducing Cytosolic mtDNA Levels: Implications for Occlusive Vascular Diseases. Diabetes & Metabolism Journal 2026; 50(1) doi: 10.4093/dmj.2024.0632
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