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M. Mezei · SciRah

Researcher profile · Semantic Scholar

M. Mezei

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M. Mezei — researcher profile on SciRah

h-index: 18
Works: 51
Citations: 4,036

Most-cited papers

Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis
D. Adams, A. González-Duarte, W. O'Riordan, Chih-Chao Yang +32 more
2018New England Journal of Medicine2,404 citations Open access
Semantic Scholar
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG size.
R. Brinkman, M. Mezei, J. Theilmann, E. Almqvist +1 more
1997American Journal of Human Genetics411 citations
Semantic Scholar
A Genome-wide Association Study of Myasthenia Gravis
A. Renton, H. Pliner, C. Provenzano, A. Evoli +51 more
2015JAMA Neurology165 citations Open access
Semantic Scholar
Influence of lamotrigine on progression of early Huntington disease
B. Kremer, C. Clark, E. Almqvist, L. Raymond +7 more
1999Neurology153 citations
Semantic Scholar
Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
G. Harlalka, A. Lehman, B. Chioza, E. Baple +19 more
2013Brain : a journal of neurology136 citations Open access
Semantic Scholar
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study.
David John Adams, M. Polydefkis, A. González-Duarte, J. Wixner +25 more
2020Lancet Neurology119 citations
Semantic Scholar
SOD1 gene mutations in ALS patients from British Columbia, Canada: Clinical features, neurophysiology and ethical issues in management
A. Eisen, M. Mezei, H. Stewart, Marife Fabros +2 more
2008Amyotrophic Lateral Sclerosis84 citations
Semantic Scholar
Sensory ataxic neuropathy with ophthalmoparesis caused by POLG mutations.
M. Milone, N. Brunetti-Pierri, Lin-ya Tang, Neeraj Kumar +5 more
2008Neuromuscular Disorders79 citations
Semantic Scholar
Eosinophilic ulcer of the oral mucosa.
M. Mezei, V. Tron, W. Stewart, Jason K. Rivers
1995Journal of American Academy of Dermatology67 citations
Semantic Scholar
OPHTHALMOPLEGIA AND PTOSIS: MITOCHONDRIAL TOXICITY IN PATIENTS RECEIVING HIV THERAPY
G. Pfeffer, H. Côté, J. Montaner, C.-C. Li +2 more
2009Neurology46 citations Open access
Semantic Scholar
A Role for Amplified Protein Kinase C Activity in the Pathogenesis of Amyotrophic Lateral Sclerosis
Ruth A. Lanius, H. Paddon, M. Mezei, R. Wagey +3 more
1995Journal of Neurochemistry40 citations
Semantic Scholar
Concurrent inflammatory myopathy and myasthenia gravis with or without thymic pathology: A case series and literature review.
Kun-Yun Huang, K. Shojania, K. Chapman, N. Amiri +2 more
2019Seminars in Arthritis & Rheumatism38 citations
Semantic Scholar
Choline acetyltransferase mutations causing congenital myasthenic syndrome: molecular findings and genotype-phenotype correlations
J. Arredondo, Marian Lara, S. Gospe, C. Mazia +6 more
2015Human Mutation29 citations Open access
Semantic Scholar
Canadian Guidelines for Hereditary Transthyretin Amyloidosis Polyneuropathy Management
M. Alcantara, M. Mezei, S. Baker, A. Breiner +12 more
2021Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques26 citations Open access
Semantic Scholar
Mitochondrial disease clinical manifestations : An overview
A. Mattman, S. Sirrs, M. Mezei, R. Salvarinova-Zivkovic +2 more
201124 citations
Semantic Scholar
A National Spinal Muscular Atrophy Registry for Real-World Evidence
V. Hodgkinson, M. Oskoui, J. Lounsberry, S. M'Dahoma +46 more
2020Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques23 citations Open access
Semantic Scholar
The Canadian Neuromuscular Disease Registry 2010–2019: A Decade of Facilitating Clinical Research Througha Nationwide, Pan-NeuromuscularDisease Registry
V. Hodgkinson, J. Lounsberry, S. M'Dahoma, A. Russell +59 more
2020Journal of Neuromuscular Diseases22 citations Open access
Semantic Scholar
Performance of serum and dried blood spot acylcarnitine profiles for detection of fatty acid β-oxidation disorders in adult patients with rhabdomyolysis
K. Al-Thihli, G. Sinclair, S. Sirrs, M. Mezei +2 more
2014Journal of Inherited Metabolic Disease19 citations
Semantic Scholar
Epidemiological evidence for a hereditary contribution to myasthenia gravis: a retrospective cohort study of patients from North America
Joshua D. Green, R. Barohn, Emanuela Bartoccion, M. Benatar +36 more
2020BMJ Open18 citations Open access
Semantic Scholar
Electromyography of respiratory muscles in amyotrophic lateral sclerosis.
H. Stewart, A. Eisen, J. Road, M. Mezei +1 more
2001Journal of Neurological Sciences18 citations
Semantic Scholar
Increased Prevalence of Hypertension in Young Adults with High Heteroplasmy Levels of the MELAS m.3243A>G Mutation.
Fady Hannah-Shmouni, S. Sirrs, M. Mezei, P. Waters +1 more
2013JIMD Reports16 citations Open access
Semantic Scholar
Superficial siderosis--a cause of audiovestibular failure.
N. Longridge, S. Hashimoto, T. Marotta, M. Mezei
1996The Journal of Otolaryngology16 citations
Semantic Scholar
Motor system abnormalities in heterozygous relatives of a D90A homozygous CuZn-SOD ALS patient of finnish extraction.
M. Mezei, P. Andersen, H. Stewart, Markus Weber +1 more
1999Journal of Neurological Sciences15 citations
Semantic Scholar
High rate of hypertension in patients with m.3243A>G MELAS mutations and POLG variants.
Andrew D. Pauls, Vikrant Sandhu, D. Young, Dayna-Lynn Nevay +7 more
2020Mitochondrion (Amsterdam. Print)11 citations
Semantic Scholar
Practice Guidelines for Canadian Neurophysiology Laboratories During the COVID-19 Pandemic
J. Appendino, S. Baker, K. Chapman, Tamara Dykstra +14 more
2020Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques10 citations Open access
Semantic Scholar
Cardiac screening investigations in adult‐onset progressive external ophthalmoplegia patients
G. Pfeffer, M. Mezei
2012Muscle and Nerve9 citations
Semantic Scholar
Mitochondrial pseudomyasthenia.
J. Barton, J. Maguire, M. Mezei, T. Hurwitz +1 more
2010Journal of neuro-ophthalmology9 citations Open access
Semantic Scholar
A Case of Good Syndrome Presumed Secondary to Metastatic Pancreatic Thymoma in a Patient Presenting With a Myasthenic Crisis Postthymectomy
Kristin L Jack, Matthew Kula, J. Flint, M. Mezei
2015Journal of Clinical Neuromuscular Disease7 citations
Semantic Scholar
Levator Palpebrae Biopsy and Diagnosis of Progressive External Ophthalmoplegia
G. Pfeffer, P. Waters, J. Maguire, H. Vallance +2 more
2012Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques7 citations Open access
Semantic Scholar
Minimal expansion of the GCG repeat in the PABP2 gene does not predispose to sporadic inclusion body myositis
M. Mezei, A. Mankodi, B. Brais, C. Marineau +3 more
1999Neurology7 citations
Semantic Scholar
Safety of statin therapy in patients with mitochondrial diseases.
Fady Hannah-Shmouni, A. Alsarraf, J. Frohlich, M. Mezei +2 more
2013Journal of Clinical Lipidology6 citations
Semantic Scholar
Diagnosis and management of patients with mitochondrial disease
A. Mattman, M. O’Riley, P. Waters, G. Sinclair +5 more
20114 citations
Semantic Scholar
Loss-of-function mitochondrial DNA polymerase gamma variants cause vascular smooth muscle cells to secrete a diffusible mitogenic factor
Samantha Rothwell, Irvin Ng, Sophia Shalchy-Tabrizi, Pola Kalinowski +8 more
2025Frontiers in Physiology3 citations Open access
Semantic Scholar
Macrocytosis in Mitochondrial DNA Deletion Syndromes
Farida Almarzooqi, H. Vallance, M. Mezei, A. Lehman +4 more
2023Acta Haematologica3 citations
Semantic Scholar
Self-initiated lifestyle interventions lead to potential insight into an effective, alternative, non-surgical therapy for mitochondrial disease associated multiple symmetric lipomatosis.
E. Nadeau, M. Mezei, M. Cresswell, Sida Zhao +7 more
2020Mitochondrion (Amsterdam. Print)2 citations
Semantic Scholar
Ketogenic diet for mitochondrial disease: potential role in treating the Multiple Symmetric Lipomatosis phenotype associated with the common MT-TK genetic mutation
A. Mattman, E. Nadeau, M. Mezei, M. Cresswell +7 more
2022Orphanet Journal of Rare Diseases1 citations Open access
Semantic Scholar
Guillian–Barré syndrome in high tetraplegia following acute respiratory illness
C. Grant, N. Briscoe, M. Mezei, A. Krassioukov
2011Spinal Cord1 citations
Semantic Scholar
Errata
Michelle M Mezey, M. Mezei
20111 citations
Semantic Scholar
P.058 Spinal arachnoiditis as a complication of cryptococcal meningitis
O. Marais, M. Mezei, M. Alhalabi, S. Belga
2022Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques0 citations Open access
Semantic Scholar
P.040 Value-based approach to the management of Inflammatory Neuropathies: Incorporating objective outcome measures in clinical care
CB Smith, K. Chapman, M. Mezei, K. Beadon
2022Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques0 citations Open access
Semantic Scholar
P.0438 Saccadik eye movements in simple and complex visual environments differenciate mild cognitive impairment: preliminary clinical results
I. Kovács, S. Somoskeoy, M. Mezei, I. Hoffmann +7 more
2021European Neuropsychopharmacology0 citations
Semantic Scholar
Response from Authors to the Letter to the Editor
J. Appendino, S. Baker, K. Chapman, Tamara Dykstra +14 more
2020Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques0 citations Open access
Semantic Scholar
AB0778 Clinical characteristics and prognosis of polymyositis and dermatomyositis associated with malignancy: a 25-year retrospective study
K. Huang, M. Mezei, K. Shojania, Kristine M. Chapman +2 more
2018Scleroderma, myositis and related syndromes0 citations Open access
Semantic Scholar
P.075 Inflammatory Myositis associated with Myasthenia Gravis with and without thymic pathology: case series and literature review
Kun Huang, M. Mezei, Kam Shojania, Neda Amiri +2 more
2018Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques0 citations Open access
Semantic Scholar
How a Drug is Assessed Once It ’ s in Clinical Trials : A Perspective from a Clinical Pharmacology Reviewer
A. González-Duarte, D. Adams, C.-C. Yang, M. Ueda +29 more
20180 citations
Semantic Scholar
MELAS and POLG exhibit high rates of hypertension with differential resistance to anti‐hypertensive drugs suggesting divergent pathogenic mechanisms
Andrew D. Pauls, Dayna-Lynn Nevay, D. Young, Vikrant Sandhu +6 more
2017The FASEB Journal0 citations Open access
Semantic Scholar
45. Recurrent rhabdomyolysis and exercise intolerance: Variable presentation in siblings with late onset very long-chain acylcoa dehydrogenase deficiency
C. F. E. Brunel-Guitton, G. Sinclair, P. Waters, R. Wanders +2 more
20120 citations
Semantic Scholar
PEO1 Gene (Twinkle) Mutation and Multi-Organ Failure Following Propofol Infusion (P07.205)
Rebecca A Harrison, Jason Valerio, F. Buffam, M. Mezei
20120 citations
Semantic Scholar
from mild to severe and can involve more than one organ system.
A. Mattman, S. Sirrs, M. Mezei, R. Salvarinova-Zivkovic +1 more
20110 citations
Semantic Scholar
Errata
Michelle M Mezey, M. Mezei
20110 citations Open access
Semantic Scholar

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