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Andrés Berardo

Heterogeneity of Coenzyme Q10Deficiency: Patient Study and Literature Review
2012 · Valentina Emmanuele, Luis C. López, et al. · Archives of Neurology · 223
A Diagnostic Algorithm for Metabolic Myopathies
2010 · Andres Berardo, Salvatore DiMauro, et al. · Current Neurology and Neuroscience Reports · 178
Hereditary myopathy with early respiratory failure: occurrence in various populations
2013 · J. Palmio, A. Evila, et al. · Journal of Neurology Neurosurgery & Psychiatry · 88
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Expanding the importance of HMERF titinopathy: new mutations and clinical aspects
2019 · Johanna Palmio, Sarah Leonard-Louis, et al. · Journal of Neurology · 53
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HNRNPDL-related muscular dystrophy: expanding the clinical, morphological and MRI phenotypes
2019 · Andrés Berardo, Xavière Lornage, et al. · Journal of Neurology · 48
Advances in Thymidine Kinase 2 Deficiency: Clinical Aspects, Translational Progress, and Emerging Therapies
2022 · Andres Berardo, Cristina Domínguez-González, et al. · Journal of Neuromuscular Diseases · 45
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Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathy
2020 · Cristina Dominguez-Gonzalez, Carmen Badosa, et al. · Scientific Reports · 43
Cardiological manifestations of mitochondrial respiratory chain disorders.
2011 · A Berardo, O Musumeci, et al. · PubMed Central · 34
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Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6
2019 · Andres Berardo, Valentina Emmanuele, et al. · Journal of Neurology · 27
Anti-glycan antibodies halt axon regeneration in a model of Guillain Barrè Syndrome axonal neuropathy by inducing microtubule disorganization via RhoA–ROCK-dependent inactivation of CRMP-2
2016 · Victoria Rozés Salvador, Florencia Heredia, et al. · Experimental Neurology · 25
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Severe axonal neuropathy is a late manifestation of SPG11
2016 · Andreea Manole, Viorica Chelban, et al. · Journal of Neurology · 19
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A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO)
2010 · Andres Berardo, Jorida Çoku, et al. · Neuromuscular Disorders · 18
Redefining infantile-onset multisystem phenotypes of coenzyme Q10-deficiency in the next-generation sequencing era
2020 · Andres Berardo, Catarina M. Quinzii · Journal of Translational Genetics and Genomics · 12
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Blockade of Rho-associated kinase prevents inhibition of axon regeneration of peripheral nerves induced by anti-ganglioside antibodies
2023 · Andrés Berardo, Cristian R. Bacaglio, et al. · Neural Regeneration Research · 7
Expanding importance of HMERF titinopathy: new mutations and clinical aspects
2017 · J. Palmio, S. Leonard, et al. · Neuromuscular Disorders · 5
Utilidad de la identificación de anticuerpos en miopatías inflamatorias: revisión
2023 · Laura Pirra, Belen Tillard, et al. · Neurología Argentina · 3
Regulatory environment for novel therapeutic development in mitochondrial diseases
2020 · Michio Hirano, Andres Berardo, et al. · Journal of Inherited Metabolic Disease · 3
Utilidad de la identificación de anticuerpos en neuropatías periféricas, neuronopatías y ganglionopatías: revisión
2020 · Ricardo C. Reisin, Valeria L. Salutto, et al. · Neurología Argentina · 3
[Argentine consensus on late-onset Pompe's disease].
2018 · Alberto Dubrovsky, Ernesto Fulgenzi, et al. · PubMed · 3
Caracterización clínica, electrofisiológica y molecular en un paciente con parálisis periódica hipocalémica tipo 2, nueva mutación en SCN4A
2016 · Andrés Berardo, Sebastián Ianardi, et al. · Neurología Argentina · 2
Use of nucleoside therapy for mitochondrial DNA depletion/deletion syndrome (MDDS)
2026 · Michio Hirano, Andres Berardo, et al. · Neurotherapeutics · 1
Long‐Chain Fatty Acid Beta‐Oxidation Defects: A Case Series and Literature Review
2025 · Juan Politei, Andrés Berardo, et al. · Lipids · 1
Utilidad de los anticuerpos en las enfermedades de la unión neuromuscular: revisión
2021 · Valeria L. Salutto, Mariana Bendersky, et al. · Neurología Argentina · 1
Nueva mutación en C10Orf2 (PEO1) en paciente con oftalmoplejía crónica progresiva mitocondrial dominante (adCPEO), primer caso argentino
2012 · Andrés Berardo, Henry Rivera, et al. · Neurología Argentina · 1
El espectro clínico de las mutaciones en POLG
2011 · Andrés Berardo · Neurología Argentina · 1
Works count: 36
Citation count: 844
H-index: 12
I10-index: 13
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