Cargando…

Correction to: Molecular basis of Leigh syndrome: a current look

Detalles Bibliográficos
Autores principales:	Schubert Baldo, Manuela, Vilarinho, Laura
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2020
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7098111/ https://www.ncbi.nlm.nih.gov/pubmed/32213199 http://dx.doi.org/10.1186/s13023-020-1351-7

Ejemplares similares

Molecular basis of Leigh syndrome: a current look
por: Schubert Baldo, Manuela, et al.
Publicado: (2020)

Leigh Syndrome Spectrum: A Portuguese Population Cohort in an Evolutionary Genetic Era
por: Baldo, Manuela Schubert, et al.
Publicado: (2023)

LEIGH SYNDROME: A CASE REPORT WITH A MITOCHONDRIAL DNA MUTATION
por: Lopes, Tânia, et al.
Publicado: (2018)

Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia
por: Kistol, Denis, et al.
Publicado: (2023)

Correction: The Cellular and Molecular Basis of Bitter Tastant-Induced Bronchodilation
por: Zhang, Cheng-Hai, et al.
Publicado: (2013)

An interesting case of Leigh-like syndrome
por: Bharani, K., et al.
Publicado: (2012)

Leigh syndrome with atypical cerebellar lesions
por: Veiga, Marcos Gil Alberto da, et al.
Publicado: (2019)

MELAS or Leigh syndrome, that’s the question
por: Finsterer, Josef
Publicado: (2021)

Leigh syndrome associated with TRMU gene mutations
por: Sala-Coromina, Júlia, et al.
Publicado: (2020)

Leigh Syndrome: A Tale of Two Genomes
por: Bakare, Ajibola B., et al.
Publicado: (2021)

Leigh syndrome: MRI findings in two children
por: Kartikasalwah, AL, et al.
Publicado: (2010)

Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations
por: Lee, Sunho, et al.
Publicado: (2019)

Why does Leigh syndrome respond to immunotherapy?
por: Finsterer, Josef, et al.
Publicado: (2016)

Leigh Syndrome with atypical cerebellum imaging features
por: da Veiga, Marcos Gil Alberto, et al.
Publicado: (2019)

Leigh syndrome in an infant: autopsy and histopathology findings
por: Saini, Arushi Gahlot, et al.
Publicado: (2021)

Correction: Molecular Time-Course and the Metabolic Basis of Entry into Dauer in Caenorhabditis elegans
por: Jeong, Pan-Young, et al.
Publicado: (2009)

Correction: Molecular Basis of Impaired Glycogen Metabolism during Ischemic Stroke and Hypoxia
Publicado: (2014)

Correction: Unravelling the Structural and Molecular Basis Responsible for the Anti-Biofilm Activity of Zosteric Acid
Publicado: (2015)

Correction: Uncovering the Differential Molecular Basis of Adaptive Diversity in Three Echinochloa Leaf Transcriptomes
Publicado: (2015)

Correction: Molecular basis for a new bovine model of Niemann-Pick type C disease
por: Woolley, Shernae A., et al.
Publicado: (2021)

Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome
por: Wang, Junling, et al.
Publicado: (2021)

Leigh Syndrome in Childhood: Neurologic Progression and Functional Outcome
por: Lee, Jin Sook, et al.
Publicado: (2016)

Phenotypic and genotypic peculiarities in Chinese patients with Leigh syndrome
por: Finsterer, Josef
Publicado: (2019)

Management of Leigh syndrome due to NDUFAF6 variants
por: Finsterer, Josef, et al.
Publicado: (2019)

Commentary: Epilepsy in Leigh Syndrome With Mitochondrial DNA Mutations
por: Finsterer, Josef
Publicado: (2019)

Expression signature of the Leigh syndrome French-Canadian type
por: Bchetnia, Mbarka, et al.
Publicado: (2022)

Leigh syndrome can manifest with intracranial calcifications and bleedings
por: Finsterer, Josef, et al.
Publicado: (2022)

Schizophrenia-Like Psychotic Symptoms Associated to Leigh Syndrome
por: Jaballah, F., et al.
Publicado: (2023)

Leigh syndrome is the main clinical characteristic of PTCD3 deficiency
por: Muñoz‐Pujol, Gerard, et al.
Publicado: (2022)

Corrigendum: Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome
por: Wang, Junling, et al.
Publicado: (2021)

Leigh Syndrome Mimicking Wernicke's Encephalopathy: A Case Report
Publicado: (2020)

A case report of Leigh syndrome diagnosed by endomyocardial biopsy
por: Maruo, Yuji, et al.
Publicado: (2021)

Activated microglia and neuroinflammation as a pathogenic mechanism in Leigh syndrome
por: Daneshgar, Nastaran, et al.
Publicado: (2023)

Dr. Leigh H. Hunt
Publicado: (1883)

SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey
por: Kose, Melis, et al.
Publicado: (2020)

Author Correction: Molecular basis for heat desensitization of TRPV1 ion channels
por: Luo, Lei, et al.
Publicado: (2020)

Clinical Characteristics of Early-Onset and Late-Onset Leigh Syndrome
por: Hong, Chan-Mi, et al.
Publicado: (2020)

Novel mutation in mitochondrial DNA in 2 siblings with Leigh syndrome
por: Veerapandiyan, Aravindhan, et al.
Publicado: (2016)

Leigh Syndrome and SURF1 Gene Presenting with Febrile Seizure
por: Panda, Prateek Kumar, et al.
Publicado: (2021)

Genetic and Mitochondrial Metabolic Analyses of an Atypical Form of Leigh Syndrome
por: Uittenbogaard, Martine, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_2vqf6fpsr22j8n1nlk2a8g1sqm