Anesthetic management in Charcot-Marie-Tooth disease type 2 due to a mutation in the mitofusin-2 gene

Anesthetic management in Charcot-Marie-Tooth disease type 2 due to a mutation in the mitofusin-2 gene

Bibliographic Details
Main Authors:	Paolo Vinci, Giovanni Lapi
Format:	Article
Language:	English
Published:	Wolters Kluwer Medknow Publications 2011-01-01
Series:	Journal of Anaesthesiology Clinical Pharmacology
Online Access:	http://www.joacp.org/article.asp?issn=0970-9185;year=2011;volume=27;issue=2;spage=286;epage=287;aulast=Vinci

Similar Items

Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (<it>MFN2</it>)
by: Haas Gerhard, et al.
Published: (2006-06-01)

Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutation
by: Paola Zanfardino, et al.
Published: (2022-12-01)

Charcot–Marie–Tooth Disease
by: Hafiz Muhammad Noman, Haleema Akbar et al
Published: (2018-06-01)

CHARCOT-MARIE-TOOTH DISEASE
by: Lea Leonardis, et al.
Published: (2003-09-01)

Charcot-Marie-Tooth disease
by: Alulin Tácio Quadros Santos Monteiro Fonseca, MD, et al.
Published: (2018-09-01)

Atypical presentation of Charcot-Marie-Tooth disease type 2Q by mutations on DHTKD1 and NTRK2 genes
by: Dulce M. Castro-Coyotl, et al.
Published: (2021-01-01)

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.
by: Bolino, A, et al.
Published: (2000)

Charcot-Marie-Tooth 2F (Hsp27 mutations): A review
by: Nicholas U. Schwartz
Published: (2019-10-01)

Novel mutation in the periaxin gene causal to Charcot–Marie–Tooth disease type 4F
by: Yu-hui Chen, et al.
Published: (2020-10-01)

Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking
by: Haicui Wang, et al.
Published: (2019-10-01)

Rehabilitation in Charcot-Marie-Tooth disease type 1
by: Manoj Mannil, et al.
Published: (2014-09-01)

A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.
by: Young Bin Hong, et al.
Published: (2016-02-01)

Physiotherapy of Charcot–Marie–Tooth disease
by: N. A. Shnayder, et al.
Published: (2015-02-01)

Alterações audiológicas na doença de Charcot-Marie-Tooth Audiological findings in the Charcot-Marie-Tooth disease
by: Erika Fukushima, et al.
Published: (2011-02-01)

Enfermedad de Charcot Marie Tooth en un niño Charcot-Marie-Tooth disease in a child
by: Teresa Vidal Pérez, et al.
Published: (2012-11-01)

Novel homozygous mutations in Pakistani families with Charcot–Marie–Tooth disease
by: Sumaira Kanwal, et al.
Published: (2021-06-01)

Dominant mutations in ITPR3 cause Charcot‐Marie‐Tooth disease
by: Julius Rönkkö, et al.
Published: (2020-10-01)

Human Rab7 mutation mimics features of Charcot–Marie–Tooth neuropathy type 2B in Drosophila
by: Katrien Janssens, et al.
Published: (2014-05-01)

Therapeutic Development in Charcot Marie Tooth Type 1 Disease
by: Pierre Miniou, et al.
Published: (2021-06-01)

Multiple respiratory complications in a patient with Charcot-Marie-Tooth disease with MFN2 mutation
by: Tomoya Sano, et al.
Published: (2022-01-01)

Charcot-Marie-Tooth 2B mutations in rab7 cause dosage-dependent neurodegeneration due to partial loss of function
by: Smita Cherry, et al.
Published: (2013-12-01)

Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients
by: Na Young Jung, et al.
Published: (2022-07-01)

Neurofilaments in health and Charcot-Marie-Tooth disease
by: Farah Kotaich, et al.
Published: (2023-12-01)

Progress in treatment of Charcot-Marie-Tooth disease
by: Ru-xu ZHANG, et al.
Published: (2017-08-01)

Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth disease.
by: Duane L Guernsey, et al.
Published: (2010-08-01)

A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease
by: Abdoulaye Yalcouyé, et al.
Published: (2019-07-01)

Pé cavo adquirido na doença de Charcot-Marie-Tooth Acquired pes cavus in Charcot-Marie-Tooth disease
by: Daniel Augusto Carvalho Maranho, et al.
Published: (2009-01-01)

Two novel missense mutations in the myelin protein zero gene causes Charcot-Marie-Tooth type 2 and Déjérine-Sottas syndrome
by: Sand Jette C, et al.
Published: (2010-04-01)

Correction: The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan
Published: (2012-01-01)

Correction: The Mutational Spectrum in a Cohort of Charcot-Marie-Tooth Disease Type 2 among the Han Chinese in Taiwan.
by: Kon-Ping Lin, et al.
Published: (2012-01-01)

Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation
by: Hideki Hayashi, et al.
Published: (2023-12-01)

X-linked Charcot Marie Tooth mutations alter CO2 sensitivity of connexin32 hemichannels
by: Jack Butler, et al.
Published: (2023-12-01)

Peripheral myelin protein 2 – a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy
by: Paulius Palaima, et al.
Published: (2019-08-01)

Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2
by: Salla Ruskamo, et al.
Published: (2017-07-01)

CASE REPORT OF ADULT-ONSET CHARCOT MARIE TOOTH TYPE X
by: Richard Suherlim, et al.
Published: (2022-01-01)

Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1)
by: Fairweather, N, et al.
Published: (1994)

Targeting muscle to treat Charcot-Marie-Tooth disease
by: David Villarroel-Campos, et al.
Published: (2024-01-01)

The Current State of Charcot–Marie–Tooth Disease Treatment
by: Yuji Okamoto, et al.
Published: (2023-07-01)

Emerging Therapies for Charcot-Marie-Tooth Inherited Neuropathies
by: Marina Stavrou, et al.
Published: (2021-06-01)

Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease
by: Cara R. Schiavon, et al.
Published: (2021-02-01)