Cargando…

Long-term outcomes after surgery to prevent aspiration for patients with amyotrophic lateral sclerosis

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease that affects motor neurons selectively. In particular, weakness in respiratory and swallowing muscles occasionally causes aspiration pneumonia and choking, which can be lethal. Surgery to prevent aspiration, w...

Descripción completa

Detalles Bibliográficos
Autores principales:	Soga, Temma, Suzuki, Naoki, Kato, Kengo, Kawamoto-Hirano, Ai, Kawauchi, Yuko, Izumi, Rumiko, Toyoshima, Masaya, Mitsuzawa, Shio, Shijo, Tomomi, Ikeda, Kensuke, Warita, Hitoshi, Katori, Yukio, Aoki, Masashi, Kato, Masaaki
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8925201/ https://www.ncbi.nlm.nih.gov/pubmed/35296264 http://dx.doi.org/10.1186/s12883-022-02619-z

Ejemplares similares

TARDBP p.G376D mutation, found in rapid progressive familial ALS, induces mislocalization of TDP-43
por: Mitsuzawa, Shio, et al.
Publicado: (2018)

Interstitial pneumonia and other adverse events in riluzole-administered amyotrophic lateral sclerosis patients: a retrospective observational study
por: Inoue-Shibui, Aya, et al.
Publicado: (2019)

AMPK Complex Activation Promotes Sarcolemmal Repair in Dysferlinopathy
por: Ono, Hiroya, et al.
Publicado: (2020)

Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations
por: Mitsuzawa, Shio, et al.
Publicado: (2021)

Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons
por: Akiyama, Tetsuya, et al.
Publicado: (2019)

Spinal Cord Infarction in an Adolescent with Protein S Deficiency: A Case Report and Literature Review
por: Kubota, Takafumi, et al.
Publicado: (2023)

Genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing
por: Izumi, Rumiko, et al.
Publicado: (2015)

Sporadic Inclusion Body Myositis Manifesting as Isolated Muscle Weakness of the Finger Flexors Three Years after Disease Onset
por: Suwa, Yuichi, et al.
Publicado: (2016)

Malignant otitis externa presenting cerebral infarction from pseudoaneurysm: A case report and a review of the literature
por: Koshiba, Yasutoshi, et al.
Publicado: (2022)

Omics Approach to Axonal Dysfunction of Motor Neurons in Amyotrophic Lateral Sclerosis (ALS)
por: Suzuki, Naoki, et al.
Publicado: (2020)

Genetics of amyotrophic lateral sclerosis: seeking therapeutic targets in the era of gene therapy
por: Suzuki, Naoki, et al.
Publicado: (2022)

Improvement of a delayed swallowing reflex following treatment for advanced head and neck cancer
por: Ohkoshi, Akira, et al.
Publicado: (2020)

Proteasome dysfunction induces muscle growth defects and protein aggregation
por: Kitajima, Yasuo, et al.
Publicado: (2014)

Efficacy confirmation study of aceneuramic acid administration for GNE myopathy in Japan
por: Mori-Yoshimura, Madoka, et al.
Publicado: (2023)

Phase II/III Study of Aceneuramic Acid Administration for GNE Myopathy in Japan
por: Suzuki, Naoki, et al.
Publicado: (2023)

Changes in tongue pressure and dysphagia at oral cancer patients by palatal augmentation prosthesis
por: Kuniyuki, Izumita, et al.
Publicado: (2021)

Characteristics of aspiration pneumonia patients in acute care hospitals: A multicenter, retrospective survey in Northern Japan
por: Suzuki, Jun, et al.
Publicado: (2021)

Prevalence and association of self-reported anxiety, pain, and oral parafunctional habits with temporomandibular disorders in Japanese children and adolescents: a cross-sectional survey
por: Karibe, Hiroyuki, et al.
Publicado: (2015)

Comparison of self-reported pain intensity, sleeping difficulty, and treatment outcomes of patients with myofascial temporomandibular disorders by age group: a prospective outcome study
por: Karibe, Hiroyuki, et al.
Publicado: (2014)

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan
por: Suzuki, Naoki, et al.
Publicado: (2016)

Investigation of non-motor symptoms in patients with amyotrophic lateral sclerosis
por: Hirayama, Takehisa, et al.
Publicado: (2022)

An Amyotrophic Lateral Sclerosis-Associated Mutant of C21ORF2 Is Stabilized by NEK1-Mediated Hyperphosphorylation and the Inability to Bind FBXO3
por: Watanabe, Yasuaki, et al.
Publicado: (2020)

Postoperative Swallowing Function in Patients with Deep Neck Infection
por: Ashizawa, Shohei, et al.
Publicado: (2023)

Isolated inclusion body myopathy caused by a multisystem proteinopathy–linked hnRNPA1 mutation
por: Izumi, Rumiko, et al.
Publicado: (2015)

The precursor osteoblast-like cell, MC3T3-E1 cell line, enhances sodium–calcium exchanger 1 (Ncx1) gene expression by stretch stimuli prior to osteoblast differentiation
por: WARITA, Katsuhiko, et al.
Publicado: (2019)

Randomized phase 2 study of perampanel for sporadic amyotrophic lateral sclerosis
por: Aizawa, Hitoshi, et al.
Publicado: (2021)

Colocalization of 14-3-3 Proteins with SOD1 in Lewy Body-Like Hyaline Inclusions in Familial Amyotrophic Lateral Sclerosis Cases and the Animal Model
por: Okamoto, Yoko, et al.
Publicado: (2011)

Evaluation of 3-Borono-l-Phenylalanine as a Water-Soluble Boron Neutron Capture Therapy Agent
por: Kondo, Naoya, et al.
Publicado: (2022)

The updated retrospective questionnaire study of sporadic inclusion body myositis in Japan
por: Suzuki, Naoki, et al.
Publicado: (2019)

Osseous Hamartoma Arising from the Eustachian Tube
por: Kawamoto, Ai, et al.
Publicado: (2013)

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes
por: Takeuchi, Ryoko, et al.
Publicado: (2016)

TDP-43 Accumulation Within Intramuscular Nerve Bundles of Patients With Amyotrophic Lateral Sclerosis
por: Kurashige, Takashi, et al.
Publicado: (2022)

Centromere Plasmid: A New Genetic Tool for the Study of Plasmodium falciparum
por: Iwanaga, Shiroh, et al.
Publicado: (2012)

Identification of an AP2-family Protein That Is Critical for Malaria Liver Stage Development
por: Iwanaga, Shiroh, et al.
Publicado: (2012)

An In Vitro Model for Lewy Body-Like Hyaline Inclusion/Astrocytic Hyaline Inclusion: Induction by ER Stress with an ALS-Linked SOD1 Mutation
por: Yamagishi, Satoru, et al.
Publicado: (2007)

A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features
por: Sainouchi, Makoto, et al.
Publicado: (2021)

New real-time patient radiation dosimeter for use in radiofrequency catheter ablation
por: Kato, Mamoru, et al.
Publicado: (2019)

Control of Genetically Prescribed Protein Tyrosine Kinase Activities by Environment-Linked Redox Reactions
por: Nakashima, Izumi, et al.
Publicado: (2011)

Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis
por: Yamashita, Satoshi, et al.
Publicado: (2015)

Correction to: A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features
por: Sainouchi, Makoto, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_0g3p7d76vgnvurqfg432hai28l