Aya Kitou: Resilience capacity according to the Boris Cyrulnik biopsychosocial model

Aya Kitou: Resilience capacity according to the Boris Cyrulnik biopsychosocial model

Abstract Objective: Spinocerebellar ataxia type 2, an orphan disease also known as spinocerebellar degeneration, is characterized by a degenerative process of the cerebellum and spinal cord. Method Biographical review of a Japanese woman known as Aya Kitou, using a qualitative approach of discours...

Full description

Bibliographic Details
Main Authors:	Stephanie Ginneth Martínez-Rojas, Nolly Nataly Castañeda-Ibáñez
Format:	Article
Language:	English
Published:	Pontifícia Universidade Católica de Campinas 2023-09-01
Series:	Estudos de Psicologia (Campinas)
Subjects:	Models, biopsychosocial Emotional intelligence Quality of life Resilience, psychological Spinocerebellar ataxia
Online Access:	http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-166X2023000100603&tlng=en

Similar Items

Otoneurological Abnormalities in Patients with Friedreich's Ataxia
by: Bianca Simone Zeigelboim, et al.
Published: (2017-01-01)

Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype
by: Christopher L. Groth, et al.
Published: (2018-01-01)

Clinical profile and genetic correlation of patients with spinocerebellar ataxia: A study from a tertiary care centre in Eastern India
by: Debabrata Pulai, et al.
Published: (2014-01-01)

Professor Wadia’s contributions to neurology and spinocerebellar ataxia type 2
by: Fernando Spina Tensini, et al.

Research progress of spinocerebellar ataxia type 1
by: Lin-wei ZHANG, et al.
Published: (2014-05-01)

Understanding the Pathophysiology of Spinocerebellar Ataxias through genetics, neurophysiology, structural and functional neuroimaging
by: Pramod Kumar Pal
Published: (2015-12-01)

Twenty-five years since the identification of the first SCA gene: history, clinical features and perspectives for SCA1
by: Carlos Roberto Martins Junior, et al.

Hereditary Cerebellar Ataxias: A Korean Perspective
by: Ji Sun Kim, et al.
Published: (2015-05-01)

Collaborative Efforts for Spinocerebellar Ataxia Research in the United States: CRC-SCA and READISCA
by: Chih-Chun Lin, et al.
Published: (2020-08-01)

A case of Spinocerebellar Ataxia from ethnic tribe of Assam
by: Kayal Ashok, et al.
Published: (2011-01-01)

Dystonia and dysphagia in spinocerebellar ataxia 1 portends a severe phenotype
by: Sahil Mehta, et al.
Published: (2020-01-01)

The history of spinocerebellar ataxia type 10 in Brazil: travels of a gene A história da ataxia espinocerebelar tipo 10 no Brasil: as viagens de um gene
by: Hélio A.G. Teive, et al.
Published: (2007-12-01)

La résilience comme attitude face au malheur : succès et usages des ouvrages de Boris Cyrulnik
by: Nicolas Marquis
Published: (2018-03-01)

Informe preliminar acerca de ataxia espinocerebelosa en la provincia de Ciego de Ávila A preliminary report on the spinocerebellar ataxia in Ciego de Avila province
by: Aldo Amado Sigler Villanueva, et al.
Published: (2011-06-01)

Effectiveness of Robotic Exoskeleton-Assisted Gait Training in Spinocerebellar Ataxia: A Case Report
by: San-Ha Kim, et al.
Published: (2021-07-01)

A trial of topiramate for patients with hereditary spinocerebellar ataxia
by: Shiroh Miura, et al.
Published: (2023-02-01)

New Nonsense Variant c.2983G>T; p.Glu995* in the Gene Causes Progressive Autosomal Dominant Ataxia
by: Yannic Saathoff, et al.
Published: (2021-01-01)

Preliminary Clinical Trial of Balance Compensation System for Improvement of Balance in Patients With Spinocerebellar Ataxia
by: Ji Seon Hong, et al.
Published: (2020-08-01)

Pseudoproptosis in a case of familial hereditary cerebellar ataxia
by: Pratheeba D Nivean, et al.
Published: (2022-01-01)

Itajaí, Santa Catarina – Azorean ancestry and spinocerebellar ataxia type 3
by: Hélio A. G. Teive, et al.

Clinical phenotype and genetic mutation of one case with head tremor and cerebellar atrophy
by: Kun-ming XIE, et al.
Published: (2017-07-01)

The History of Gene Hunting in Hereditary Spinocerebellar Degeneration: Lessons From the Past and Future Perspectives
by: Ashraf Yahia, et al.
Published: (2021-03-01)

Genetic Screening for Spinocerebellar Ataxia Genes in a Japanese Single-Hospital Cohort
by: Ryuji Sakakibara, et al.
Published: (2017-09-01)

Clinical and genetic profile in index patients with spinocerebellar ataxia type 3 in Indonesia: case report
by: Siti Aminah, et al.
Published: (2021-07-01)

Biopsychosocial Benefits of Physical Activity in Children
by: Ayse Meydanlioglu
Published: (2015-06-01)

Validity of the biopsychosocial model in contemporary psychiatry
by: Joel Philip, et al.
Published: (2020-01-01)

The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population
by: Nejat Mahdieh, et al.
Published: (2024-04-01)

A Difficult Case to Diagnose: Machado-Joseph Disease/Spinocerebellar Ataxia Type III
by: Muhammad Sohail Ajmal Ghoauri, et al.
Published: (2023-12-01)

MRI Findings in a Patient with Known SCAR-16 Type STUB1 Associated Cerebellar Ataxia
by: Alexander Thorvaldsson, et al.
Published: (2022-12-01)

Evaluation of various movement disorders in patients of genetically proven spinocerebellar ataxia: A study from a Tertiary Care Center in Northern India
by: Divya M Radhakrishnan, et al.
Published: (2018-01-01)

Evidence and practices of the use of next generation sequencing in patients with undiagnosed autosomal dominant cerebellar ataxias: a review
by: Luiz Eduardo NOVIS, et al.
Published: (2020-07-01)

Transcriptome Profile of a New Mouse Model of Spinocerebellar Ataxia Type 14 Implies Changes in Cerebellar Development
by: Szilvia E. Mezey, et al.
Published: (2022-08-01)

Use of Riluzole for the Treatment of Hereditary Ataxias: A Systematic Review
by: Iván Nicolas Ayala, et al.
Published: (2022-08-01)

Increased Actin Binding Is a Shared Molecular Consequence of Numerous SCA5 Mutations in β-III-Spectrin
by: Alexandra E. Atang, et al.
Published: (2023-08-01)

Magnetic resonance in the diagnosis of the most common forms of spinocerebellar ataxia
by: Tamaš Olivera, et al.
Published: (2023-01-01)

Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population
by: Szu‐Ju Chen, et al.
Published: (2019-10-01)

Spinocerebellar ataxia type 6 in eastern India: Some new observations
by: Kalyan B Bhattacharyya, et al.
Published: (2016-01-01)

Computational neurobiology is a useful tool in translational neurology: the example of ataxia
by: Sherry-Ann eBrown, et al.
Published: (2015-01-01)

Quantitative gait analysis in patients with spinocerebellar ataxia—An explorative analysis
by: Tittu Thomas James, et al.
Published: (2022-01-01)

The evaluation of swallowing in patients with spinocerebellar ataxia and oropharyngeal dysphagia: A comparison study of videofluoroscopic and sonar doppler
by: Abdulmassih, Edna Márcia da Silva, et al.
Published: (2013-01-01)