نتایج جستجو برای: oculomotor apraxia

تعداد نتایج: 7081  

Journal: :Journal of neurophysiology 2009
Scott A Stevenson James K Elsley Brian D Corneil

The "gap effect" describes a phenomenon whereby saccadic reaction times are expedited by the removal of a visible fixation point prior to target presentation. Here we investigated whether processes controlling saccade cancellation are also subjected to a gap effect. Human subjects performed a countermanding experiment that required them to try to cancel an impending saccade in the presence of a...

Journal: :Brain : a journal of neurology 2005
Cindy Zadikoff Anthony E Lang

The definition of apraxia specifies that the disturbance of performed skilled movements cannot be explained by the more elemental motor disorders typical of patients with movement disorders. Generally this does not present a significant diagnostic problem when dealing with 'higher-level' praxic disturbances (e.g. ideational apraxia), but it can be a major confound in establishing the presence o...

Journal: :Developmental Medicine & Child Neurology 2007

2013
Lorenzo Nanetti Simona Cavalieri Viviana Pensato Alessandra Erbetta Davide Pareyson Marta Panzeri Giovanna Zorzi Carlo Antozzi Isabella Moroni Cinzia Gellera Alfredo Brusco Caterina Mariotti

OBJECTIVES/BACKGROUND Ataxia with oculomotor apraxia defines a group of genetically distinct recessive ataxias including ataxia-telangectasia (A-T, ATM gene), ataxia with oculomotor apraxia type 1 (AOA1, APTX gene) and type 2 (AOA2, SETX gene). Although, a few unique clinical features differentiate each of these forms, the patients also share common clinical signs, such as the presence of cereb...

Journal: :European Journal of Radiology 2019

Journal: :Acta medica Iranica 2017
Amene Saghazadeh Sina Hafizi Firouzeh Hosseini Mahmoud Reza Ashrafi Nima Rezaei

Friedreich's ataxia (FRDA) is a rare autosomal recessive spinocerebellar ataxia which in the majority of cases is associated with a GAA-trinucleotide repeat expansion in the first intron of Frataxin gene located on chromosome 9. The clinical features include progressive gait and limb ataxia, cerebellar dysarthria, neuropathy, optic atrophy, and loss of vibration and proprioception. Ataxia with ...

Journal: :Brain : a journal of neurology 2009
M Anheim B Monga M Fleury P Charles C Barbot M Salih J P Delaunoy M Fritsch L Arning M Synofzik L Schöls J Sequeiros C Goizet C Marelli I Le Ber J Koht J Gazulla J De Bleecker M Mukhtar N Drouot L Ali-Pacha T Benhassine M Chbicheb A M'Zahem A Hamri B Chabrol J Pouget R Murphy M Watanabe P Coutinho M Tazir A Durr A Brice C Tranchant M Koenig

Ataxia with oculomotor apraxia type 2 (AOA2) is an autosomal recessive disease due to mutations in the senataxin gene, causing progressive cerebellar ataxia with peripheral neuropathy, cerebellar atrophy, occasional oculomotor apraxia and elevated alpha-feto-protein (AFP) serum level. We compiled a series of 67 previously reported and 58 novel ataxic patients who underwent senataxin gene sequen...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2018
Emer O'Connor Jana Vandrovcova Enrico Bugiardini Viorica Chelban Andreea Manole Indran Davagnanam Sarah Wiethoff Alan Pittman David S Lynch Stephanie Efthymiou Silvia Marino Adnan Y Manzur Mark Roberts Michael G Hanna Henry Houlden Emma Matthews Nicholas W Wood

Letter Mutations in genes involved in singlestrand break repair (SSBR) have been linked to hereditary cerebellar ataxias. Notably, Ataxia-oculomotor apraxia 1 (AOA1 (MIM: 2 08 920)), Spinocerebellar ataxia with axonal neuropathy 1 (SCAN1 (MIM: 6 07 250)) and Ataxia-oculomotor apraxia 4 (AOA4 (MIM: 616267616267616267)) are associated with mutations in APTX (MIM: 606350), TDP1 (MIM: 607198) and P...

Journal: :American journal of human genetics 2001
M C Moreira C Barbot N Tachi N Kozuka P Mendonça J Barros P Coutinho J Sequeiros M Koenig

Ataxia with oculomotor apraxia (AOA) is characterized by early-onset cerebellar ataxia, ocular apraxia, early areflexia, late peripheral neuropathy, slow progression, severe motor handicap, and absence of both telangiectasias and immunodeficiency. We studied 13 Portuguese families with AOA and found that the two largest families show linkage to 9p, with LOD scores of 4.13 and 3.82, respectively...

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