Works matching DE "ATAXIA"

Results: 3016

Gait ataxia in alcohol use disorder: A systematic review.

Published in:

2024

By:

Mistarz, Nicolaj;
Canfield, Lind;
Nielsen, Dorthe Grüner;
Skøt, Lotte;
Mellentin, Angelina Isabella

Publication type:

Journal Article

Children use common knowledge to solve coordination problems.

Published in:

2023

By:

Deutchman, Paul;
McAuliffe, Katherine

Publication type:

Journal Article

Movement drift in optic ataxia reveals deficits in hand state estimation in oculocentric coordinates.

Published in:

2021

By:

Mikula, Laura;
Blohm, Gunnar;
Koun, Éric;
Khan, Aarlenne Z.;
Pisella, Laure

Publication type:

Journal Article

Implicit contextual learning in spinocerebellar ataxia.

Published in:

2020

By:

Ulasoglu-Yildiz, Cigdem;
Gurvit, Hakan

Publication type:

Journal Article

Autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCA-DN) associated with progressive cognitive and behavioral deterioration.

Published in:

2017

By:

Walker, Lisa A. S.;
Bourque, Pierre;
Smith, Andra M.;
Warman Chardon, Jodi

Publication type:

Journal Article

Mutational ataxia resulting from abnormal vestibular acquisition and processing is partially compensated for.

Published in:

2012

By:

Kopecky, Benjamin;
DeCook, Rhonda;
Fritzsch, Bernd

Publication type:

Journal Article

Capturing the fragile X premutation phenotypes: A collaborative effort across multiple cohorts.

Published in:

2012

By:

Hunter, Jessica Ezzell;
Sherman, Stephanie;
Grigsby, Jim;
Kogan, Cary;
Cornish, Kim

Publication type:

Journal Article

Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome.

Published in:

2011

By:

Allen, Emily Graves;
Hunter, Jessica E.;
Rusin, Michele;
Juncos, Jorge;
Novak, Gloria;
Hamilton, Debra;
Shubeck, Lisa;
Charen, Krista;
Sherman, Stephanie L.

Publication type:

Journal Article

Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome.

Published in:

2008

By:

Grigsby, Jim;
Brega, Angela G.;
Engle, Karen;
Leehey, Maureen A.;
Hagerman, Randi J;
Tassone, Flora;
Hessl, David;
Hagerman, Paul J.;
Cogswell, Jennifer B.;
Bennett, Rachael E.;
Cook, Kylee;
Hall, Deborah A.;
Bounds, Lanee S.;
Paulich, Marsha J.;
Reynolds, Ann

Publication type:

Journal Article

Screening for ENU-induced mutations in mice that result in aberrant ethanol-related phenotypes.

Published in:

2007

By:

Hamre, Kristin M.;
Goldowitz, Daniel;
Wilkinson, Sarah;
Matthews, Douglas B.

Publication type:

Journal Article

Self-administration cues as signals: Drug self-administration and tolerance.

Published in:

2001

By:

Weise-Kelly, Lorraine;
Siegel, Shepard

Publication type:

Journal Article

Genetic determinants of sensitivity to diazepam in inbred mice.

Published in:

1998

By:

Crabbe, John C.;
Gallaher, Edward J.;
Cross, Stephen J.;
Belknap, John K.

Publication type:

Journal Article

Associative learning in patients with cerebellar ataxia.

Published in:

1996

By:

Tucker, J.;
Harding, A. E.;
Jahanshahi, M.;
Nixon, P. D.;
Rushworth, M.;
Quinn, N. P.;
Thompson, P. D.;
Passingham, R. E.

Publication type:

Journal Article

Stress controllability influences the ataxic properties of both ethanol and midazolam in the rat.

Published in:

1996

By:

Drugan, Robert C.;
Coyle, Tara S.;
Healy, Denis J.;
Chen, Sako

Publication type:

Journal Article

Genetic determinants of sensitivity to ethanol in inbred mice.

Published in:

1994

By:

Crabbe, John C.;
Gallaher, Edward S.;
Phillips, Tamara J.;
Belknap, John K.

Publication type:

Journal Article

Sensitivity to ethanol in inbred mice: Genotypic correlations among several behavioral responses.

Published in:

1983

By:

Crabbe, John C.

Publication type:

Journal Article

Body sway and vision.

Published in:

1946

By:

Edwards, A. S.

Publication type:

Journal Article

Nervous and mental disorders.

Published in:: 1926
Publication type:: Abstract Collection

The clinical and psychopathological aspects of dementia praecox (ueber die dementia praecox, streifzüge durch klinik und psychopathologie.).

Published in:

1911

By:

Coriat, Isador H.

Publication type:

Review-Book

Motor pathology.

Published in:: 1905
Publication type:: Review-Book

Review of Eugenical sterilization: A reorientation of the problem.

Published in:

1939

By:

Lowrey, Lawson G.

Publication type:

Review-Book

Sedatives and suggestibility in neurotic patients.

Published in:

1961

By:

Ingham, J. G.;
White, J. M.

Publication type:

Journal Article

Review of Motor Ataxia From Emotion.

Published in:

1910

By:

Miles, Walter R.

Publication type:

Review-Book

Review of Diagnostic Symptoms in Nervous Diseases.

Published in:: 1914
Publication type:: Review-Book

Review of Locomotor ataxia (tabes dorsalis). An introduction to the study and treatment of nervous diseases. For students and practitioners.

Published in:

1921

By:

Solomon, Meyer

Publication type:

Review-Book

Childhood Chronic Progressive Ataxia with Normal Neuroimaging: Think of CONDSIAS.

Published in:

2025

By:

Bhanudeep, Singanamalla;
Koneti, Bramhini Bhargavi

Publication type:

Letter

Cerebellum-Predominant Progressive Multifocal Leukoencephalopathy: An Under-recognized Cause of Cerebellar Syndrome among People with Human Immunodeficiency Virus Infection.

Published in:

Neurology India, 2025, v. 73, n. 3, p. 519, doi. 10.4103/neurol-india.Neurol-India-D-23-00603

By:

Kumar, Selwyn Selva;
Gautam, Priyanka;
Vanjare, Harshad Arvind;
Kumar, P Prasanna;
Abraham, Asha Mary;
Karthik, Rajiv;
Manesh, Abi

Publication type:

Article

Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse.

Published in:

Neurogenetics, 2004, v. 5, n. 4, p. 229, doi. 10.1007/s10048-004-0197-9

By:

Mannan, Ashraf U.;
Roussa, Elena;
Kraus, Cornelia;
Rickmann, Micheal;
Maenner, Joerg;
Nayernia, Karim;
Krieglstein, Kerstin;
Reis, André;
Engel, Wolfgang

Publication type:

Article

Private SACS mutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) families from Turkey.

Published in:

Neurogenetics, 2004, v. 5, n. 3, p. 165, doi. 10.1007/s10048-004-0179-y

By:

Richter, Andrea M.;
Koksal Ozgul, Riza;
Poisson, Virginie C.;
Topaloglu, Hauk

Publication type:

Article

Novel splice site CACNA1A mutation causing episodic ataxia type 2.

Published in:

Neurogenetics, 2004, v. 5, n. 1, p. 69, doi. 10.1007/s10048-003-0161-0

By:

Kaunisto, M. A.;
Harno, H.;
Kallela, M.;
Somer, H.;
Sallinen, R.;
Hämäläinen, E.;
Miettinen, P. J.;
Vesa, J.;
Orpana, A.;
Palotie, A.;
Färkkilä, M.;
Wessman, M.

Publication type:

Article

Efficiency of a 3-week multicomponent rehabilitation on improving the function in a patient with Friedreich's ataxia - a case report.

Published in:

Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2023, v. 80, n. 2, p. 182, doi. 10.2298/VSP220209027S

By:

Samardžić, Vesna

Publication type:

Article

UN MODELO BASADO EN ECUACIONES DIFERENCIALES ORDINARIAS PARA ESTUDIOS DE LOS MOVIMIENTOS SACÁDICOS EN PACIENTES CON ATAXIA ESPINOCEREBELOSA DE TIPO 2 (SCA2).

Published in:

Revista Cubana de Física, 2018, v. 35, n. 1E, p. E38

By:

MORA, C.;
VELÁZQUEZ, C.;
URQUIZA, R.;
BECERRA, R.;
VÁZQUEZ, E.

Publication type:

Article

Simultaneous Axillary–Carotid and Carotid–Axillary Bypass.

Published in:

Indian Journal of Surgery, 2021, v. 83, n. 1, p. 330, doi. 10.1007/s12262-020-02325-5

By:

Qi, Yixia;
Li, Liqiang;
Cui, Shijun;
Yan, Lin;
Gu, Yongquan

Publication type:

Article

Novel Compound Heterozygous Mutation on MYORG Gene in a Chinese Patient with Primary Familial Brain Calcification.

Published in:

2025

By:

Lin, Jixiang;
Wang, Yanfei;
Gao, Xiang;
Liu, Xiaomin

Publication type:

Letter

Adult-onset Migraine and Very Late Onset Ataxia Due to a Novel Pathogenic Variant of the CACNA1A Gene.

Published in:

Neurology India, 2023, v. 71, n. 6, p. 1307, doi. 10.4103/0028-3886.391362

By:

Bhattacharjee, Shakya;
Paramanandam, Vijayshankar

Publication type:

Article

Craniovertebral Junction Anomalies: An Overlooked Cause of 'Posterior Circulation Stroke'.

Published in:

Neurology India, 2022, v. 70, p. 149, doi. 10.4103/0028-3886.360916

By:

Garg, Kanwaljeet;
Tandon, Vivek;
Kumar, Rajinder;
Chandra, P;
Kale, Shashank;
Sharma, Bhawani;
Mahapatra, Ashok;
Chandra, P Sarat;
Kale, Shashank S;
Sharma, Bhawani Shankar;
Mahapatra, Ashok K

Publication type:

Article

Clinical and Molecular Spectrum of Degenerative Cerebellar Ataxia: A Single Centre Study.

Published in:

2022

By:

Balakrishnan, Surya;
Aggarwal, Shagun;
Muthulakshmi, Mayandi;
Meena, Angamuthu;
Borgohain, Rupam;
Mridula, Kandadai;
Yareeda, Sireesha;
Ranganath, Prajnya;
Dalal, Ashwin;
Meena, Angamuthu Kanikannan;
Mridula, Kandadai Rukmini

Publication type:

Journal Article

Paroxysmal Dysarthria Ataxia-Tremor-Blepharospasm Syndrome in Bickerstaff Brainstem Encephalitis; A Variant of Paroxysmal Dysarthria Ataxia Syndrome.

Published in:

2022

By:

Maramattom, Boby;
Maramattom, Boby Varkey

Publication type:

Letter

The Effect of the Activation of the Core Muscles on Tremor in a Patient with Multiple Sclerosis.

Published in:

2021

By:

Usta, Aysegul;
Salcı, Yeliz;
Yildiz, Fatma;
Çakmaklı, Gül;
Armutlu, Kadriye;
Yildiz, Fatma Gökcem;
Çakmaklı, Gül Yalçın

Publication type:

Case Study

Lamotrigine-Associated Movement Disorder: A Literature Review.

Published in:

2021

By:

Rissardo, Jamir;
Fornari Caprara, Ana;
Rissardo, Jamir Pitton;
Fornari Caprara, Ana L

Publication type:

journal article

Mutations in the Voltage Dependent Calcium Channel (P/Q type alpha 1A subunit) Causing Neurological Disorders - An Overview.

Published in:

2021

By:

Manickam, Agaath;
Ramasamy, Sivasamy;
Manickam, Agaath Hedina

Publication type:

journal article

Paroxysmal Dysarthria Ataxia-Tremor-Blepharospasm Syndrome in Bickerstaff Brainstem Encephalitis: A Variant of Paroxysmal Dysarthria Ataxia Syndrome.

Published in:

2021

By:

Ferrante, Enrico;
Trimboli, Michele

Publication type:

Letter

Novel Compound Heterozygous SACS Mutations in a Case with a Spasticity-Lacking Phenotype of Sacsin-Related Ataxia.

Published in:

2021

By:

Chen, You;
Cen, Zhidong;
Zheng, Xiaosheng;
Chen, Si;
Xie, Fei;
Luo, Wei

Publication type:

Case Study

Tumors masquerading as neurological diseases: A caution for clinicians in planning diagnosis and treatment.

Published in:

2020

By:

Vidhya Annapoorni, C;
Retnaswami, Chandra;
Mailankody, Pooja;
Katragadda, Pavan;
Pillai, Sivakumar;
Rangarajan, Anush;
Padmanabha, Hansashree;
Pendharkar, Hima;
Vidhya Annapoorni, C S;
Retnaswami, Chandra Sadanandavalli;
Pillai, Sivakumar Krishna

Publication type:

journal article

Paroxysmal Dysarthria Ataxia-Tremor-Blepharospasm Syndrome in Bickerstaff Brainstem Encephalitis: A Variant of Paroxysmal Dysarthria Ataxia Syndrome.

Published in:

2019

By:

Maramattom, Boby;
Maramattom, Boby Varkey

Publication type:

Case Study

Opsoclonus myoclonus ataxia syndrome.

Published in:

2018

By:

Khadilkar, Satish;
Benny, Rajesh

Publication type:

journal article

Episodic ataxia in a child with senataxin mutation.

Published in:

2018

By:

Sesh, S.;
Radhakrishnan, Ashalatha

Publication type:

Case Study

Diffuse cerebellar hypometabolism in 18FDG PET-CT in two long-term followed patients with diagnosis of nonprogressive congenital ataxia.

Published in:

2018

By:

Don-Kyu Kim;
Si Hyun Kang;
Kyung Mook Seo;
Kim, Don-Kyu;
Kang, Si Hyun;
Seo, Kyung Mook

Publication type:

Case Study

Effects of Sex and Gender on Adaptation to Space: Neurosensory Systems.

Published in:

2014

By:

Reschke, Millard F.;
Cohen, Helen S.;
Cerisano, Jody M.;
Clayton, Janine A.;
Cromwell, Ronita;
Danielson, Richard W.;
Hwang, Emma Y.;
Tingen, Candace;
Allen, John R.;
Tomko, David L.

Publication type:

Journal Article

Mitochondrial dysfunction in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome: prospect use of antioxidants and mitochondrial nutrients.

Published in:

Molecular Biology Reports, 2024, v. 51, n. 1, p. 1, doi. 10.1007/s11033-024-09415-7

By:

Pagano, Giovanni;
Lyakhovich, Alex;
Pallardó, Federico V.;
Tiano, Luca;
Zatterale, Adriana;
Trifuoggi, Marco

Publication type:

Article