Works matching DE "SPASTIC paralysis"

Results: 299

The Role of a Conserved Arg-Asp Pair in the Structure and Function of Tetanus Neurotoxin.

Published in:

Toxins, 2025, v. 17, n. 6, p. 273, doi. 10.3390/toxins17060273

By:

Wilson, Elizabeth A.;
Bevans, Ashtyn N.;
Baldwin, Michael R.

Publication type:

Article

Challenges of Hip Arthroplasty in a Paretic, Spastic Limb: A Case Study on Managing Femoral Neck Fracture Following Fixation Failure in a Hemiparetic Patient.

Published in:

Journal of Clinical Medicine, 2024, v. 13, n. 14, p. 4023, doi. 10.3390/jcm13144023

By:

Dąbkowska, Izabela;
Sobiech, Lena;
Merkisz, Michał;
Turżańska, Karolina;
Blicharski, Tomasz;
Jankiewicz, Katarzyna

Publication type:

Article

The mu opioid receptor activation does not affect ischemia-induced agonal currents in rat spinal ventral horn.

Published in:

Journal of Anesthesia, 2014, v. 28, n. 6, p. 839, doi. 10.1007/s00540-014-1829-3

By:

Honda, Hiroyuki;
Baba, Hiroshi;
Kohno, Tatsuro

Publication type:

Article

Two Cases of Human T-Lymphotropic Virus Type I-Associated Myelopathy/Tropical Spastic Paraparesis Caused by Living-Donor Renal Transplantation.

Published in:

Case Reports in Neurological Medicine, 2016, p. 1, doi. 10.1155/2016/4203079

By:

Tajima, Yasutaka;
Matsumura, Mariko;
Yaguchi, Hiroaki;
Mito, Yasunori

Publication type:

Article

Spinal cord compression of primary extragonadal giant yolk sac tumor.

Published in:

Spinal Cord, 2007, v. 45, n. 3, p. 254, doi. 10.1038/sj.sc.3101942

By:

Guzel, A.;
Tatli, M.;
Belen, D.;
Seckin, H.

Publication type:

Article

Comparison of muscular and articular factors in the progression of contractures after spinal cord injury in rats.

Published in:

Spinal Cord, 2006, v. 44, n. 3, p. 174, doi. 10.1038/sj.sc.3101802

By:

Moriyama, H.;
Yoshimura, O.;
Sunahori, H.;
Tobimatsu, Y.

Publication type:

Article

Disability profile of patients with HTLV-I-associated myelopathy/tropical spastic paraparesis using the Functional Independence Measure (FIM™).

Published in:

Spinal Cord, 2005, v. 43, n. 4, p. 236, doi. 10.1038/sj.sc.3101677

By:

Franzoi, A. C.;
Araújo, A. Q. C.

Publication type:

Article

Myelopathy and amnesia following accidental electrical injury.

Published in:

Spinal Cord, 2002, v. 40, n. 5, p. 253, doi. 10.1038/sj.sc.3101275

By:

Kalita, J.;
Jose, M.;
Misra, U. K.

Publication type:

Article

Degos disease and spastic paraplegia.

Published in:

Clinical & Experimental Dermatology, 1993, v. 18, n. 4, p. 344, doi. 10.1111/j.1365-2230.1993.tb02214.x

By:

Leslie, T.A.;
Goldsmith, P.C.;
Thompson, A.J.;
Dowd, P.M.

Publication type:

Article

Sonoelastography contribution in cerebral palsy spasticity treatment assessment, preliminary report: A systematic review of the literature apropos of seven patients.

Published in:

Medical Ultrasonography, 2010, v. 12, n. 4, p. 306

By:

Vasilescu, Dan;
Vasilescu, Dana;
Dudea, Sorin;
Botar-Jid, Carolina;
Sfrângeu, Silviu;
Cosma, Dan

Publication type:

Article

Impact of an Educational Film on Parental Knowledge of Children with Cerebral Palsy.

Published in:

International Journal of Pediatrics, 2014, p. 1, doi. 10.1155/2014/573698

By:

Arora, Shilpa Khanna;
Aggarwal, Anju;
Mittal, Hema

Publication type:

Article

Prevalence of developmental enamel defects in children with cerebral palsy.

Published in:

1992

By:

Bhat, Mohandas;
Nelson, Karin B.;
Cummins, Susan K.;
Grether, Judith K.;
Bhat, M;
Nelson, K B;
Cummins, S K;
Grether, J K

Publication type:

journal article

The Effects of Dalfampridine on Hereditary Spastic Paraparesis.

Published in:

European Neurology, 2016, v. 76, n. 3/4, p. 152, doi. 10.1159/000449375

By:

Uygunoglu, Ugur;
Gunduz, Aysegul;
Tutuncu, Melih;
Akalin, Mehmet Ali;
Saip, Sabahattin;
Siva, Aksel

Publication type:

Article

Frequency and Nature of Cerebellar Injury in the Extremely Premature Survivor With Cerebral Palsy.

Published in:

Journal of Child Neurology, 2005, v. 20, n. 1, p. 60, doi. 10.1177/08830738050200011001

By:

Johnsen, Stanley D.

Publication type:

Article

Reduction of pain sensitivity after somatosensory therapy in adults with cerebral palsy.

Published in:

Frontiers in Human Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnhum.2013.00276

By:

Riquelme, Inmaculada;
Zamorano, Anna;
Montoya, Pedro

Publication type:

Article

Human T Lymphotropic Virus Type 1—Associated Myelopathy/Tropical Spastic Paraparesis in an HIV-Positive Patient Coinfected with Human T Lymphotropic Virus Type 2 Following Initiation of Antiretroviral Therapy.

Published in:

Clinical Infectious Diseases, 2007, v. 45, n. 9, p. e118, doi. 10.1086/522172

By:

Toro, Carlos;
Blanco, Francisco;
García-Gascó, Pilar;
Sheldon, Julie;
Benito, José M.;
Rallón, Norma I.;
Soriano, Vincent

Publication type:

Article

Juvenile Human T Lymphotropic Virus Type 1-Associated Myelopathy.

Published in:

2002

By:

Araujo, Alexander P.Q.C.;
Fontenelle, Lucia M.C.;
Padua, Paula A.B.;
Filho, Heber S. Maia;
Araujo, Aberlardo de Q.C.

Publication type:

Case Study

UDRUŽENI ETIOLOŠKI FAKTORI DJEČIJE CEREBRALNE PARALIZE.

Published in:

Medical Journal / Medicinski Žurnal, 2009, v. 15, n. 1/2, p. 40

By:

Švraka, Emira

Publication type:

Article

Late-onset hereditary spastic paraplegia associated with a genetic variant in interferon induced with helicase c domain 1 (IFIH1) gene.

Published in:

QJM: An International Journal of Medicine, 2023, v. 116, n. 7, p. 574, doi. 10.1093/qjmed/hcad055

By:

Zhang, S -Y;
Zhu, L;
Fan, L -L;
Xiang, R;
Zeng, L;
Jin, J -Y

Publication type:

Article

Saccharomyces boulardii improves the behaviour and emotions of spastic cerebral palsy rats through the gut-brain axis pathway.

Published in:

2021

By:

Tao, Deshuang;
Zhong, Tangwu;
Pang, Wei;
li, Xiaojie

Publication type:

journal article

Causal Mechanisms Underlying Periventricular Leukomalacia and Cerebral Palsy.

Published in:

Current Pediatric Reviews, 2005, v. 1, n. 1, p. 1, doi. 10.2174/1573396052953471

By:

Kadhim, Hazim;
Sébire, Guillaume;
Kahn, André;
Evrard, Philippe;
Dan, Bernard

Publication type:

Article

Trunk and Hip Muscle Activation Patterns Are Different During Walking in Young Children With and Without Cerebral Palsy.

Published in:

Physical Therapy, 2010, v. 90, n. 7, p. 986, doi. 10.2522/ptj.20090161

By:

Prosser, Laura A.;
Lee, Samuel C. K.;
VanSant, Ann F.;
Barbe, Mary F.;
Lauer, Richard T.

Publication type:

Article

Social and Community Participation of Children and Youth With Cerebral Palsy Is Associated With Age and Gross Motor Function Classification.

Published in:

Physical Therapy, 2009, v. 89, n. 12, p. 1304, doi. 10.2522/ptj.20090162

By:

Palisano, Robert J.;
Kang, Lin-Ju;
Chiarello, Lisa A.;
Orlin, Margo;
Oeffinger, Donna;
Maggs, Jill

Publication type:

Article

Complications of Intrathecal Baclofen Pumps in Children.

Published in:

Pediatric Neurosurgery, 2003, v. 39, n. 1, p. 1, doi. 10.1159/000070870

By:

Gooch, Judith L.;
Oberg, Wende A.;
Grams, Barbara;
Ward, Lorrie A.;
Walker, Marion L.

Publication type:

Article

Upper Extremity Performance and Self-Care Skill Changes in Children with Spastic Cerebral Palsy following Selective Posterior Rhizotomy.

Published in:

Pediatric Neurosurgery, 1998, v. 29, n. 4, p. 191, doi. 10.1159/000028720

By:

Loewen, Patricia;
Steinbok, Paul;
Holsti, Liisa;
MacKay, Margot

Publication type:

Article

Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant.

Published in:

2018

By:

Helal, Mayada;
Mazaheri, Neda;
Shalbafan, Bita;
Malamiri, Reza Azizi;
Dilaver, Nafi;
Buchert, Rebecca;
Mohammadiasl, Javad;
Golchin, Neda;
Sedaghat, Alireza;
Mehrjardi, Mohammad Yahya Vahidi;
Haack, Tobias B.;
Riess, Olaf;
Chung, Wendy K.;
Galehdari, Hamid;
Shariati, Gholamreza;
Maroofian, Reza

Publication type:

journal article

Novel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysis.

Published in:

2015

By:

Xie, Fei;
Cen, Zhi-dong;
Xiao, Jian-feng;
Luo, Wei

Publication type:

Letter

Mutation of Proteolipid Protein 1 Gene: From Severe Hypomyelinating Leukodystrophy to Inherited Spastic Paraplegia.

Published in:

Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071709

By:

Khalaf, Guy;
Mattern, Claudia;
Begou, Mélina;
Boespflug-Tanguy, Odile;
Massaad, Charbel;
Massaad-Massade, Liliane

Publication type:

Article

PHYSIOTHERAPY TREATMENT IN RESIDENCE TO THE PATIENT WITH SEVERE SPINAL CORD INJURY.

Published in:

Studia Universitatis Vasile Goldis, Physical Education & Physical Therapy Series, 2016, v. 5, n. 1, p. 53

By:

TOMA, Ștefan

Publication type:

Article

Assessment of the Saccular Function in Children with Spastic Cerebral Palsy.

Published in:

Neurophysiology, 2016, v. 48, n. 2, p. 141, doi. 10.1007/s11062-016-9580-z

By:

Akbarfahimi, N.;
.Hosseini, S.;
Rassafiani, M.;
Rezazadeh, N.;
Shahshahani, S.;
Ghomsheh, F.;
Karimlou, M.

Publication type:

Article

Candidate single-nucleotide polymorphisms and cerebral palsy: A case-control study.

Published in:

Biomedical Reports, 2015, v. 3, n. 6, p. 849, doi. 10.3892/br.2015.519

By:

XIAO-GUANG HE;
QI PENG;
YAN-HUA CHEN;
TING HE;
HUI HUANG;
ZE-KE MA;
XUE-JIN FAN;
LING LUO;
SHAO-JI LIU;
XIAO-MEI LU

Publication type:

Article

A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesis.

Published in:

Neuropathology, 2007, v. 27, n. 3, p. 228, doi. 10.1111/j.1440-1789.2007.00766.x

By:

Shrimpton, Antony E.;
Schelper, Robert L.;
Linke, Reinhold P.;
Hardy, John;
Crook, Richard;
Dickson, Dennis W.;
Ishizawa, Takashi;
Davis, Richard L.

Publication type:

Article

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 3, p. 163, doi. 10.1038/jhg.2013.139

By:

Ishiura, Hiroyuki;
Takahashi, Yuji;
Hayashi, Toshihiro;
Saito, Kayoko;
Furuya, Hirokazu;
Watanabe, Mitsunori;
Murata, Miho;
Suzuki, Mikiya;
Sugiura, Akira;
Sawai, Setsu;
Shibuya, Kazumoto;
Ueda, Naohisa;
Ichikawa, Yaeko;
Kanazawa, Ichiro;
Goto, Jun;
Tsuji, Shoji

Publication type:

Article

Four mutations of the spastin gene in Japanese families with spastic paraplegia.

Published in:

Journal of Human Genetics, 2006, v. 51, n. 8, p. 711, doi. 10.1007/s10038-006-0412-7

By:

Basri, Rehana;
Yabe, Ichiro;
Soma, Hiroyuki;
Takei, Asako;
Nishimura, Hiroyuki;
Machino, Yuka;
Kokubo, Yasumasa;
Kosugi, Masafumi;
Okada, Ryuichirou;
Yukitake, Motohiro;
Tachibana, Hisao;
Kuroda, Yasuo;
Kuzuhara, Shigeki;
Sasaki, Hidenao

Publication type:

Article

A novel missense mutation (I344K) in the SPG4 gene in a Korean family with autosomal-dominant hereditary spastic paraplegia.

Published in:

Journal of Human Genetics, 2002, v. 47, n. 9, p. 473, doi. 10.1007/s100380200068

By:

Ki, C.-S.;
Lee, W. Y.;
Han, D. H.;
Sung, D. H.;
Lee, K.-B.;
Lee, K.-A;
Cho, S. S.;
Cho, S.;
Hwang, H.;
Sohn, K. M.;
Choi, Y. J.;
Kim, J.-W.

Publication type:

Article

A Pyramidal Cause of a Cerebellar Ataxia: HSP-7.

Published in:

Case Reports in Neurology, 2020, v. 12, n. 3, p. 329, doi. 10.1159/000509346

By:

Lagrand, Tjerk Joppe;
Hageman, Gerard

Publication type:

Article

Parkinsonism in Association with Dihydropteridine Reductase Deficiency.

Published in:

2017

By:

Takahashi, Yoshiaki;
Manabe, Yasuhiro;
Nakano, Yumiko;
Yunoki, Taijun;
Kono, Syoichiro;
Narai, Hisashi;
Furujo, Mahoko;
Abe, Koji

Publication type:

Case Study

CSF CXCL10, CXCL9, and Neopterin as Candidate Prognostic Biomarkers for HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis.

Published in:

PLoS Neglected Tropical Diseases, 2013, v. 7, n. 10, p. 1, doi. 10.1371/journal.pntd.0002479

By:

Sato, Tomoo;
Coler-Reilly, Ariella;
Utsunomiya, Atae;
Araya, Natsumi;
Yagishita, Naoko;
Ando, Hitoshi;
Yamauchi, Junji;
Inoue, Eisuke;
Ueno, Takahiko;
Hasegawa, Yasuhiro;
Nishioka, Kusuki;
Nakajima, Toshihiro;
Jacobson, Steven;
Izumo, Shuji;
Yamano, Yoshihisa

Publication type:

Article

Clinical and molecular spectrum of a large Egyptian cohort with ALS2‐related disorders of infantile‐onset of clinical continuum IAHSP/JPLS.

Published in:

Clinical Genetics, 2023, v. 104, n. 2, p. 238, doi. 10.1111/cge.14338

By:

Zaki, Maha S.;
Sharaf‐Eldin, Wessam E.;
Rafat, Karima;
Elbendary, Hasnaa M.;
Kamel, Mona;
Elkhateeb, Nour;
Noureldeen, Mahmoud M.;
Abdeltawab, Mohamed A.;
Sadek, Abdelrahim A.;
Essawi, Mona L.;
Lau, Tracy;
Murphy, David;
Abdel‐Hamid, Mohamed S.;
Holuden, Henry;
Issa, Mahmoud Y.;
Gleeson, Joseph G.

Publication type:

Article

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.

Published in:

Clinical Genetics, 2013, v. 83, n. 3, p. 257, doi. 10.1111/j.1399-0004.2012.01896.x

By:

Sánchez‐Ferrero, E;
Coto, E;
Beetz, C;
Gámez, J;
Corao, AI;
Díaz, M;
Esteban, J;
del Castillo, E;
Moris, G;
Infante, J;
Menéndez, M;
Pascual‐Pascual, SI;
López de Munaín, A;
Garcia‐Barcina, MJ;
Alvarez, V

Publication type:

Article

Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.

Published in:

Clinical Genetics, 2012, v. 82, n. 2, p. 157, doi. 10.1111/j.1399-0004.2011.01717.x

By:

Crimella, C;
Baschirotto, C;
Arnoldi, A;
Tonelli, A;
Tenderini, E;
Airoldi, G;
Martinuzzi, A;
Trabacca, A;
Losito, L;
Scarlato, M;
Benedetti, S;
Scarpini, E;
Spinicci, G;
Bresolin, N;
Bassi, MT

Publication type:

Article

Novel homozygous ALS2 nonsense mutation (p.Gln715X) in sibs with infantile-onset ascending spastic paralysis: the first cases from northwestern Europe.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 11, p. 1407, doi. 10.1038/ejhg.2008.108

By:

Verschuuren-Bemelmans, Corien C.;
Winter, Pia;
Sival, Deborah A.;
Elting, Jan-Willem;
Brouwer, Oebele F.;
Müller, Ulrich

Publication type:

Article

Mental deficiency in three families with SPG4 spastic paraplegia.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 1, p. 97, doi. 10.1038/sj.ejhg.5201922

By:

Ribaï, Pascale;
Depienne, Christel;
Fedirko, Estelle;
Jothy, Anne-Catherine;
Viveweger, Caterine;
Hahn-Barma, Valérie;
Brice, Alexis;
Durr, Alexandra

Publication type:

Article

Hereditary spastic paraplegia caused by mutations in the SPG4 gene.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 10, p. 771, doi. 10.1038/sj.ejhg.5200528

By:

Bürger, Joachim;
Fonknechten, Nuria;
Hoeltzenbein, Maria;
Neumann, Luitgart;
Bratanoff, Elfriede;
Hazan, Jamilé;
Reis, André

Publication type:

Article

A refined physical and transcriptional map of the SPG9 locus on 10q23.3–q24.2.

Published in:

European Journal of Human Genetics, 2000, v. 8, n. 10, p. 777, doi. 10.1038/sj.ejhg.5200546

By:

Lo Nigro, Cristiana;
Cusano, Roberto;
Scaranari, Monica;
Cinti, Roberta;
Forabosco, Paola;
Morra, Vincenzo Brescia;
De Michele, Giuseppe;
Santoro, Lucio;
Davies, Sally;
Hurst, Jane;
Devoto, Marcella;
Ravazzolo, Roberto;
Seri, Marco

Publication type:

Article

Risk factors for cerebral palsy in children born at term.

Published in:

Acta Obstetricia et Gynecologica Scandinavica, 2011, v. 90, n. 10, p. 1070, doi. 10.1111/j.1600-0412.2011.01217.x

By:

HIMMELMANN, KATE;
AHLIN, KRISTINA;
JACOBSSON, BO;
CANS, CHRISTINE;
THORSEN, POUL

Publication type:

Article

Quantitative and Functional Analyses of Spastin in the Nervous System: Implications for Hereditary Spastic Paraplegia.

Published in:

Journal of Neuroscience, 2008, v. 28, n. 9, p. 2147, doi. 10.1523/JNEUROSCI.3159-07.2008

By:

Solowska, Joanna M.;
Morfini, Gerardo;
Falnikar, Aditi;
Himes, B. Timothy;
Brady, Scott T.;
Dongyang Huang;
Baas, Peter W.

Publication type:

Article

Clinical Manifestations Associated with the Domain-Containing Protein 2 Gene Mutation in an Iranian Family with Spastic Paraplegia 54.

Published in:

Neurodegenerative Diseases, 2023, v. 22, n. 3/4, p. 139, doi. 10.1159/000530375

By:

Yari, Abolfazl;
Etesam, Shokoofeh;
Zarifi, Shannaz;
Parvizpour, Sepideh;
Miri-Moghaddam, Ebrahim

Publication type:

Article

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 326, doi. 10.1038/ng758

By:

Zhao, Xinping;
Alvarado, David;
Rainier, Shirley;
Lemons, Rosemary;
Hedera, Peter;
Weber, Christian H.;
Tukel, Turgut;
Apak, Memnune;
Heiman-Patterson, Terry;
Ming, Lei;
Bui, Melanie;
Fink, John K.

Publication type:

Article

Prevalence of major depressive disorder and its associated factors among adult patients with neurolathyrism in Dawunt District, Ethiopia; 2022: community-based cross-sectional study.

Published in:

BMC Psychiatry, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12888-024-05755-7

By:

Bimerew, Melaku;
Gebremeskel, Teshome;
Beletew, Biruk;
Ayaliew, Wondye;
Wodaje, Mulugeta;
Ayalneh, Manay

Publication type:

Article