Works matching IS 03405354 AND DT 2015 AND VI 262 AND IP 8

Results: 28

Neurogenic muscle cramps.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1814, doi. 10.1007/s00415-015-7659-x

By:

Katzberg, Hans

Publication type:

Article

Progress in Huntington's disease: the search for markers of disease onset and progression.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1990, doi. 10.1007/s00415-015-7700-0

By:

Mason, Sarah;
Barker, Roger

Publication type:

Article

Henri Gastaut (1915-1995).

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1999, doi. 10.1007/s00415-015-7765-9

By:

Mahmoudi Nezhad, Golnoush Sadat;
Dalfardi, Behnam

Publication type:

Article

Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1822, doi. 10.1007/s00415-015-7772-x

By:

Keogh, M.;
Steele, H.;
Douroudis, K.;
Pyle, A.;
Duff, J.;
Hussain, R.;
Smertenko, T.;
Griffin, H.;
Santibanez-Koref, M.;
Horvath, R.;
Chinnery, P.

Publication type:

Article

Gaze holding deficits discriminate early from late onset cerebellar degeneration.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1837, doi. 10.1007/s00415-015-7773-9

By:

Tarnutzer, Alexander;
Weber, K.;
Schuknecht, B.;
Straumann, D.;
Marti, S.;
Bertolini, G.

Publication type:

Article

Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1899, doi. 10.1007/s00415-015-7778-4

By:

Bansagi, Boglarka;
Antoniadi, Thalia;
Burton-Jones, Sarah;
Murphy, Sinead;
McHugh, John;
Alexander, Michael;
Wells, Richard;
Davies, Joanna;
Hilton-Jones, David;
Lochmüller, Hanns;
Chinnery, Patrick;
Horvath, Rita

Publication type:

Article

Neuroimaging evidence of gray and white matter damage and clinical correlates in progressive supranuclear palsy.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1850, doi. 10.1007/s00415-015-7779-3

By:

Piattella, Maria;
Upadhyay, N.;
Bologna, M.;
Sbardella, E.;
Tona, F.;
Formica, A.;
Petsas, N.;
Berardelli, A.;
Pantano, P.

Publication type:

Article

Normalization of sensorimotor integration by repetitive transcranial magnetic stimulation in cervical dystonia.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1883, doi. 10.1007/s00415-015-7789-1

By:

Zittel, S.;
Helmich, R.;
Demiralay, C.;
Münchau, A.;
Bäumer, T.

Publication type:

Article

Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1961, doi. 10.1007/s00415-015-7791-7

By:

Lindig, Tobias;
Bender, Benjamin;
Hauser, Till-Karsten;
Mang, Sarah;
Schweikardt, Daniel;
Klose, Uwe;
Karle, Kathrin N.;
Schüle, Rebecca;
Schöls, Ludger;
Rattay, Tim W.

Publication type:

Article

Magnetization transfer ratio in lesions rather than normal-appearing brain relates to disability in patients with multiple sclerosis.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1909, doi. 10.1007/s00415-015-7793-5

By:

Amann, Michael;
Papadopoulou, Athina;
Andelova, Michaela;
Magon, Stefano;
Mueller-Lenke, Nicole;
Naegelin, Yvonne;
Stippich, Christoph;
Radue, Ernst;
Bieri, Oliver;
Kappos, Ludwig;
Sprenger, Till

Publication type:

Article

Eye-tracking controlled cognitive function tests in patients with amyotrophic lateral sclerosis: a controlled proof-of-principle study.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1918, doi. 10.1007/s00415-015-7795-3

By:

Keller, Jürgen;
Gorges, Martin;
Horn, Hannah;
Aho-Özhan, Helena;
Pinkhardt, Elmar;
Uttner, Ingo;
Kassubek, Jan;
Ludolph, Albert;
Lulé, Dorothée

Publication type:

Article

Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1927, doi. 10.1007/s00415-015-7788-2

By:

Doss, Sarah;
Rinnenthal, Jan;
Schmitz-Hübsch, Tanja;
Brandt, Alexander;
Papazoglou, Sebastian;
Lux, Silke;
Maul, Stephan;
Würfel, Jens;
Endres, Matthias;
Klockgether, Thomas;
Minnerop, Martina;
Paul, Friedemann

Publication type:

Article

Treatment and outcome of children and adolescents with N-methyl- d-aspartate receptor encephalitis.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1859, doi. 10.1007/s00415-015-7781-9

By:

Zekeridou, Anastasia;
Karantoni, Evgenia;
Viaccoz, Aurélien;
Ducray, François;
Gitiaux, Cyril;
Villega, Frédéric;
Deiva, Kumaran;
Rogemond, Veronique;
Mathias, Elodie;
Picard, Géraldine;
Tardieu, Marc;
Antoine, Jean-Christophe;
Delattre, Jean-Yves;
Honnorat, Jerome

Publication type:

Article

Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1828, doi. 10.1007/s00415-015-7782-8

By:

Ueda, Akihiko;
Ueda, Mitsuharu;
Nagatoshi, Akihito;
Hirano, Teruyuki;
Ito, Takaaki;
Arai, Nobutaka;
Uyama, Eiichiro;
Mori, Kota;
Nakamura, Masaaki;
Shinriki, Satoru;
Ikeda, Katsuyoshi;
Ando, Yukio

Publication type:

Article

Tailored care for somatoform vertigo/dizziness: study protocol for a randomised controlled trial evaluating integrative group psychotherapy.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1867, doi. 10.1007/s00415-015-7784-6

By:

Lahmann, Claas;
Henningsen, P.;
Dieterich, M.;
Radziej, K.;
Schmid, G.

Publication type:

Article

Progression of subcortical atrophy and iron deposition in multiple system atrophy: a comparison between clinical subtypes.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1876, doi. 10.1007/s00415-015-7785-5

By:

Lee, Jae-Hyeok;
Kim, Tae-Hyung;
Mun, Chi-Woong;
Kim, Tae-Hyoung;
Han, Yong-Hee

Publication type:

Article

Olfactory dysfunction in neuromyelitis optica spectrum disorders.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1890, doi. 10.1007/s00415-015-7787-3

By:

Zhang, Lin-Jie;
Zhao, Ning;
Fu, Ying;
Zhang, Da-Qi;
Wang, Jing;
Qin, Wen;
Zhang, Ningnannan;
Wood, Kristofer;
Liu, Yaou;
Yu, Chunshui;
Shi, Fu-Dong;
Yang, Li

Publication type:

Article

Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1936, doi. 10.1007/s00415-015-7797-1

By:

Allart, Etienne;
Benoit, Anne;
Blanchard-Dauphin, Anne;
Tiffreau, Vincent;
Thevenon, André;
Zephir, Hélène;
Outteryck, Olivier;
Lacour, Arnaud;
Vermersch, Patrick

Publication type:

Article

Unchanged gastric emptying and visceral perception in early Parkinson's disease after a high caloric test meal.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1946, doi. 10.1007/s00415-015-7799-z

By:

Epprecht, L.;
Schreglmann, S.;
Goetze, O.;
Woitalla, D.;
Baumann, C.;
Waldvogel, D.

Publication type:

Article

Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation.

Published in:

2015

By:

Koutsis, Georgios;
Lynch, David;
Manone, Andreea;
Karadima, Georgia;
Reilly, Mary;
Houlden, Henry;
Panas, Marios

Publication type:

Letter

Ambiguous value of anti-ganglioside IgM autoantibodies in Guillain-Barré syndrome and its variants.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1954, doi. 10.1007/s00415-015-7806-4

By:

Koga, Michiaki;
Takahashi, Masaki;
Yokoyama, Keiko;
Kanda, Takashi

Publication type:

Article

Functional dizziness: diagnostic keys and differential diagnosis.

Published in:

2015

By:

Brandt, Thomas;
Huppert, Doreen;
Strupp, Michael;
Dieterich, Marianne

Publication type:

Letter

Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation.

Published in:

2015

By:

Koutsis, Georgios;
Lynch, David;
Manole, Andreea;
Karadima, Georgia;
Reilly, Mary;
Houlden, Henry;
Panas, Marios

Publication type:

Erratum

Radiotherapy treatment of sialorrhea in patients with amyotrophic lateral sclerosis requiring non-invasive ventilation.

Published in:

2015

By:

Amador, Maria;
Assouline, Avi;
Gonzalez-Bermejo, Jésus;
Pradat, Pierre-François

Publication type:

Letter

Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathies.

Published in:

2015

By:

Horga, Alejandro;
Cottenie, Ellen;
Tomaselli, Pedro;
Rojas-García, Ricard;
Salvado, Maria;
Villarreal-Pérez, Liliana;
Gamez, Josep;
Márquez-Infante, Celedonio;
Houlden, Henry;
Reilly, Mary

Publication type:

Letter

Hereditary spastic paraplegia type 11 with a very late onset.

Published in:

2015

By:

Rubegni, Anna;
Storti, Eugenia;
Tessa, Alessandra;
Federico, Antonio;
Santorelli, Filippo

Publication type:

Letter

Testing new treatments for paediatric epilepsies.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1996, doi. 10.1007/s00415-015-7857-6

By:

Thomas, R.;
Robertson, N.

Publication type:

Article

Diagnosis and differential diagnosis of MSA: boundary issues.

Published in:

Journal of Neurology, 2015, v. 262, n. 8, p. 1801, doi. 10.1007/s00415-015-7654-2

By:

Kim, Han-Joon;
Jeon, Beom;
Jellinger, Kurt

Publication type:

Article