Diagnosis and differential diagnosis of MSA: boundary issues Han-Joon KimBeom S. JeonKurt A. Jellinger Review 07 February 2015 Pages: 1801 - 1813
Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia M. J. KeoghH. SteeleP. F. Chinnery Original Communication Open access 16 May 2015 Pages: 1822 - 1827
Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014 Akihiko UedaMitsuharu UedaYukio Ando Original Communication 16 May 2015 Pages: 1828 - 1836
Gaze holding deficits discriminate early from late onset cerebellar degeneration Alexander A. TarnutzerK. P. WeberG. Bertolini Original Communication 16 May 2015 Pages: 1837 - 1849
Neuroimaging evidence of gray and white matter damage and clinical correlates in progressive supranuclear palsy Maria Cristina PiattellaN. UpadhyayP. Pantano Original Communication 16 May 2015 Pages: 1850 - 1858
Treatment and outcome of children and adolescents with N-methyl-d-aspartate receptor encephalitis Anastasia ZekeridouEvgenia KarantoniJerome Honnorat Original Communication 19 May 2015 Pages: 1859 - 1866
Tailored care for somatoform vertigo/dizziness: study protocol for a randomised controlled trial evaluating integrative group psychotherapy Claas LahmannP. HenningsenG. Schmid Original Communication 23 May 2015 Pages: 1867 - 1875
Progression of subcortical atrophy and iron deposition in multiple system atrophy: a comparison between clinical subtypes Jae-Hyeok LeeTae-Hyung KimYong-Hee Han Original Communication 28 May 2015 Pages: 1876 - 1882
Normalization of sensorimotor integration by repetitive transcranial magnetic stimulation in cervical dystonia S. ZittelR. C. HelmichT. Bäumer Original Communication 28 May 2015 Pages: 1883 - 1889
Olfactory dysfunction in neuromyelitis optica spectrum disorders Lin-Jie ZhangNing ZhaoLi Yang Original Communication 28 May 2015 Pages: 1890 - 1898
Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland Boglarka BansagiThalia AntoniadiRita Horvath Original Communication Open access 02 June 2015 Pages: 1899 - 1908
Magnetization transfer ratio in lesions rather than normal-appearing brain relates to disability in patients with multiple sclerosis Michael AmannAthina PapadopoulouTill Sprenger Original Communication 05 June 2015 Pages: 1909 - 1917
Eye-tracking controlled cognitive function tests in patients with amyotrophic lateral sclerosis: a controlled proof-of-principle study Jürgen KellerMartin GorgesDorothée Lulé Original Communication 05 June 2015 Pages: 1918 - 1926
Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency Sarah DossJan Leo RinnenthalFriedemann Paul Original Communication 05 June 2015 Pages: 1927 - 1935
Sustained-released fampridine in multiple sclerosis: effects on gait parameters, arm function, fatigue, and quality of life Etienne AllartAnne BenoitPatrick Vermersch Original Communication 05 June 2015 Pages: 1936 - 1945
Unchanged gastric emptying and visceral perception in early Parkinson's disease after a high caloric test meal L. EpprechtS. R. SchreglmannD. Waldvogel Original Communication 06 June 2015 Pages: 1946 - 1953
Ambiguous value of anti-ganglioside IgM autoantibodies in Guillain-Barré syndrome and its variants Michiaki KogaMasaki TakahashiTakashi Kanda Original Communication 09 June 2015 Pages: 1954 - 1960
Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations Tobias LindigBenjamin BenderTim W. Rattay Original Communication 09 June 2015 Pages: 1961 - 1971
Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation Georgios KoutsisDavid LynchMarios Panas Letter to the Editors 06 June 2015 Pages: 1972 - 1975
Erratum to: Charcot-Marie-Tooth disease type 2C and scapuloperoneal muscular atrophy overlap syndrome in a patient with the R232C TRPV4 mutation Georgios KoutsisDavid LynchMarios Panas Erratum 11 July 2015 Pages: 1976 - 1976
Functional dizziness: diagnostic keys and differential diagnosis Thomas BrandtDoreen HuppertMarianne Dieterich Letter to the Editors 30 June 2015 Pages: 1977 - 1980
Radiotherapy treatment of sialorrhea in patients with amyotrophic lateral sclerosis requiring non-invasive ventilation Maria del Mar AmadorAvi AssoulinePierre-François Pradat Letter to the Editors 15 July 2015 Pages: 1981 - 1983
Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathies Alejandro HorgaEllen CottenieMary M. Reilly Letter to the Editors 21 July 2015 Pages: 1984 - 1986
Hereditary spastic paraplegia type 11 with a very late onset Anna RubegniEugenia StortiFilippo M. Santorelli Letter to the Editors 17 July 2015 Pages: 1987 - 1989
Progress in Huntington’s disease: the search for markers of disease onset and progression Sarah MasonRoger A. Barker Neurological Update 21 March 2015 Pages: 1990 - 1995
Testing new treatments for paediatric epilepsies R. H. ThomasN. P. Robertson Journal club 21 July 2015 Pages: 1996 - 1998
Henri Gastaut (1915–1995) Golnoush Sadat Mahmoudi NezhadBehnam Dalfardi Pioneers in Neurology 01 May 2015 Pages: 1999 - 2000
