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Papers authored by Djarmati A

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ATP13A2 variants in early-onset Parkinson's disease patients and controls.

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Djarmati A, Hagenah J, Reetz K, Winkler S, Behrens MI, Pawlack H, Lohmann K, Ramirez A, Tadić V, Brüggemann N, Berg D, Siebner HR, Lang AE, Pramstaller PP, Binkofski F, Kostić VS,

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Movement disorders : official journal of the Movement Disorder Society 24(14):2104-11, 2009 Oct 30 - Who cited this? | PubMed ID: 19705361 | Fulltext

Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers.

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Brüggemann N, Mitterer M, Lanthaler AJ, Djarmati A, Hagenah J, Wiegers K, Winkler S, Pawlack H, Lohnau T, Pramstaller PP, Klein C, and Lohmann K

Parkinsonism & related disorders 15(6):425-9, 2009 Jul - Who cited this? | PubMed ID: 19162522 | Fulltext

Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

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Djarmati A, Schneider SA, Lohmann K, Winkler S, Pawlack H, Hagenah J, Brüggemann N, Zittel S, Fuchs T, Raković A, Schmidt A, Jabusch HC, Wilcox R, Kostić VS, Siebner H, Altenmüller E,

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Lancet neurology 8(5):447-52, 2009 May - Who cited this? | PubMed ID: 19345148 | Fulltext

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.

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Rakovic A, Stiller B, Djarmati A, Flaquer A, Freudenberg J, Toliat MR, Linnebank M, Kostic V, Lohmann K, Paus S, Nürnberg P, Kubisch C, Klein C, Wüllner U, and Ramirez A

Movement disorders : official journal of the Movement Disorder Society 24(3):429-33, 2009 Feb 15 - Who cited this? | PubMed ID: 19097176 | Fulltext

{alpha}-Synuclein gene duplication is present in sporadic Parkinson disease.

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Brueggemann N, Odin P, Gruenewald A, Tadic V, Hagenah J, Seidel G, Lohmann K, Klein C, Djarmati A, Jeon BS, Ahn TB, and Park SS

Neurology 71(16):1294, 2008 Oct 14 - Who cited this? | PubMed ID: 18852448 | Fulltext

Transcranial sonography findings in a large family with homozygous and heterozygous PINK1 mutations.

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Hagenah JM, Becker B, Brüggemann N, Djarmati A, Lohmann K, Sprenger A, Klein C, and Seidel G

Journal of neurology, neurosurgery, and psychiatry 79(9):1071-4, 2008 Sep - Who cited this? | PubMed ID: 18469032 | Fulltext

Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers.

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Reetz K, Lencer R, Steinlechner S, Gaser C, Hagenah J, Büchel C, Petersen D, Kock N, Djarmati A, Siebner HR, Klein C, and Binkofski F

Biological psychiatry 64(3):241, 2008 Aug 1 - Who cited this? | PubMed ID: 18261714 | Fulltext

LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlation.

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Marras C, Klein C, Lang AE, Wakutani Y, Moreno D, Sato C, Yip E, Munhoz RP, Lohmann K, Djarmati A, Bi A, and Rogaeva E

Neurobiology of aging, 2008 Jul 19 - Who cited this? | PubMed ID: 18644660 | Fulltext

A heterozygous frameshift mutation in PRKRA (DYT16) associated with generalised dystonia in a German patient.

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Seibler P, Djarmati A, Langpap B, Hagenah J, Schmidt A, Brüggemann N, Siebner H, Jabusch HC, Altenmüller E, Münchau A, Lohmann K, and Klein C

Lancet neurology 7(5):380-1, 2008 May - Who cited this? | PubMed ID: 18420150 | Fulltext

Evidence for linkage of restless legs syndrome to chromosome 9p: Are there two distinct loci?.

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Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, and Klein C

Neurology 70(9):686-94, 2008 Feb 26 - Who cited this? | PubMed ID: 18032746 | Fulltext

Myoclonus-dystonia: significance of large SGCE deletions.

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Grünewald A, Djarmati A, Lohmann-Hedrich K, Farrell K, Zeller JA, Allert N, Papengut F, Petersen B, Fung V, Sue CM, O'Sullivan D, Mahant N, Kupsch A, Chuang RS, Wiegers K, Pawlack H,

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Human mutation 29(2):331-2, 2008 Feb - Who cited this? | PubMed ID: 18205193 | Fulltext

MECP2 mutations in Serbian Rett syndrome patients.

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Djarmati A, Dobricić V, Kecmanović M, Marsh P, Jancić-Stefanović J, Klein C, Djurić M, and Romac S

Acta neurologica Scandinavica 116(6):413-9, 2007 Dec - Who cited this? | PubMed ID: 17986102 | Fulltext

Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene.

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Orth M, Djarmati A, Bäumer T, Winkler S, Grünewald A, Lohmann-Hedrich K, Kabakci K, Hagenah J, Klein C, and Münchau A

Movement disorders : official journal of the Movement Disorder Society 22(14):2090-6, 2007 Oct 31 - Who cited this? | PubMed ID: 17702041 | Fulltext

Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification.

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Djarmati A, Guzvić M, Grünewald A, Lang AE, Pramstaller PP, Simon DK, Kaindl AM, Vieregge P, Nygren AO, Beetz C, Hedrich K, and Klein C

Movement disorders : official journal of the Movement Disorder Society 22(12):1708-14, 2007 Sep 15 - Who cited this? | PubMed ID: 17674414 | Fulltext

Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations.

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Steinlechner S, Stahlberg J, Völkel B, Djarmati A, Hagenah J, Hiller A, Hedrich K, König I, Klein C, and Lencer R

Journal of neurology, neurosurgery, and psychiatry 78(5):532, 2007 May - Who cited this? | PubMed ID: 17202228 | Fulltext

Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.

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Hiller A, Hagenah JM, Djarmati A, Hedrich K, Reetz K, Schneider-Gold C, Kress W, Münchau A, and Klein C

Movement disorders : official journal of the Movement Disorder Society 22(1):145-7, 2007 Jan - Who cited this? | PubMed ID: 17013904 | Fulltext

Intrafamilial phenotypic and genetic heterogeneity of dystonia.

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Kostić VS, Svetel M, Kabakci K, Ristić A, Petrović I, Schüle B, Kock N, Djarmati A, Romac S, and Klein C

Journal of the neurological sciences 250(1-2):92-6, 2006 Dec 1 - Who cited this? | PubMed ID: 17027035 | Fulltext

Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.

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Stefanova E, Djarmati A, Momcilović D, Dragasević N, Svetel M, Klein C, and Kostić VS

Movement disorders : official journal of the Movement Disorder Society 21(11):2010-5, 2006 Nov - Who cited this? | PubMed ID: 16972263 | Fulltext

Heterozygous PINK1 mutations: a susceptibility factor for Parkinson disease?.

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Djarmati A, Hedrich K, Svetel M, Lohnau T, Schwinger E, Romac S, Pramstaller PP, Kostić V, and Klein C

Movement disorders : official journal of the Movement Disorder Society 21(9):1526-30, 2006 Sep - Who cited this? | PubMed ID: 16755580 | Fulltext

Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?.

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Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grünewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R,

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Archives of neurology 63(6):833, 2006 Jun - Who cited this? | PubMed ID: 16769864 | Fulltext

Homozygous and heterozygous PINK1 mutations: considerations for diagnosis and care of Parkinson's disease patients.

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Zadikoff C, Rogaeva E, Djarmati A, Sato C, Salehi-Rad S, St George-Hyslop P, Klein C, and Lang AE

Movement disorders : official journal of the Movement Disorder Society 21(6):875-9, 2006 Jun - Who cited this? | PubMed ID: 16547921 | Fulltext

Co-occurrence of restless legs syndrome and Parkin mutations in two families.

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Adel S, Djarmati A, Kabakci K, Pichler I, Eskelson C, Lohnau T, Kock N, Hagenah J, Hedrich K, Schwinger E, Kramer PL, Pramstaller PP, and Klein C

Movement disorders : official journal of the Movement Disorder Society 21(2):258-63, 2006 Feb - Who cited this? | PubMed ID: 16161156 | Fulltext

Significance of recurrent mutations in the myofibrillogenesis regulator 1 gene.

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Djarmati A, Svetel M, Momcilovic D, Kostic V, and Klein C

Archives of neurology 62(10):1641, 2005 Oct - Who cited this? | PubMed ID: 16216955 | Fulltext

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.

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Klein C, Djarmati A, Hedrich K, Schäfer N, Scaglione C, Marchese R, Kock N, Schüle B, Hiller A, Lohnau T, Winkler S, Wiegers K, Hering R, Bauer P, Riess O, Abbruzzese G,

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European journal of human genetics : EJHG 13(9):1086, 2005 Sep - Who cited this? | PubMed ID: 15970950 | Fulltext

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.

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Djarmati A, Hedrich K, Svetel M, Schäfer N, Juric V, Vukosavic S, Hering R, Riess O, Romac S, Klein C, and Kostic V

Human mutation 23(5):525, 2004 May - Who cited this? | PubMed ID: 15108293 | Fulltext

Spinocerebellar ataxia type 17 in the Yugoslav population.

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Alendar A, Euljković B, Savić D, Djarmati A, Keckarević M, Ristić A, Dragasević N, Kosić V, and Romac S

Acta neurologica Scandinavica 109(3):185-7, 2004 Mar - Who cited this? | PubMed ID: 14763955 | Fulltext

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

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Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss PH, Hilker R, Vieregge P, Ozelius LJ, Heutink P, Bonifati V, Schwinger E, Lang AE, Noth J, Bressman SB, Pramstaller PP,

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Neurology 62(3):389-94, 2004 Feb 10 - Who cited this? | PubMed ID: 14872018 | Fulltext

SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism.

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Svetel M, Djarmati A, Dragasević N, Savić D, Culjković B, Romac S, and Kostić VS

European journal of neurology : the official journal of the European Federation of Neurological Societies 10(5):597, 2003 Sep - Who cited this? | PubMed ID: 12940846 | Fulltext

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Papers authored by Djarmati A

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