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A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
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A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism

Westenberger, Ana ; Reyes, Charles Jourdan ; Saranza, Gerard ; Dobricic, Valerija ; Hanssen, Henrike ; Domingo, Aloysius ; Laabs, Björn‐Hergen ; Schaake, Susen ; Pozojevic, Jelena ; Rakovic, Aleksandar ; Grütz, Karen ; Begemann, Kimberly ; Walter, Uwe ; Dressler, Dirk ; Bauer, Peter ; Rolfs, Arndt ; Münchau, Alexander ; Kaiser, Frank J. ; Ozelius, Laurie J. ; Jamora, Roland Dominic ; Rosales, Raymond L. ; Diesta, Cid Czarina E. ; Lohmann, Katja ; König, Inke R. ; Brüggemann, Norbert ; Klein, Christine

Annals of neurology, 2019-06, Vol.85 (6), p.812-822 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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2
Characterizing mixed location hemorrhages/microbleeds with CSF markers
Characterizing mixed location hemorrhages/microbleeds with CSF markers
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Characterizing mixed location hemorrhages/microbleeds with CSF markers

Jensen-Kondering, Ulf ; Margraf, Nils G ; Weiler, Caroline ; Maetzler, Walter ; Dargvainiene, Justina ; Falk, Kim ; Philippen, Sarah ; Bartsch, Thorsten ; Flüh, Charlotte ; Röcken, Christoph ; Möller, Bettina ; Royl, Georg ; Neumann, Alexander ; Brüggemann, Norbert ; Roeben, Benjamin ; Schulte, Claudia ; Bender, Benjamin ; Berg, Daniela ; Kuhlenbäumer, Gregor

International journal of stroke, 2023-07, Vol.18 (6), p.728-735 [Periódico revisado por pares]

London, England: SAGE Publications

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3
Sonographic alteration of substantia nigra is related to parkinsonism-predominant course of X-linked dystonia-parkinsonism
Sonographic alteration of substantia nigra is related to parkinsonism-predominant course of X-linked dystonia-parkinsonism
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Sonographic alteration of substantia nigra is related to parkinsonism-predominant course of X-linked dystonia-parkinsonism

Walter, Uwe ; Rosales, Raymond ; Rocco, Alessandro ; Westenberger, Ana ; Domingo, Aloysius ; Go, Criscely L ; Brüggemann, Norbert ; Klein, Christine ; Lee, Lillian V ; Dressler, Dirk

Parkinsonism & related disorders, 2017-04, Vol.37, p.43-49 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Characterisation and differential diagnosis of neurological complications in adults with phenylketonuria: literature review and expert opinion
Characterisation and differential diagnosis of neurological complications in adults with phenylketonuria: literature review and expert opinion
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Characterisation and differential diagnosis of neurological complications in adults with phenylketonuria: literature review and expert opinion

Merkel, Martin ; Berg, Daniela ; Brüggemann, Norbert ; Classen, Joseph ; Mainka, Tina ; Zittel, Simone ; Muntau, Ania C.

Journal of neurology, 2023-08, Vol.270 (8), p.3675-3687 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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5
Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD)
Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD)
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Psychiatric comorbidity and functional impairment in a clinically referred sample of adults with attention-deficit/hyperactivity disorder (ADHD)

Sobanski, Esther ; Brüggemann, Daniel ; Alm, Barbara ; Kern, Sebastian ; Deschner, Monika ; Schubert, Thomas ; Philipsen, Alexandra ; Rietschel, Marcella

European archives of psychiatry and clinical neuroscience, 2007-10, Vol.257 (7), p.371-377 [Periódico revisado por pares]

Germany: Springer Nature B.V

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6
Basal Ganglia Atrophy as a Marker for Prodromal X‐Linked Dystonia‐Parkinsonism
Basal Ganglia Atrophy as a Marker for Prodromal X‐Linked Dystonia‐Parkinsonism
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Basal Ganglia Atrophy as a Marker for Prodromal X‐Linked Dystonia‐Parkinsonism

Hanssen, Henrike ; Diesta, Cid C. E. ; Heldmann, Marcus ; Dy, Jackson ; Tantianpact, Jeffrey ; Steinhardt, Julia ; Sauza, Rosanna ; Manalo, Hans T. S. ; Sprenger, Andreas ; Reyes, Charles Jourdan ; Tuazon, Raphael ; Laabs, Björn‐Hergen ; Domingo, Aloysius ; Rosales, Raymond L. ; Klein, Christine ; Münte, Thomas F. ; Westenberger, Ana ; Oropilla, Jean Q. ; Brüggemann, Norbert

Annals of neurology, 2023-05, Vol.93 (5), p.999-1011 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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7
Longitudinal evaluations of somatosensory-motor inhibition in Dopa-responsive dystonia
Longitudinal evaluations of somatosensory-motor inhibition in Dopa-responsive dystonia
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Longitudinal evaluations of somatosensory-motor inhibition in Dopa-responsive dystonia

Weissbach, Anne ; Steinmeier, Annika ; Pauly, Martje ; Al-Shorafat, Duha M. ; Saranza, Gerard ; Lang, Anthony ; Brüggemann, Norbert ; Tadic, Vera ; Klein, Christine ; Münchau, Alexander ; Bäumer, Tobias ; Brown, Matt J.N.

Parkinsonism & related disorders, 2022-02, Vol.95, p.40-46 [Periódico revisado por pares]

England: Elsevier Ltd

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8
Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls
Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls
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Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls

Prasuhn, Jannik ; Borsche, Max ; Hicks, Andrew A. ; Gögele, Martin ; Egger, Clemens ; Kritzinger, Cleo ; Pichler, Irene ; Castelo-Rueda, Maria Paulina ; Langlott, Lynn ; Kasten, Meike ; Mascalzoni, Deborah ; Klein, Christine ; Pramstaller, Peter P. ; Brüggemann, Norbert

Parkinsonism & related disorders, 2021-05, Vol.86, p.101-104 [Periódico revisado por pares]

England: Elsevier Ltd

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9
No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients
No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients
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No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients

Richter, Julia ; Appenzeller, Silke ; Ammerpohl, Ole ; Deuschl, G. ; Paschen, Steffen ; Brüggemann, Norbert ; Klein, Christine ; Kuhlenbäumer, Gregor

Movement disorders, 2012-04, Vol.27 (4), p.590-591 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only
Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only
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Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only

Wilcox, Robert ; Brænne, Ingrid ; Brüggemann, Norbert ; Winkler, Susen ; Wiegers, Karin ; Bertram, Lars ; Anderson, Tim ; Lohmann, Katja

Journal of neurology, 2015, Vol.262 (1), p.187-193 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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