Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease.

Sascha Hering; Clemens Achmüller; Andrea Köhler; Werner Poewe; Raine Schneider; Sylvia M Boesch

doi:10.1002/mds.22465

Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease.

Sascha Hering (Erstautor/-in)
, Clemens Achmüller
, Andrea Köhler
, Werner Poewe
, Raine Schneider
, Sylvia M Boesch

Universitätsklinik für Neurologie, neurologische Intensivmedizin und Neurorehabilitation

Publikation: Beitrag in Fachzeitschrift › Kurzbericht / Notes › Begutachtung

4 Quellenangaben (Web of Science)

Originalsprache	Englisch
Seiten (von - bis)	774-777
Fachzeitschrift	MOVEMENT DISORDERS
Jahrgang	24
Ausgabenummer	5
DOIs	https://doi.org/10.1002/mds.22465
Publikationsstatus	Veröffentlicht - 2009

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10.1002/mds.22465

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Hering, S., Achmüller, C., Köhler, A., Poewe, W., Schneider, R., & Boesch, S. M. (2009). Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease. MOVEMENT DISORDERS , 24(5), 774-777. https://doi.org/10.1002/mds.22465

Hering, Sascha ; Achmüller, Clemens ; Köhler, Andrea et al. / Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease. in: MOVEMENT DISORDERS 2009 ; Jahrgang 24, Nr. 5. S. 774-777.

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Hering, S, Achmüller, C, Köhler, A, Poewe, W, Schneider, R & Boesch, SM 2009, 'Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease.', MOVEMENT DISORDERS , Jg. 24, Nr. 5, S. 774-777. https://doi.org/10.1002/mds.22465

Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease. / Hering, Sascha (Erstautor/-in); Achmüller, Clemens; Köhler, Andrea et al.
in: MOVEMENT DISORDERS , Jahrgang 24, Nr. 5, 2009, S. 774-777.

Publikation: Beitrag in Fachzeitschrift › Kurzbericht / Notes › Begutachtung

TY - JOUR

T1 - Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease.

AU - Hering, Sascha

AU - Achmüller, Clemens

AU - Köhler, Andrea

AU - Poewe, Werner

AU - Schneider, Raine

AU - Boesch, Sylvia M

PY - 2009

Y1 - 2009

KW - REPEAT

KW - SCA2

KW - LITHIUM

KW - EXPANSION

KW - NEURODEGENERATION

KW - AUTOPHAGY

KW - ONSET

KW - ROLES

KW - AGE

U2 - 10.1002/mds.22465

DO - 10.1002/mds.22465

M3 - Short comment / notes

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SN - 0885-3185

VL - 24

SP - 774

EP - 777

JO - MOVEMENT DISORDERS

JF - MOVEMENT DISORDERS

IS - 5

ER -

Hering S, Achmüller C, Köhler A, Poewe W, Schneider R, Boesch SM. Phenotype variability in spinocerebellar ataxia type 2: a longitudinal family survey and a case featuring an unusual benign course of disease. MOVEMENT DISORDERS . 2009;24(5):774-777. doi: 10.1002/mds.22465