Suchergebnisse - "Hjermind, Lena Elisabeth"

PubPharm (33)

1

A randomised double-blind controlled study of Deep Brain Stimulation for dystonia in STN or GPi - A long term follow-up after up to 15 years

enthalten in: Parkinsonism & related disorders | 2022

von Hock, A. | Jensen, S. | Svaerke, K. | +6

2

Corrigendum: combining literature review with a ground truth approach for diagnosing huntington's disease phenocopy

Erschienen: Ulm, Universität Ulm, 2022

von Nguyen, Q. | Ortigoza Escobar, J. | Burgunder, J. | +6

3

Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy

enthalten in: Frontiers in neurology | 2022

von Nguyen, Q. | Ortigoza Escobar, J. | Burgunder, J. | +6

ErratumIn: Front Neurol. 2022 Mar 30;13:891800. - PMID 35432158

4

Corrigendum : Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy

enthalten in: Frontiers in neurology | 2022

von Nguyen, Q. | Ortigoza Escobar, J. | Burgunder, J. | +6

ErratumFor: Front Neurol. 2022 Feb 10;13:817753. - PMID 35222250

5

Intellectual curiosity and action initiation are subtypes of apathy affected in Huntington’s disease gene expansion carriers

enthalten in: Alzheimer's & Dementia | 2021

von Hendel, R. | Hellem, M. | Hjermind, L. | +2

6

Quantitative Measurements of Motor Function in Alzheimer's Disease, Frontotemporal Dementia, and Dementia with Lewy Bodies : A Proof-of-Concept Study

enthalten in: Dementia and geriatric cognitive disorders | 2018

von Jeppesen Kragh, F. | Bruun, M. | Budtz-Jørgensen, E. | +5

7

P1‐062 : TWELVE YEARS OF EVOLUTION IN PRESCRIPTION PATTERNS OF ANTI‐DEMENTIA DRUGS IN A TERTIARY REFERRAL MEMORY CLINIC

enthalten in: Alzheimer's & Dementia | 2018

von Johannsen, P. | Andersen, B. | Almer Bromann, J. | +8

8

Defining active progressive multiple sclerosis

enthalten in: Multiple sclerosis (Houndmills, Basingstoke, England) | 2017

von Sellebjerg, F. | Börnsen, L. | Ammitzbøll, C. | +7

CommentIn: Mult Scler. 2017 Nov;23(13):1660-1661. - PMID 28984535

9

SCA28 : Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy

enthalten in: Cerebellum (London, England) | 2017

von Svenstrup, K. | Nielsen, T. | Aidt, F. | +9

10

A Novel TTBK2 De Novo Mutation in a Danish Family with Early-Onset Spinocerebellar Ataxia

enthalten in: Cerebellum (London, England) | 2017

von Lindquist, S. | Møller, L. | Dali, C. | +4