Suchergebnisse - "Ballegaard, Martin"

PubPharm (37)

1

Postictal EEG changes following focal seizures : Interrater agreement and comparison to frequency analysis

enthalten in: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | 2019

von Zibrandtsen, I. | Weisdorf, S. | Ballegaard, M. | +2

2

Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants

enthalten in: Journal of neurology | 2019

von Toft, A. | Birk, S. | Ballegaard, M. | +4

3

Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants

enthalten in: Journal of neurology | 2019

von Toft, A. | Birk, S. | Ballegaard, M. | +4

4

Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants

enthalten in: Journal of neurology | 2019

von Toft, A. | Birk, S. | Ballegaard, M. | +4

5

Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants

enthalten in: Journal of neurology | 2019

von Toft, A. | Birk, S. | Ballegaard, M. | +4

6

Do you define the limits of normalcy from looking at the patient or the healthy subject?

enthalten in: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | 2018

von Ballegaard, M.

CommentOn: Clin Neurophysiol. 2018 Mar;129(3):672-675. - PMID 29289442

7

The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease

enthalten in: Scandinavian journal of clinical and laboratory investigation | 2017

von Hasholt, L. | Ballegaard, M. | Bundgaard, H. | +9

8

The Effect of Local Anesthetic Volume Within the Adductor Canal on Quadriceps Femoris Function Evaluated by Electromyography : A Randomized, Observer- and Subject-Blinded, Placebo-Controlled Study in Volunteers

enthalten in: Anesthesia and analgesia | 2016

von Grevstad, U. | Jæger, P. | Sørensen, J. | +5

9

Contact Heat Evoked Potentials (CHEPs) in Patients with Mild-Moderate Alzheimer's Disease and Matched Control--A Pilot Study

enthalten in: Pain medicine (Malden, Mass.) | 2016

von Jensen-Dahm, C. | Madsen, C. | Waldemar, G. | +4

10

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

enthalten in: Brain : a journal of neurology | 2016

von Zaharieva, I. | Thor, M. | Oates, E. | +37

CommentIn: Brain. 2016 Mar;139(Pt 3):642-4. - PMID 26917582