Andreas Ferbert
Overview
Explore the profile of Andreas Ferbert including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
45
Citations
908
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Laabs B, Lohmann K, Vollstedt E, Reinberger T, Nuxoll L, Kilic-Berkmen G, et al.
Mov Disord
. 2024 Sep;
39(11):2110-2116.
PMID: 39287592
Background: Despite considerable heritability, previous smaller genome-wide association studies (GWASs) have not identified any robust genetic risk factors for isolated dystonia. Objective: The objective of this study was to perform...
2.
Roth C, Yavuz R, Maschita C, Ferbert A, Matthaei J
J Neurol
. 2024 Apr;
271(7):4423-4429.
PMID: 38676723
Background: Acute basilar artery occlusion is a life-threatening medical emergency with a highly elevated mortality rate when left untreated. Little is known about symptoms and clinical progression of chronic occlusions....
3.
Thomsen M, Marth K, Loens S, Everding J, Junker J, Borngraber F, et al.
Mov Disord
. 2024 Jan;
39(3):526-538.
PMID: 38214203
Background: Pathogenic variants in several genes have been linked to genetic forms of isolated or combined dystonia. The phenotypic and genetic spectrum and the frequency of pathogenic variants in these...
4.
Bremer J, Meinhardt A, Katona I, Senderek J, Kammerer-Gassler E, Roos A, et al.
Brain Pathol
. 2023 Aug;
34(1):e13200.
PMID: 37581289
Myelin protein zero (MPZ/P0) is a major structural protein of peripheral nerve myelin. Disease-associated variants in the MPZ gene cause a wide phenotypic spectrum of inherited peripheral neuropathies. Previous nerve...
5.
Mair D, Biskup S, Kress W, Abicht A, Bruck W, Zechel S, et al.
Brain Pathol
. 2020 May;
30(5):877-896.
PMID: 32419263
Altered autophagy accompanied by abnormal autophagic (rimmed) vacuoles detectable by light and electron microscopy is a common denominator of many familial and sporadic non-inflammatory muscle diseases. Even in the era...
6.
Kleffmann J, Pahl R, Ferbert A, Roth C
Clin Neurol Neurosurg
. 2020 May;
195:105869.
PMID: 32353664
Objectives: Percutaneous tracheostomy (PT) is common on ICUs. An increase of intracranial pressure (ICP) can be observed in patients with acute cerebral diseases. Factors determining ICP increase remain unclear. Patients...
7.
Klein C, Baumann H, Olschewski L, Hanssen H, Munchau A, Ferbert A, et al.
Parkinsonism Relat Disord
. 2019 Apr;
64:337-339.
PMID: 30935829
No abstract available.
8.
Roth C, Ferbert A, Matthaei J, Kaestner S, Engel H, Gehling M
J Neurol Sci
. 2019 Feb;
398:171-175.
PMID: 30731304
Background: Clinical investigations of brain death are supposed to prove absence of cerebral perfusion. However, only limited data are available documenting intracranial pressure (ICP) and cerebral perfusion pressure (CPP) during...
9.
Olschewski L, Jesus S, Kim H, Tunc S, Lons S, Junker J, et al.
Parkinsonism Relat Disord
. 2019 Feb;
62:196-200.
PMID: 30712998
Background: The role of ANO3 variants as a monogenic cause of dystonia is still under debate because of its relatively high frequency also in controls. Objective: To screen >1000 patients...
10.
Roth C, Ferbert A, Huegens-Penzel M, Siekmann R, Freilinger T
J Neurol Sci
. 2018 Aug;
392:22-27.
PMID: 30097147
Background: Familial hemiplegic migraine (FHM) is a rare monogenic form of migraine with aura with three distinct genetic subtypes (FHM1-3). Imaging studies during acute FHM attacks are scarce in the...