C Van Broeckhoven
Overview
Explore the profile of C Van Broeckhoven including associated specialties, affiliations and a list of published articles.
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Articles
376
Citations
10718
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Recent Articles
1.
Lofgren A, de Vos A, Sermon K, Liebaers I, VAN Steirteghem A, Van Broeckhoven C
Ann N Y Acad Sci
. 2017 Nov;
883(1):460-462.
PMID: 29086984
No abstract available.
2.
Meuleman J, Kuhlenbaumer G, Schirmacher A, Wehnert M, Young P, Stogbauer F, et al.
Ann N Y Acad Sci
. 2017 Nov;
883(1):443-444.
PMID: 29086982
No abstract available.
3.
Kochanski A, Timmerman V, Jedrzejowska H, Ryniewicz B, Lofgren A, De Vriendt E, et al.
Ann N Y Acad Sci
. 2017 Nov;
883(1):493-496.
PMID: 29086975
No abstract available.
4.
Timmerman V, Beuten J, Irobi J, De Jonghe P, Martin J, Van Broeckhoven C
Ann N Y Acad Sci
. 2017 Nov;
883(1):60-64.
PMID: 29086966
The distal hereditary motor neuropathies (distal HMN) are clinically and genetically heterogeneous and are subdivided in seven subtypes according to the mode of inheritance, age at onset and clinical evolution....
5.
Kuhlenbaumer G, Young P, Kiefer R, Timmerman V, Wang J, Schroeder J, et al.
Ann N Y Acad Sci
. 2017 Nov;
883(1):445-448.
PMID: 29086959
No abstract available.
6.
De Jonghe P, Nelis E, Timmerman V, Lofgren A, Martin J, Van Broeckhoven C
Ann N Y Acad Sci
. 2017 Nov;
883(1):389-396.
PMID: 29086951
The inherited neuropathies of the peripheral nervous system are clinically and genetically a heterogeneous group of disorders. Molecular genetic studies have made major breakthroughs in unraveling the underlying gene defects,...
7.
Leonardis L, Zidar J, Popovic M, Timmerman V, Lofgren A, Van Broeckhoven C, et al.
Pflugers Arch
. 2017 Feb;
439(Suppl 1):r208-r210.
PMID: 28176125
In a Slovene Gypsy family of 19 subjects from four generations three patients with clinical characteristics compatible with hereditary motor and sensory neuropathy -Lom (HMSNL), were found. They had severe...
8.
Schonecker S, Brendel M, van der Zee J, Van Broeckhoven C, Rominger A, Danek A, et al.
Fortschr Neurol Psychiatr
. 2016 Aug;
84(8):494-8.
PMID: 27570907
We report on a pair of siblings with frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) and a novel Thr462Lysfs mutation in the TANK-binding kinase 1 (TBK1) gene identified through...
9.
Theuns J, Van Broeckhoven C
Acta Neuropsychiatr
. 2016 Mar;
11(2):60-2.
PMID: 26976255
Alzheimer disease (AD), the most common form of dementia in the elderly, is rapidly becoming a major health problem in developed countries where the number of elderly people continuously grows...
10.
Gijselinck I, Van Mossevelde S, van der Zee J, Sieben A, Engelborghs S, De Bleecker J, et al.
Mol Psychiatry
. 2015 Oct;
21(8):1112-24.
PMID: 26481318
Pathological expansion of a G4C2 repeat, located in the 5' regulatory region of C9orf72, is the most common genetic cause of frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS)....