An E Vanhaesebrouck
Overview
Explore the profile of An E Vanhaesebrouck including associated specialties, affiliations and a list of published articles.
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13
Citations
146
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Recent Articles
1.
Walker P, Freeman P, Monforte Monteiro S, Bexfield N, Harris G, Radke H, et al.
Vet Rec
. 2022 Jan;
190(9):e1268.
PMID: 34993971
Background: Clinicians observe that cats and dogs referred to neurology services often do not have an underlying neurological disorder. There has been no analysis of the frequency or categorisation of...
2.
Webster R, Vanhaesebrouck A, Maxwell S, Cossins J, Liu W, Ueta R, et al.
Hum Mol Genet
. 2020 Jun;
29(14):2325-2336.
PMID: 32543656
Congenital myasthenic syndromes (CMS) are characterized by fatigable muscle weakness resulting from impaired neuromuscular transmission. β2-adrenergic agonists are an effective treatment for DOK7-CMS. DOK7 is a component within the AGRN-LRP4-MUSK-DOK7...
3.
Monforte Monteiro S, Rossmeisl J, Russell J, Holmes M, Wessmann A, Morris J, et al.
J Vet Intern Med
. 2020 Feb;
34(2):821-827.
PMID: 32032456
Background: Seizures are a common presenting sign in dogs with brain tumors. Hypothesis/objectives: To investigate the effect of radiotherapy on freedom from brain tumor-associated seizures and survival time in dogs....
4.
Vanhaesebrouck A, Webster R, Maxwell S, Rodriguez Cruz P, Cossins J, Wickens J, et al.
Brain
. 2019 Oct;
142(12):3713-3727.
PMID: 31633155
Acetylcholine receptor deficiency is the most common form of the congenital myasthenic syndromes, a heterogeneous collection of genetic disorders of neuromuscular transmission characterized by fatiguable muscle weakness. Most patients with...
5.
Vanhaesebrouck A, Beeson D
Curr Opin Neurol
. 2019 Jul;
32(5):696-703.
PMID: 31361628
Purpose Of Review: Congenital myasthenic syndromes (CMS) are a group of heterogeneous inherited disorders caused by mutations in genes encoding proteins whose function is essential for the integrity of neuromuscular...
6.
Monforte Monteiro S, Gallucci A, Rousset N, Freeman P, Ives E, Gandini G, et al.
J Am Vet Med Assoc
. 2016 Nov;
249(10):1180-1186.
PMID: 27823364
CASE DESCRIPTION 5 dogs were examined because of clinical signs of myelopathy, including signs of pain associated with the spinal region and rapidly progressive neurologic deficits. CLINICAL FINDINGS In all...
7.
Ives E, Vanhaesebrouck A, Cian F
J Feline Med Surg
. 2013 Jun;
15(12):1149-53.
PMID: 23744728
A 4-month-old female entire domestic shorthair cat presented with an acute onset of blindness, tetraparesis and subsequent generalised seizure activity. Haematology and serum biochemistry demonstrated a moderate, poorly regenerative anaemia,...
8.
Vanhaesebrouck A, Bhatti S, Franklin R, Van Ham L
Vet J
. 2013 Apr;
197(2):153-62.
PMID: 23583699
Involuntary muscle hyperactivity can result from muscle or peripheral nerve hyperexcitability or central nervous system dysfunction. In humans, diseases causing hyperexcitability of peripheral nerves are grouped together under the term...
9.
Vanhaesebrouck A, Posch B, Baker S, Plessas I, Palmer A, Constantino-Casas F
J Feline Med Surg
. 2012 Jul;
14(12):932-7.
PMID: 22791561
A 14-year-old male domestic shorthair cat presented with an acute onset of aggressive behaviour, fear and hypersalivation. Neurological examination revealed bilateral mydriasis and left-sided facial twitching and hemiparesis. Magnetic resonance...
10.
Van Poucke M, Vanhaesebrouck A, Peelman L, Van Ham L
Neuromuscul Disord
. 2012 Feb;
22(6):558-65.
PMID: 22342001
KCNA1, KCNA2, KCNA6 and KCNQ2 are associated with peripheral nerve hyperexcitability in humans. In order to determine if these genes are also involved in Jack Russell Terriers with a similar...