Veronique Humbertclaude
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Explore the profile of Veronique Humbertclaude including associated specialties, affiliations and a list of published articles.
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15
Citations
538
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Recent Articles
1.
Russet F, Humbertclaude V, Davidovic Vrljicak N, Dieleman G, Dodig-Curkovic K, Franic T, et al.
Front Psychiatry
. 2022 Feb;
12:768206.
PMID: 35222101
Background: In mental health, transition refers to the pathway of young people from child and adolescent to adult services. Training of mental health psychiatrists on transition-related topics offers the opportunity...
2.
Gur-Hartman T, Berkowitz O, Yosovich K, Roubertie A, Zanni G, Macaya A, et al.
Eur J Paediatr Neurol
. 2020 Dec;
30:144-154.
PMID: 33349592
Background: CACNA1A-related disorders present with persistent progressive and non-progressive cerebellar ataxia and paroxysmal events: epileptic seizures and non-epileptic attacks. These phenotypes overlap and co-exist in the majority of patients. Objective:...
3.
Piarroux J, Riant F, Humbertclaude V, Remerand G, Hadjadj J, Rejou F, et al.
Ann Clin Transl Neurol
. 2020 Mar;
7(4):565-572.
PMID: 32162847
We report four patients from two families who presented attacks of childhood-onset episodic ataxia associated with pathogenic mutations in the FGF14 gene. Attacks were triggered by fever, lasted several days,...
4.
Russet F, Humbertclaude V, Dieleman G, Dodig-Curkovic K, Hendrickx G, Kovac V, et al.
BMC Med Educ
. 2019 Jun;
19(1):204.
PMID: 31196080
Background: Profound clinical, conceptual and ideological differences between child and adult mental health service models contribute to transition-related discontinuity of care. Many of these may be related to psychiatry training....
5.
Humbertclaude V, Riant F, Krams B, Zimmermann V, Nagot N, Annequin D, et al.
Dev Med Child Neurol
. 2019 May;
62(3):330-337.
PMID: 31115040
Aim: To describe the clinico-radiological phenotype of children with a CACNA1A mutation and to precisely evaluate their learning ability and cognitive status. Method: Children between the ages of 3 and...
6.
Humbertclaude V, Krams B, Nogue E, Nagot N, Annequin D, Tourniaire B, et al.
Dev Med Child Neurol
. 2018 Jun;
60(12):1256-1263.
PMID: 29926469
Aim: Benign paroxysmal torticollis (BPT), benign paroxysmal vertigo (BPV), and benign tonic upward gaze (BTU) are characterized by transient and recurrent episodes of neurological manifestations. The purpose of this study...
7.
Delcourt M, Riant F, Mancini J, Milh M, Navarro V, Roze E, et al.
J Neurol Neurosurg Psychiatry
. 2015 Jan;
86(7):782-5.
PMID: 25595153
Background: Heterozygous dominant mutations of PRRT2 have been associated with various types of paroxysmal neurological manifestations, including benign familial infantile convulsions and paroxysmal kinesigenic dyskinesia. The phenotype associated with biallelic...
8.
van den Bergen J, Hiller M, Bohringer S, Vijfhuizen L, Ginjaar H, Chaouch A, et al.
J Neurol Neurosurg Psychiatry
. 2014 Dec;
86(10):1060-5.
PMID: 25476005
Objective: Duchenne muscular dystrophy (DMD) is characterised by progressive muscle weakness. It has recently been reported that single nucleotide polymorphisms (SNPs) located in the SPP1 and LTBP4 loci can account...
9.
Ishmukhametova A, Khau Van Kien P, Mechin D, Thorel D, Vincent M, Rivier F, et al.
Eur J Hum Genet
. 2012 Apr;
20(10):1096-100.
PMID: 22510846
We report on the effectiveness of a custom-designed oligonucleotide-based comparative genomic hybridization microarray (array-CGH) to interrogate copy number across the entire 2.2-Mb genomic region of the DMD gene and its...
10.
Humbertclaude V, Hamroun D, Bezzou K, Berard C, Boespflug-Tanguy O, Bommelaer C, et al.
Eur J Paediatr Neurol
. 2011 Sep;
16(2):149-60.
PMID: 21920787
Aims: Our objective was to clarify the clinical heterogeneity in Duchenne muscular dystrophy (DMD). Methods: The French dystrophinopathy database provided clinical, histochemical and molecular data of 278 DMD patients (mean...