I Desguerre
Overview
Explore the profile of I Desguerre including associated specialties, affiliations and a list of published articles.
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Articles
73
Citations
1303
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0
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Recent Articles
1.
Barrois R, Tervil B, Cacioppo M, Barnerias C, Deladriere E, Leloup-Germa V, et al.
J Neuroeng Rehabil
. 2024 Oct;
21(1):183.
PMID: 39415296
Background: Onasemnogene abeparvovec gene replacement therapy (GT) has changed the prognosis of patients with spinal muscular atrophy (SMA) with variable outcome regarding motor development in symptomatic patients. This pilot study...
2.
Richard M, Barrois R, Desguerre I, Deladriere E, Leloup-Germa V, Barnerias C, et al.
Arch Pediatr
. 2023 Nov;
31(1):26-31.
PMID: 37989659
Background: Spinal muscular atrophy (SMA) is a neuromuscular disorder characterized by the degeneration of the anterior horn cells of the spinal cord. Nusinersen for the treatment of SMA has been...
3.
Barrois R, Barnerias C, Deladriere E, Leloup-Germa V, Tervil B, Audic F, et al.
Neuromuscul Disord
. 2023 Mar;
33(4):309-314.
PMID: 36881951
Spinal muscular atrophy 1 (SMA1) is a severe early genetic disease with degeneration of motor neurons. Motor development is still suboptimal after gene replacement therapy in symptomatic patients. In this...
4.
Millischer A, Grevent D, Sonigo P, Bahi-Buisson N, Desguerre I, Mahallati H, et al.
AJNR Am J Neuroradiol
. 2021 Dec;
43(1):132-138.
PMID: 34949593
Background And Purpose: Prognosis of isolated short corpus callosum is challenging. Our aim was to assess whether fetal DTI tractography can distinguish callosal dysplasia from variants of normal callosal development...
5.
Voermans N, Vriens-Munoz Bravo M, Padberg G, Laforet P, van Alfen N, Attarian S, et al.
Neuromuscul Disord
. 2021 Aug;
31(9):907-918.
PMID: 34404575
No abstract available.
6.
Dangles M, Malan V, Dumas G, Romana S, Raoul O, Coste-Zeitoun D, et al.
Clin Neurophysiol
. 2021 Mar;
132(5):1126-1137.
PMID: 33773177
Objective: We aimed to describe epilepsy and EEG patterns related to vigilance states and age, in chromosome15-long-arm-duplication-syndrome (dup15q) children with epilepsy, in both duplication types: interstitial (intdup15) and isodicentric (idic15)....
7.
Chabrol B, Desguerre I
Arch Pediatr
. 2020 Dec;
27(7S):7S50-7S53.
PMID: 33357599
The pediatrician has a privileged relationship with a child with infantile spinal muscular atrophy (SMA). At all times, he/she must be the child's mentor, promoting a comprehensive approach and support...
8.
Chabrol B, Desguerre I
Arch Pediatr
. 2020 Dec;
27(7S):7S1-7S2.
PMID: 33357590
No abstract available.
9.
Guimaraes-Costa R, Fernandez-Eulate G, Wahbi K, Leturcq F, Malfatti E, Behin A, et al.
Eur J Neurol
. 2020 Oct;
28(2):660-669.
PMID: 33051934
Background And Purpose: To describe a large series of patients with α, β, and γ sarcoglycanopathies (LGMD-R3, R4, and R5) and study phenotypic correlations and disease progression. Methods: A multicentric...
10.
Bodemer C, Diociaiuti A, Hadj-Rabia S, Robert M, Desguerre I, Maniere M, et al.
J Eur Acad Dermatol Venereol
. 2020 Jul;
34(7):1415-1424.
PMID: 32678511
Background: Incontinentia pigmenti (IP) is a rare multisystemic X-linked dominant genetic disorder characterized by highly diagnostic skin lesions. The disease can be misdiagnosed in infants, and complications affecting the eyes...