Isaac Adanyeguh
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Explore the profile of Isaac Adanyeguh including associated specialties, affiliations and a list of published articles.
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10
Citations
127
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Recent Articles
1.
Robertson J, Adanyeguh I, Bender B, Boesch S, Brunetti A, Cocozza S, et al.
Mov Disord
. 2025 Feb;
PMID: 39927598
Background: Spinocerebellar ataxia type 2 (SCA2) is a rare, inherited neurodegenerative disease characterized by progressive deterioration in both motor coordination and cognitive function. Atrophy of the cerebellum, brainstem, and spinal...
2.
Robertson J, Adanyeguh I, Bender B, Boesch S, Brunetti A, Cocozza S, et al.
bioRxiv
. 2024 Sep;
PMID: 39345594
Objective: Spinocerebellar ataxia type 2 (SCA2) is a rare, inherited neurodegenerative disease characterised by progressive deterioration in both motor coordination and cognitive function. Atrophy of the cerebellum, brainstem, and spinal...
3.
Pandolfo M, Reetz K, Darling A, Rodriguez de Rivera F, Henry P, Joers J, et al.
Neurol Genet
. 2022 Dec;
8(6):e200034.
PMID: 36524101
Background And Objectives: Friedreich ataxia (FRDA) is an autosomal recessive ataxia with no approved treatments. Leriglitazone is a selective peroxisome proliferator-activated receptor γ agonist that crosses the blood-brain barrier and,...
4.
Wiehler A, Branzoli F, Adanyeguh I, Mochel F, Pessiglione M
Curr Biol
. 2022 Aug;
32(16):3564-3575.e5.
PMID: 35961314
Behavioral activities that require control over automatic routines typically feel effortful and result in cognitive fatigue. Beyond subjective report, cognitive fatigue has been conceived as an inflated cost of cognitive...
5.
Ekmen A, Meneret A, Valabregue R, Beranger B, Worbe Y, Lamy J, et al.
Neurology
. 2022 Jan;
98(10):e1077-e1089.
PMID: 35058336
Background And Objectives: The main culprit gene for paroxysmal kinesigenic dyskinesia, characterized by brief and recurrent attacks of involuntary movements, is . The location of the primary dysfunction associated with...
6.
Coarelli G, Darios F, Petit E, Dorgham K, Adanyeguh I, Petit E, et al.
Neurobiol Dis
. 2021 Feb;
153:105311.
PMID: 33636389
Neurofilament light chain (NfL) is a marker of brain atrophy and predictor of disease progression in rare diseases such as Huntington Disease, but also in more common neurological disorders such...
7.
Ward J, Stoyas C, Switonski P, Ichou F, Fan W, Collins B, et al.
Cell Rep
. 2019 Jan;
26(5):1189-1202.e6.
PMID: 30699348
Spinocerebellar ataxia type 7 (SCA7) is a retinal-cerebellar degenerative disorder caused by CAG-polyglutamine (polyQ) repeat expansions in the ataxin-7 gene. As many SCA7 clinical phenotypes occur in mitochondrial disorders, and...
8.
Petiet A, Adanyeguh I, Aigrot M, Poirion E, Nait-Oumesmar B, Santin M, et al.
J Comp Neurol
. 2018 Dec;
527(13):2179-2189.
PMID: 30520034
Specific magnetic resonance imaging (MRI) markers of myelin are critical for the evaluation and development of regenerative therapies for demyelinating diseases. Several MRI methods have been developed for myelin imaging,...
9.
Masingue M, Adanyeguh I, Tchikviladze M, Maisonobe T, Jardel C, Galanaud D, et al.
Mitochondrion
. 2018 Feb;
45:22-28.
PMID: 29474836
Mutations in the gene encoding polymerase gamma (POLG) are a common cause of mitochondrial diseases in adults. We retrospectively analyzed volumetric and diffusion tensor imaging data from 20 adult POLG-mutated...
10.
Hainque E, Caillet S, Leroy S, Flamand-Roze C, Adanyeguh I, Charbonnier-Beaupel F, et al.
Orphanet J Rare Dis
. 2017 Oct;
12(1):160.
PMID: 28969699
Background: Based on the hypothesis of a brain energy deficit, we investigated the safety and efficacy of triheptanoin on paroxysmal episodes in patients with alternating hemiplegia of childhood due to...