Danielle Seilhean
Overview
Explore the profile of Danielle Seilhean including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
128
Citations
4900
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Vicario R, Fragkogianni S, Pokrovskii M, Meyer C, Lopez-Rodrigo E, Hu Y, et al.
Neuron
. 2025 Mar;
PMID: 40081365
Langerhans cell histiocytosis (LCH) and Erdheim-Chester disease (ECD) are clonal myeloid disorders associated with mitogen-activated protein (MAP)-kinase-activating mutations and an increased risk of neurodegeneration. We found microglial mutant clones in...
2.
Delorme C, Pegat A, Theuriet J, Brandel J, Roze E, Viala K, et al.
Ann Clin Transl Neurol
. 2025 Jan;
PMID: 39799963
Objective: To describe peripheral neuropathy associated with familial Creutzfeldt-Jakob disease. Methods: We report two unrelated patients with genetic Creutzfeldt-Jakob disease with demyelinating peripheral neuropathy as initial presentation, with a comprehensive...
3.
Pellerin D, Mereaux J, Boluda S, Danzi M, Dicaire M, Davoine C, et al.
Brain
. 2024 Oct;
PMID: 39378335
Spinocerebellar ataxia 27B (SCA27B) is a common autosomal dominant ataxia caused by an intronic GAA•TTC repeat expansion in FGF14. Neuropathological studies have shown that neuronal loss is largely restricted to...
4.
Vicario R, Fragkogianni S, Pokrovskii M, Mayer C, Lopez-Rodrigo E, Hu Y, et al.
bioRxiv
. 2024 Aug;
PMID: 39131366
Langerhans cell Histiocytosis (LCH) and Erdheim-Chester disease (ECD) are clonal myeloid disorders, associated with MAP-Kinase activating mutations and an increased risk of neurodegeneration. Surprisingly, we found pervasive PU.1 microglia mutant...
5.
Pellerin D, Mereaux J, Boluda S, Danzi M, Dicaire M, Davoine C, et al.
medRxiv
. 2024 Jul;
PMID: 39006414
Spinocerebellar ataxia 27B (SCA27B) is a common autosomal dominant ataxia caused by an intronic GAA•TTC repeat expansion in . Neuropathological studies have shown that neuronal loss is largely restricted to...
6.
Denouel A, Brandel J, Peckeu-Abboud L, Seilhean D, Bouaziz-Amar E, Quadrio I, et al.
Euro Surveill
. 2023 Dec;
28(50).
PMID: 38099349
BackgroundPrion diseases are rare, fatal disorders that have repeatedly raised public health concerns since the early 1990s. An active prion disease surveillance network providing national level data was implemented in...
7.
Fourgeaud J, Regnault B, Ok V, Da Rocha N, Sitterle E, Mekouar M, et al.
Lancet Microbe
. 2023 Dec;
5(1):e52-e61.
PMID: 38048804
Background: Metagenomic next-generation sequencing (mNGS) allows untargeted identification of a broad range of pathogens, including rare or novel microorganisms. Despite the recognition of mNGS as a valuable diagnostic tool for...
8.
Maximova O, Weller M, Krogmann T, Sturdevant D, Ricklefs S, Virtaneva K, et al.
PLoS Pathog
. 2023 Aug;
19(8):e1011544.
PMID: 37595007
Astroviruses (AstVs) can cause of severe infection of the central nervous system (CNS) in immunocompromised individuals. Here, we identified a human AstV of the VA1 genotype, HAstV-NIH, as the cause...
9.
Duyckaerts C, Maisonobe T, Hauw J, Seilhean D
Free Neuropathol
. 2023 Jun;
2.
PMID: 37284640
Jean-Martin Charcot described what he called amyotrophic lateral sclerosis in his 12 and 13 lessons published in 1873 by Bourneville. He distinguished the symptoms that were related to the lesion...
10.
Boluda S, Mokhtari K, Megarbane B, Annane D, Mathon B, Cao A, et al.
Free Neuropathol
. 2023 Jun;
4.
PMID: 37283933
In a neuropathological series of 20 COVID-19 cases, we analyzed six cases (three biopsies and three autopsies) with multiple foci predominantly affecting the white matter as shown by MRI. The...