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Centre hospitalier universitaire (CHU) de Dijon Bourgogne
Hospital
Location:
Dijon
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:
https://ror.org/0377z4z10
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Publications
(35)
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Journal article
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Management of Local Skin Reactions Caused by 5-FU 4% Cream for the Treatment of Actinic Keratosis: A Delphi Consensus (2025)
Brancaccio G, Briatico G, Apalla Z, Dummer R, Eklind J, Seguin NB, Dreno B, et al.
Journal article
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors (2024)
Willim J, Woike D, Greene D, Das S, Pfeifer K, Yuan W, Lindsey A, et al.
Journal article
Hematopoietic stem cell transplantation for DLBCL: a report from the European Society for Blood and Marrow Transplantation on more than 40,000 patients over 32 years (2024)
Berning P, Fekom M, Ngoya M, Goldstone AH, Dreger P, Montoto S, Finel H, et al.
Journal article
MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway (2024)
Gong M, Li J, Qin Z, Machado Bressan Wilke MV, Liu Y, Li Q, Liu H, et al.
Journal article
Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (2024)
Paulet A, Bennett-Ness C, Ageorges F, Trost D, Green A, Goudie D, Jewell R, et al.
Journal article
DNA methylation episignature and comparative epigenomic profiling for Pitt-Hopkins syndrome caused by TCF4 variants (2024)
van der Laan L, Lauffer P, Rooney K, Silva A, Haghshenas S, Relator R, Levy MA, et al.
Journal article
Developmental epileptic encephalopathy in DLG4-related synaptopathy. (2024)
Kassabian B, Levy AM, Gardella E, Aledo-Serrano A, Ananth AL, Brea-Fernández AJ, Caumes R, et al.
Journal article
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features (2024)
Li D, Wang Q, Bayat A, Battig MR, Zhou Y, Bosch DG, van Haaften G, et al.
Journal article
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 (2024)
Paul MS, Michener SL, Pan H, Chan H, Pfliger JM, Rosenfeld JA, Lerma VC, et al.
Journal article
Further delineation of the SCAF4-associated neurodevelopmental disorder (2024)
Schmid CM, Gregor A, Ruiz A, Manso Bazús C, Herman I, Ammouri F, Kotzaeridou U, et al.
Journal article
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