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authFullName_s : Pascale Marcorelles

Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis

F. Démurger , L. Pasquier , C. Dubourg , V. Dupé , I. Gicquel et al.
Molecular Syndromology, 2013, 4 (6), pp.267--272. ⟨10.1159/000353878⟩
Journal articles hal-01064054v1
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Comparison of Characteristics of Neuropathic and Non-neuropathic Pruritus to Develop a Tool for the Diagnosis of Neuropathic Pruritus The NP5

Johanna Huguen , Emilie Brenaut , Caroline-Jade Clerc , Florence Poizeau , Pascale Marcorelles et al.
Frontiers in Medicine, 2019, 6, pp.79. ⟨10.3389/fmed.2019.00079⟩
Journal articles hal-02156251v1

VEGFR1 and NRP1 endothelial expressions predict distant relapse after radical prostatectomy in clinically localized prostate cancer.

Matthieu Talagas , Arnaud Uguen , Ronan Garlantezec , Georges Fournier , Laurent Doucet et al.
Anticancer Research, 2013, 33 (5), pp.2065-75
Journal articles hal-00876427v1
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The neuronal endopeptidase ECEL1 is associated with a distinct form of recessive distal arthrogryposis.

Klaus Dieterich , Susana Quijano-Roy , Nicole Monnier , Jie Zhou , Julien Fauré et al.
Human Molecular Genetics, 2013, 22 (8), pp.1483-92. ⟨10.1093/hmg/dds514⟩
Journal articles inserm-00904747v1
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Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review

Laïla El Khattabi , Sylvie Jaillard , Joris Andrieux , Laurent Pasquier , Laurence Perrin et al.
American Journal of Medical Genetics Part A, 2015, 167 (6), pp.1252--1261. ⟨10.1002/ajmg.a.36932⟩
Journal articles istex hal-01165441v1

Inversion duplication deletions involving the long arm of chromosome 13: phenotypic description of additional three fetuses and genotype-phenotype correlation.

Chloe Quelin , Emmanuel Spaggiari , Suonavy Khung-Savatovsky , Celine Dupont , Laurent Pasquier et al.
American Journal of Medical Genetics Part A, 2014, 164A (10), pp.2504-9. ⟨10.1002/ajmg.a.36658⟩
Journal articles istex hal-01116584v1

The transcription coactivator ASC-1 is a regulator of skeletal myogenesis, and its deficiency causes a novel form of congenital muscle disease

Laurianne Davignon , Claire Chauveau , Cédric Julien , Corinne Dill , Isabelle Duband-Goulet et al.
Human Molecular Genetics, 2016, 25 (8), pp.1559--1573. ⟨10.1093/hmg/ddw033⟩
Journal articles hal-01295646v1

Fluorescent In Situ Hybridization Must be Preferred to pan-TRK Immunohistochemistry to Diagnose NTRK3-rearranged Gastrointestinal Stromal Tumors (GIST)

Marine Castillon , Solene-Florence Kammerer-Jacquet , Mélanie Cariou , Sebastian Costa , Gwenael Conq et al.
Applied Immunohistochemistry and Molecular Morphology : Aimm, 2021, ⟨10.1097/PAI.0000000000000933⟩
Journal articles hal-03229092v1

Presence of putative stem cells in Merkel cell carcinomas.

Gilles Lemasson , Nolwenn Coquart , Nicolas Lebonvallet , Nicholas Boulais , Marie-Dominique Galibert et al.
Journal of the European Academy of Dermatology and Venereology, 2012, 26 (6), pp.789-95. ⟨10.1111/j.1468-3083.2011.04132.x⟩
Journal articles istex inserm-00604469v1

An Original Case of an Association of Eosinophilic Fasciitis with Cholangitis Induced by Nivolumab

Erwan Le Tallec , Charles Ricordel , Louise Triquet , Arnaud Deniel , Pascale Marcorelles et al.
Journal of Thoracic Oncology, 2019, 14 (1), pp.E13-E15. ⟨10.1016/j.jtho.2018.09.016⟩
Journal articles hal-01978479v1

Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases.

Laurent Pasquier , Pascale Marcorelles , Philippe Loget , Fanny Pelluard , Dominique Carles et al.
Acta Neuropathologica, 2009, 117 (2), pp.185-200. ⟨10.1007/s00401-008-0469-9⟩
Journal articles inserm-00353294v1
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Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.

Claude Bendavid , Lucie Rochard , Christèle Dubourg , Jonathan Seguin , Isabelle Gicquel et al.
Human Mutation, 2009, 30 (8), pp.1175-82. ⟨10.1002/humu.21016⟩
Journal articles inserm-00404487v1