Statins and the Brain: More than Lipid Lowering Agents? von Fracassi, Anna, Marangoni, Martina, Rosso, Pamela, Pallottini, Valentina, Fioramonti, Marco, Siteni, Silvia, Segatto, Marco

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Deficiency of Nrf2 exacerbates white matter damage and microglia/macrophage levels in a mouse model of vascular cognitive impairment von Sigfridsson, Emma, Marangoni, Martina, Hardingham, Giles E., Horsburgh, Karen, Fowler, Jill H.

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Dimethyl fumarate improves white matter function following severe hypoperfusion: Involvement of microglia/macrophages and inflammatory mediators von Fowler, Jill H, McQueen, Jamie, Holland, Philip R, Manso, Yasmina, Marangoni, Martina, Scott, Fiona, Chisholm, Emma, Scannevin, Robert H, Hardingham, Giles E, Horsburgh, Karen

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Astrocyte-specific overexpression of Nrf2 protects against optic tract damage and behavioural alterations in a mouse model of cerebral hypoperfusion von Sigfridsson, Emma, Marangoni, Martina, Johnson, Jeffrey A., Hardingham, Giles E., Fowler, Jill H., Horsburgh, Karen

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Minocycline reduces microgliosis and improves subcortical white matter function in a model of cerebral vascular disease von Manso, Yasmina, Holland, Philip R., Kitamura, Akihiro, Szymkowiak, Stefan, Duncombe, Jessica, Hennessy, Edel, Searcy, James L., Marangoni, Martina, Randall, Andrew D., Brown, Jon T., McColl, Barry W., Horsburgh, Karen

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Prenatal diagnosis of cystinuria with a heterozygous pathogenic variant in SLC7A9 gene associated with isolated hyperechogenic fetal kidneys: A case report von Aigbogun, Osaretin Pamela, Vancoppenolle, Noémie, Coppens, Sandra, Marangoni, Martina, Elsen, Elodie, Cassart, Marie, Gounongbe, Caroline

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Case Report: Homozygous Pathogenic Variant P209L in the TTC21B Gene: A Rare Cause of End Stage Renal Disease and Biliary Cirrhosis Requiring Combined Liver-Kidney Transplantation.... von Gambino, Giuseppe, Catalano, Concetta, Marangoni, Martina, Geers, Caroline, Moine, Alain Le, Boon, Nathalie, Smits, Guillaume, Ghisdal, Lidia

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Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants von Hurni, Yannick, Marangoni, Martina, Garofalo, Giulia, Cassart, Marie, Tomasi, Lisa, Vandernoot, Isabelle, Smits, Guillaume, Gounongbé, Caroline

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Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis von Sassi, Asma, Désir, Julie, Janssens, Véronique, Marangoni, Martina, Daneels, Dorien, Gheldof, Alexander, Bonduelle, Maryse, Van Dooren, Sonia, Costagliola, Sabine, Delbaere, Anne

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Middle interhemispheric variant of holoprosencephaly: First prenatal report of a ZIC2 missense mutation von Gounongbé, Caroline, Marangoni, Martina, Gouder de Beauregard, Vanessa, Delaunoy, Mélanie, Jissendi, Patrice, Cassart, Marie, Désir, Julie

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Efficiency of clinical exome sequencing in the diagnosis of pediatric genodermatoses: A prospective cohort study von Salik, Deborah, Marangoni, Martina, Dangoisse, Chantal, Richert, Bertrand, Smits, Guillaume

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Switching OnabotulinumtoxinA to Monoclonal Anti-CGRP Antibodies in Drug-Resistant Chronic Migraine von Iannone, Luigi Francesco, Fattori, Davide, Marangoni, Martina, Benemei, Silvia, Chiarugi, Alberto, Geppetti, Pierangelo, De Cesaris, Francesco

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Peripheral Nerve Resident Macrophages and Schwann Cells Mediate Cancer-Induced Pain von De Logu, Francesco, Marini, Matilde, Landini, Lorenzo, de Araujo, Daniel Souza Monteiro, Bartalucci, Niccolo, Trevisan, Gabriela, Bruno, Gennaro, Marangoni, Martina, Schmidt, Brian Lee, Bunnett, Nigel W., Geppetti, Pierangelo, Nassini, Romina

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Novel Mixed NOP/Opioid Receptor Peptide Agonists von Pacifico, Salvatore, Albanese, Valentina, Illuminati, Davide, Marzola, Erika, Fabbri, Martina, Ferrari, Federica, Holanda, Victor A.D, Sturaro, Chiara, Malfacini, Davide, Ruzza, Chiara, Trapella, Claudio, Preti, Delia, Lo Cascio, Ettore, Arcovito, Alessandro, Della Longa, Stefano, Marangoni, Martina, Fattori, Davide, Nassini, Romina, Calò, Girolamo, Guerrini, Remo

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Salt-losing tubulopathy worsening the prognosis of renal sarcoidosis von Abu Ayyach, Anis, Le Moine, Alain, Kaci, Louiza, Royer-Chardon, Claire, Ghisdal, Lidia, Marangoni, Martina, Smits, Guillaume, Nortier, Joëlle

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Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis von Ghesh, Leïla, Désir, Julie, Haye, Damien, Le Tanno, Pauline, Devillard, Françoise, Cogné, Benjamin, Marangoni, Martina, Tecco, Laura, Heron, Delphine, Le Vaillant, Claudine, Joubert, Madeleine, Beneteau, Claire

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Evaluation of neurodevelopmental symptoms in 10 cases of neonatal ichthyosis and sclerosing cholangitis syndrome von Salik, Deborah, Hadj‐Rabia, Smail, Hohl, Daniel, Vahidnezhad, Hassan, Youssefian, Leila, Rakosi, Adèle, Dangoisse, Chantal, Marangoni, Martina, Vilain, Catheline, Smits, Guillaume

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Age-related axonal swellings precede other neuropathological hallmarks in a knock-in mouse model of Huntington's disease von Marangoni, Martina, Adalbert, Robert, Janeckova, Lucie, Patrick, Jane, Kohli, Jaskaren, Coleman, Michael P, Conforti, Laura

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Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohorts von Marangoni, Martina, Smits, Guillaume, Ceysens, Gilles, Costa, Elena, Coulon, Robert, Daelemans, Caroline, De Coninck, Caroline, Derisbourg, Sara, Gajewska, Kalina, Garofalo, Giulia, Gounongbe, Caroline, Guizani, Meriem, Holoye, Anne, Houba, Catherine, Makhoul, Jean, Norgaard, Christian, Regnard, Cecile, Romée, Stephanie, Soto, Jamil, Stagel-Trabbia, Aurore, Van Rysselberge, Michel, Vercoutere, An, Zaytouni, Siham, Bouri, Sarah, D'Haene, Nicky, D'Onle, Dominique, Dugauquier, Christian, Racu, Marie-Lucie, Rocq, Laureen, Segers, Valérie, Verocq, Camille, Avni, Ephraim Freddy, Cassart, Marie, Massez, Anne, Blaumeiser, Bettina, Brischoux-Boucher, Elise, Bulk, Saskia, De Ravel, Thomy, Debray, Guillaume, Dimitrov, Boyan, Janssens, Sandra, Keymolen, Kathelijn, Laterre, Marie, van Berkel, Kim, Van Maldergem, Lionel, Vandernoot, Isabelle, Vilain, Catheline, Donner, Catherine, Tecco, Laura, Thomas, Dominique, Désir, Julie, Abramowicz, Marc, Migeotte, Isabelle

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Novel features of PIK3CA-Related Overgrowth Spectrum: Lesson from an aborted fetus presenting a de novo constitutional PIK3CA mutation von De Graer, Celine, Marangoni, Martina, Romnée, Stephanie, Delaunoy, Mélanie, Zaytouni, Siham, D'Haene, Nicky, Désir, Julie, Donner, Catherine

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