Effects of Positive Psychology Interventions on the Well-Being of Young Children: A Systematic Literature Review von Benoit, Valérie, Gabola, Piera

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Role of Callous and Unemotional (CU) Traits on the Development of Youth with Behavioral Disorders: A Systematic Review von Squillaci, Myriam, Benoit, Valérie

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Shaping the Future of Probiotics and Prebiotics von Cunningham, Marla, Azcarate-Peril, M. Andrea, Barnard, Alan, Benoit, Valerie, Grimaldi, Roberta, Guyonnet, Denis, Holscher, Hannah D., Hunter, Kirsty, Manurung, Sarmauli, Obis, David, Petrova, Mariya I., Steinert, Robert E., Swanson, Kelly S., van Sinderen, Douwe, Vulevic, Jelena, Gibson, Glenn R.

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Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome von Lederer, Damien, Grisart, Bernard, Digilio, Maria Cristina, Benoit, Valérie, Crespin, Marianne, Ghariani, Sophie Claire, Maystadt, Isabelle, Dallapiccola, Bruno, Verellen-Dumoulin, Christine

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Consumption of Yogurts Fortified in Vitamin D and Calcium Reduces Serum Parathyroid Hormone and Markers of Bone Resorption: A Double-Blind Randomized Controlled Trial in Institutio... von Bonjour, Jean-Philippe, Benoit, Valérie, Payen, Flore, Kraenzlin, Marius

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Consumption of Vitamin D-and Calcium-Fortified Soft White Cheese Lowers the Biochemical Marker of Bone Resorption TRAP 5b in Postmenopausal Women at Moderate Risk of Osteoporosis F... von BONJOUR, Jean-Philippe, BENOIT, Valérie, ROUSSEAU, Brigitte, SOUBERBIELLE, Jean-Claude

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Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome von Belge, Hendrica, Dahan, Karin, Cambier, Jean-François, Benoit, Valérie, Morelle, Johann, Bloch, Julie, Vanhille, Philippe, Pirson, Yves, Demoulin, Nathalie

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De novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability von Parker, Michael J., Fryer, Alan E., Shears, Deborah J., Lachlan, Katherine L., McKee, Shane A., Magee, Alex C., Mohammed, Shehla, Vasudevan, Pradeep C., Park, Soo-Mi, Benoit, Valérie, Lederer, Damien, Maystadt, Isabelle, study, DDD, FitzPatrick, David R.

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Effects of Vitamin D and Calcium Fortified Yogurts on Gait, Cognitive Performances, and Serum 25-Hydroxyvitamin D Concentrations in Older Community-Dwelling Females: Results from t... von Beauchet, Olivier, Launay, Cyrille P, Galery, Kevin, Vilcocq, Christine, Dontot-Payen, Flore, Rousseau, Brigitte, Benoit, Valérie, Allali, Gilles

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Eight further individuals with intellectual disability and epilepsy carrying bi-allelic CNTNAP2 aberrations allow delineation of the mutational and phenotypic spectrum von Smogavec, Mateja, Cleall, Alison, Hoyer, Juliane, Lederer, Damien, Nassogne, Marie-Cécile, Palmer, Elizabeth E, Deprez, Marie, Benoit, Valérie, Maystadt, Isabelle, Noakes, Charlotte, Leal, Alejandro, Shaw, Marie, Gecz, Jozef, Raymond, Lucy, Reis, André, Shears, Deborah, Brockmann, Knut, Zweier, Christiane

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A second case of Okamoto syndrome caused by HNRNPK mutation von Maystadt, Isabelle, Deprez, Marie, Moortgat, Stéphanie, Benoît, Valérie, Karadurmus, Deniz

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Broadening the phenotypic spectrum and physiological insights related to EIF2S3 variants von Moortgat, Stephanie, Manfroid, Isabelle, Pendeville, Hélène, Freeman, Stephen, Bourdouxhe, Jordane, Benoit, Valérie, Merhi, Ahmad, Philippe, Christophe, Faivre, Laurence, Maystadt, Isabelle

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Clinical delineation, sex differences, and genotype–phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2 von Faundes, Víctor, Goh, Stephanie, Akilapa, Rhoda, Bezuidenhout, Heidre, Bjornsson, Hans T., Bradley, Lisa, Brady, Angela F., Brischoux-Boucher, Elise, Brunner, Han, Bulk, Saskia, Canham, Natalie, Cody, Declan, Dentici, Maria Lisa, Digilio, Maria Cristina, Elmslie, Frances, Fry, Andrew E., Gill, Harinder, Hurst, Jane, Johnson, Diana, Julia, Sophie, Lachlan, Katherine, Lebel, Robert Roger, Byler, Melissa, Gershon, Eric, Lemire, Edmond, Gnazzo, Maria, Lepri, Francesca Romana, Marchese, Antonia, McEntagart, Meriel, McGaughran, Julie, Mizuno, Seiji, Okamoto, Nobuhiko, Rieubland, Claudine, Rodgers, Jonathan, Sasaki, Erina, Scalais, Emmanuel, Scurr, Ingrid, Suri, Mohnish, van der Burgt, Ineke, Matsumoto, Naomichi, Miyake, Noriko, Benoit, Valérie, Lederer, Damien, Banka, Siddharth

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A three generation X-linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A von Lederer, Damien, Shears, Debbie, Benoit, Valérie, Verellen-Dumoulin, Christine, Maystadt, Isabelle

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Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy von Moortgat, Stéphanie, Désir, Julie, Benoit, Valérie, Boulanger, Sébastien, Pendeville, Hélène, Nassogne, Marie-Cécile, Lederer, Damien, Maystadt, Isabelle

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Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literature von Carmignac, Virginie, Nambot, Sophie, Lehalle, Daphné, Callier, Patrick, Moortgat, Stephanie, Benoit, Valérie, Ghoumid, Jamal, Delobel, Bruno, Smol, Thomas, Thuillier, Caroline, Zordan, Cécile, Naudion, Sophie, Bienvenu, Thierry, Touraine, Renaud, Ramond, Francis, Zweier, Christiane, Reis, André, Kraus, Cornelia, Nizon, Mathilde, Cogné, Benjamin, Verloes, Alain, Tran Mau‐Them, Frédéric, Sorlin, Arthur, Jouan, Thibaud, Duffourd, Yannis, Tisserant, Emilie, Philippe, Christophe, Vitobello, Antonio, Thevenon, Julien, Faivre, Laurence, Thauvin‐Robinet, Christel

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Antenatal diagnosis of CHARGE syndrome: Prenatal ultrasound findings and crucial role of fetal dysmorphic signs. About a series of 10 cases and review of literature von Biard, Jean-Marc, Payrat, Stéphanie, Clapuyt, Philippe, Barrea, Catherine, Benoit, Valérie, Baldin, Pamela, Bernard, Pierre, Van Grambezen, Bénédicte, Sznajer, Yves

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Case report: Thirty-year progression of an EMPF1 encephalopathy due to defective mitochondrial and peroxisomal fission caused by a novel de novo heterozygous DNM1L variant von Lhuissier, Charlène, Wagner, Bart E., Vincent, Amy, Garraux, Gaëtan, Hougrand, Olivier, Van Coster, Rudy, Benoit, Valerie, Karadurmus, Deniz, Lenaers, Guy, Gueguen, Naïg, Chevrollier, Arnaud, Maystadt, Isabelle

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Case Report: Inactivating PTH/PTHrP Signaling Disorder Type 1 Presenting With PTH Resistance von Demaret, Tanguy, Wintjens, René, Sana, Gwenaelle, Docquir, Joachim, Bertin, Frederic, Ide, Christophe, Monestier, Olivier, Karadurmus, Deniz, Benoit, Valerie, Maystadt, Isabelle

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Protein quality affects bone status during moderate protein restriction in growing mice von Rouy, Emilien, Vico, Laurence, Laroche, Norbert, Benoit, Valérie, Rousseau, Brigitte, Blachier, François, Tomé, Daniel, Blais, Anne

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