Foxg1-Cre Mediated Lrp2 Inactivation in the Developing Mouse Neural Retina, Ciliary and Retinal Pigment Epithelia Models Congenital High Myopia von Cases, Olivier, Joseph, Antoine, Obry, Antoine, Santin, Mathieu D, Ben-Yacoub, Sirine, Pâques, Michel, Amsellem-Levera, Sabine, Bribian, Ana, Simonutti, Manuel, Augustin, Sébastien, Debeir, Thomas, Sahel, José Alain, Christ, Annabel, de Castro, Fernando, Lehéricy, Stéphane, Cosette, Pascal, Kozyraki, Renata

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Intronic mutations outside of Alu-repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia von AMSELLEM, Sabine, BRIFFAUT, Dorothée, DE GENNES, Jean Luc, BRUKERT, Eric, BENLIAN, Pascale, CARRIE, Alain, RABES, Jean Pierre, GIRARDET, Jean Philippe, FREDENRICH, Alexandre, MOULIN, Philippe, KREMPF, Michel, REZNIK, Yves, VIALETTES, Bernard

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Cubilin Is Essential for Albumin Reabsorption in the Renal Proximal Tubule von AMSELLEM, Sabine, GBUREK, Jakub, HAMARD, Ghislaine, NIELSEN, Rikke, WILLNOW, Thomas E, DEVUYST, Olivier, NEXO, Ebba, VERROUST, Pierre J, CHRISTENSEN, Erik I, KOZYRAKI, Renata

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Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia von Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre

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Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia von Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre

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Cubilin, a High Affinity Receptor for Fibroblast Growth Factor 8, Is Required for Cell Survival in the Developing Vertebrate Head von Cases, Olivier, Perea-Gomez, Aitana, Aguiar, Diego P., Nykjaer, Anders, Amsellem, Sabine, Chandellier, Jacqueline, Umbhauer, Muriel, Cereghini, Silvia, Madsen, Mette, Collignon, Jérôme, Verroust, Pierre, Riou, Jean-François, Creuzet, Sophie E., Kozyraki, Renata

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Detailed investigations of proximal tubular function in Imerslund-Gräsbeck syndrome von Storm, Tina, Zeitz, Christina, Cases, Olivier, Amsellem, Sabine, Verroust, Pierre J, Madsen, Mette, Benoist, Jean-François, Passemard, Sandrine, Lebon, Sophie, Jønsson, Iben Møller, Emma, Francesco, Koldsø, Heidi, Hertz, Jens Michael, Nielsen, Rikke, Christensen, Erik I, Kozyraki, Renata

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An alcoholic binge causes massive degradation of hepatic mitochondrial DNA in mice von Mansouri, Abdellah, Gaou, Isabelle, de Kerguenec, Caroline, Amsellem, Sabine, Haouzi, Delphine, Berson, Alain, Moreau ‡, Alain, Feldmann ‡, Gérard, Lettéron, Philippe, Pessayre, Dominique, Fromenty, Bernard

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Diagnosis Scoring for Clinical Identification of Children With Heterozygous Familial Hypercholesterolemia von Benlian, Pascale, Turquet, Anne, Carrat, Fabrice, Amsellem, Sabine, Sanchez, Lydie, Briffaut, Dorothée, Girardet, Jean Philippe

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Erratum: Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia von Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre

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Magnitude of HDL Cholesterol Variation After High-Dose Atorvastatin Is Genetically Determined at the LDL Receptor Locus in Patients With Homozygous Familial Hypercholesterolemia von Sposito, Andrei C, Gonbert, Sophie, Bruckert, Eric, Atassi, Marielle, Beucler, Isabel, Amsellem, Sabine, Khallouf, Oumayma, Benlian, Pascale, Turpin, Gerard

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Foxg1-Cre Mediated Lrp2 Inactivation in the Developing Mouse Neural Retina, Ciliary and Retinal Pigment Epithelia Models Congenital High Myopia: e0129518 von Cases, Olivier, Joseph, Antoine, Obry, Antoine, Santin, Mathieu D, Ben-Yacoub, Sirine, Paques, Michel, Amsellem-Levera, Sabine, Bribian, Ana, Simonutti, Manuel, Augustin, Sebastien

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Erratum: Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia von Allard, Delphine, Amsellem, Sabine, Abifadel, Marianne, Trillard, Mélanie, Devillers, Martine, Luc, Gérald, Krempf, Michel, Reznik, Yves, Girardet, Jean-Philippe, Fredenrich, Alexandre, Junien, Claudine, Varret, Mathilde, Boileau, Catherine, Benlian, Pascale, Rabès, Jean-Pierre

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Detailed investigations of proximal tubular function in Imerslund-Graesbeck syndrome von Storm, Tina, Zeitz, Christina, Cases, Olivier, Amsellem, Sabine, Verroust, Pierre J, Madsen, Mette, Benoist, Jean-Francois, Passemard, Sandrine, Lebon, Sophie, Joensson, Iben Moeller, Emma, Francesco, Koldsoe, Heidi, Hertz, Jens Michael, Nielsen, Rikke, Christensen, Erik I, Kozyraki, Renata

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Telomere Dysfunction Causes Sustained Inflammation in Chronic Obstructive Pulmonary Disease von AMSELLEM, Valerie, GARY-BOBO, Guillaume, HUE, Sophie, LE CORVOISIER, Philippe, LE GOUVELLO, Sabine, DUBOIS-RANDE, Jean-Luc, BOCZKOWSKI, Jorge, ADNOT, Serge, MARCOS, Elisabeth, MAITRE, Bernard, CHAAR, Vicky, VALIDIRE, Pierre, STERN, Jean-Baptiste, NOUREDDINE, Hiba, SAPIN, Elise, RIDEAU, Dominique

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Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric population von El Allali, Yasmine, Hermetet, Coralie, Bacchetta, Justine, Amouroux, Cyril, Rothenbuhler, Anya, Porquet-Bordes, Valérie, Champigny, Marie-Alexandrine, Baron, Sabine, Barat, Pascal, Bony-Trifunovic, Hélène, Bourdet, Karine, Busiah, Kanetee, Cartigny-Maciejewski, Maryse, Compain, Florence, Coutant, Régis, Amsellem-Jager, Jessica, De Kerdanet, Marc, Magontier, Nathalie, Mignot, Brigitte, Richard, Odile, Rossignol, Sylvie, Soskin, Sylvie, Berot, Aurélie, Naud-Saudreau, Catherine, Salles, Jean-Pierre, Linglart, Agnès, Edouard, Thomas, Lienhardt-Roussie, Anne

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The Severity of Congenital Hypothyroidism with Gland-in-situ Predicts Molecular Yield by Targeted NGS von Levaillant, Lucie, Bouhours-Nouet, Natacha, Illouz, Frédéric, Jager, Jessica Amsellem, Bachelot, Anne, Barat, Pascal, Baron, Sabine, Bensignor, Candace, De La Perriere, Aude Brac, Djellas, Yasmine Braik, Caillot, Morgane, Caldagues, Emmanuelle, Campas, Marie-Neige, Caquard, Marylène, Cartault, Audrey, Cheignon, Julie, Decrequy, Anne, Delemer, Brigitte, Dieckmann, Katherine, Donzeau, Aurélie, Doye, Emilie, Fradin, Mélanie, Gaudillière, Mélanie, Gatelais, Frédérique, Gorce, Magali, Hazart, Isabelle, Houcinat, Nada, Houdon, Laure, Ister-Salome, Marielle, Jozwiak, Lucie, Jeannoel, Patrick, Labarthe, Francois, Lacombe, Didier, Lambert, Anne-Sophie, Lefevre, Christine, Leheup, Bruno, Leroy, Clara, Maisonneuve, Benedicte, Marchand, Isis, Marquant, Emeline, Muszlak, Matthias, Pantalone, Letitia, Pochelu, Sandra, Quelin, Chloé, Radet, Catherine, Renoult-Pierre, Peggy, Reynaud, Rachel, Rouleau, Stéphanie, Teinturier, Cécile, Thevenon, Julien, Turlotte, Caroline, Valle, Aline, Vierge, Melody, Villanueva, Carine, Ziegler, Alban, Dieu, Xavier, Bouzamondo, Nathalie, Rodien, Patrice, Prunier-Mirebeau, Delphine, Coutant, Régis

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