Clinical and genetic spectrums of 413 North African families with inherited retinal dystrophies and optic neuropathies by Aymane Bouzidi, Hicham Charoute, Majida Charif, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers

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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 by Charlène Lhuissier, Bart E. Wagner, Amy Vincent, Gaëtan Garraux, Gaëtan Garraux, Olivier Hougrand, Rudy Van Coster, Valerie Benoit, Deniz Karadurmus, Guy Lenaers, Guy Lenaers, Naïg Gueguen, Naïg Gueguen, Arnaud Chevrollier, Isabelle Maystadt, Isabelle Maystadt

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Recessive TBC1D24 Mutations Are Frequent in Moroccan Non-Syndromic Hearing Loss Pedigrees. by Amina Bakhchane, Majida Charif, Sara Salime, Redouane Boulouiz, Halima Nahili, Rachida Roky, Guy Lenaers, Abdelhamid Barakat

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Neurotoxins Acting on TRPV1—Building a Molecular Template for the Study of Pain and Thermal Dysfunctions by Florian Beignon, Margaux Notais, Sylvie Diochot, Anne Baron, Ziad Fajloun, Hélène Tricoire-Leignel, Guy Lenaers, César Mattei

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Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss. by Amina Bakhchane, Majida Charif, Amale Bousfiha, Redouane Boulouiz, Halima Nahili, Hassan Rouba, Hicham Charoute, Guy Lenaers, Abdelhamid Barakat

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Microcebus murinus retina: A new model to assess prion-related neurotoxicity in primates by Joan Torrent, Chadi Soukkarieh, Guy Lenaers, Carl Arndt, Valérie Forster, Serge Picaud, Nadine Mestre-Francés, Jean-Michel Verdier

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Pitfalls in Monitoring Mitochondrial Temperature Using Charged Thermosensitive Fluorophores by Dominique Chrétien, Paule Bénit, Christine Leroy, Riyad El-Khoury, Sunyou Park, Jung Yeol Lee, Young-Tae Chang, Guy Lenaers, Pierre Rustin, Malgorzata Rak

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Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission by Charlène Lhuissier, Valérie Desquiret-Dumas, Anaïs Girona, Jennifer Alban, Justine Faure, Julien Cassereau, Philippe Codron, Guy Lenaers, Olivier R. Baris, Naïg Gueguen, Arnaud Chevrollier

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Resveratrol Directly Binds to Mitochondrial Complex I and Increases Oxidative Stress in Brain Mitochondria of Aged Mice. by Naïg Gueguen, Valérie Desquiret-Dumas, Géraldine Leman, Stéphanie Chupin, Stéphanie Baron, Valérie Nivet-Antoine, Emilie Vessières, Audrey Ayer, Daniel Henrion, Guy Lenaers, Pascal Reynier, Vincent Procaccio

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Characterization of SSBP1-related optic atrophy and foveopathy by Isabelle Meunier, Béatrice Bocquet, Sabine Defoort-Dhellemmes, Vasily Smirnov, Carl Arndt, Marie Christine Picot, Hélène Dollfus, Majida Charif, Isabelle Audo, Hélèna Huguet, Xavier Zanlonghi, Guy Lenaers

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Hereditary spastic paraplegia and prominent sensorial involvement: think MAG mutations! by Agathe Roubertie, Majida Charif, Pierre Meyer, Gael Manes, Isabelle Meunier, Guillaume Taieb, Raul Junta Morales, Agnès Guichet, Cecile Delettre, Emmanuelle Sarzi, Nicolas Leboucq, François Rivier, Guy Lenaers

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Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy by Majida Charif, Yvette C. Wong, Soojin Kim, Agnès Guichet, Catherine Vignal, Xavier Zanlonghi, Philippe Bensaid, Vincent Procaccio, Dominique Bonneau, Patrizia Amati-Bonneau, Pascal Reynier, Dimitri Krainc, Guy Lenaers

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The Long Non-Coding RNA SAMMSON Is a Regulator of Chemosensitivity and Metabolic Orientation in MCF-7 Doxorubicin-Resistant Breast Cancer Cells by Charlotte Orre, Xavier Dieu, Jordan Guillon, Naïg Gueguen, Seyedeh Tayebeh Ahmadpour, Jean-François Dumas, Salim Khiati, Pascal Reynier, Guy Lenaers, Olivier Coqueret, Arnaud Chevrollier, Delphine Mirebeau-Prunier, Valérie Desquiret-Dumas

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Cyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy by Stéphanie Leruez, Christophe Verny, Dominique Bonneau, Vincent Procaccio, Guy Lenaers, Patrizia Amati-Bonneau, Pascal Reynier, Clarisse Scherer, Adriana Prundean, Christophe Orssaud, Xavier Zanlonghi, Marie-Bénédicte Rougier, Caroline Tilikete, Dan Miléa

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Expanding the genetic spectrum of mitochondrial diseases in Tunisia: novel variants revealed by whole-exome sequencing by Ismail Gouiza, Ismail Gouiza, Ismail Gouiza, Ismail Gouiza, Meriem Hechmi, Meriem Hechmi, Abir Zioudi, Abir Zioudi, Abir Zioudi, Hamza Dallali, Hamza Dallali, Nadia Kheriji, Nadia Kheriji, Nadia Kheriji, Majida Charif, Morgane Le Mao, Said Galai, Said Galai, Lilia Kraoua, Lilia Kraoua, Ilhem Ben Youssef-Turki, Ilhem Ben Youssef-Turki, Ilhem Ben Youssef-Turki, Ichraf Kraoua, Ichraf Kraoua, Ichraf Kraoua, Guy Lenaers, Guy Lenaers, Rym Kefi, Rym Kefi

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Data-Mining Approach on Transcriptomics and Methylomics Placental Analysis Highlights Genes in Fetal Growth Restriction by Floris Chabrun, Floris Chabrun, Noémie Huetz, Noémie Huetz, Xavier Dieu, Xavier Dieu, Guillaume Rousseau, Guillaume Rousseau, Guillaume Bouzillé, Guillaume Bouzillé, Juan Manuel Chao de la Barca, Juan Manuel Chao de la Barca, Vincent Procaccio, Vincent Procaccio, Guy Lenaers, Guy Lenaers, Odile Blanchet, Guillaume Legendre, Delphine Mirebeau-Prunier, Delphine Mirebeau-Prunier, Marc Cuggia, Marc Cuggia, Philippe Guardiola, Pascal Reynier, Pascal Reynier, Geraldine Gascoin, Geraldine Gascoin

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OPA1: 516 unique variants and 831 patients registered in an updated centralized Variome database by Bastien Le Roux, Guy Lenaers, Xavier Zanlonghi, Patrizia Amati-Bonneau, Floris Chabrun, Thomas Foulonneau, Angélique Caignard, Stéphanie Leruez, Philippe Gohier, Vincent Procaccio, Dan Milea, Johan T. den Dunnen, Pascal Reynier, Marc Ferré

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OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions by Valentina Del Dotto, Prashant Mishra, Sara Vidoni, Mario Fogazza, Alessandra Maresca, Leonardo Caporali, J. Michael McCaffery, Martina Cappelletti, Enrico Baruffini, Guy Lenaers, David Chan, Michela Rugolo, Valerio Carelli, Claudia Zanna

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A Data Mining Metabolomics Exploration of Glaucoma by Judith Kouassi Nzoughet, Khadidja Guehlouz, Stéphanie Leruez, Philippe Gohier, Cinzia Bocca, Jeanne Muller, Odile Blanchet, Dominique Bonneau, Gilles Simard, Dan Milea, Vincent Procaccio, Guy Lenaers, Juan M. Chao de la Barca, Pascal Reynier

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ACO2 clinicobiological dataset with extensive phenotype ontology annotation by Khadidja Guehlouz, Thomas Foulonneau, Patrizia Amati-Bonneau, Majida Charif, Estelle Colin, Céline Bris, Valérie Desquiret-Dumas, Dan Milea, Philippe Gohier, Vincent Procaccio, Dominique Bonneau, Johan T. den Dunnen, Guy Lenaers, Pascal Reynier, Marc Ferré

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