부산대학교 도서관

Damaj, Gandhi; de Masson, Adèle; Dreger, Peter; Bazarbachi, Ali; Berning, Philipp; Duarte, Rafael F.; Fox, Christopher P.; Guenova, Emmanuella; Hermine, Olivier; Kyriakou, Charalampia; Tanase, Alina; Tournilhac, Olivier; Jurczak, Wojiech; Karsten, Imke E.; Quoc, Stéphanie Nguyen; Serroukh, Yasmina; Stella, Federico; Wulf, Gerald; Sureda, Anna; Papadavid, Evangelia; Ortiz-Romero, Pablo L.; Ruggeri, Annalisa; Sánchez-Ortega, Isabel; Scarisbrick, Julia J.; Yakoub-Agha, Ibrahim; Onida, Francesco; Schmitz, Norbert

Bone Marrow Transplantation: Official journal of the European Society for Blood and Marrow Transplantation. 60(12):1565-1573

Jaster, Alaina M.; Hadlock, Thomas M.; Buzzi, Belle; Maltman, Jessica L.; Silva, Gabriella M.; Saha, Somdatta; Koseli, Eda; Pondelick, Abby M.; Thakur, Nikita; Zhang, Xin; Li, Gaoshan; Ledesma-Corvi, Sandra; Moore, Karah N.; Peterson, Hannah R.; Fujita, Barbara; Zylko, Alexia L.; Lewis, Melissa R.; Poklis, Justin L.; Halquist, Matthew S.; Wolstenholme, Jennifer T.; Selley, Dana E.; Hamilton, Peter J.; Lu, Chang; Damaj, M. Imad; González-Maeso, Javier

Nature Communications. 16(1)

P. Rollier; A. Cospain; M. Barth; V. Milon; N. Gueguen; C. Homedan; V. Desquiret; C. Bris; E. Colin; L. Damaj; A. Ryckewaert; P. Reynier; S. Odent; P. Amati-Bonneau; V. Procaccio; D. Bonneau; A. Ziegler

Molecular Genetics and Metabolism Reports, Vol 43, Iss , Pp 101214- (2025)

Blin M; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France.; Tardieu M; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France.; Lacombe D; Inserm U1211, Université de Bordeaux, Centre de Compétences Maladies Héréditaires du Métabolisme, CHU de Bordeaux, Bordeaux, France.; Gorce M; Centre de Référence Maladies Héréditaires du Métabolisme, CHU Toulouse, Toulouse, France.; Damaj L; Centre de Compétences Maladies Héréditaires du Métabolisme, CHU Rennes, Rennes, France.; Barth M; Centre de Compétences Maladies Héréditaires du Métabolisme, CHU Angers, Angers, France.; Genevaz D; Vaincre les Maladies Lysosomales (VML), Massy, France.; Vibet S; Centre d'Évaluation et de Traitement de la Douleur, CHRU Tours, Tours, France.; Labarthe F; Centre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France. labarthe@univ-tours.fr.; N2C, Inserm U1069, Université François Rabelais de Tours, Tours, France. labarthe@univ-tours.fr.

Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

Pacot L; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Fédération de Génétique et Médecine Génomique, DMU BioPhyGen, Hôpital Cochin, AP-HP.Centre-Université Paris Cité, Paris, France.; Blok M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands.; Vidaud D; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Fédération de Génétique et Médecine Génomique, DMU BioPhyGen, Hôpital Cochin, AP-HP.Centre-Université Paris Cité, Paris, France.; Fertitta L; Department of Dermatology, Hôpital Henri Mondor, Assistance Publique-Hôpital Paris (AP-HP), Créteil, France.; INSERM U955, Université Paris Est Créteil (UPEC), Créteil, France.; Laurendeau I; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Coustier A; Fédération de Génétique et Médecine Génomique, DMU BioPhyGen, Hôpital Cochin, AP-HP.Centre-Université Paris Cité, Paris, France.; Maillard T; Fédération de Génétique et Médecine Génomique, DMU BioPhyGen, Hôpital Cochin, AP-HP.Centre-Université Paris Cité, Paris, France.; Barbance C; Fédération de Génétique et Médecine Génomique, DMU BioPhyGen, Hôpital Cochin, AP-HP.Centre-Université Paris Cité, Paris, France.; Hadjadj D; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Ye M; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Lallemand D; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Ferkal S; Department of Dermatology, Hôpital Henri Mondor, Assistance Publique-Hôpital Paris (AP-HP), Créteil, France.; INSERM U955, Université Paris Est Créteil (UPEC), Créteil, France.; Funalot B; Department of Genetics, AP-HP (Assistance Publique-Hôpitaux de Paris), Henri Mondor University Hospital, Créteil, France.; Lunati-Rozie A; Department of Genetics, AP-HP (Assistance Publique-Hôpitaux de Paris), Henri Mondor University Hospital, Créteil, France.; Hebrard B; Department of Genetics, AP-HP (Assistance Publique-Hôpitaux de Paris), Henri Mondor University Hospital, Créteil, France.; Bhouri R; Department of Ophthalmology, Centre Hospitalier Intercommunal de Créteil (CHIC), Créteil, France.; Spruijt L; Department of Clinical Genetics, Radboud University Medical Centre, Nijmegen, The Netherlands.; Bessis D; Department of Dermatology and Reference Center for Rare Skin Diseases MAGEC-Sud Montpellier, Filière Maladies Rares Dermatologiques (FIMARAD), Saint-Eloi Hospital, and University of Montpellier, Montpellier, France.; Geneviève D; Inserm U1183, Department of Clinical Genetics, Reference center for rare disease developmental anomaly and malformative syndrome, CHU Montpellier, and Montpellier University, Montpellier, France.; Vernimmen V; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, The Netherlands.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, The Netherlands.; Broen MPG; Department of Neurology, GROW School for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, The Netherlands.; Sigaudy S; Department of Medical Genetics, Children's Hospital La Timone, Assistance Publique des Hôpitaux de Marseille, Marseille, France.; Odent S; Service de génétique clinique, CLAD Ouest, CHU Rennes, Hôpital Sud, Rennes, France.; Damaj L; Service de génétique clinique, CLAD Ouest, CHU Rennes, Hôpital Sud, Rennes, France.; Quélin C; Service de génétique clinique, CLAD Ouest, CHU Rennes, Hôpital Sud, Rennes, France.; Pasquier L; Service de génétique clinique, CLAD Ouest, CHU Rennes, Hôpital Sud, Rennes, France.; Layet V; Consultations de Génétique, Groupe Hospitalier du Havre, Le Havre, France.; Gilbert-Dussardier B; Service de Génétique, CHU de Poitiers, Poitiers, France.; Nicolas G; Department of Genetics and reference center for developmental abnormalities, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.; Guerrot AM; Department of Genetics and reference center for developmental abnormalities, Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Rouen, France.; Leheup B; Service de Génétique Médicale, Hôpitaux de Brabois, CHRU de Nancy, Vandoeuvre-lès-Nancy, France.; Bursztejn AC; Department of Dermatology, CHRU Nancy, Vandoeuvre-lès-Nancy, France.; Petit F; Clinique de Génétique, Centre de Référence Anomalies du Développement, Univ. Lille, CHU Lille, Lille, France.; Boute-Bénéjean O; Clinique de Génétique, Centre de Référence Anomalies du Développement, Univ. Lille, CHU Lille, Lille, France.; Capri Y; UF de Génétique Clinique, CHU Robert Debré, Paris, France.; Guimier A; Service de Médecine Génomique des Maladies Rares et Institut Imagine UMR-1163 Inserm, Université Paris Cité, Hôpital Necker-Enfants Malades, Assistance Publique des Hôpitaux de Paris, Paris, France.; Lyonnet S; Service de Médecine Génomique des Maladies Rares et Institut Imagine UMR-1163 Inserm, Université Paris Cité, Hôpital Necker-Enfants Malades, Assistance Publique des Hôpitaux de Paris, Paris, France.; Baujat G; Service de Médecine Génomique des Maladies Rares et Institut Imagine UMR-1163 Inserm, Université Paris Cité, Hôpital Necker-Enfants Malades, Assistance Publique des Hôpitaux de Paris, Paris, France.; Bourrat E; Department of Dermatology, MAGEC-Nord Hôpital Saint Louis, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.; Isidor B; Medical Genetics Department, CHU de Nantes, Hôtel Dieu Hospital, Nantes, France.; Nizon M; Medical Genetics Department, CHU de Nantes, Hôtel Dieu Hospital, Nantes, France.; Barbarot S; Department of Dermatology, CHU Nantes, INRAE, UMR 1280, PhAN, Nantes University, Nantes, France.; Toutain A; Department of Genetics, Bretonneau University Hospital, Tours, France.; UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Blesson S; Department of Genetics, Bretonneau University Hospital, Tours, France.; Van-Gils J; Département de Génétique Médicale, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.; Morice-Picard F; Pediatric Dermatology Unit, National Center for Rare Skin Disorders, University Hospital of Bordeaux, Bordeaux, France.; Audebert-Bellanger S; Service de Pédiatrie et de Génétique Médicale, CHRU Morvan, Brest, France.; Mazereeuw-Hautier J; Service de Dermatologie, Centre de Référence des Maladies rares de la peau, Hôpital Larrey, Toulouse, France.; Ziegler A; Department of Genetics, University Hospital of Toulouse, Toulouse, France.; Alembik Y; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Piard J; Centre de Génétique Humaine, Centre Hospitalier Universitaire de Besançon, Besançon, France.; UMR1231 GAD, Inserm, Université de Bourgogne, Dijon, France.; Brischoux-Boucher E; Centre de Génétique Humaine, Centre Hospitalier Universitaire de Besançon, Besançon, France.; Guerrini-Rousseau L; Department of Children and Adolescents Oncology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.; Morera J; Department of Endocrinology and Diabetology, CHU Côte de Nacre, Caen, France.; Paquis-Flucklinger V; Inserm U1081, CNRS UMR7284, IRCAN, Université Côte d'Azur, CHU de Nice, Nice, France.; Delobel B; Service de génétique médicale, GH de l'Institut Catholique de Lille, Lille, France.; Alessandri JL; service de pédiatrie, CHU Féleix Guyon, Saint-Denis, France.; Parfait B; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France.; Fédération de Génétique et Médecine Génomique, DMU BioPhyGen, Hôpital Cochin, AP-HP.Centre-Université Paris Cité, Paris, France.; Wolkenstein P; Department of Dermatology, Hôpital Henri Mondor, Assistance Publique-Hôpital Paris (AP-HP), Créteil, France.; INSERM U955, Université Paris Est Créteil (UPEC), Créteil, France.; Pasmant E; Institut Cochin, Inserm U1016, CNRS UMR8104, Université Paris Cité, CARPEM, Paris, France eric.pasmant@inserm.fr.; Genetics Department, Institut Curie, Paris, France.

Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

Kumble, S; Levy, AM; Punetha, J; Gao, H; Ah Mew, N; Anyane-Yeboa, K; Benke, PJ; Berger, SM; Bjerglund, L; Campos-Xavier, B; Ciliberto, M; Cohen, JS; Comi, AM; Curry, C; Damaj, L; Denommé-Pichon, AS; Emrick, L; Faivre, L; Fasano, MB; Fiévet, A; Finkel, RS; García-Miñaúr, S; Gerard, A; Gomez-Puertas, P; Guillen Sacoto, MJ; Hoffman, TL; Howard, L; Iglesias, AD; Izumi, K; Larson, A; Leiber, A; Lozano, R; Marcos-Alcalde, I; Mintz, CS; Mullegama, SV; Møller, RS; Odent, S; Oppermann, H; Ostergaard, E; Pacio-Míguez, M; Palomares-Bralo, M; Parikh, S; Paulson, AM; Platzer, K; Posey, JE; Potocki, L; Revah-Politi, A; Rio, M; Ritter, AL; Robinson, S; Rosenfeld, JA; Santos-Simarro, F; Sousa, SB; Wéber, M; Xie, Y; Chung, WK; Brown, NJ; Tümer, Z; Acosta, MT; Adam, M; Adams, DR; Agrawal, PB; Alejandro, ME; Alvey, J; Amendola, L; Andrews, A; Ashley, EA; Azamian, MS; Bacino, CA; Bademci, G; Baker, E; Balasubramanyam, A; Baldridge, D; Bale, J; Bamshad, M; Barbouth, D; Bayrak-Toydemir, P; Beck, A; Beggs, AH; Behrens, E; Bejerano, G; Bennet, J; Berg-Rood, B; Bernstein, JA; Berry, GT; Bican, A; Bivona, S; Blue, E; Bohnsack, J; Bonnenmann, C; Bonner, D; Botto, L; Boyd, B; Briere, LC; Brokamp, E; Brown, G; Burke, EA; Burrage, LC; Butte, MJ; Byers, P

DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
Universidad Francisco de Vitoria
instname
Human mutation, vol. 43, no. 2, pp. 266-282
Kumble, S & Undiagnosed Diseases Network 2022, ' The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder ', Human Mutation, vol. 43, no. 2, pp. 266-282 . https://doi.org/10.1002/humu.24308
Tümer, Z & Undiagnosed Diseases Network 2022, ' The clinical and molecular spectrum of QRICH1 associated neurodevelopmental disorder ', Human Mutation, vol. 43, no. 2, pp. 266-282 . https://doi.org/10.1002/humu.24308

Mouffok, L.; Damaj, L.; Begaud, X.; Lepage, A.C; Diez, H.

Proceedings of the 5th European Conference on Antennas and Propagation (EUCAP) Antennas and Propagation (EUCAP), Proceedings of the 5th European Conference on. :909-912 Apr, 2011

Haidar, I.M.; Sliman, L.; Damaj, I.W.; Haidar, A.M.

IEEE Access Access, IEEE. 12:50517-50536 2024

Khan K; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Tavares E; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.; Bishara K; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Ozanturk A; Center for Human Disease Modeling, Duke University Medical Center, Durham, NC, USA.; Qebibo L; Malformations and Cerebellar Congenital Diseases Reference Center, Sorbonne Université, Hôpital Trousseau, Paris, France.; Pediatric Molecular Neurogenetics Laboratory, Genetics Department, AP-HP, Sorbonne Université, Hôpital Trousseau, Paris, France.; Frangakis S; Center for Human Disease Modeling, Duke University Medical Center, Durham, NC, USA.; Calame DG; Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Meunier I; Institute for Neurosciences of Montpellier (INM), Univ. Montpellier, INSERM, Montpellier, France.; Bocquet B; Institute for Neurosciences of Montpellier (INM), Univ. Montpellier, INSERM, Montpellier, France.; Ploski R; Department of Medical Genetics, Medical University of Warsaw, Warsaw Poland.; Al Khateeb MA; Women's Wellness Research Center and Neonatal Intensive Care Unit, Hamad Medical Corporation, Weill Cornell Medicine, Doha, Qatar.; Marafi D; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.; Mansard L; Molecular Genetics Laboratory, University of Montpellier, Montpellier University Hospital, Montpellier, France.; Auragen Laboratory, Plan France Medecine Genomique 2025, Lyon, France.; Damaj L; Department of Clinical Genetics, Competence Center of Inherited Metabolic Disorders, Rennes Hospital, Rennes, France.; Lewis RA; Texas Children's Hospital, Houston, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Ophthalmology, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Ullah F; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Arbogast T; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Ogden JP; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Harion M; Malformations and Cerebellar Congenital Diseases Reference Center, Sorbonne Université, Hôpital Trousseau, Paris, France.; Neuropediatrics Department, AP-HP, Sorbonne Université, Hôpital Trousseau, Paris, France.; Willems M; Institute for Neurosciences of Montpellier (INM), Univ. Montpellier, INSERM, Montpellier, France.; Department of Medical Genetics, University of Montpellier, Montpellier University Hospital, Montpellier, France.; Zaki MS; Department of Clinical Genetics, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt.; Bartolomaeus T; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Roux AF; Molecular Genetics Laboratory, University of Montpellier, Montpellier University Hospital, Montpellier, France.; Auragen Laboratory, Plan France Medecine Genomique 2025, Lyon, France.; Lupski JR; Texas Children's Hospital, Houston, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.; Rydzanicz M; Department of Medical Genetics, Medical University of Warsaw, Warsaw Poland.; Jamra RA; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.; Ramond F; Auragen Laboratory, Plan France Medecine Genomique 2025, Lyon, France.; Department of Genetics, Centre Hospitalier Universitaire de Saint-Étienne, Saint-Étienne, France.; Heon E; Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Canada.; Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.; Burglen L; Pediatric Molecular Neurogenetics Laboratory, Genetics Department, AP-HP, Sorbonne Université, Hôpital Trousseau, Paris, France.; Developmental Brain Disorders Laboratory, Imagine Institute, INSERM UMR1163, 75015 Paris, France.; Davis EE; Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Department of Pediatrics and Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.

Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 101653440 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2375-2548 (Electronic) Linking ISSN: 23752548 NLM ISO Abbreviation: Sci Adv Subsets: MEDLINE

Menicucci L; Reference Center of Leukodystrophies, Department of Medical Genetics, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.; Mane M; Reference Center of Leukodystrophies, Department of Medical Genetics, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France; Reference Center of Neurogenetics, Department of Neuropediatrics, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; Roubertie A; Reference Center of Neurogenetics, Department of Neuropediatrics, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; Boespflug-Tanguy O; Assistance Publique - Hôpitaux de Paris (APHP), Centre de Reference LEUKOFRANCE, Service de Neuropédaitrie, Hôpital Robert Debré, Paris, France; Université Paris Cité, UMR, INSERM 1141, Hôpital Robert Debré, Paris, France.; Damaj L; Competence Center of Leukodystrophies, Department of Neuropediatrics, Centre Hospitalier Universitaire de Rennes, Rennes, France.; Delignieres A; Maison du développement de l'enfant La Colline, Vannes, France.; Perrin L; Departments of Pediatrics, Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne, France.; Rodriguez D; Reference Center of Neurogenetics, Department of Neuropediatrics, Hôpital Armand Trousseau, Assistance Publique - Hôpitaux de Paris, Paris, France.; Dorboz I; Assistance Publique - Hôpitaux de Paris (APHP), Centre de Reference LEUKOFRANCE, Service de Neuropédaitrie, Hôpital Robert Debré, Paris, France; Université Paris Cité, UMR, INSERM 1141, Hôpital Robert Debré, Paris, France.; Koenig M; Department of Molecular Biology, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.; Burglen L; Departments of Molecular Biology, Hôpital Armand Trousseau Assistance Publique - Hôpitaux de Paris, Paris, France.; Durand N; Reference Center of Leukodystrophies, Department of Medical Genetics, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.; Sarret C; Reference Center of Leukodystrophies, Department of Medical Genetics, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France; ICCN, Therapy-guided Imaging, Institut Pascal, Université Clermont Auvergne, Clermont-Ferrand, France. Electronic address: csarret@chu-clermontferrand.fr.

Publisher: Saunders Country of Publication: England NLM ID: 9715169 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2130 (Electronic) Linking ISSN: 10903798 NLM ISO Abbreviation: Eur J Paediatr Neurol Subsets: MEDLINE

Joueidi, Y.; Peoc'H, K.; Le Lous, Maela; Bouzille, Guillaume; Rousseau, Chloé; Bardou-Jacquet, Edouard; Bendavid, Claude; Damaj, L; Fromenty, B.; Lavoué, Vincent; Moreau, Caroline

European Journal of Obstetrics & Gynecology and Reproductive Biology. 252:198-205

Leclerc, D.; Goujon, L.; Jaillard, S.; Nouyou, B.; Cluzeau, L.; Damaj, L.; Dubourg, C.; Etcheverry, A.; Levade, T.; Froissart, R.; Dreano, S.; Guillory, X.; Eriksson, Leif A, 1964; Launay, E.; Mouriaux, F.; Belaud-Rotureau, M. A.; Odent, S.; Gilot, D.

Crispr Journal. 6(1)

Renous, A.-S.; Tardieu, M.; Labarthe, F.; Damaj, L.; Pasquier, L.; Gorce, M.; Barth, M.; Bedu, A.; Laroche-Raynaud, C.; Sacaze, E.; Lamireau, D.; Maakaroun-Vermesse, Z.

In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, December 2025, 20(1))

Damaj, Ziad; Naveau, Aude; Dupont, Laurent; Henon, Eric; Rogez, Guillaume; Guillon, Emmanuel

Inorganic Chemistry Communications. Jan, 2009, Vol. 12 Issue 1, p17, 4 p.

Mckiver, Bryan D.; Herz, Sara M.; Patel, Shivani; Bryan, Tayla; Mann, Jared; Poklis, Justin L.; Bigbee, John W.; Windle, Jolene J.; Salem, Aliasger K.; Sarkar, Devanand; Damaj, M.Imad

Brain Behavior and Immunity. 127:329-340

Karin, Kimberly N.; Mustafa, Mohammed A.; Poklis, Justin L.; Buzzi, Belle; Schlosburg, Joel E.; Parker, Linda; Damaj, M. Imad; Lichtman, Aron H.

Drug and Alcohol Dependence. 259

Akinola, Lois S.; Gonzales, Jada; Buzzi, Belle; Mathews, Hunter L.; Papke, Roger L.; Stitzel, Jerry A.; Damaj, M. Imad

Drug and Alcohol Dependence. 257

Delapierre, B.; Troussard, X.; Damaj, G.; Dejardin, O.; Tron, L.

Cancer Epidemiology. 82

Caillaud, Martial; Patel, Nipa H.; White, Alyssa; Wood, Mackinsey; Contreras, Katherine M.; Toma, Wisam; Alkhlaif, Yasmin; Roberts, Jane L.; Tran, Tammy H.; Jackson, Asti B.; Poklis, Justin; Gewirtz, David A.; Damaj, M. Imad

Brain Behavior and Immunity. 93:172-185

Godin, Jean-Rémi; Roy, Patrick; Quadri, Marta; Bagdas, Deniz; Toma, Wisam; Narendrula-Kotha, Ramya; Kishta, Osama A.; Damaj, M. Imad; Horenstein, Nicole A.; Papke, Roger L.; Simard, Alain R.

Brain Behavior and Immunity. 87:286-300