نتائج البحث - Matteo Cassina

  • يعرض 1 - 17 نتائج من 17
تنقيح النتائج
  1. 1
    First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis

    First-trimester exposure to metformin and risk of birth defects: a systematic review and meta-analysis حسب Matteo Cassina, Marta Donà, Elena Di Gianantonio, Pietro Litta, Maurizio Clementi

    منشور في 2014
    احصل على النص الكامل احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  2. 2
    Genetics of Coenzyme Q10 Deficiency

    Genetics of Coenzyme Q10 Deficiency حسب Mara Doimo, María Andrea Desbats, Cristina Cerqua, Matteo Cassina, Eva Trevisson, Leonardo Salviati

    منشور في 2014
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  3. 3
    Treatment of Hyperthyroidism in Pregnancy and Birth Defects

    Treatment of Hyperthyroidism in Pregnancy and Birth Defects حسب Maurizio Clementi, Elena Di Gianantonio, Matteo Cassina, Emanuele Leoncini, Lorenzo D. Botto, Pierpaolo Mastroiacovo

    منشور في 2010
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  4. 4
    Epigenetics of pregnancy: looking beyond the DNA code

    Epigenetics of pregnancy: looking beyond the DNA code حسب Daniela Zuccarello, Ugo Sorrentino, Valeria Brasson, Loris Marin, C. Piccolo, Antonio Capalbo, Alessandra Andrisani, Matteo Cassina

    منشور في 2022
    احصل على النص الكامل احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  5. 5
    Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations

    Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations حسب Matteo Cassina, Luisa Frizziero, Enrico Opocher, Raffaele Parrozzani, Ugo Sorrentino, Elisabetta Viscardi, Giacomo Miglionico, Edoardo Midena, Maurizio Clementi, Eva Trevisson

    منشور في 2019
    احصل على النص الكامل احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  6. 6
    The<i>COQ2</i>genotype predicts the severity of coenzyme Q<sub>10</sub>deficiency

    The<i>COQ2</i>genotype predicts the severity of coenzyme Q<sub>10</sub>deficiency حسب María Andrea Desbats, Valeria Morbidoni, Micol Silic‐Benussi, Mara Doimo, Vincenzo Ciminale, Matteo Cassina, Sabrina Sacconi, Michio Hirano, Giuseppe Basso, Fabien Pierrel, Plácido Navas, Leonardo Salviati, Eva Trevisson

    منشور في 2016
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  7. 7
    Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function

    Mutations in COQ8B (ADCK4) found in patients with steroid-resistant nephrotic syndrome alter COQ8B function حسب Luis Vázquez-Fonseca, Mara Doimo, Cristina Calderan, María Andrea Desbats, M.J. Acosta, Cristina Cerqua, Matteo Cassina, Shazia Ashraf, Friedhelm Hildebrandt, Geppo Sartori, Plácido Navas, Eva Trevisson, Leonardo Salviati

    منشور في 2017
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  8. 8
    Catechol‐<i>O</i>‐Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta‐Analysis of Previously Published Studies

    Catechol‐<i>O</i>‐Methyltransferase (COMT) Val158Met Polymorphism and Eating Disorders: Data From a New Biobank and Meta‐Analysis of Previously Published Studies حسب Enrico Collantoni, Marco Solmi, Davide Gallicchio, Paolo Santonastaso, Paolo Meneguzzo, André F. Carvalho, Brendon Stubbs, Maurizio Clementi, Claudia Pinato, Monica Forzan, Matteo Cassina, Francesca Fontana, I. Piva, Roberta Siani, Pierandrea Salvo, Elena Tenconi, Nicola Veronese, Christoph U. Correll, Angela Favaro

    منشور في 2017
    احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  9. 9
    Haploinsufficiency of<i>COQ4</i>causes coenzyme Q<sub>10</sub>deficiency

    Haploinsufficiency of<i>COQ4</i>causes coenzyme Q<sub>10</sub>deficiency حسب Leonardo Salviati, Eva Trevisson, María Hernández, Alberto Casarin, Vanessa Pertegato, Mara Doimo, Matteo Cassina, Caterina Agosto, María Andrea Desbats, Geppo Sartori, Sabrina Sacconi, Luigi Memo, Orsetta Zuffardi, Rafael Artuch, Catarina M. Quinzii, Salvatore DiMauro, Michio Hirano, Carlos Santos–Ocaña, Plácido Navas

    منشور في 2012
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  10. 10
    A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes

    A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes حسب Silvia Russo, Luciano Calzari, Alessandro Mussa, Ester Mainini, Matteo Cassina, Stefania Di Candia, Maurizio Clementi, Sara Guzzetti, Silvia Tabano, Monica Miozzo, Silvia Maria Sirchia, Palma Finelli, Paolo Prontera, Silvia Maitz, Giovanni Sorge, Annalisa Calcagno, Mohamad Maghnie, Maria Teresa Divizia, Daniela Melis, Emanuela Manfredini, Giovanni Battista Ferrero, Vanna Pecile, Lidia Larizza

    منشور في 2016
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  11. 11
    Pregnancy outcomes in women on metformin for diabetes or other indications among those seeking teratology information services

    Pregnancy outcomes in women on metformin for diabetes or other indications among those seeking teratology information services حسب Alice Panchaud, Valentin Rousson, Thierry Vial, Nathalie Bernard, David Baud, Emmanuelle Amar, Marco De Santis, Alessandra Pistelli, Anne Dautriche, F. Beau-Salinas, Matteo Cassina, Hannah J. Dunstan, Anneke Passier, Yusuf Cem Kaplan, Mine Kadıoğlu, Eva Maňáková, Georgios Eleftheriou, Gil Klinger, Ursula Winterfeld, Laura E. Rothuizen, Thierry Buclin, Chantal Csajka, Sonia Hernández–Dı́az

    منشور في 2017
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  12. 12
    Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes

    Genome-wide association studies of binge-eating behaviour and anorexia nervosa yield insights into the unique and shared biology of eating disorder phenotypes حسب Jet D. Termorshuizen, Helena L. Davies, Sang Hyuck Lee, Jessica Dennis, Christopher Hübel, Jessica Johnson, Yi Lu, Melissa A. Munn‐Chernoff, Triinu Peters, Baiyu Qi, Katherine Schaumberg, Rebecca Signer, Karanvir Singh, Abigail ter Kuile, Laura M. Thornton, Jiayi Xu, Shuyang Yao, Zeynep Yılmaz, Ruyue Zhang, Johan Zvrskovec, Mohamed Abdulkadir, Ziada Ayorech, Elizabeth C. Corfield, Alexandra Havdahl, Kristi Krebs, Taralynn Mack, Maria Niarchou, Teemu Palviainen, Julia Sealock, Jessica H. Baker, Andrew W. Bergen, Andreas Birgegård, Vesna Boraska Perica, Katharina Bühren, Roland Burghardt, Matteo Cassina, Enrico Collantoni, James J. Crowley, Unna N. Danner, Franziska Degenhardt, Janiece DeSocio, Christian Dina, Monika Dmitrzak‐Węglarz, Laramie E. Duncan, Karin Egberts, Lenka Foretová, Ina Giegling, Fragiskos Gonidakis, Scott D. Gordon, Jakob Grove, Sébastien Guillaume, Jerry Guintivano, Annette M. Hartman, Konstantinos Hatzikotoulas, Stefan Herms, Hartmut Imgart, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Leila Karhunen, Kirsty Kiezebrink, Theresa Kolb, Janne Tidselbak Larsen, Dong Li, Lisa Lilenfeld, Mario Maj, Morten Mattingsdal, Paolo Meneguzzo, Allison L. Miller, Karen S. Mitchell, Alessio Maria Monteleone, Catherine M. Olsen, Leonid Padyukov, Jacques Pantel, Richard Parker, Dalila Pinto, Anu Raevuori, Samuli Ripatti, Marion Roberts, Paolo Santonastaso, Androula Savva, Ulrike Schmidt, Alexandra Schosser, Jochen Seitz, Lenka Šlachtová, Agnieszka Słopień, Sandro Sorbi, Péter Straub, Jin Szatkiewicz, Friederike I. Tam, Elena Tenconi, Alfonso Tortorella, Άρτεμις Τσίτσικα, Annemarie Elburg, Gudrun Wagner, Hunna J. Watson, Roger A.H. Adan, Lars Alfredsson, Ole A. Andreassen

    منشور في 2025
    احصل على النص الكامل
    Pré-impressão
    أضف إلى المفضلة
    محفوظ في:
  13. 13
    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

    Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa حسب Laramie Duncan, Zeynep Yılmaz, Helena Gaspar, Raymond K. Walters, Jackie Goldstein, Verneri Anttila, Brendan Bulik‐Sullivan, Stephan Ripke, Laura Thornton, Anke Hinney, Mark J. Daly, Patrick F. Sullivan, Eleftheria Zeggini, Gerome Breen, Cynthia M. Bulik, Laramie Duncan, Zeynep Yılmaz, Héléna A. Gaspar, Raymond K. Walters, Jackie Goldstein, Verneri Anttila, Brendan Bulik‐Sullivan, Stephan Ripke, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, H.N. Aschauer, Jessica H. Baker, Jeffrey C. Barrett, Vladimír Bencko, Andrew W. Bergen, Wade Berrettini, Andreas Birgegård, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Roland Burghardt, Laura Carlberg, Matteo Cassina, Carolyn E. Cesta, Sven Cichon, Maurizio Clementi, Sarah Cohen‐Woods, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Bo Ding, Monika Dmitrzak‐Węglarz, Elisa Docampo, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Thomas Espeseth, Xavier Estivill, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Chris Finan, Krista Fischer, James Floyd, Manuel Föcker, Lenka Foretová, Monica Forzan, Caroline S. Fox, C. Franklin, Valérie Gaborieau, Steven Gallinger, Giovanni Gambaro, Ina Giegling, Fragiskos Gonidakis, Philip Gorwood, Mónica Gratacòs, Sébastien Guillaume, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Rebecca Harrison, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Judith Hendriks, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Christopher Hilliard

    منشور في 2017
    احصل على النص الكامل احصل على النص الكامل
    Revisão
    أضف إلى المفضلة
    محفوظ في:
  14. 14
    Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches

    Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches حسب Shuyang Yao, Ralf Kuja‐Halkola, Joanna Martin, Yi Lu, Paul Lichtenstein, Claes Norring, Andreas Birgegård, Zeynep Yılmaz, Christopher Hübel, Hunna J. Watson, Jessica Baker, Catarina Almqvist, Laura M. Thornton, Patrik K. E. Magnusson, Cynthia M. Bulik, Henrik Larsson, Roger A.H. Adan, Tetsuya Ando, Jessica Baker, Andrew W. Bergen, Wade Berrettini, Andreas Birgegård, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Roland Burghardt, Matteo Cassina, Carolyn E. Cesta, Maurizio Clementi, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Monika Dmitrzak‐Węglarz, Elisa Docampo, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Chris Finan, Krista Fischer, Manuel Föcker, Lenka Foretová, Monica Forzan, C. Franklin, Héléna A. Gaspar, Fragiskos Gonidakis, Philip Gorwood, Mónica Gratacòs, Sébastien Guillaume, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Judith Hendriks, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Christopher Hilliard, Anke Hinney, Laura M. Huckins, James I. Hudson, Julia Huemer, Hartmut Imgart, Hidetoshi Inoko, Susana Jiménez‐Múrcia, Craig Johnson, Jennifer Jordan, Anders Juréus, Gursharan Kalsi, Debora Kaminska, Allan S. Kaplan, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J. Kas, Walter H. Kaye, James L. Kennedy, Martin A. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Kelly L. Klump, Gun Peggy Knudsen

    منشور في 2019
    احصل على النص الكامل احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  15. 15
    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa

    Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa حسب Hunna J. Watson, Zeynep Yılmaz, Laura M. Thornton, Christopher Hübel, Jonathan R. I. Coleman, Héléna A. Gaspar, Julien Bryois, Anke Hinney, Virpi Leppä, Manuel Mattheisen, Sarah E. Medland, Stephan Ripke, Shuyang Yao, Paola Giusti‐Rodríguez, Ken B. Hanscombe, Kirstin L. Purves, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, Jessica H. Baker, Wade H. Berrettini, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Katharina Buehren, Roland Burghardt, Matteo Cassina, Sven Cichon, Maurizio Clementi, Roger D. Cone, Philippe Courtet, Scott J. Crow, James J. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred M. Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, Christopher S. Franklin, Steven Gallinger, Ina Giegling, Johanna Giuranna, Fragiskos Gonidakis, Philip Gorwood, Monica Gratacos Mayora, Sébastien Guillaume, Yiran Guo, Hákon Hákonarson, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Jaakko Kaprio, Leila Karhunen, Andreas Karwautz, Martien J. Kas, James L. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Lars Klareskog, Kelly L. Klump, Gun Peggy Knudsen, Maria C. La Via, Stéphanie Le Hellard, Robert D. Levitan

    منشور في 2019
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  16. 16
    Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

    Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease حسب Julien Bryois, Nathan Skene, Thomas Hansen, Lisette J. A. Kogelman, Hunna J. Watson, Zijing Liu, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, Jessica H. Baker, Andrew W. Bergen, Wade H. Berrettini, Andreas Birgegård, Joseph M. Boden, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Harry Brandt, Gerome Breen, Julien Bryois, Katharina Buehren, Cynthia M. Bulik, Roland Burghardt, Matteo Cassina, Sven Cichon, Maurizio Clementi, Jonathan R. I. Coleman, Roger D. Cone, Philippe Courtet, Steven Crawford, Scott J. Crow, James L. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo Martínez, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, C. Franklin, Steven Gallinger, Héléna A. Gaspar, Ina Giegling, Johanna Giuranna, Paola Giusti-Rodríquez, Fragiskos Gonidakis, Scott D. Gordon, Philip Gorwood, Monica Gratacos Mayora, Jakob Grove, Sébastien Guillaume, Yiran Guo, Hákon Hákonarson, Katherine A. Halmi, Ken B. Hanscombe, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Anjali K. Henders, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Anke Hinney, L. John Horwood, Christopher Hübel, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Craig Johnson, Jennifer Jordan, Antonio Julià, Anders Juréus, Gursharan Kalsi, Deborah Kaminská, Allan S. Kaplan, Jaakko Kaprio

    منشور في 2020
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:
  17. 17
    Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies

    Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies حسب Melissa A. Munn‐Chernoff, Emma C. Johnson, Yi‐Ling Chou, Jonathan R. I. Coleman, Laura M. Thornton, Raymond K. Walters, Zeynep Yılmaz, Jessica H. Baker, Christopher Hübel, Scott D. Gordon, Sarah E. Medland, Hunna J. Watson, Héléna A. Gaspar, Julien Bryois, Anke Hinney, Virpi Leppä, Manuel Mattheisen, Stephan Ripke, Shuyang Yao, Paola Giusti‐Rodríguez, Ken B. Hanscombe, Roger A.H. Adan, Lars Alfredsson, Tetsuya Ando, Ole A. Andreassen, Wade H. Berrettini, Ilka Boehm, Claudette Boni, Vesna Boraska Perica, Katharina Buehren, Roland Burghardt, Matteo Cassina, Sven Cichon, Maurizio Clementi, Roger D. Cone, Philippe Courtet, Scott J. Crow, James J. Crowley, Unna N. Danner, Oliver S. P. Davis, Martina de Zwaan, George Dedoussis, Daniela Degortes, Janiece E. DeSocio, Danielle M. Dick, Dimitris Dikeos, Christian Dina, Monika Dmitrzak‐Węglarz, Elisa Docampo, Laramie E. Duncan, Karin Egberts, Stefan Ehrlich, Geòrgia Escaramís, Tõnu Esko, Xavier Estivill, Anne Farmer, Angela Favaro, Fernando Fernández‐Aranda, Manfred M. Fichter, Krista Fischer, Manuel Föcker, Lenka Foretová, Andreas J. Forstner, Monica Forzan, Christopher S. Franklin, Steven Gallinger, Ina Giegling, Johanna Giuranna, Fragiskos Gonidakis, Philip Gorwood, Monica Gratacos Mayora, Sébastien Guillaume, Yiran Guo, Hákon Hákonarson, Konstantinos Hatzikotoulas, Joanna Hauser, Johannes Hebebrand, Sietske G. Helder, Stefan Herms, Beate Herpertz‐Dahlmann, Wolfgang Herzog, Laura M. Huckins, James I. Hudson, Hartmut Imgart, Hidetoshi Inoko, Vladimí­r Janout, Susana Jiménez‐Múrcia, Antonio Julià, Gursharan Kalsi, Deborah Kaminská, Leila Karhunen, Andreas Karwautz, Martien J. Kas, James L. Kennedy, Anna Keski‐Rahkonen, Kirsty Kiezebrink, Youl‐Ri Kim, Kelly L. Klump, Gun Peggy Knudsen, Maria C. La Via

    منشور في 2020
    احصل على النص الكامل
    Artigo
    أضف إلى المفضلة
    محفوظ في:

أدوات البحث: