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1. Association between upper and lower respiratory disease among patients with primary ciliary dyskinesia: an international study

Author

Lam, Yin Ting, primary, Papon, Jean-François, additional, Alexandru, Mihaela, additional, Anagiotos, Andreas, additional, Armengot, Miguel, additional, Boon, Mieke, additional, Burgess, Andrea, additional, Calmes, Doriane, additional, Crowley, Suzanne, additional, Dheyauldeen, Sinan Ahmed. D., additional, Emiralioglu, Nagehan, additional, Erdem Eralp, Ela, additional, van Gogh, Christine, additional, Gokdemir, Yasemin, additional, Haarman, Eric G., additional, Harris, Amanda, additional, Hayn, Isolde, additional, Ismail-Koch, Hasnaa, additional, Karadag, Bülent, additional, Kempeneers, Céline, additional, Kieninger, Elisabeth, additional, Kim, Sookyung, additional, Lorent, Natalie, additional, Ozcelik, Ugur, additional, Pioch, Charlotte, additional, Raidt, Johanna, additional, Reula, Ana, additional, Roehmel, Jobst, additional, Sperstad Kennelly, Synne, additional, Yiallouros, Panayiotis, additional, and Goutaki, Myrofora, additional

Published
2024
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3. Association between upper and lower respiratory disease among patients with primary ciliary dyskinesia: an international study

Author

Lam, Yin Ting, primary, Papon, Jean-François, additional, Alexandru, Mihaela, additional, Anagiotos, Andreas, additional, Armengot, Miguel, additional, Boon, Mieke, additional, Burgess, Andrea, additional, Calmes, Doriane, additional, Crowley, Suzanne, additional, Dheyauldeen, Sinan Ahmed. D., additional, Emiralioglu, Nagehan, additional, Erdem Eralp, Ela, additional, van Gogh, Christine, additional, Gokdemir, Yasemin, additional, Haarman, Eric G., additional, Harris, Amanda, additional, Hayn, Isolde, additional, Ismail-Koch, Hasnaa, additional, Karadag, Bülent, additional, Kempeneers, Céline, additional, Kieninger, Elisabeth, additional, Kim, Sookyung, additional, Lorent, Natalie, additional, Ozcelik, Ugur, additional, Pioch, Charlotte, additional, Raidt, Johanna, additional, Reula, Ana, additional, Roehmel, Jobst, additional, Sperstad Kennelly, Synne, additional, Yiallouros, Panayiotis, additional, and Goutaki, Myrofora, additional

Published
2023
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6. Association between upper and lower respiratory disease among patients with primary ciliary dyskinesia: an international study.

Author

Yin Ting Lam, Papon, Jean-François, Alexandru, Mihaela, Anagiotos, Andreas, Armengot, Miguel, Boon, Mieke, Burgess, Andrea, Calmes, Doriane, Crowley, Suzanne, Dheyauldeen, Sinan Ahmed D., Emiralioglu, Nagehan, Eralp, Ela Erdem, van Gogh, Christine, Gokdemir, Yasemin, Haarman, Eric G., Harris, Amanda, Hayn, Isolde, Ismail-Koch, Hasnaa, Karadag, Bülent, and Kempeneers, Céline

Published
2024
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7. Characteristics of Otologic Disease Among Patients With Primary Ciliary Dyskinesia

Author

Goutaki, Myrofora, primary, Lam, Yin Ting, additional, Alexandru, Mihaela, additional, Anagiotos, Andreas, additional, Armengot, Miguel, additional, Boon, Mieke, additional, Burgess, Andrea, additional, Caversaccio, Nathalie, additional, Crowley, Suzanne, additional, Dheyauldeen, Sinan Ahmed D., additional, Emiralioglu, Nagehan, additional, Erdem, Ela, additional, van Gogh, Christine, additional, Gunaydin, Onder, additional, Haarman, Eric G., additional, Harris, Amanda, additional, Hayn, Isolde, additional, Ismail-Koch, Hasnaa, additional, Karadag, Bulent, additional, Kempeneers, Céline, additional, Kim, Sookyung, additional, Lorent, Natalie, additional, Ozcelik, Ugur, additional, Pioch, Charlotte, additional, Poirrier, Anne-Lise M. L., additional, Reula, Ana, additional, Roehmel, Jobst, additional, Yiallouros, Panayiotis, additional, Yumusakhuylu, Ali Cemal, additional, and Papon, Jean-François, additional

Published
2023
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11. Sinonasal disease among patients with primary ciliary dyskinesia – an international study

Author

Lam, Yin Ting, primary, Papon, Jean-François, additional, Alexandru, Mihaela, additional, Anagiotos, Andreas, additional, Armengot, Miguel, additional, Boon, Mieke, additional, Burgess, Andrea, additional, Crowley, Suzanne, additional, Dheyauldeen, Sinan Ahmed. D., additional, Emiralioglu, Nagehan, additional, Eralp, Ela Erdem, additional, van Gogh, Christine, additional, Gokdemir, Yasemin, additional, Gunaydın, Onder, additional, Haarman, Eric G., additional, Harris, Amanda, additional, Hayn, Isolde, additional, Ismail-Koch, Hasnaa, additional, Karadag, Bülent, additional, Kempeneers, Céline, additional, Kim, Sookyung, additional, Latzin, Philipp, additional, Lorent, Natalie, additional, Ozcelik, Ugur, additional, Pioch, Charlotte, additional, Poirrier, Anne-Lise ML, additional, Reula, Ana, additional, Roehmel, Jobst, additional, Yiallouros, Panayiotis, additional, and Goutaki, Myrofora, additional

Published
2022
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12. Otologic disease among patients with primary ciliary dyskinesia - an international observational study

Author

Goutaki, Myrofora, primary, Lam, Yin Ting, additional, Alexandru, Mihaela, additional, Anagiotos, Andreas, additional, Armengot, Miguel, additional, Boon, Mieke, additional, Burgess, Andrea, additional, Caversaccio, Nathalie, additional, Crowley, Suzanne, additional, Dheyauldeen, Sinan Ahmed D., additional, Emiralioglu, Nagehan, additional, Erdem, Ela, additional, van Gogh, Christine, additional, Gunaydın, Onder, additional, Haarman, Eric G., additional, Harris, Amanda, additional, Hayn, Isolde, additional, Ismail-Koch, Hasnaa, additional, Karadag, Bulent, additional, Kempeneers, Céline, additional, Kim, Sookyung, additional, Lorent, Natalie, additional, Ozcelik, Ugur, additional, Pioch, Charlotte, additional, Poirrier, Anne-Lise ML, additional, Reula, Ana, additional, Roehmel, Jobst, additional, Yiallouros, Panayiotis, additional, Yumusakhuylu, Ali Cemal, additional, and Papon, Jean-François, additional

Published
2022
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15. The disease-specific clinical trial network for primary ciliary dyskinesia:PCD-CTN

Author

Raidt, Johanna, Maitre, Bernard, Pennekamp, Petra, Altenburg, Josje, Anagnostopoulou, Pinelopi, Armengot, Miguel, Bloemsma, Lizan D., Boon, Mieke, Borrelli, Melissa, Brinkmann, Folke, Carr, Siobhan B., Carroll, Mary P., Castillo-Corullón, Silvia, Coste, André, Cutrera, Renato, Dehlink, Eleonora, Destouches, Damien M.S., Di Cicco, Maria E., Dixon, Lucy, Emiralioglu, Nagehan, Eralp, Ela Erdem, Haarman, Eric G., Hogg, Claire, Karadag, Bulent, Kobbernagel, Helene E., Lorent, Natalie, Mall, Marcus A., Marthin, June K., Martinu, Vendula, Narayanan, Manjith, Ozcelik, Ugur, Peckham, Daniel, Pifferi, Massimo, Pohunek, Petr, Polverino, Eva, Range, Simon, Ringshausen, Felix C., Robson, Evie, Roehmel, Jobst, Rovira-Amigo, Sandra, Santamaria, Francesca, Schlegtendal, Anne, Szépfalusi, Zsolt, Tempels, Petra, Thouvenin, Guillaume, Ullmann, Nicola, Walker, Woolf T., Wetzke, Martin, Yiallouros, Panayiotis, Omran, Heymut, Nielsen, Kim G., Raidt, Johanna, Maitre, Bernard, Pennekamp, Petra, Altenburg, Josje, Anagnostopoulou, Pinelopi, Armengot, Miguel, Bloemsma, Lizan D., Boon, Mieke, Borrelli, Melissa, Brinkmann, Folke, Carr, Siobhan B., Carroll, Mary P., Castillo-Corullón, Silvia, Coste, André, Cutrera, Renato, Dehlink, Eleonora, Destouches, Damien M.S., Di Cicco, Maria E., Dixon, Lucy, Emiralioglu, Nagehan, Eralp, Ela Erdem, Haarman, Eric G., Hogg, Claire, Karadag, Bulent, Kobbernagel, Helene E., Lorent, Natalie, Mall, Marcus A., Marthin, June K., Martinu, Vendula, Narayanan, Manjith, Ozcelik, Ugur, Peckham, Daniel, Pifferi, Massimo, Pohunek, Petr, Polverino, Eva, Range, Simon, Ringshausen, Felix C., Robson, Evie, Roehmel, Jobst, Rovira-Amigo, Sandra, Santamaria, Francesca, Schlegtendal, Anne, Szépfalusi, Zsolt, Tempels, Petra, Thouvenin, Guillaume, Ullmann, Nicola, Walker, Woolf T., Wetzke, Martin, Yiallouros, Panayiotis, Omran, Heymut, and Nielsen, Kim G.

Abstract

Primary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by impaired mucociliary clearance leading to irreversible lung damage. In contrast to other rare lung diseases like cystic fibrosis (CF), there are only few clinical trials and limited evidence-based treatments. Management is mainly based on expert opinions and treatment is challenging due to a wide range of clinical manifestations and disease severity. To improve clinical and translational research and facilitate development of new treatments, the clinical trial network for PCD (PCD-CTN) was founded in 2020 under the framework of the European Reference Network (ERN)-LUNG PCD Core. Applications from European PCD sites interested in participating in the PCD-CTN were requested. Inclusion criteria consisted of patient numbers, membership of ERN-LUNG PCD Core, use of associated standards of care, experience in PCD and/or CF clinical research, resources to run clinical trials, good clinical practice (GCP) certifications and institutional support. So far, applications from 22 trial sites in 18 European countries have been approved, including >1400 adult and >1600 paediatric individuals with PCD. The PCD-CTN is headed by a coordinating centre and consists of a steering and executive committee, a data safety monitoring board and committees for protocol review, training and standardisation. A strong association with patient organisations and industrial companies are further cornerstones. All participating trial sites agreed on a code of conduct. As CTNs from other diseases have demonstrated successfully, this newly formed PCD-CTN operates to establish evidence-based treatments for this orphan disease and to bring new personalised treatment approaches to patients.

Published
2022

18. The disease-specific clinical trial network for primary ciliary dyskinesia: PCD-CTN

Author

Raidt, Johanna, primary, Maitre, Bernard, additional, Pennekamp, Petra, additional, Altenburg, Josje, additional, Anagnostopoulou, Pinelopi, additional, Armengot, Miguel, additional, Bloemsma, Lizan D., additional, Boon, Mieke, additional, Borrelli, Melissa, additional, Brinkmann, Folke, additional, Carr, Siobhan B., additional, Carroll, Mary P., additional, Castillo-Corullón, Silvia, additional, Coste, André, additional, Cutrera, Renato, additional, Dehlink, Eleonora, additional, Destouches, Damien M.S., additional, Di Cicco, Maria E., additional, Dixon, Lucy, additional, Emiralioglu, Nagehan, additional, Erdem Eralp, Ela, additional, Haarman, Eric G., additional, Hogg, Claire, additional, Karadag, Bulent, additional, Kobbernagel, Helene E., additional, Lorent, Natalie, additional, Mall, Marcus A., additional, Marthin, June K., additional, Martinu, Vendula, additional, Narayanan, Manjith, additional, Ozcelik, Ugur, additional, Peckham, Daniel, additional, Pifferi, Massimo, additional, Pohunek, Petr, additional, Polverino, Eva, additional, Range, Simon, additional, Ringshausen, Felix C., additional, Robson, Evie, additional, Roehmel, Jobst, additional, Rovira-Amigo, Sandra, additional, Santamaria, Francesca, additional, Schlegtendal, Anne, additional, Szépfalusi, Zsolt, additional, Tempels, Petra, additional, Thouvenin, Guillaume, additional, Ullmann, Nicola, additional, Walker, Woolf T., additional, Wetzke, Martin, additional, Yiallouros, Panayiotis, additional, Omran, Heymut, additional, and Nielsen, Kim G., additional

Published
2022
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28. Study protocol: the ear-nose-throat (ENT) prospective international cohort of patients with primary ciliary dyskinesia (EPIC-PCD)

Author

Goutaki, Myrofora, Lam, Yin Ting, Alexandru, Mihaela, Anagiotos, Andreas, Armengot, Miguel, Bequignon, Emilie, Boon, Mieke, Burgess, Andrea, Coste, Andre, Emiralioglu, Nagehan, Erdem, Ela, Haarman, Eric G, Harris, Amanda, Hool, Sara-Lynn, Karadag, Bulent, Kim, Sookyung, Latzin, Philipp, Lorent, Natalie, Ozcelik, Ugur, Reula, Ana, Roehmel, Jobst, van Gogh, Christine, Yiallouros, Panayiotis, Zappe, Soeren Marian, and Papon, Jean Francois

Subjects
Science & Technology, education, 610 Medicine & health, OTOLOGIC FEATURES, CHILDREN, DEFECTS, OTITIS-MEDIA, Medicine, General & Internal, MANIFESTATIONS, 360 Social problems & social services, General & Internal Medicine, chronic airways disease, paediatric thoracic medicine, audiology, paediatric otolaryngology, otorhinolaryngologic diseases, respiratory medicine (see thoracic medicine), epidemiology, Life Sciences & Biomedicine
Abstract

INTRODUCTION: Primary ciliary dyskinesia (PCD) is a rare, genetic, multiorgan disease with an estimated prevalence of 1 in 10 000. It affects mainly the upper and lower airways due to impaired mucociliary clearance. Almost all patients have sinonasal or otologic (ear-nose-throat, ENT) problems, although the ENT clinical phenotype may present great variability. Despite that, data on PCD ENT manifestations are scarce and based on small single-centre studies. To date, we know little about the spectrum and severity of PCD ENT disease, its association with lung disease, its course over life and its determinants of prognosis.This study protocol describes the aims and methods of the first prospective, observational, multinational cohort study focusing on ENT disease in patients with PCD. METHODS AND ANALYSIS: The ENT prospective international cohort of patients with PCD (EPIC-PCD) is a prospective standardised observational clinical cohort set up as a multinational multicentre study, embedded into routine patient care. It aims to longitudinally characterise ENT disease in patients with PCD and its association with lung disease, and to identify determinants of its prognosis. Patients of all ages, diagnosed with PCD who undergo an ENT clinical assessment at least once a year at one of the participating centres will be invited to participate. Collected data include diagnostic test results, results of ENT examinations, lung function measurements, information on management of ENT disease and patient-reported data on clinical symptoms and health-related quality of life (QoL). Data are collected using the standardised PCD-specific FOLLOW-PCD form and the validated QoL-PCD questionnaire. ETHICS AND DISSEMINATION: The study has been reviewed and approved by the Human Research Ethics Committees at all participating centres, based on local legislation. The results of the study will be published in scientific journals, presented at scientific conferences and disseminated to participants and national patient organisations. TRIAL REGISTRATION: NCT04611516. ispartof: BMJ OPEN vol:11 issue:10 ispartof: location:England status: published

Published
2021
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36. The ear-nose-throat (ENT) prospective international cohort of patients with primary ciliary dyskinesia (EPIC-PCD)

Author

Goutaki, Myrofora., Lam, Yin-Ting., Alexandru, Mihaela., Anagiotos, Andreas., Armengot, Miguel., Bequignon, Emilie., Reula Martín, Ana., Producción Científica UCH 2021, and UCH. Departamento de Ciencias Biomédicas

Subjects
Kartagener, Síndrome de, Disquinesia ciliar, Síndrome de, Primary ciliary dyskinesia, Respiratory organs - Diseases in children, Enfermedades crónicas en los niños, Pediatric otolaryngology, Kartagener's syndrome, Aparato respiratorio - Enfermedades en los niños, Otorrinolaringología pediátrica, Chronic diseases in children
Abstract

Este artículo se encuentra disponible en la siguiente URL: https://bmjopen.bmj.com/content/bmjopen/11/10/e051433.full.pdf En este artículo de investigación también participan: Mieke Boon, Andrea Burgess, Andre Coste, Nagehan Emiralioglu, Ela Erdem, Eric G. Haarman, Amanda Harris, Sara-Lynn Hool, Bulent Karadag, Sookyung Kim, Philipp Latzin, Natalie Lorent, Ugur Ozcelik, Jobst Roehmel, Christine van Gogh, Panayiotis Yiallouros, Soeren Marian Zappe, On behalf of the EPIC-PCD team, Jean Francois Papon. Introduction Primary ciliary dyskinesia (PCD) is a rare, genetic, multiorgan disease with an estimated prevalence of 1 in 10 000. It affects mainly the upper and lower airways due to impaired mucociliary clearance. Almost all patients have sinonasal or otologic (ear–nose–throat, ENT) problems, although the ENT clinical phenotype may present great variability. Despite that, data on PCD ENT manifestations are scarce and based on small single-centre studies. To date, we know little about the spectrum and severity of PCD ENT disease, its association with lung disease, its course over life and its determinants of prognosis. This study protocol describes the aims and methods of the first prospective, observational, multinational cohort study focusing on ENT disease in patients with PCD. Methods and analysis The ENT prospective international cohort of patients with PCD (EPIC-PCD) is a prospective standardised observational clinical cohort set up as a multinational multicentre study, embedded into routine patient care. It aims to longitudinally characterise ENT disease in patients with PCD and its association with lung disease, and to identify determinants of its prognosis. Patients of all ages, diagnosed with PCD who undergo an ENT clinical assessment at least once a year at one of the participating centres will be invited to participate. Collected data include diagnostic test results, results of ENT examinations, lung function measurements, information on management of ENT disease and patient-reported data on clinical symptoms and health-related quality of life (QoL). Data are collected using the standardised PCD-specific FOLLOW-PCD form and the validated QoL-PCD questionnaire.

Published
2021
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43. New Laboratory Protocol to Determine the Oxidative Stress Profile of Human Nasal Epithelial Cells Using Flow Cytometry

Author

Reula, Ana, primary, Pellicer, Daniel, additional, Castillo, Silvia, additional, Magallón, María, additional, Armengot, Miguel, additional, Herrera, Guadalupe, additional, O’Connor, José-Enrique, additional, Bañuls, Lucía, additional, Navarro-García, María Mercedes, additional, Escribano, Amparo, additional, and Dasí, Francisco, additional

Published
2021
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45. X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3

Author

Olcese, Chiara, Patel, Mitali P., Shoemark, Amelia, Kiviluoto, Santeri, Legendre, Marie, Williams, Hywel J., Vaughan, Cara K., Hayward, Jane, Goldenberg, Alice, Emes, Richard D., Munye, Mustafa M., Dyer, Laura, Cahill, Thomas, Bevillard, Jeremy, Gehrig, Corinne, Guipponi, Michel, Chantot, Sandra, Duquesnoy, Philippe, Thomas, Lucie, Jeanson, Ludovic, Copin, Bruno, Tamalet, Aline, Thauvin-Robinet, Christel, Papon, Jean-Francois, Garin, Antoine, Pin, Isabelle, Vera, Gabriella, Aurora, Paul, Fassad, Mahmoud R., Jenkins, Lucy, Boustred, Christopher, Cullup, Thomas, Dixon, Mellisa, Onoufriadis, Alexandros, Bush, Andrew, Chung, Eddie M. K., Antonarakis, Stylianos E., Loebinger, Michael R., Wilson, Robert, Armengot, Miguel, Escudier, Estelle, Hogg, Claire, Amselem, Serge, Sun, Zhaoxia, Bartoloni, Lucia, Blouin, Jean-Louis, Mitchison, Hannah M., and UK10K Rare Grp

Subjects
Science, PROTEIN, DEFECTS, VARIANTS, R2TP COMPLEX, respiratory tract diseases, ARMS, IDENTIFIES MUTATIONS, MOTILITY, OF-FUNCTION MUTATIONS, otorhinolaryngologic diseases, INNER, OUTER
Abstract

By moving essential body fluids and molecules, motile cilia and flagella govern respiratory mucociliary clearance, laterality determination and the transport of gametes and cerebrospinal fluid. Primary ciliary dyskinesia (PCD) is an autosomal recessive disorder frequently caused by non-assembly of dynein arm motors into cilia and flagella axonemes. Before their import into cilia and flagella, multi-subunit axonemal dynein arms are thought to be stabilized and pre-assembled in the cytoplasm through a DNAAF2DNAAF4- HSP90 complex akin to the HSP90 co-chaperone R2TP complex. Here, we demonstrate that large genomic deletions as well as point mutations involving PIH1D3 are responsible for an X-linked form of PCD causing disruption of early axonemal dynein assembly. We propose that PIH1D3, a protein that emerges as a new player of the cytoplasmic pre-assembly pathway, is part of a complementary conserved R2TP-like HSP90 co-chaperone complex, the loss of which affects assembly of a subset of inner arm dyneins.

Published
2017

48. A Ciliary Motility Index for Activity Measurement in Cell Cultures With Respiratory Syncytial Virus

Author

Universitat Politècnica de València. Departamento de Física Aplicada - Departament de Física Aplicada, Universitat Politècnica de València. Departamento de Ingeniería Electrónica - Departament d'Enginyeria Electrònica, Universitat Politècnica de València. Departamento de Matemática Aplicada - Departament de Matemàtica Aplicada, European Commission, Instituto de Salud Carlos III, European Regional Development Fund, Ministerio de Economía y Competitividad, Parrilla Bernabé, Eduardo, Armengot, Miguel, Mata, Manuel, Carda, Carmen, Cortijo, Julio, Moratal, David, Ginestar Peiro, Damián, Hueso, José L., Riera Guasp, Jaime, Universitat Politècnica de València. Departamento de Física Aplicada - Departament de Física Aplicada, Universitat Politècnica de València. Departamento de Ingeniería Electrónica - Departament d'Enginyeria Electrònica, Universitat Politècnica de València. Departamento de Matemática Aplicada - Departament de Matemàtica Aplicada, European Commission, Instituto de Salud Carlos III, European Regional Development Fund, Ministerio de Economía y Competitividad, Parrilla Bernabé, Eduardo, Armengot, Miguel, Mata, Manuel, Carda, Carmen, Cortijo, Julio, Moratal, David, Ginestar Peiro, Damián, Hueso, José L., and Riera Guasp, Jaime

Abstract

[EN] Background: The respiratory epithelium is frequently infected by the respiratory syncytial virus, resulting in inflammation, a reduction in cilia activity and an increase in the production of mucus. Methods: In this study, an automatic method has been proposed to characterize the ciliary motility from cell cultures by means of a motility index using a dense optical flow algorithm. This method allows us to determine the ciliary beat frequency (CBF) together with a ciliary motility index of the cells in the cultures. The object of this analysis is to automatically distinguish between normal and infected cells in a culture. Results: The method was applied in 2 stages. It was concluded from the first stage that the CBF is not a good enough indicator to discriminate between the control and infected cultures. However, the ciliary motility index does succeed in discriminating between the control and infected cultures using the t test with a value t ¿ 6.46 and P <.001. In the second stage, it has been shown that the ciliary motility index did not differ significantly between patients, and the analysis of variance test gives a ¿ 0.05, F ¿ 1.61, P ¿.20. A threshold for this index has been determined using a receiver operating characteristics analysis that gives an area under the curve of 0.93. Conclusions: We have obtained a ciliary motility index that is able to discriminate between control and infected cultures after the eighth postinfection day. After infection, there is a rapid cilia loss of the cells and the measured CBF corresponds to the remaining noninfected cells. This is why the CBF does not discriminate between the control and the infected cells.

Published
2019

49. Preliminary results of high-speed video-microscopy and immunofluorescence analysis in a Spanish cohort of patients with primary ciliary dyskinesia

Author

Rovira Amigo, Sandra, primary, Baz Redon, Noelia, additional, Camats Tarruella, Núria, additional, Fernández Cancio, Mónica, additional, Garrido, Marta, additional, Antolin, María, additional, Cols, Maria, additional, Caballero, Araceli, additional, Asensio, Oscar, additional, Vizmanos, Gerardo, additional, Reula, Ana, additional, Escribano, Amparo, additional, Dasí, Francisco, additional, Armengot, Miguel, additional, and Moreno Galdo, Antonio, additional

Published
2019
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