Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Patricia Costa Reis"'
Autor:
Helena Fonseca, Cláudia Marques, Raquel Campanilho-Marques, Filipa Oliveira-Ramos, Luis Graca, Sandra Sousa, Patricia Costa-Reis, Catarina Tomé, Ana F. Mourão, Ana T. Melo, Rui L. Teixeira, Ana P. Martins, Sofia Moeda, Rita P. Torres, Matilde Bandeira, Miroslava Gonçalves, Maria J. Santos, João E. Fonseca, Rita A. Moura
Publikováno v:
RMD Open, Vol 9, Iss 3 (2023)
Objectives The main goal of this study was to characterise the frequency and phenotype of B, T follicular helper (Tfh) and T follicular regulatory (Tfr) cells in peripheral blood and the cytokine environment present in circulation in children with ex
Externí odkaz:
https://doaj.org/article/f335f2f4ff2a4e0184a487ea4b064cd1
Autor:
Michelle A Petri, Emily von Scheven, Marisa S Klein-Gitelman, Patricia Costa-Reis, Kelly Maurer, Kathleen E Sullivan, Daniella Levy Erez, Xue Zhao, Walter Faig, Jon Burnham, Kathleen O'Neil
Publikováno v:
Lupus Science and Medicine, Vol 9, Iss 1 (2022)
Objective Lupus nephritis is a key driver of morbidity and mortality in SLE. Detecting active nephritis on a background of pre-existing renal damage is difficult, leading to potential undertreatment and accumulating injury. An unmet need is a biomark
Externí odkaz:
https://doaj.org/article/65699cef0c59422a86921fb9a6855bc0
Publikováno v:
ARP rheumatology. 1(1)
Kikuchi-Fujimoto disease is usually a self-limited cause of lymphadenitis. It is a prevalent disease amongst Asian individuals, but rare in other parts of the world. It affects especially young women, with limited cases described in children. Kikuchi
Autor:
Patricia Costa-Reis, Kelly Maurer, Michelle A Petri, Daniella Levy Erez, Xue Zhao, Walter Faig, Jon Burnham, Kathleen O'Neil, Marisa S Klein-Gitelman, Emily von Scheven, Laura Eve Schanberg, Kathleen E Sullivan
Publikováno v:
Lupus sciencemedicine. 9(1)
ObjectiveLupus nephritis is a key driver of morbidity and mortality in SLE. Detecting active nephritis on a background of pre-existing renal damage is difficult, leading to potential undertreatment and accumulating injury. An unmet need is a biomarke
Autor:
Blanca Elena Rios Gomes Bica, Mahesh Janarthanan, Patricia Costa Reis, B. Hinrichs, Natalia Vasquez-Canizares, Valda Stanevicha, Vanessa Smith, Susan Nielsen, Anjali Patwardhan, Mikhail Kostik, Ekaterina Alexeeva, Amra Adrovic, Edoardo Marrani, Lillemor Berntson, Kathryn S. Torok, Tadej Avcin, Flavio Sztajnbok, Dieneke Schonenberg-Meinema, Maria Teresa Terreri, Despina Eleftheriou, Simone Appenzeller, Sujata Sawhney, N. Helmus, W.A. Sifuentes-Giraldo, Cristina Battagliotti, Kirsten Minden, Thomas J. A. Lehman, Ozgur Kasapcopur, Yosef Uziel, María M Katsicas, Raju Khubchandani, Farzana Nuruzzaman, Jens Klotsche, Ivan Foeldvari, Brian M. Feldman, Jordi Anton, Tilmann Kallinich, Maria José Santos
Publikováno v:
Arthritis Care and Research, 74(3), 364-370. John Wiley and Sons Inc.
ARTHRITIS CARE & RESEARCH
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
ARTHRITIS CARE & RESEARCH
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
OBJECTIVE: Utilizing data obtained from a prospective, international, juvenile systemic sclerosis (SSc) cohort, the present study was undertaken to determine if pulmonary screening with forced vital capacity (FVC) and diffusing capacity for carbon mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53fa6c2c68cb3f36f890f44b50b34820
https://pure.amc.nl/en/publications/underdetection-of-interstitial-lung-disease-in-juvenile-systemic-sclerosis(3543b1bc-68ff-401b-8fb7-052bf46f495e).html
https://pure.amc.nl/en/publications/underdetection-of-interstitial-lung-disease-in-juvenile-systemic-sclerosis(3543b1bc-68ff-401b-8fb7-052bf46f495e).html
Autor:
Jessica Durkee-Shock, Anqing Zhang, Hua Liang, Hannah Wright, Julieann Magnusson, Elizabeth Garabedian, Rebecca A. Marsh, Kathleen E. Sullivan, Michael D. Keller, Jennifer Puck, Elizabeth Secord, Javeed Akhter, Tamara Pozos, Ramsay Fuleihan, Karin Chen, Rebecca Buckley, Niraj Patel, Daniel Suez, Megan Cooper, Manish Butte, Francisco Bonilla, Kelly Walkovich, Elie Haddad, Charlotte Cunningham-Rundles, Gary Kleiner, Hey Chong, Zuhair Ballas, Burcin Uygungil, Vivian Hernandez-Trujillo, Elizabeth A. Secord, Nicholas Hartog, Morna Dorsey, Ralph Shapiro, Susan Schuval, Luigi Notarangelo, John Routes, Adina Knight, Nicholas Bennett, Fatima Khan, Jolan Walter, Christine Seroogy, Hans Ochs, Kathleen Haines, Mica Muskat, Patricia Costa Reis, Laurence Cheng
Publikováno v:
The journal of allergy and clinical immunology. In practice. 10(5)
Optimal management of patients with combined immunodeficiency, especially pertaining to hematopoietic stem cell transplantation (HSCT), remains unclear.To identify factors influencing HSCT and mortality in the population with combined immunodeficienc
Autor:
Ivan Foeldvari, Jens Klotsche, Ozgur Kasapcopur, Amra Adrovic, Maria Teresa Terreri, Ana Paula Sakamoto, Valda Stanevicha, Jordi Anton, Brian M Feldman, Flavio Sztajnbok, Raju Khubchandani, Ekaterina Alexeeva, Maria Katsicas, Sujata Sawhney, Vanessa Smith, Simone Appenzeller, Tadej Avcin, Mikhail Kostik, Thomas Lehman, Edoardo Marrani, Dieneke Schonenberg-Meinema, Walter-Alberto Sifuentes-Giraldo, Natalia Vasquez-Canizares, Mahesh Janarthanan, Monika Moll, Dana Nemcova, Anjali Patwardhan, Maria Jose Santos, Cristina Battagliotti, Lillemor Berntson, Blanca Bica, Jürgen Brunner, Rolando Cimaz, Patricia Costa-Reis, Despina Eleftheriou, Liora Harel, Gerd Horneff, Sindhu R Johnson, Daniela Kaiser, Tilmann Kallinich, Dragana Lazarevic, Kirsten Minden, Susan Nielsen, Farzana Nuruzzaman, Siri Opsahl Hetlevik, Yosef Uziel, Nicola Helmus, Kathryn S Torok
Publikováno v:
Journal of Scleroderma and Related Disorders. SAGE Publications Ltd
Foeldvari, I, Klotsche, J, Kasapcopur, O, Adrovic, A, Terreri, M T, Sakamoto, A P, Stanevicha, V, Anton, J, Feldman, B M, Sztajnbok, F, Khubchandani, R, Alexeeva, E, Katsicas, M, Sawhney, S, Smith, V, Appenzeller, S, Avcin, T, Kostik, M, Lehman, T, Marrani, E, Schonenberg-Meinema, D, Sifuentes-Giraldo, W-A, Vasquez-Canizares, N, Janarthanan, M, Moll, M, Nemcova, D, Patwardhan, A, Santos, M J, Battagliotti, C, Berntson, L, Bica, B, Brunner, J R, Cimaz, R, Costa-Reis, P, Eleftheriou, D, Harel, L, Horneff, G, Johnson, S R, Kaiser, D, Kallinich, T, Lazarevic, D, Minden, K, Nielsen, S, Nuruzzaman, F, Opsahl Hetlevik, S, Uziel, Y, Helmus, N & Torok, K S 2022, ' Gender differences in juvenile systemic sclerosis patients : Results from the international juvenile scleroderma inception cohort ', Journal of Scleroderma and Related Disorders . https://doi.org/10.1177/23971983221143244
Foeldvari, I, Klotsche, J, Kasapcopur, O, Adrovic, A, Terreri, M T, Sakamoto, A P, Stanevicha, V, Anton, J, Feldman, B M, Sztajnbok, F, Khubchandani, R, Alexeeva, E, Katsicas, M, Sawhney, S, Smith, V, Appenzeller, S, Avcin, T, Kostik, M, Lehman, T, Marrani, E, Schonenberg-Meinema, D, Sifuentes-Giraldo, W-A, Vasquez-Canizares, N, Janarthanan, M, Moll, M, Nemcova, D, Patwardhan, A, Santos, M J, Battagliotti, C, Berntson, L, Bica, B, Brunner, J R, Cimaz, R, Costa-Reis, P, Eleftheriou, D, Harel, L, Horneff, G, Johnson, S R, Kaiser, D, Kallinich, T, Lazarevic, D, Minden, K, Nielsen, S, Nuruzzaman, F, Opsahl Hetlevik, S, Uziel, Y, Helmus, N & Torok, K S 2022, ' Gender differences in juvenile systemic sclerosis patients : Results from the international juvenile scleroderma inception cohort ', Journal of Scleroderma and Related Disorders . https://doi.org/10.1177/23971983221143244
Objective: To compare organ involvement and disease severity between male and female patients with juvenile onset systemic sclerosis. Methods: Demographics, organ involvement, laboratory evaluation, patient-reported outcomes and physician assessment
Autor:
Marta Melgosa Hijosa, Elisa Benetti, Daniele Doná, Jacek Toporski, Maribel Barrios, Jelena Rascon, Luis Garcia Guereta, Ulrich Baumann, Nicolaus Schwerk, Björn Fischler, Alastair Baker, Etienne Sokal, Federica De Corti, Olivia Boyer, Lars Wennberg, Antonio Pérez Martínez, Caroline A. Lindemans, Emanuele Nicastro, Xavier Stéphenne, Maria Francelina Lopes, Paloma Jara, Ana Teixeira, Peter Bárány, Sophie Branchereau, Piotr Kaliciński, Juan Torres Canizales, Mara Cananzi, Esther Ramos Boluda, Loreto Hierro, Dominque Debray, Patricia Costa Reis, Marco Sciveres, Marius Miglinas, Elisabetta Calore, Manila Candusso
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Clinical Transplantation
Clinical Transplantation, Vol. 34, no. 10, p. e14063 [1-8] (2020)
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Clinical Transplantation
Clinical Transplantation, Vol. 34, no. 10, p. e14063 [1-8] (2020)
The current pandemic SARS-CoV-2 has required an unusual allocation of resources that can negatively impact chronically ill patients and high-complexity procedures. Across the European Reference Network on Pediatric Transplantation (ERN TransplantChil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a3bb6544f37bcf8ee001b0bb858c8cf
https://hdl.handle.net/10400.16/2566
https://hdl.handle.net/10400.16/2566
Autor:
Mahesh Janarthanan, Anjali Patwardhan, N. Helmus, Maria T. Tererri, Dana Nemcova, Valda Stanevicha, Patricia Costa Reis, Tadej Avcin, Blanca Elena Rios Gomes Bica, Yosef Uziel, Jens Klotsche, Despina Eleftheriou, Kirsten Minden, M. Moll, Susan Nielsen, Amra Adrovic, Jordi Anton, Lillemor Berntson, M. Katsikas, Dieneke Schonenberg, Ekaterina Alexeeva, Maria José Santos, Simone Appenzeller, Vanessa Smith, Mikhail Kostik, Dragana Lazarevic, Thomas J. A. Lehman, J. Brunner, Rolando Cimaz, Ivan Foeldvari, Gerd Horneff, Ozgur Kasapcopur, Cristina Battagliotti, Liora Harel, Kathryn S. Torok, Walter Alberto Sifuentes-Giraldo, Tilmann Kallinich, Flavio Sztajnbok, Farzana Nuruzzaman
Publikováno v:
Saturday, 15 June 2019.
Background Juvenile systemic scleroderma (jSSc) is an orphan disease with a prevalence of 3 in 1 000 000 children. There are limited data regarding the clinical presentation of jSSc. The Juvenile Systemic Scleroderma Inception Cohort (JSSIC) is a mul
Autor:
Anne M. Stevens, Kim Fligelstone, LI Suzanne, Brandi E. Stevens, Jordi Anton, Clarissa Pilkington, Michael Blakley, Ozgur Kasapcopur, Vanessa Smith, B. Hinrichs, Patricia Costa Reis, Daniel E. Furst, Christopher P. Denton, Megan L. Curran, Dinesh Khanna, Francesco Del Galdo, Antonia Höger, Dana Nemcova, Ivan Foeldvari, Christian Beyer, Catherine H. Orteu, Allison Zheng, Maurizio Cutolo, Tamás Constantin, Kathryn S. Torok, Lusine Ambartsumyan, Francesca Ingegnoli
Publikováno v:
Abstracts Accepted for Publication.
Background Juvenile systemic sclerosis (jSSc) is an orphan disease, associated with high morbidity and mortality. New treatment strategies are much needed. To develop an open label drug trial for the treatment of jSSc patients, it is necessary to cle