Zobrazeno 1 - 10
of 202
pro vyhledávání: '"Anemia, Sickle Cell/complications"'
Autor:
Patricia Reparaz, Idoya Serrano, Rosa Adan-Pedroso, Itziar Astigarraga, Jimena de Pedro Olabarri, Aizpea Echebarria-Barona, Miguel Garcia-Ariza, Ricardo Lopez-Almaraz, Rafael Andrés del Orbe-Barreto, Miriam Vara-Pampliega, Paula Gonzalez-Urdiales
Publikováno v:
Anales de Pediatría, Vol 97, Iss 1, Pp 4-11 (2022)
Resumen: Introducción: La drepanocitosis es una anemia emergente en Europa que condiciona una elevada morbilidad con complicaciones agudas y crónicas. El manejo de estos pacientes es complejo y requiere atención interdisciplinar. El objetivo del e
Externí odkaz:
https://doaj.org/article/795552aded8940b294f21743164edce1
Autor:
Carreira, Pedro, Loureiro, Tomás, Moraes, Filipe, Carreira, Rita, Sampaio, Audrey, Cabral, Diogo, Vide Escada, Ana, Campos, Nuno
Publikováno v:
Revista Sociedade Portuguesa de Oftalmologia; Vol. 46 No. 4 (2022); 239-244
Revista Sociedade Portuguesa de Oftalmologia; Vol. 46 N.º 4 (2022); 239-244
Revista Sociedade Portuguesa de Oftalmologia; Vol. 46 N.º 4 (2022); 239-244
INTRODUCTION: Retinopathy is the most frequent ophthalmological manifestation of sickle cell disease (SCD). Advances in retinal multimodal imaging have revealed the presence of retinopathy in asymptomatic patients. The present study aims to character
Autor:
Karin Fijnvandraat, Vera Bongaerts, H. Heijboer, Bart J. Biemond, Erfan Nur, Jorn J. Gerritsma, Corien L. Eckhardt, Ellen van der Schoot
Publikováno v:
British journal of haematology, 196(3), 769-776. Wiley-Blackwell
Delayed haemolytic transfusion reaction (DHTR) is a potentially life-threatening complication of red blood cell (RBC) transfusions in sickle cell disease (SCD) and is classically induced by reactivation of previously formed antibodies. Improved antig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6559b58cd1a9234f5af908a180afac23
https://pure.amc.nl/en/publications/extended-phenotyping-does-not-preclude-the-occurrence-of-delayed-haemolytic-transfusion-reactions-in-sickle-cell-disease(6ec653d3-8b03-4ec9-85a0-ac7a3307abcb).html
https://pure.amc.nl/en/publications/extended-phenotyping-does-not-preclude-the-occurrence-of-delayed-haemolytic-transfusion-reactions-in-sickle-cell-disease(6ec653d3-8b03-4ec9-85a0-ac7a3307abcb).html
Autor:
Reparaz Goñi, Patricia, Serrano Pejenaute, Idoya, Adán Pedroso, Rosa, Astigarraga Aguirre, María Iciar, De Pedro Olabarri, Jimena, Echebarria Barona, Aizpea Beatriz, García Ariza, Miguel, López Almaraz, Ricardo, Del Orbe Barreto, Rafael Andrés, Vara Pampliega, Miriam, González Urdiales, Paula
Publikováno v:
Addi. Archivo Digital para la Docencia y la Investigación
instname
instname
Sickle cell disease is an emerging anemia in Europe leading to high morbidity with severe acute complications requiring hospital admission and chronic consequences. The management of these patients is complex and needs interdisciplinary care. The obj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c55006fa5aa3e52c0a6f23cca3255df7
http://hdl.handle.net/10810/57803
http://hdl.handle.net/10810/57803
Autor:
Rodrigues, Jorge, Milheiro Silva, Tiago, Garcia, Ana Margarida, Soares, Eugénia, Brito, Maria João
Publikováno v:
Portuguese Journal of Pediatrics, Vol 53, Iss 1 (2022)
Acute chest syndrome (ACS) is a life-threatening complication in sickle cell disease (SCD). Infections are frequently implied and like other viruses, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may be a trigger. Additionally, due to
Autor:
Rafael Pereira de Paula, Alana Ferreira Nascimento, Sandra Mara Bispo Sousa, Paulo Roberto Velasco Bastos, Ana Angelica Leal Barbosa
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 35, Iss 5, Pp 349-351 (2013)
BACKGROUND Renal failure is common among older patients with sickle cell disease; this is preceded by subclinical glomerular hyperfiltration. Data about renal function of adults with sickle cell disease have been reported, but data on children is sca
Externí odkaz:
https://doaj.org/article/56fcbc5a3cb34520bf46e4554c2e60f9
Autor:
Tine Vervoort, Lori E. Crosby, Zina Trost, Adam T. Hirsh, Anna M Hood, Deanna Rumble, Megan M. Miller, Avi Madan-Swain, Jeffrey D. Lebensburger
Publikováno v:
Pain Med
Miller, M M, Rumble, D D, Hirsh, A T, Vervoort, T, Crosby, L E, Madan-Swain, A, Lebensburger, J, Hood, A M & Trost, Z 2021, ' Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease : A Preliminary Investigation ', Pain Medicine, vol. 22, no. 10, pp. 2207-2217 . https://doi.org/10.1093/pm/pnab001
Miller, M M, Rumble, D D, Hirsh, A T, Vervoort, T, Crosby, L E, Madan-Swain, A, Lebensburger, J, Hood, A M & Trost, Z 2021, ' Pain-Related Injustice Appraisals in Youth with Sickle Cell Disease : A Preliminary Investigation ', Pain Medicine, vol. 22, no. 10, pp. 2207-2217 . https://doi.org/10.1093/pm/pnab001
Objectives Sickle cell disease (SCD) is a genetic disorder that affects approximately 100,000 Americans, the majority of whom are African American. SCD-related pain often has deleterious effects on functioning and quality of life. The inherited natur
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Diyar Z. Akkaynak, Yeşim Oymak, Gonul Aydogan, Tuğba Gürleyen Eren, Gülsün Karasu, Bahattin Tunç, Fatma Gumruk, Selma Unal, Umran Caliskan, Turkan Patiroglu, Adalet Meral Güneş, Zafer Salcioglu, Ahmet Koç, Yusuf Ziya Aral, Yasemin Isik Balci, Mehmet Akin, Aylin Canbolat Ayhan, Vedat Uygun, Osman Alphan Küpesiz, Gönül Oktay, Canan Vergin, Betül Biner, İlgen Şaşmaz, Mehmet Ertem, Hilmi Apak, Emine Türkkan, Yıldız Yildirmak, Cetin Timur, Elif Güler Kazanci, Gülersu Irken, Ülker Koçak, Murat Söker, Erdal Kurtoğlu, Mehmet Akif Yesilipek, Bülent Antmen, Zeynep Karakas
PubMedID: 30300449 Objectives: To evaluate the long-term efficacy and safety of deferasirox therapy in a large observational cohort of children with transfusion-dependent thalassemia (TDT) and sickle cell anemia (SCA) in Turkey. Methods: This was a m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b5a731b446ddb4e25ef6dbad909d7cf