Zobrazeno 1 - 10
of 37 125
pro vyhledávání: '"A. fc"'
Publikováno v:
Journal of Asthma and Allergy, Vol Volume 17, Pp 801-811 (2024)
Craig LaForce,1 Frank C Albers,2 Mark Cooper,3 Anna Danilewicz,4 Lynn Dunsire,3 Robert Rees,4 Christy Cappelletti5 1North Carolina Clinical Research, Chapel Hill, NC, USA; 2Avillion, Northbrook, IL, USA; 3BioPharmaceuticals Research and Development,
Externí odkaz:
https://doaj.org/article/f3a1870b43c34835acf51dbcd7fac7bc
Publikováno v:
Nigerian Journal of Paediatrics, Vol 46, Iss 4, Pp 195-199 (2024)
Background: Missed Opportunity for Vaccination (MOV) is a significant cause of low immunisation coverage and resurgence of vaccine preventable diseases. Hence, identifying the causes of MOV in our health facilities and eliminating them will help impr
Externí odkaz:
https://doaj.org/article/b0a25d60e62a4dc084f0dc86a2811f05
Publikováno v:
Nigerian Journal of Paediatrics, Vol 46, Iss 4, Pp 189-194 (2024)
Background: The patterns and outcome of under-five morbidity in health care facilities are invaluable tools that reflect the disease burden and health care needs of the children in the community. Efforts are being made over the past few years to impr
Externí odkaz:
https://doaj.org/article/1bf4f10464fb4c889cb3162380dbbcda
Autor:
Stoleriu MG, Pienn M, Joerres RA, Alter P, Fero T, Urschler M, Kovacs G, Olschewski H, Kauczor HU, Wielpütz M, Jobst B, Welte T, Behr J, Trudzinski FC, Bals R, Watz H, Vogelmeier CF, Biederer J, Kahnert K
Publikováno v:
International Journal of COPD, Vol Volume 19, Pp 1515-1529 (2024)
Mircea Gabriel Stoleriu,1,2,* Michael Pienn,3,4,* Rudolf A Joerres,5 Peter Alter,6 Tamas Fero,7 Martin Urschler,8 Gabor Kovacs,3,9 Horst Olschewski,3,9 Hans-Ulrich Kauczor,7,10 Mark Wielpütz,7,10 Bertram Jobst,7,10 Tobias Welte,11 Jürgen Be
Externí odkaz:
https://doaj.org/article/ff4bd68bbfb64a7db54791ce1212dcdc
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S44-S45 (2024)
Recent evidence has demonstrated that the gut microbiota plays an important role in the pathophysiology of sickle cell disease (SCD). Enterocyte damage, increased permeability and intestinal dysbiosis may be directly involved in modulating inflammato
Externí odkaz:
https://doaj.org/article/63e25845fbef4a8ea88e27403e0ab400
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S55-S56 (2024)
Introduction: Sickle cell anemia (SCA) is a hereditary condition characterized by morphological changes in erythrocytes, which increase their fragility and susceptibility to rupture, releasing intracellular components, including the heme molecule. Re
Externí odkaz:
https://doaj.org/article/b4ab26b1c37c4cbc82084fff3b4b8c4b
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S59- (2024)
Introduction: Intravascular hemolysis (IVH) results in the release of damage-associated molecular patterns (DAMPs) into the circulation, particularly hemoglobin (Hb) and heme, which can trigger NLRP3 inflammasome activation and a sterile inflammatory
Externí odkaz:
https://doaj.org/article/f614eccc80164f91bb728c9a407d68c4
Autor:
LFS Gushiken, SL Linguet, EMF Gotardo, PL Brito, FC Leonardo, CLV Kim, S Laurance, B Koehl, FF Costa, N Conran
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S99-S100 (2024)
Introduction: Sickle cell disease (SCD), the most common inherited hemoglobinopathy worldwide, results in the production of abnormal hemoglobin S. Polymerization of this hemoglobin causes red blood cell sickling and pathophysiological consequences. V
Externí odkaz:
https://doaj.org/article/62e5740a40504b8f93dac87b926fde3a
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S291-S292 (2024)
Objetivo: Relatar caso de paciente com diagnóstico de Linfoma Difuso de Grandes Células B (LDGCB) com histórico de Púrpura trombocitopênica trombótica (PTT). Relato de caso: Paciente do sexo feminino, 44 anos, com diagnóstico de PTT em 2016. R
Externí odkaz:
https://doaj.org/article/edd96359bcdf40939c25e9a2a16b9f7d
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S381-S382 (2024)
Introdução: Neoplasias mielodisplásicas (SMD) são doenças clonais, caracterizadas por citopenias, displasias, anomalias genéticas recorrentes e risco elevado de progressão para leucemia mieloide aguda (LMA). Estudos sugerem que SMDs com del20q
Externí odkaz:
https://doaj.org/article/9b53f246a50c4639b8364f7f7b60a63a