Results 131 to 140 of about 94,881 (302)

Prevalence of Associated Extraoral Symptoms and Comorbidities in Burning Mouth Syndrome Patients: A Systematic Review

Oral Diseases, EarlyView.
ABSTRACT Objective Patients with burning mouth syndrome (BMS) suffer from oral pain in the absence of oral lesions. Although less frequently, they may also experience extraoral symptoms that are not readily apparent to clinicians. This study aimed to systematically assess the prevalence of associated extraoral symptoms and comorbid disorders in BMS ...
João Paulo Gonçalves de Paiva, Caique Mariano Pedroso, Rosa María López‐Pintor Muñoz, Milda Chmieliauskaite, Alessandro Villa, Jacks Jorge, Alan Roger Santos‐Silva   +6 more
wiley   +1 more source

Protein S Enhances the Phagocytosis of Phosphatidylserine-Exposing Erythrocytes: Implications in Sickle Cell Disease. [PDF]

Am J Hematol
ABSTRACT The major anticoagulant Protein S (PROS1) also contributes to the phagocytosis of apoptotic cells by bridging exposed phosphatidylserine (PtdSer) to the MerTK receptor on macrophages (efferocytosis). Whether PROS1 is involved in the splenic clearance of PtdSer‐positive senescent and altered erythrocytes such as erythrocyte ghosts (eryghosts ...
Auditeau C, Fricot A, Gauthier R, Sissoko A, Cacan Z, Gounou C, Joseph L, Manceau S, Allali S, Dussiot M, Marin M, Lavergne A, Khamari M, Moog S, Bianchini E, Claer L, Laurance S, Brousse V, Eymieux S, Roingeard P, Amireault P, Trovati Maciel T, Brisson A, Buffet P, Saller F, Borgel D, Roussel C.   +26 more
europepmc   +2 more sources

Porphyromonas gingivalis GroEL exacerbates orthotopic allograft transplantation vasculopathy via impairment of endothelial cell function

Molecular Oral Microbiology, EarlyView.
Abstract Orthotopic allograft transplantation (OAT) is a significant approach to addressing organ failure. However, persistent immune responses to the allograft affect chronic rejection, which induces OAT vasculopathy (OATV) and organ failure. Porphyromonas gingivalis can infiltrate remote organs via the bloodstream, thereby intensifying the severity ...
Chien‐Sung Tsai, Chun‐Yao Huang, Yi‐Ting Tsai, Chun‐Ming Shih, Ze‐Hao Lai, Chen‐Wei Liu, Yi‐Wen Lin, Feng‐Yen Lin   +7 more
wiley   +1 more source

MANAGEMENT OF CHILDREN WITH SICKLE CELL DISEASE IN EUROPE: CURRENT SITUATION AND FUTURE PERSPECTIVES

European Medical Journal Hematology, 2016
Sickle cell disease (SCD) is the most common haemoglobinopathy worldwide and its frequency has steadily increased in Europe in the past decades. SCD is a complex multisystem disorder characterised by chronic haemolytic anaemia, vaso-occlusive crisis, and
Raffaella Colombatti, Laura Sainati
doaj  

Landscape of Current Transplant Infectious Disease Training Programs

Transplant Infectious Disease, EarlyView.
ABSTRACT Background Transplant infectious disease (TID) training is not accredited by the Accreditation Council for Graduate Medical Education (ACGME) and is not standardized. Prior surveys of the training landscape in TID have focused on fellow responses; we sought description of programs from program directors and coordinators. Methods Along with the
Michael J. Scolarici, Jessica Tischendorf, Rachel Filipiak, Lara Danziger‐Isakov, Benjamin Hanisch, Alice Sato, Saman Nematollahi, Christopher Saddler   +7 more
wiley   +1 more source

Genotype Differences and Hydroxyurea Utilization Among Adults With Moderate to Severe Sickle Cell Disease. [PDF]

Pharmacotherapy
ABSTRACT Backgrounds Hydroxyurea (HU) remains underutilized in adults with sickle cell disease (SCD) despite proven benefits. Current HU guidelines primarily target sickle cell anemia (SCA), overlooking other genotypes. Objectives This study examined HU utilization patterns across genotypes among adults considered to have moderate to severe SCD ...
Cheng SH, Novelli EM, Kang HA, Newman TV, Suh K.   +4 more
europepmc   +2 more sources

Perspectives in genomics and sickle cell disease therapeutics [PDF]

Ambroise Wonkam
openalex   +1 more source

Malaria Screening and Treatment in Hematopoietic Cell Transplant Donors and Sickle Cell Disease Candidates/Recipients: A Case Series Using Malaria Polymerase Chain Reaction Testing and a Literature Review

Transplant Infectious Disease, EarlyView.
Malaria polymerase chain reaction (PCR) testing is more sensitive than conventional diagnostics. Routine PCR screening of at‐risk asymptomatic hematopoietic cell donors and transplant candidates may prevent unnecessary deferrals or treatment. In our experience, PCR negativity during screening or after treatment supports donor/candidate eligibility ...
Mary M. Czech, Sanchita Das, Emily Limerick, Courtney Fitzhugh, Matthew Hsieh, Jennifer Cuellar‐Rodriguez   +5 more
wiley   +1 more source

HEALTHCARE PROFESSIONAL (HCP) PERCEPTIONS OF SICKLE CELL DISEASE (SCD): INTERNATIONAL SICKLE CELL WORLD ASSESSMENT SURVEY (SWAY)

Hematology, Transfusion and Cell Therapy, 2020
M.R. Abboud, J. James, N. Ramscar, I. Osunkwo, S.C. Sway   +4 more
doaj   +1 more source

Hemolysis inhibits humoral B-cell responses and modulates alloimmunization risk in patients with sickle cell disease [PDF]

, 2020
Mouli Pal, Weili Bao, Rikang Wang, Yunfeng Liu, Xiuli An, William B. Mitchell, Cheryl A. Lobo, Caterina P. Minniti, Patricia A. Shi, Deepa Manwani, Karina Yazdanbakhsh, Hui Zhong   +11 more
openalex   +1 more source