Results 161 to 170 of about 2,781 (251)

Hypervirulent Klebsiella pneumoniae Infections: A Systematic Review of Clinical, Microbiological, and Outcome Data From Reported Cases

MicrobiologyOpen, Volume 15, Issue 3, June 2026.
Distribution of organ involvement in reported hypervirulent Klebsiella pneumoniae cases. Studies restricted to isolated liver abscess cases were excluded. Percentages represent the proportion of cases with documented involvement of each anatomical site among cases with available data.
Nermin Sakru, Ender Cetinkaya, Feza Irem Aldi, Mervenur Inan, Canan Eryildiz   +4 more
wiley   +1 more source

Severe Pain Phenotype in Hemoglobin C (HbC)/Beta-Zero (β⁰) Thalassemia Without Hemoglobin S (HbS): A Clinical and Diagnostic Challenge. [PDF]

Cureus
Martinez MJ, Friedland BN, Jha A, Zagoruychenko T, Berman S.   +4 more
europepmc   +1 more source

Visual Identity, Social Branding, and Advocacy: Development of the PEN‐Plus Logo for Severe Non‐Communicable Disease Care in Nepal

Public Health Challenges, Volume 5, Issue 2, June 2026.
Nepal's PEN‐Plus logo, developed through a participatory process, serves as a unifying visual identity for severe non‐communicable disease care. Integrating social branding and behavioral insights, it uses symbolic elements to raise awarness to reduce stigma, promote inclusion, and address barriers to care. It fosters community engagement, builds trust,
Dhurba Khatri, Shishir Paudel, Yamuna Chhetri, Bhakta Bahadur K. C., Rudra Prakash Hada, Sheela Shrestha, Leela Khanal, Sandeepa Karki   +7 more
wiley   +1 more source

Gene Expression Profiles at Early vs Late Stages After Cervical Artery Dissection. [PDF]

Neurol Genet
Ferguson RB, Green IE, Mcmurry TL, Keene KL, Williams SR, Hsu FC, Bekiranov S, Hyacinth HI, Jickling GC, Sale MM, Worrall BB, Southerland AM.   +11 more
europepmc   +1 more source

On‐Chip Evaluation of Red Blood Cell Deformability Through Transit Velocity Index in Hematological Diseases

Small, Volume 22, Issue 33, 12 June 2026.
The deformability of red blood cell is essential for smooth microcirculation. We propose a deformability index using a microfluidic platform with capillary‐like constrictions, based on the relationship between cell deformation and transit velocity through the constrictions. Its effectiveness and clinical potential have been demonstrated in applications
Kenji Kajitani, Chia‐Hung Dylan Tsai, Tomohito Ohtani, Shigeo Wada, Ivan Cimrák, Misato Chimura, Tatsunori Taniguchi, Yasutaka Ueda, Jun‐ichi Nishimura, Yasushi Sakata   +9 more
wiley   +1 more source

Exploring the protective effects of thalassemia against malaria in Africa: a systematic review. [PDF]

Syst Rev
Donkor AB, Nyarko SB, Asare KK, Asa-Atiemo CKM, Kusi KA, Afrane YA, Amoah LE.   +6 more
europepmc   +1 more source

Red blood cell membrane proteome as a reporter of disease severity, transfusion impact and genetic background in transfusion‐dependent β‐thalassaemia

British Journal of Haematology, Volume 208, Issue 6, Page 1980-1992, June 2026.
Summary Omics technologies have transformed research in haemoglobinopathies, yet the proteome of RBCs remains largely unexplored in transfusion‐dependent thalassaemia (TDT). In this proteomic analysis, Red blood cell (RBC) membranes from 48 adults with TDT were compared with healthy controls.
Konstantina Theocharaki, Sophia Delicou, Aikaterini Ntzoura‐Kani, Nikolaos Simantiris, Marianna Politou, Veroniki Komninaka, Martina Samiotaki, Jerome Zoidakis, Marianna H. Antonelou   +8 more
wiley   +1 more source

Editorial: Micro-nano-materials for drug delivery, disease diagnosis, and therapeutic treatment. [PDF]

Front Bioeng Biotechnol
Guo B, Peng T, Mi C, Ye L.
europepmc   +1 more source

A genetic risk score based on BCL11A and HBS1L‐MYB variants predicts clinical severity in Brazilian sickle cell anaemia patients

British Journal of Haematology, Volume 208, Issue 6, Page 2203-2211, June 2026.
Summary Individuals with sickle cell anaemia (SCA) exhibit significant clinical heterogeneity influenced by several factors, especially fetal haemoglobin (HbF) levels. Variations in adult HbF levels are partly explained by the co‐inheritance of genetic variants that regulate globin expression.
Gabriela S. Arcanjo, Alexsandro P. Silva, Madi V. Diniz, Igor F. Domingos, Diego A. Pereira‐Martins, Amanda B. Araújo, Talita S. S. França, Ana C. Anjos, Aderson S. Araujo, Edis Belini‐Junior, Sara T. O. Saad, Fernando F. Costa, Antonio R. Lucena‐Araujo, Marcos André C. Bezerra   +13 more
wiley   +1 more source

Luspatercept Treatment in a β-Thalassemia Patient with Pulmonary Arterial Hypertension: A Case Report. [PDF]

Mediterr J Hematol Infect Dis
Yang B, Liu D, Yang C, Zhou Y, Liao G, Huang J, Li Y, Tang Y, Yin X.   +8 more
europepmc   +1 more source