Results 41 to 50 of about 7,492,718 (206)

Chipmunk parvovirus is distinct from members in the genus Erythrovirus of the family Parvoviridae. [PDF]

PLoS ONE, 2010
The transcription profile of chipmunk parvovirus (ChpPV), a tentative member of the genus Erythrovirus in the subfamily Parvovirinae of the family Parvoviridae, was characterized by transfecting a nearly full-length genome.
Zhaojun Chen, Aaron Yun Chen, Fang Cheng, Jianming Qiu   +3 more
doaj   +1 more source

Parvovirus B19 [PDF]

, 2013
B19, database# 1S58. Parvovirus B19 virus is part of the parvovirus family and causes a childhood rash called fifth disease or erythema infectiosum that is commonly called slapped cheek syndrome.
Hatice Türk Dağı, Hall, David J.
core   +3 more sources

Parvovirus B19 infections in paediatric sickle cell disease patients: Genotype and hydroxyurea treatment influence disease severity

British Journal of Haematology, EarlyView.
Summary In patients with sickle cell disease (SCD), parvovirus B19 infection (B19V) leads to acute anaemia (aplastic crisis), but may also be associated with other serious complications. We retrospectively analysed clinical data from paediatric SCD patients with B19V infections between 2023 and 2025, including symptoms, laboratory parameters ...
Matthias Bleeke, Arne Simon, Beate Winkler, Sabine Heine, Anna Eichinger, Ulrich von Both, Meinolf Siepermann, Sonya El Amouri, Arndt Borkhardt, Yvonne Pritschow, Wolfgang Novak, Michael Dworzak, Sarah Goretzki, Clara Held, Karin Beutel, Franziska Gams, Henriette Rudolph, Leila Koscher, Piet E. Beusker, Eckard Hamelmann, Stefan Weichert, Svenja Häuser, Maximilian Mauritz, Malik Aydin, Verena Wiegering, Regine Grosse, Rainer Misgeld, Martina Stiefel, Nicole Töpfner, Uta Falke, Lara Imhof, Laura Tagliaferri, Daniel Ebrahimi‐Fakhari, Andreas Groll, Marion Appel, Nora Naumann‐Bartsch, Michaela Nathrath, Olaf Beck, Solvej Heidtmann, Philipp Tischer, Ulf Schulze‐Sturm, Urs Mücke, Holger Cario   +42 more
wiley   +1 more source

ICSH Guidance on Bone Marrow Examination and Reporting

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Examination of the bone marrow (BM) remains fundamental to the diagnosis, classification, prognostication, and monitoring of hematolymphoid and other disorders affecting blood cell production. Since publication of the International Council for Standardization in Haematology (ICSH) guideline in 2008, advances in diagnostic technologies, disease
Wendy N. Erber, Alexandar Tzankov, Olga Pozdnyakova, Hiromichi Matsushita, Gina Zini, Leonie Saft, on behalf of the International Council for Standardization in Haematology   +6 more
wiley   +1 more source

A descriptive case series of hepatotoxicity associated with CFTR modulators and possible relevance of pharmacogenetic polymorphisms in cystic fibrosis patients

British Journal of Clinical Pharmacology, Volume 92, Issue 9, Page 3257-3264, September 2026.
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators are widely used in patients with cystic fibrosis and significantly improve respiratory function and quality of life. However, their effectiveness may be limited by liver damage, which sometimes leads to treatment discontinuation, and the mechanisms underlying this remain poorly ...
Clara Laffitte Redondo, Venceslas Bourdin, Abd El Kader Ait Tayeb, Sihem Benaboud, Inès Martins, Caroline Joyau, Myriam Benhamida, Isabelle Sermet‐Gaudelus, Clémence Martin, Pierre Régis Burgel, Céline Verstuyft, Laurent Chouchana, Estelle Ayme‐Dietrich   +12 more
wiley   +1 more source

Mirror Syndrome (Ballantyne Syndrome): Prenatal Diagnosis, Pathophysiology, and the Role of Fetal Therapy—A Narrative Review

Prenatal Diagnosis, Volume 46, Issue 10, Page 1617-1625, September 2026.
ABSTRACT Mirror syndrome is a rare maternal–fetal condition associated with fetal hydrops and a high risk of adverse maternal and fetal perinatal outcomes. Its diagnosis is challenging due to the lack of standardized diagnostic criteria and its clinical and biochemical overlap with preeclampsia.
Riccardo Tudisco, Pauline Latapie, Anita Romiti, Alexandra Benachi, Maelig Abgral, Alexandre J. Vivanti   +5 more
wiley   +1 more source

Without parvovirus B19 infection of thyroid tissues, no Hashimoto's thyroiditis

, 2021
Aim: Whether a Parvovirus B19 viral infection is responsible for Hashimoto's thyroiditis remains unclear. Studies addressing this issue were reanalysed. Materials and methods: The electronic database PubMed has been searched for appropriate studies. New
Barukčić, Ilija
core   +1 more source

Seroprevalence of Toxoplasma gondii, Rubella Virus, Cytomegalovirus, and Herpes Simplex Virus Among Children and Women in Bhutan's National Referral Hospital: A Cross‐Sectional Study

Public Health Challenges, Volume 5, Issue 3, September 2026.
Congenital infections caused by Toxoplasma gondii, rubella virus, cytomegalovirus, and herpes simplex virus were assessed in 624 children and women at JDWNRH (2019–2022). HSV (83.8%) and CMV (82.7%) were most prevalent, whereas T. gondii was the lowest (14.7%).
Karma Norbu, Sonam Wangzin Rabjay, Karma Galey, Thinley Dorji, Ugyen Chophel, Jamyang Wangmo, Binita Rai, Yeshey Dorjey, Tshokey Tshokey   +8 more
wiley   +1 more source

Parvovirus B19 Prevalence among Children of African Descent in Sokoto North Western Nigeria

Sokoto Journal of Medical Laboratory Science, 2019
Human Parvovirus B19 (HPVB19) belongs to the family Parvoviridae and it causes Erythema infectiosum, aplastic crises in persons with blood disorder and prolonged anaemia in immuno compromised persons.
Ibrahim, K.* , Muhammad, M.B. , Erhabor, O. , Adias, T.C. , Udomah, F. , Abdulrahaman, Y. , Onuigwe, U. , Okwesili, A. , Ibrahim, B.A. , Buhari, H. , Zama, I. , Erhabor, T . Egenti, B.N.
doaj  

Phenotype‐specific immune profiles and outcomes in childhood autoimmune neutropenia: A 20‐year cohort study

British Journal of Haematology, Volume 209, Issue 3, Page 1158-1165, September 2026.
Summary Childhood autoimmune neutropenia (AIN) encompasses heterogeneous entities; phenotype‐specific immunological profiles and their relationship to infection outcomes remain incompletely defined. To characterise clinical, immunological and long‐term outcomes across distinct phenotypes of childhood AIN.
Ioanna Saougou, Chrysoula Kosmeri, Nikolaos Chaliasos, Irene Mavroudi, Charalampos Pontikoglou, Alexandros Makis   +5 more
wiley   +1 more source