Results 41 to 50 of about 9,824 (158)

Origins of T‐cell‐mediated autoimmunity in acquired aplastic anaemia

British Journal of Haematology, Volume 206, Issue 4, Page 1035-1053, April 2025.
Acquired aplastic anaemia (AA) is an autoimmune bone marrow failure disease caused by a cytotoxic T‐cell–mediated attack on haematopoietic stem and progenitor cells (HSPCs). Despite significant progress in understanding T‐cell repertoire alterations in AA, the identification of specific pathogenic T cells remains elusive.
Aura Enache, Shannon A. Carty, Daria V. Babushok   +2 more
wiley   +1 more source

A New Diagnostic Approach for Myelodysplastic Neoplasms Using a Combination of Scores Based on Flow Cytometry and Automated Hematology Sysmex XN Analyzers

International Journal of Laboratory Hematology, Volume 47, Issue 2, Page 236-245, April 2025.
ABSTRACT Introduction The first‐step in diagnosis of myelodysplastic neoplasms (MDS) is essentially based on bone marrow cytomorphology. However, cytomorphology of MDS is often a difficult exercise, subject to inter‐operator variability. Our study aims to evaluate whether the combination of two dysplasia scores, the extended Ogata score and the MDS‐CBC
Ludovic Firrera, Benjamin Podvin, Julien Herlem, Marion Magierowicz, Alexandre Willaume, Vincent Thibaud, Agnès Charpentier   +6 more
wiley   +1 more source

Chemotherapy in a Patient with Prior History of Idiopathic Thrombocytopenic Purpura

Acta Medica, 2003
We described a 67 years old small-cell lung cancer patient with a prior history of idiopathic thrombocytopenic purpura (ITP) who was treated with successful chemotherapy.
Kouji Kanemoto, Hiroaki Satoh, Kiyohisa Sekizawa   +2 more
doaj   +1 more source

Occurrence of immune thrombocytopenic purpura in a patient with essential thrombocythemia: How the immune system can overcome a neoplastic clone

Clinical Case Reports, 2020
Our case highlights the possible coexistence of essential thrombocythemia (ET) and idiopathic thrombocytopenic purpura (ITP), two pathological entities with opposite clinical and laboratory manifestations.
Antonio Carruale, Francesco Longu, Francesca Mura, Giovanni Caocci, Giorgio La Nasa, Claudio Fozza   +5 more
doaj   +1 more source

Childhood Idiopathic Thrombocytopenic Purpura: A Retrospective Analysis Of Clinical Features And Response To Treatment

مجلة كلية الطب, 2006
Background : A retrospective study was done in the Pediatric ward /AL-Kadhimiyia Teaching Hospital on cases diagnosed as idiopathic thrombocytopenic Purpura admitted since the first of January1992 – the end of December 2004.
Sawsan S. Abbas
doaj  

A Case Associated with Comorbidities Among Cerebral Infarction, Idiopathic Thrombocytopenic Purpura, and Triple X Syndrome

Turkish Journal of Hematology, 2014
A 46-year-old female presented to the emergency room due to the chief complaint of left-sided weakness. By imaging study, she was diagnosed with cerebral infarction.
Hanjun Kim, Sang Sun Hwang, Young Uh, Juwon Kim, Kap Jun Yoon, Ji Yong Lee   +5 more
doaj   +1 more source

Whole exome sequencing reveals an FCGBP variant associated with spontaneous intraabdominal hemorrhage in severe acute pancreatitis

iMetaOmics, Volume 2, Issue 1, March 2025.
A large cohort of acute pancreatitis patients (n = 600) underwent whole‐exome sequencing, which identified a genetic mutation in FCGBP strongly associated with a predisposition of spontaneous intraabdominal hemorrhage. Incorporating the FCGBP mutation as a clinical indicator enhances the assessment for complications and mortality risk in acute ...
Qiu‐Yi Tang, Yue‐Peng Hu, Qi Yang, Jing Zhou, Jing‐Zhu Zhang, Jie Yang, Hai‐Bin Hao, Gang Li, Bai‐Qiang Li, Lu Ke, Zhi‐Hui Tong, Yu‐Xiu Liu, Evan Yi‐Wen Yu, Wei‐Qin Li   +13 more
wiley   +1 more source

CAUSES OF DEVELOPMENT OF ACUTE AND CHRONIC THROMBOCYTOPENIA IN CHILDREN OF IRKUTSK REGION

Acta Biomedica Scientifica, 2018
Background. Immune thrombocytopenia in children is not a rare disease. Currently, this diagnosis is found in 2 times more often than 5-10 years ago. Acute immune thrombocytopenia is increasingly taking on a chronic course. Aims.
N. N. Martynovich, O. P. Tolmacheva, V. A. Khyshova   +2 more
doaj   +1 more source

Association of Helicobacter pylori Infection and Risk of Dyslipidemia: A Systematic Review and Meta‐Analysis

JGH Open, Volume 9, Issue 3, March 2025.
ABSTRACT Background Although Helicobacter pylori (H. pylori) infections are widespread throughout the world, it is yet unknown whether they are linked to systemic illnesses like dyslipidemia. The purpose of this systematic review and meta‐analysis was to examine the connection between lipid metabolism and H. pylori infection, with a particular emphasis
Ankita Gaonkar, Quazi Syed Zahiruddin, Muhammed Shabil, Soumya V. Menon, Mandeep Kaur, Mukesh Kumari, Puneet Sudan, K. Satyam Naidu, Shailendra Thapliyal, Jyoti Uikey, Rachna Kathuria, Sanjay Singh Chauhan, Lokesh Verma, Amritpal Sidhu, Ganesh Bushi, Rohimah Binti Md Yusoff, Rachana Mehta, Prakasini Satapathy, Sanjit Sah   +18 more
wiley   +1 more source