Results 41 to 50 of about 10,507 (124)
Journal of Gastroenterology and Hepatology, Volume 41, Issue 5, Page 1403-1414, May 2026.ABSTRACT Background High antibiotic resistance and limited tetracycline accessibility severely restrict the clinical application of classic bismuth quadruple therapy (BQT), creating an urgent demand for alternative regimens. Methods A systematic search was conducted in PubMed, Embase, Cochrane Library, and Web of Science up to June 3, 2025, for trials ...
Qi‐Qi Guo +7 more
wiley +1 more source
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
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 +2 more
doaj +1 more source
A Difficult‐to‐Manage Case of Primary Idiopathic Erythromelalgia—Case Report
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Erythromelalgia is a rare condition with symptoms of erythema, warmth, and painful extremities exacerbated by warmth and relieved by cooling. Pain management is often challenging. The sodium channel blocker, lacosamide, was most effective in this patient.
Sarah Wide +3 more
wiley +1 more source
Successful Treatment of Aplastic Anemia With Eltrombopag During Pregnancy: A Short Report
eJHaem, Volume 7, Issue 2, April 2026.ABSTRACT Introduction Aplastic anemia (AA) is a rare bone marrow failure syndrome with pancytopenia, mainly due to immune‐mediated stem cell destruction. First‐line therapy for acquired severe AA ≥ 50 years/non‐severe AA (NSAA) requiring treatment is immunosuppressive therapy with horse anti‐thymocyte globulin, cyclosporine A (CSA), and eltrombopag ...
Sandra M. Frey +3 more
wiley +1 more source
Immunology, Volume 177, Issue 4, Page 736-748, April 2026.A constant rate of DNA damage that is not perfectly repaired will cause a constant rate of DNA mutations. The chance of mutation will increase if DNA is prone to damage, such as occurs in somatic hypermutation (SHM) hotspots and GC‐rich DNA. Thus, if one mutation‐prone DNA site drives disease, the age of onset of disease and degree of penetrance should
Piet C. de Groen
wiley +1 more source
Indian Journal of Anaesthesia, 2007 Acute immune thrombocytopenic purpura in children, though a benign self limiting condition, at times complicated with life threatening haemorrhage. In spite of bleeding episode it is inevitable that surgical procedure will be performed on patients with ...
Minati Choudhury, Nirvik Pal, Usha Kiran
doaj
Pulmonary Circulation, 2020 While the prognosis of idiopathic pulmonary arterial hypertension has improved significantly due to newer medications, lung transplantation remains a critical therapeutic option for severe pulmonary arterial hypertension.
Takayuki Kobayashi +8 more
doaj +1 more source
Recurrent Acute Myocardial Infarction in Patients with Immune Thrombocytopenic Purpura
Journal of Patient-Centered Research and Reviews, 2014 Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura, is an acquired immune-mediated disease of adults and children characterized by a transient or persistent decrease of platelets and, depending upon the degree of ...
Fengyi Shen, Tonga Nfor, Tanvir Bajwa
doaj +1 more source
Idiopathic thrombocytopenic purpura. Clinical case
Zaporožskij Medicinskij Žurnal, 2015 Aim. To draw the attention of physicians - internists to the problem of thrombocytopenia and hemorrhagic vasculitis. To describe the clinical case of idiopathic thrombocytopenic purpura, features of diagnostics and treatment of this disease at various ...
V. V. Syvolap +2 more
doaj +1 more source