Results 91 to 100 of about 26,371 (219)
Idiopathic Thrombocytopenic Purpura Misdiagnosed as Hereditary Angioedema [PDF]
, 2015 Hereditary angioedema is a rare, but potentially life-threatening genetic disorder that results from an autosomal dominant trait. It is characterized by acute, recurrent attacks of severe local edema, most commonly affecting the skin and mucosa. Swelling
Andersen, Michelle Fog, Bygum, Anette
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Trombocitopenia inmune primaria en pacientes de edad avanzada : experiencia en un centro [PDF]
, 2011 Estudi descriptiu dels pacients majors de 60 anys amb diagnòstic de trombocitopènia immune primària en un centre. S'han revisat característiques bàsiques en el moment de l'inici de la malaltia, així com les diferents línies de tractament, resposta ...
López Pavía, María de la Encarnación +2 more
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Journal of Medical Case Reports, 2018 Background Thrombotic thrombocytopenic purpura is a very rare hereditary blood deficiency disorder of ADAMTS13 (von Willebrand factor-cleaving protease) and a life-threatening thrombotic microangiopathy characterized by thrombocytopenia and ...
Valter Romão de Souza +9 more
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The comparison of perceived stress in idiopathic thrombocytopenic purpura patients referred to Seyed Al-Shohada Hospital with healthy people in Isfahan, Iran, 2013. [PDF]
, 2015 BACKGROUND Mental stress and daily crises comprise a part of physical and mental threats. Perceived stress is a physical and mental threat, as well.
Hemati, Z., Kiani, D.
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Complement and cytokine response in acute Thrombotic Thrombocytopenic Purpura [PDF]
, 2013 Complement dysregulation is key in the pathogenesis of atypical Haemolytic Uraemic Syndrome (aHUS), but no clear role for complement has been identified in Thrombotic Thrombocytopenic Purpura (TTP).
Heelas, E +4 more
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Hematology, Transfusion and Cell TherapyBackground: Immune thrombocytopenic purpura, a recurrent autoimmune disease, is characterized by thrombocytopenia, purpura and hemorrhagic episodes with the main factor in the pathogenesis of this disease being autoantibodies against platelets. Since the
Esra Seçkin, Rafiye Ciftciler
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Helicobacter pylori Eradication in Patients with Immune Thrombocytopenic Purpura: A Review and the Role of Biogeography [PDF]
, 2015 Idiopathic thrombocytopenic purpura (ITP) is typically a diagnosis of exclusion, assigned by clinicians after ruling out other identifiable etiologies. Since a report by Gasbarrini et al.
Beck, Paul L. +3 more
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Infection and Drug Resistance, 2023 Fei Lv,1,2 Yue Zhao,2 Xing-Di Yang,2 Han-Zhu Chen,2 Wen-Ya Ren,2 Ling-Xia Chen,2 Qiao-Qiao Yi,2 Wei Zheng,2 Hong-Ying Pan2 1The Second Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, 310053, People’s Republic of China ...
Lv F +8 more
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Successful use of rituximab in Evans syndrome and refractory immune thrombocytopenic purpura [PDF]
, 2010 Immune cytopenias are mediated by auto-antibodies produced by B-lymphocytes. Conventional treatment of immune-mediated haematological disorders includes immunosuppression with steroids and other immune modulating therapies and in some refractory cases ...
Adil, Salman Naseem +3 more
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تظاهرات بالينی و نتايج درمان در ايمون ترومبوسيتوپنی پورپورای شيرخواران [PDF]
, 2004 هدف از اين مطالعه بررسی تظاهرات بالينی، عوامل مستعد کننده، نتايج درمان و ميزان مزمن شدن بيماری در شيرخواران 23-1 ماهه مبتلا به ايمون ترومبوسيتوپنی پورپورا بوده است. در اين مطالعه گذشتهنگر تعداد 62 شيرخوار مبتلا به ITP از سال 1377 لغايت 1381 به مدت 5 سال،
ارجمندی رفسنجانی, خدیجه +3 more
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