Results 51 to 60 of about 10,614 (201)
Síndrome de Evans: reporte de un caso [PDF]
El Síndrome de Evans es un trastorno inmunológico atípico y poco frecuente causado por anticuerpos contra antígeno de membrana, de hematíes y plaquetas cursando con manifestaciones hemorrágicas en piel y mucosas generalmente de evolución no siempre ...
Alarcón Martínez, Yanet +3 more
core +1 more source
ABSTRACT Background Neonatal alloimmune thrombocytopaenia (NAIT) is a rare but potentially serious condition where maternal antibodies result in destruction of foetal and neonatal platelets. At Middlemore Hospital in south Auckland, routine cord blood platelet counts were performed over many years.
Galama Vela +2 more
wiley +1 more source
IDIOPATHIC THROMBOCYTOPENIC PURPURA (i.T.P.) [PDF]
The course of t he disorder is acute and chronic.The acute form o f the disease occurs most c ommonly in children , but is seen i n adults as well . The chronic recurrent f orm occurs most o f t e n in women between t wenty and forty years of age.
Sh. MOHAMEDI M ZAMANIANPOUR ML GHASEMI
doaj +1 more source
Abstract Background Studies suggest an increase in autoimmune diseases following SARS‐CoV‐2 infection and/or COVID‐19‐vaccination. We aimed to describe possible associations in Norway. Methods We used information from the emergency preparedness register for COVID‐19, BeredtC19, for all residents aged 18–64 (N = 3,450,080).
Håkon Bøås +4 more
wiley +1 more source
European Code Against Cancer, 5th edition – cancer‐causing infections and related interventions
The 5th edition of the European Code Against Cancer (ECAC5) contains 14 recommendations on cancer prevention. Here, we update the cancer prevention recommendations related to cancer‐causing infections, namely H. pylori, HPV, HBV, HCV and HIV, positioned as recommendation number 12.
Catharina Johanna Alberts +18 more
wiley +1 more source
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 +5 more
doaj +1 more source
Púrpura Trombocitopénica Idiopática y sangramiento gingival. Presentación de un caso. [PDF]
Se realiza la presentación de un caso de una paciente con antecedentes de púrpura trombocitopénica idiopática por defecto en el factor F3p de la coagulación, que acudió a la consulta de Periodoncia porque presentaba sangramiento de las encías.
Grisel Isabel Echenagusía López +2 more
core +1 more source
Timeline of events ABSTRACT Moderate‐to‐severe ulcerative colitis can be effectively treated with JAK‐1 inhibition, but platelet counts should be closely monitored, especially in active disease. We confirmed immune‐mediated thrombocytopenia (ITP) in one of our patients after the initiation of filgotinib. Whether this was drug‐induced is uncertain.
M. J. van der Hoff +2 more
wiley +1 more source
Hemostatic changes by thrombopoietin-receptor agonists in immune thrombocytopenia patients [PDF]
Thrombopoietin receptor agonist (TPO-RA) treatment increases the thrombosis rate in immune thrombocytopenia (ITP). We hypothesize that TPO-RAs influence platelet function, global and secondary hemostasis and/or fibrinolysis.
Brandwijk, Odila N +5 more
core

