Results 11 to 20 of about 2,566 (179)
Insights into the clinical, platelet and genetic landscape of inherited thrombocytopenia with malignancy risk [PDF]
Inherited thrombocytopenia (IT) caused by germline variants in RUNX1, ETV6 or ANKRD26 carries a high risk of developing haematological malignancy. This study examined the clinical, platelet and molecular characteristics of 66 patients with these conditions, who carried 24 distinct genetic variants in the corresponding genes.
Ana Marín‐Quílez +34 more
wiley +2 more sources
Risk Profile of Patients with Spontaneous Cervical Artery Dissection
Objective Epidemiological data to characterize the individual risk profile of patients with spontaneous cervical artery dissection (sCeAD) are rather inconsistent. Methods and Results In the setting of the Italian Project on Stroke in Young Adults Cervical Artery Dissection (IPSYS CeAD), we compared the characteristics of 1,468 patients with sCeAD ...
Elisabetta Del Zotto +45 more
wiley +1 more source
Trombosis is seen in children with acute lymphoblastic leukemia during or after L-asparaginase treatment. Posterior reversible encephalopathy syndrome (PRES) is a complex syndrome characterized with sudden hypertension, headache, nausea, vomiting, alteration in the state of consciousness, vision defect and seizures.
Kartal, Vural +5 more
openaire +2 more sources
Dilemmas on emicizumab in children with haemophilia A: A survey of strategies from PedNet centres
Abstract Introduction Haemophilia A care has changed with the introduction of emicizumab. Experience on the youngest children is still scarce and clinical practice varies between haemophilia treatment centres. Aim We aimed to assess the current clinical practice on emicizumab prophylaxis within PedNet, a collaborative research platform for ...
Susanna Ranta +17 more
wiley +1 more source
Deep sequencing of circulating miRNAs and target mRNAs level in deep venous thrombosis patients
Eight differentially expressed miRNAs including hsa‐miR‐150‐5p, hsa‐miR‐326, hsa‐miR‐144‐3p, hsa‐miR‐199a‐5p, hsa‐miR‐199b‐5p, hsa‐miR‐125a‐5p, hsa‐let‐7e‐5p and hsa‐miR‐381‐3p and their target mRNAs (PRKCA, SP1, TP53, SLC27A4, PDE1B, EPHB3, IRS1, HIF1A, MTUS1 and ZNF652) were found associated with deep venous thrombosis for the first time ...
Qingxian Wang +3 more
wiley +1 more source
Se presenta el caso de un hombre de 63 años con antecedentes de cardiopatía isquémica intervenida, portador de prótesis mecánica mitral, que acude a urgencias por focalidad neurológica. En la ecocardiografía se observa una masa sobre válvula mitral protésica que sugiere la presencia de un trombo protésico.
José Eduardo Ramírez Batista +4 more
openaire +1 more source
Trombosis Sinus Kavernosus Akibat Komplikasi Furunkulosis Hidung
Trombosis sinus kavernosus merupakan kasus yang jarang, tetapi dapat mengancam kehidupan. Penyebab trombosis dapat berasal dari infeksi daerah sinonasal, midface atau orbita. Gejala klinis meliputi gejala yang melibatkan mata dan beberapa nervus kranial.
Bestari Jaka Budiman +3 more
doaj +1 more source
Well’S syndrome and trombosis [PDF]
The well rsquo s syndrome or recurrent granulomatous dermatitis is reported the first time by Dr George Wells in United Kingdom of the department of dermatology at St Thomas Hospital in the report was about four patients who had turret skin with plaques red violet slightlypruritic edematous recurrent character and disappear in weeks months without ...
openaire +1 more source
Defisiensi Protein S pada Trombosis Vena Dalam
Trombosis vena dalam (TVD) merupakan penyebab kematian yang utama di Amerika Serikat dan negara barat. Sekitar 2 juta orang meninggal akibat trombosis vena maupun komplikasinya.
Rinni Andriani, Irza Wahid
doaj +1 more source
PB2652: EVALUATION OF 6 CASES WITH FXIII DEFICIENCY: SINGLE CENTRE EXPERIENCE
HemaSphere, Volume 7, Issue S3, August 2023.
Fahri Sahin +3 more
wiley +1 more source

