How I treat patients with a history of heparin-induced thrombocytopenia
Blood. 2016;128(3):348-359
מאמרים נבחרים המטולוגיה
How I treat patients with inherited bleeding disorders who need anticoagulant therapy
16:53
סגור לתגובות על How I treat patients with inherited bleeding disorders who need anticoagulant therapy
Situations that ordinarily necessitate consideration of anticoagulation, such as arterial and venous thrombotic events and prevention of stroke in atrial fibrillation, become
How I treat MDS and AML in Fanconi anemia
17:13
סגור לתגובות על How I treat MDS and AML in Fanconi anemia
Fanconi anemia (FA) is the most frequent genetic cause of bone marrow failure (BMF).1 More than 18 FA
How I treat hypereosinophilic syndromes
12:18
סגור לתגובות על How I treat hypereosinophilic syndromes
BLOOD, 27 AUGUST 2015 x VOLUME 126, NUMBER 9
Paroxysmal Nocturnal Hemoglobinuria: A Complement-Mediated Hemolytic Anemia
10:34
סגור לתגובות על Paroxysmal Nocturnal Hemoglobinuria: A Complement-Mediated Hemolytic Anemia
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, clonal, hematopoietic stem cell disorder that manifests with a hemolytic anemia
טיפול בטסיות דם בילודים
11:59
סגור לתגובות על טיפול בטסיות דם בילודים
המלצות אלו גובשו באיגוד הנאונטולוגי במשותף עם האיגוד להמטולוגיה/אונקולוגיה ילדים.
How I treat refractory thrombotic thrombocytopenic purpura
17:21
סגור לתגובות על How I treat refractory thrombotic thrombocytopenic purpura
Acquired thrombotic thrombocytopenic purpura (TTP) is characterized by thrombocytopenia and microangiopathic hemolytic anemia (MAHA) without an obvious
cause, and may
How I treat and manage strokes in sickle cell disease
12:31
סגור לתגובות על How I treat and manage strokes in sickle cell disease
Neurologic complications are a major cause of morbidity and mortality in sickle
cell disease (SCD). In children with sickle cell
Guideline on the management of acute chest syndrome in sickle cell disease
12:53
סגור לתגובות על Guideline on the management of acute chest syndrome in sickle cell disease
Sickle cell disease (SCD) affects 12 000–15 000 individuals in the UK. Whilst homozygous SCD (sickle cell anaemia — HbSS)
How I treat incidental pulmonary embolism
17:00
סגור לתגובות על How I treat incidental pulmonary embolism
The identification of pulmonary embolism (PE) on computed tomography scans performed for indications other than identification of thromboembolism is a
