How I treat hemophagocytic lymphohistiocytosis
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation, occurring as either a familial disorder or a
BLOOD, 13 OCTOBER 2011 , VOLUME 118, NUMBER 15
The purpose of this article is to set forth our approach to diagnosing and managing the
thalassemias, including b-thalassemia intermedia and
BLOOD, 11 AUGUST 2011 , VOLUME 118, NUMBER 6
Since 2004, a national observational study has been aiming to thoroughly describe cases and identify prognostic factors. Patients
The appropriate classification of hypoplastic BM disorders in young patients continues to be a great challenge. Accurate diagnosis
The guideline writing group was selected to be representative of UK-based medical experts.
doi:10.1111/j.1365-2141.2011.08793.x British Journal of Haematology, 155,
Acute chest syndrome describes new respiratory symptoms and findings, often severe and progressive, in a child with sickle cell disease and
Evidence-based guidelines are presented for the management of haemophilia in the fetus and neonate. This includes information regarding the
The guideline was drawn up to inform practitioners in the UK who are involved in counselling patients regarding
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הכניסה לאתר מותרת אך ורק לרופאים/ות בעלי רישיון לעסוק ברפואה בישראל
ו/או בעלי רישיון לעסוק ברוקחות ו/או אדם הנמנה על צוות רפואי או מחקר ביו-רפואי.