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American Journal of Hematology, ISSN 0361-8609, 11/2017, Volume 92, Issue 11, pp. E639 - E641
Journal Article
Blood Coagulation and Fibrinolysis, ISSN 0957-5235, 2018, Volume 29, Issue 5, pp. 423 - 428
Journal Article
Cardiovascular and Hematological Disorders - Drug Targets, ISSN 1871-529X, 04/2016, Volume 16, Issue 1, pp. 6 - 12
Journal Article
Medicina (Kaunas, Lithuania), ISSN 1010-660X, 08/2019, Volume 55, Issue 9, p. 528
Mastocytosis is a rare disease in which heightened amounts of mast cells accumulate in the skin, bone marrow, and other visceral organs. Upon activation, mast... 
zolendronic acid | thrombocythemia | hydroxyurea | osteoporosis | mastocytosis
Journal Article
Blood Coagulation & Fibrinolysis, ISSN 0957-5235, 05/2018, Volume 29, Issue 5, pp. 423 - 428
To compare the prevalence of cardiovascular diseases with other chance-associated morbidities in patients with congenital prekallikrein deficiency. Patients... 
bleeding | FLETCHER FACTOR DEFICIENCY | PARTIAL THROMBOPLASTIN TIME | CONTACT ACTIVATION | ASYMPTOMATIC PATIENT | FACTOR-XII | FAMILY | thrombosis | comorbidities | deficiency | PK DEFICIENCY | MUTATION | GRAVES-DISEASE | COAGULATION | prekallikrein | HEMATOLOGY | Prothrombin | Care and treatment | Research | Cardiovascular diseases | Health aspects | Blood plasma
Journal Article
Blood Cells, Molecules and Diseases, ISSN 1079-9796, 07/2019, Volume 77, pp. 8 - 11
To investigate the incidence of thrombotic events in patients heterozygous for FXII deficiency during a long observation period. 103 heterozygotes for FXII... 
Heterozygotes | Mutation | Factor XII | Thrombosis | CONTACT | MYOCARDIAL-INFARCTION | DEEP-VEIN THROMBOSIS | PREVALENCE | FACTOR-XII-DEFICIENCY | COAGULATION | PATIENT | HEMATOLOGY | ANTIGEN | Stroke (Disease) | Blood clot
Journal Article
Cardiovascular and Hematological Disorders, ISSN 1871-529X, 04/2016, Volume 16, Issue 1, pp. 6 - 12
Objective: To investigate the occurrence of ischemic stroke in patients with congenital bleeding disorders. Patients and Methods: Patients with congenital... 
Journal Article
Clinical and Applied Thrombosis/Hemostasis, ISSN 1076-0296, 05/2015, Volume 21, Issue 4, pp. 359 - 364
Objective:To investigate the occurrence of myocardial infarction or other acute coronary syndromes in rare congenital bleeding disorders.Patients:All patients... 
Journal Article
Hematology, ISSN 1024-5332, 07/2018, Volume 23, Issue 6, pp. 346 - 350
Objective: To investigate the structure-function relation in prekallikrein (PK) deficiency. PK is one of the proteins of the contact phase of blood coagulation... 
molecular studies | bleeding | deficiency | Prekallikrein | hypertension | THROMBOSIS | FLETCHER FACTOR DEFICIENCY | TRAIT | ARGENTINA | FAMILY | PK DEFICIENCY | MUTATION | ASN124SER | HEMATOLOGY
Journal Article
ITALIAN JOURNAL OF PEDIATRICS, ISSN 1720-8424, 08/2019, Volume 45, Issue 1, pp. 95 - 7
Background Sudden unexpected postnatal collapse of presumably healthy neonates during early skin-to-skin contact is a rare, yet recognized occurrence,... 
SUPC | HEALTHY NEWBORN-INFANTS | RISK | PEDIATRICS | LIFE-THREATENING EVENTS | DEATHS | Breast feeding | UNEXPECTED POSTNATAL COLLAPSE | Delivery room practices | Skin to skin | Neonatal collapse
Journal Article
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