Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Elvezia Maria Paraboschi
Exploring the Global Landscape of Genetic Variation in Coagulation Factor XI Deficiency
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Mycobacterium Tuberculosis Drives Expansion of Low-Density Neutrophils Equipped With Regulatory Activities
Frontiers in Immunology
Allergy
Immunology
Related publications
Genetic Variation in the Coagulation Factor v Gene and Risk of Femoral Head Osteonecrosis
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Genetic Variants of Coagulation Factor XI Show Association With Ischemic Stroke Up to 70 Years of Age
PLoS ONE
Multidisciplinary
Laboratory Investigation of a Rare Coagulation Factor Deficiency
Pathology
Forensic Medicine
Pathology
Characterization of Seven Novel Mutations Causing Factor XI Deficiency
Haematologica
Hematology
Spontaneous Regression of the Inhibitor Against the Coagulation Factor XIII a Subunit in Acquired Factor XIII Deficiency
Thrombosis and Haemostasis
Hematology
Three Factor11 Mutations Associated With Factor XI Deficiency in a Turkish Family
Turkish Journal of Haematology
Hematology
Exploring the Genetic Basis for Clinical Variation in Neurofibromatosis Type 1
Expert Review of Neurotherapeutics
Neuroscience
Neurology
Pharmacology
Factor XI Deficiency Enhances the Pulmonary Allergic Response to House Dust Mite in Mice Independent of Factor XII
American Journal of Physiology - Lung Cellular and Molecular Physiology
Pulmonary
Respiratory Medicine
Physiology
Cell Biology
Spontaneous Thrombosis in a Patient With Factor XI Deficiency Homozygous for the p.Cys398Tyr Mutation
Cumhuriyet Medical Journal
Medicine