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Publications by Gessica Fontana
Haploinsufficiency of the Platelet P2Y12 Gene in a Family With Congenital Bleeding Diathesis.
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Related publications
Haploinsufficiency of the Platelet P2Y12 Gene in a Family With Congenital Bleeding Diathesis
Haematologica
Hematology
P2Y12 Receptor Gene Mutations Associated With Bleeding
Platelets
Medicine
Hematology
Bleeding Diathesis Due to Thromboxane Synthesis Deficiency
A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly
Frontiers in Genetics
Genetics
Molecular Medicine
Waldenstrom Macroglobulinaemia Presenting as Bleeding Diathesis With Paradoxical Coagulation of Blood Samples.
Emergency Medicine Journal
Medicine
Critical Care
Emergency Medicine
Intensive Care Medicine
Combination of Cyclic Nucleotide Modulators With P2Y12 Receptor Antagonists as Anti-Platelet Therapy
Journal of Thrombosis and Haemostasis
Medicine
Hematology
Contribution of the P2Y12 Receptor-Mediated Pathway to Platelet Hyperreactivity in Hypercholesterolemia
Journal of Thrombosis and Haemostasis
Medicine
Hematology
Fatal Neonatal Respiratory Failure in an Infant With Congenital Hypothyroidism Due to Haploinsufficiency of the NKX2-1 Gene: Alteration of Pulmonary Surfactant Homeostasis
Archives of Disease in Childhood: Fetal and Neonatal Edition
Pediatrics
Gynecology
Perinatology
Obstetrics
Medicine
Child Health
A Novel MIP Gene Mutation Analysis in a Chinese Family Affected With Congenital Progressive Punctate Cataract
PLoS ONE
Multidisciplinary
