J. Perez Botero

发表

Specifications of the variant curation guidelines for ITGA2B/ITGB3: ClinGen Platelet Disorder Variant Curation Panel.

Kristy Lee, Minjie Luo, P. Bray, 2021, Blood advances.

Apixaban and dalteparin in active malignancy‐associated venous thromboembolism: The ADAM VTE trial

C. Loprinzi, T. Zemla, A. Ashrani, 2020, Journal of thrombosis and haemostasis : JTH.

Diagnostic Testing Approaches for Activated Protein C Resistance and Factor V Leiden: A Comparison of Institutional and National Provider Practices

Dong Chen, R. Pruthi, J. Perez Botero, 2017, American journal of clinical pathology.

Severe thrombocytopenia and microangiopathic hemolytic anemia in pregnancy: A guide for the consulting hematologist

J. George, J. Perez Botero, J. Reese, 2021, American journal of hematology.

von Willebrand disease type1/type 2N compound heterozygotes: diagnostic and management challenges

M. Patnaik, A. Ashrani, R. Pruthi, 2017, British journal of haematology.

Incidence of symptomatic venous thromboembolism in patients with hemophilia undergoing joint replacement surgery: a retrospective study.

A. Ashrani, R. Trousdale, R. Pruthi, 2015, Thrombosis research.

GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis

W. Ouwehand, K. Downes, D. Trégouët, 2021, Journal of thrombosis and haemostasis : JTH.

The Society for Obstetric Anesthesia and Perinatology Interdisciplinary Consensus Statement on Neuraxial Procedures in Obstetric Patients With Thrombocytopenia

Mark P. MacEachern, Christopher L. Wu, S. Segal, 2021, Anesthesia and analgesia.

Recognition of the unique bleeding pattern and laboratory findings in acquired haemophilia A facilitates prompt treatment of a life-threatening disorder

J. Perez Botero, H. Cameron, 2021, BMJ Case Reports.

Coagulation abnormalities and haemostatic surgical outcomes in 142 patients with Noonan syndrome

M. Patnaik, V. Rodriguez, R. Pruthi, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Comprehensive Platelet Phenotypic Laboratory Testing and Bleeding History Scoring for Diagnosis of Suspected Hereditary Platelet Disorders: A Single-Institution Experience

Dong Chen, S. Tian, D. Warad, 2017, American journal of clinical pathology.

Phenotypic heterogeneity associated with germline GATA2 haploinsufficiency: a comprehensive kindred study

M. Patnaik, V. Rodriguez, C. Haddox, 2019, Leukemia & lymphoma.

Gray Platelet Syndrome Presenting With Pancytopenia, Splenomegaly, and Bone Marrow Fibrosis.

E. Medina, H. Tariq, J. Perez Botero, 2021, American journal of clinical pathology.

Successful treatment with thalidomide of a patient with congenital factor V deficiency and factor V inhibitor with recurrent gastrointestinal bleeding from small bowel arteriovenous malformations

R. Pruthi, C. Thompson, J. Perez Botero, 2013, Haemophilia : the official journal of the World Federation of Hemophilia.

ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26

A. Tefferi, M. Patnaik, R. Pruthi, 2015, Blood Cancer Journal.

Practice patterns in the diagnosis of inherited platelet disorders within a single institution

M. Patnaik, Dong Chen, R. Pruthi, 2017, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Factor IX Gene (F9) Genotyping Trends and Spectrum of Mutations Identified: A Reference Laboratory Experience

Dong Chen, R. Pruthi, J. Perez Botero, 2017, Seminars in Thrombosis and Hemostasis.

Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia

M. Patnaik, Dong Chen, E. Klee, 2017, Leukemia & lymphoma.

Congenital Disorders of Platelet Function and Number.

Ruchika Sharma, S. Jobe, J. Perez Botero, 2018, Pediatric clinics of North America.

Grey platelet syndrome misdiagnosed as ITP

Dong Chen, J. Perez Botero, M. Patnaik, 2016, British journal of haematology.

Peripartum management of deep venous thrombosis in the context of antithrombin deficiency and May-Thurner syndrome.

Claire Stevens-haas, J. Perez Botero, J. Mcintosh, 2022, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Diagnostic approach to the patient with a suspected inherited platelet disorder: Who and how to test

J. Di Paola, J. Perez Botero, 2021, Journal of thrombosis and haemostasis : JTH.

Clinical and laboratory characteristics in congenital ANKRD26 mutation-associated thrombocytopenia: A detailed phenotypic study of a family

A. Tefferi, M. Patnaik, Dong Chen, 2016, Platelets.

Clinical spectrum and clonal evolution in germline syndromes with predisposition to myeloid neoplasms

A. Tefferi, M. Patnaik, Dong Chen, 2018, British journal of haematology.

Do incident and recurrent venous thromboembolism risks truly differ between heterozygous and homozygous Factor V Leiden carriers? A retrospective cohort study.

J. Heit, M. Patnaik, A. Ashrani, 2016, European journal of internal medicine.