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Journal Articles

The Mystery of "Magic Blood" - Familial Macrothrombocytopenia Associated with a Novel Variant in GP1BA Gene

Zhaohui Liao Arter, MD, Caitlin Yatogo, MS, CGC, Michael C. Chicka, PhD, Jeffrey L. Berenberg, MD

Blood (2019) 134 (Supplement_1): 2380.

https://doi.org/10.1182/blood-2019-122384

Published: 2019

Journal Articles

Bleeding Severity and Health Care Utilization in Patients with Platelet Function Disorders

Divyaswathi Citla Sridhar, MD, Sneha Butala, MD, Anjali Shekar, Robert F. Sidonio, Jr., MD, Sanjay Ahuja

Blood (2018) 132 (Supplement 1): 4994.

https://doi.org/10.1182/blood-2018-99-119403

Published: 2018

Journal Articles

TPO-logy accepted

Karin M. Hoffmeister

Blood (2018) 132 (6): 555–557.

https://doi.org/10.1182/blood-2018-06-854935

Published: 2018

Journal Articles

Validation of the Modified Self-Administered Pediatric Bleeding Assessment Questionnaire (Self-PBQ) in Children Aged 8-12 Years

Jessica Bui, BHSc, David Martyres, Paula D. James, MD, Julie Grabell, CCRP, John K. Wu, MBBS, FRCPC, MS, MacGregor Steele, MD FRCP(C), Mariana Silva, MD FRCPC, Margaret L. Rand, PhD, Victor S. Blanchette, MD, Robert J Klaassen, MD FRCPC

Blood (2017) 130 (Supplement 1): 2135.

https://doi.org/10.1182/blood.V130.Suppl_1.2135.2135

Published: 2017

Journal Articles

Comparison of Different Phenotypes of Bernard-Soulier Syndrome

Maria A. Kumskova, MD, Nadezhda Zozulya, MD PhD, Valentina N. Dvyrnik, MD PhD, Elena Likhachyova, MD PhD, Elena Yakovleva, MD PhD, Valeriy G. Savchenko

Blood (2017) 130 (Supplement 1): 4856.

https://doi.org/10.1182/blood.V130.Suppl_1.4856.4856

Published: 2017

Journal Articles

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

Suthesh Sivapalaratnam, MD PhD, Willem Ouwehand, MD PhD, Bridge Consortium, ThromboGenomics Consortium

Blood (2016) 128 (22): 1359.

https://doi.org/10.1182/blood.V128.22.1359.1359

Published: 2016

Journal Articles

Utility of Whole Exome Sequencing in Diagnosis of Pediatric Platelet Disorders: A Subanalysis of the Pediseq Study

Edward J Romasko, PhD, Sawona Biswas, MSc MS CGC, Batsal Devkota, PhD, Jayaraman Vijayakumar, Sowmyra Jairam, PhD, Christopher S Thom, MD PhD, Matthew C Dulik, PhD, Laura K Conlin, PhD, Nancy B. Spinner, PhD, Ian D Krantz, MD, Michele P. Lambert, MD MTR

Blood (2016) 128 (22): 3726.

https://doi.org/10.1182/blood.V128.22.3726.3726

Published: 2016

Journal Articles

Value of Platelet Esoteric Testing in Laboratory Diagnosis of Platelet Disorders: A Single Center Experience

Juliana Perez Botero, MD, Deepti M. Warad, M.B.B.S., Rong He, MD, Rajiv K. Pruthi, MBBS, Dong Chen, MD PhD

Blood (2015) 126 (23): 1061.

https://doi.org/10.1182/blood.V126.23.1061.1061

Published: 2015

Journal Articles

Platelet GPIba Is Important for Thrombopoietin Production and Thrombopoietin-Induced Platelet Generation

Miao Xu, MSc, MD, Li Ma, PhD, Naadiya Carrim, PhD, Issaka Yougbare, PhD, June Li, MSc, Pingguo Chen, MD PhD, Guangheng Zhu, MD, Heyu Ni, MD PhD

Blood (2015) 126 (23): 12.

https://doi.org/10.1182/blood.V126.23.12.12

Published: 2015

Journal Articles

Platelet Transmission Electron Microscopy and Flow Cytometry in the Diagnosis of Congenital/Hereditary Qualitative or Quantitative Platelet Disorders

Juliana Perez Botero, MD, Laynalee K Cardel, MT, Aneel A. Ashrani, MBBS, MSc, John A. Heit, MD, Rong He, MD, C Christopher Hook, MD, Robert D McBane, II, MD, Animesh Pardanani, MBBS, PhD, Deepti M. Warad, M.B.B.S., Waldemar E Wysokinski, MD PhD, Vilmarie Rodriguez, MD, William L. Nichols, Jr., MD, Rajiv K. Pruthi, MBBS, Dong Chen, MD PhD, Mrinal M Patnaik, MBBS

Blood (2015) 126 (23): 3476.

https://doi.org/10.1182/blood.V126.23.3476.3476

Published: 2015

Journal Articles

Autosomal Recessive Inherited Bleeding Disorders in Pakistan, a Cross Sectional Study from Selected Regions

Arshi Naz, MSc.PhD, Mohammad younus Jamal, M.B;B.S, PhD, Samina Tufail Amanat, FCPS, MB, BS, Humayun Patel, MSc., Akbar Agha, M.B;B.S, fazal-E- Razik, Nisar Ahmed, FCPS haematology, Ayisha Imran, M.B;B.S, FCPS haematology, Tahir Shamsi, MBBS, MRCPath,FRCPath

Blood (2015) 126 (23): 4708.

https://doi.org/10.1182/blood.V126.23.4708.4708

Published: 2015

Journal Articles

Inherited Giant Platelet Disorder, Kashmiri Thrombocytopenia, a Common Syndrome Found in Srinagar, India

Felipe R Lorenzo, PhD, Tsewang Tashi, MD, Parvaiz Koul, MD, Nicola J Camp, PhD, Perumal Thiagarajan, MD, Josef T. Prchal, MD

Blood (2014) 124 (21): 4211.

https://doi.org/10.1182/blood.V124.21.4211.4211

Published: 2014

Journal Articles

Thrombin-Dependent Incorporation of Von Willebrand Factor into a Fibrin Network

Adam Miszta, PhD, Leonie Pelkmans, Theo Lindhout, PhD, Philip De Groot, Coenraad Hemker, PhD, Johan Heemskerk, PhD, Hilde Kelchtermans, PhD, Bas De Laat, PhD

Blood (2014) 124 (21): 101.

https://doi.org/10.1182/blood.V124.21.101.101

Published: 2014

Journal Articles

Childhood myelodysplastic syndrome associated with an acquired Bernard-Soulier–like platelet dysfunction

Marco Frigeni, Monica Galli

Blood (2014) 124 (16): 2609.

https://doi.org/10.1182/blood-2014-08-587832

Published: 2014

Journal Articles

Mutation Analysis and Clinical Sprectrum Of Patients With Glanzmann’s Thrombasthenia and Bernard Soulier Syndrome

Huseyin Tokgoz, Umran Caliskan, MD, Akar Nejat, Erdem Ak

Blood (2013) 122 (21): 4751.

https://doi.org/10.1182/blood.V122.21.4751.4751

Published: 2013

Journal Articles

Normal Range Of Bleeding Scores For The ISTH-BAT: Adult and Pediatric Data From The Merging Project

Malak Elbatarny, Shamim Mollah, Julie Grabell, Margaret L. Rand, PhD, Dewi S. Clark, BSc, Andreas Mauer, Pamela A. Christopherson, Robert R. Montgomery, MD, Zimmerman Program Investigators, Barry S. Coller, MD, Paula D. James, MD

Blood (2013) 122 (21): 1107.

https://doi.org/10.1182/blood.V122.21.1107.1107

Published: 2013

Journal Articles

A Novel Molecular Mechanism In The Interplay Of Platelet GPIb-VWF-Fibrin In Thrombus Formation

Miguel A. Cruz, PhD, Perumal Thiagarajan, MD, Swapan Kumar Dasgupta, Sameer Thacker

Blood (2013) 122 (21): 1065.

https://doi.org/10.1182/blood.V122.21.1065.1065

Published: 2013

Journal Articles

Bleeding Phenotype of Murine Bernard Soulier Syndrome Is Potentially Corrected by Non-Myeloablative Hematopoietic Stem Cell Transplantation

Sachiko Kanaji, MD, PhD, Scot A. Fahs, Jerry Ware, PhD, Robert R. Montgomery, MD, Qizhen Shi, MD, PhD

Blood (2012) 120 (21): 3340.

https://doi.org/10.1182/blood.V120.21.3340.3340

Published: 2012

Journal Articles

Platelet Glycoprotein VI: An Adenine Insertion in Exon 6 Generates a Truncated Form of the Protein Associated with Bleeding Disorder in 4 Chilean Unrelated Patients

Valeria Matus, PhD, José Guillermo Valenzuela, Claudia G Sáez, PhD, Patricia Hidalgo, Olga Panes, Jaime Pereira, M.D., Diego Mezzano, M.D.

Blood (2012) 120 (21): 3302.

https://doi.org/10.1182/blood.V120.21.3302.3302

Published: 2012

Journal Articles

Genetic Diagnosis of Inherited Bleeding Disorders in 1250 Probands From India: A Single Centre Experience

Giridhara R Jayandharan, Ph.D, Govindanattar Sankari Devi, S RajKumar, Everette Nelson, Ramachandran V Shaji, Neeraj Arora, P Shenbagaapriya, Sukesh C Nair, MD, Auro Viswabandya, MD, Biju George, MD, Vikram Mathews, Alok Srivastava, MD

Blood (2012) 120 (21): 1127.

https://doi.org/10.1182/blood.V120.21.1127.1127

Published: 2012

NARROW

The Mystery of "Magic Blood" - Familial Macrothrombocytopenia Associated with a Novel Variant in GP1BA Gene

Bleeding Severity and Health Care Utilization in Patients with Platelet Function Disorders

TPO-logy accepted

Validation of the Modified Self-Administered Pediatric Bleeding Assessment Questionnaire (Self-PBQ) in Children Aged 8-12 Years

Comparison of Different Phenotypes of Bernard-Soulier Syndrome

Rare Variants in GP1BB underlie Autosomal Dominant Macrothrombocytopenia; Findings of Large Unique Bleeding and Platelet Disorders Cohort

Utility of Whole Exome Sequencing in Diagnosis of Pediatric Platelet Disorders: A Subanalysis of the Pediseq Study

Value of Platelet Esoteric Testing in Laboratory Diagnosis of Platelet Disorders: A Single Center Experience

Platelet GPIba Is Important for Thrombopoietin Production and Thrombopoietin-Induced Platelet Generation

Platelet Transmission Electron Microscopy and Flow Cytometry in the Diagnosis of Congenital/Hereditary Qualitative or Quantitative Platelet Disorders

Autosomal Recessive Inherited Bleeding Disorders in Pakistan, a Cross Sectional Study from Selected Regions

Inherited Giant Platelet Disorder, Kashmiri Thrombocytopenia, a Common Syndrome Found in Srinagar, India

Thrombin-Dependent Incorporation of Von Willebrand Factor into a Fibrin Network

Childhood myelodysplastic syndrome associated with an acquired Bernard-Soulier–like platelet dysfunction

Mutation Analysis and Clinical Sprectrum Of Patients With Glanzmann’s Thrombasthenia and Bernard Soulier Syndrome

Normal Range Of Bleeding Scores For The ISTH-BAT: Adult and Pediatric Data From The Merging Project

A Novel Molecular Mechanism In The Interplay Of Platelet GPIb-VWF-Fibrin In Thrombus Formation

Bleeding Phenotype of Murine Bernard Soulier Syndrome Is Potentially Corrected by Non-Myeloablative Hematopoietic Stem Cell Transplantation

Platelet Glycoprotein VI: An Adenine Insertion in Exon 6 Generates a Truncated Form of the Protein Associated with Bleeding Disorder in 4 Chilean Unrelated Patients

Genetic Diagnosis of Inherited Bleeding Disorders in 1250 Probands From India: A Single Centre Experience

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American Society of Hematology

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ASH Publications

American Society of Hematology

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