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Journal Articles

Time Is Quality of Life (QoL): An Institutional Review of Emergency Department Management of Acute Vaso-Occlusive Episodes in Patients with Sickle Cell Disease

Jaime Baldeon Mendoza, Consuela Albright, Kristin Seastrand, Katrina Seedhouse, Rosa Young, Milvon Bryson, Ravi Talati, Rabi Hanna, Crawford John Strunk

Blood (2024) 144 (Supplement 1): 7530.

https://doi.org/10.1182/blood-2024-207564

Published: 2024

Journal Articles

An Analysis of Racial and Ethnic Backgrounds within the Casire International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research

Blood (2019) 134 (Supplement_1): 2305.

https://doi.org/10.1182/blood-2019-127613

Published: 2019

Journal Articles

History of Asthma is Associated with Albuminuria within an International Pediatric Cohort of Sickle Cell Disease Patients: A Casire Group Analysis

Immacolata Tartaglione, MD, Baba PD Inusa, MBBS, FMCPaed, FRCPCH, MRCP, DCP, Raffaella Colombatti, MD PhD, Deepa Manwani, MD, Silverio Perrotta, Eugenia Vicky Naa Kwarley Asare, MBChB, BSc, Connie M. Piccone, MD, Fredericka Sey, MB ChB, Charles Antwi-Boasiako, PhD, Laura Sainati, MD, Adetola A. Kassim, MD MS, Donna Boruchov, MD, Angela Rivers, MD PhD, William Zempsky, MD, Crawford John Strunk, MD, Biree Andemariam, MD, Andrew D. Campbell, MD

Blood (2016) 128 (22): 3668.

https://doi.org/10.1182/blood.V128.22.3668.3668

Published: 2016

Journal Articles

Hydroxyurea Shows Clinical Benefit without Alteration of Fetal Hemoglobin, MCV, or Hemoglobin in Unselected Adult and Pediatric Patients with Sickle Cell Anemia

Crawford John Strunk, MD, Biree Andemariam, MD, Fredericka Sey, MB ChB, Fatimah Farooq, BS, Rebekah Urbonya, BS, Charles Antwi-Boasiako, PhD, Adetola A. Kassim, MD MS, Onike Rodrigues, MD, Connie M. Piccone, MD, Angela Rivers, MD PhD, Deepa Manwani, MD, Imma Tartaglione, MD, Laura Sainati, MD, Raffaella Colombatti, MDPhD, Andrew D. Campbell, MD

Blood (2015) 126 (23): 2187.

https://doi.org/10.1182/blood.V126.23.2187.2187

Published: 2015

Journal Articles

Sickle Cell Disease Proteinuria Is Not Associated With Systolic Blood Pressure, CSSCD-Defined Hypertension, or Family History Of Hypertension In An International Cohort Of SCD Patients

Andrew Campbell, MD, Biree Andemariam, MD, Fredericka Sey, MD, Connie M. Piccone, MD, Baba PD Inusa, MD, FRCPCH, Silverio Perrotta, MD, Imma Tartaglione, MD, William Zempsky, MD, Crawford John Strunk, MD, Rebekah Urbonya, Laura Sainati, MD, Adetola A. Kassim, MD, Charles Antwi-Boasiako, M.S., Deepa Manwani, M.D, Raffaella Colombatti, MD PhD

Blood (2013) 122 (21): 981.

https://doi.org/10.1182/blood.V122.21.981.981

Published: 2013

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Time Is Quality of Life (QoL): An Institutional Review of Emergency Department Management of Acute Vaso-Occlusive Episodes in Patients with Sickle Cell Disease

An Analysis of Racial and Ethnic Backgrounds within the Casire International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research

History of Asthma is Associated with Albuminuria within an International Pediatric Cohort of Sickle Cell Disease Patients: A Casire Group Analysis

Hydroxyurea Shows Clinical Benefit without Alteration of Fetal Hemoglobin, MCV, or Hemoglobin in Unselected Adult and Pediatric Patients with Sickle Cell Anemia

Sickle Cell Disease Proteinuria Is Not Associated With Systolic Blood Pressure, CSSCD-Defined Hypertension, or Family History Of Hypertension In An International Cohort Of SCD Patients

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ASH Publications

American Society of Hematology

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Time Is Quality of Life (QoL): An Institutional Review of Emergency Department Management of Acute Vaso-Occlusive Episodes in Patients with Sickle Cell Disease

An Analysis of Racial and Ethnic Backgrounds within the Casire International Cohort of Sickle Cell Disease Patients: Implications for Disease Phenotype and Clinical Research

History of Asthma is Associated with Albuminuria within an International Pediatric Cohort of Sickle Cell Disease Patients: A Casire Group Analysis

Hydroxyurea Shows Clinical Benefit without Alteration of Fetal Hemoglobin, MCV, or Hemoglobin in Unselected Adult and Pediatric Patients with Sickle Cell Anemia

Sickle Cell Disease Proteinuria Is Not Associated With Systolic Blood Pressure, CSSCD-Defined Hypertension, or Family History Of Hypertension In An International Cohort Of SCD Patients

Email alerts

ASH Publications

American Society of Hematology

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