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Journal Articles

A Pilot Adult Sickle Cell Hematology Clinic in California's Inland Empire Improves Patient Outcome

Neha Chiruvolu, DO, Amie Patel, DO, Carolyn Rowley, PhD, Marsha J. Treadwell, PhD, Elliott P. Vichinsky, MD, Zahra Pakbaz, MD

Blood (2019) 134 (Supplement_1): 3470.

https://doi.org/10.1182/blood-2019-125160

Published: 2019

Journal Articles

Did the Outcome of Sicke Cell Disease Babies Screened at Birth Improved from 2000? a Single Center Experience

Clemence Peresse, MD, Laurence Dedeken, MD, Phu-Quoc Le, MD PhD, Laurence Rozen, Beatrice Gulbis, MD PhD, Sarah Wambacq, Alina Ferster, MD

Blood (2019) 134 (Supplement_1): 4847.

https://doi.org/10.1182/blood-2019-130294

Published: 2019

Journal Articles

Follow-up and Treatment Expectancy and Compliance of Y-Generation Hemophiliacs

Bulent Zulfikar, Prof, Basak Koc, MD, Yusuf Buyukpinarbasili, Fikret Bezgal, Caner Dadak, Funda Ciga, Irmak Gumustas, Haluk Zulfikar

Blood (2018) 132 (Supplement 1): 5029.

https://doi.org/10.1182/blood-2018-99-117901

Published: 2018

Journal Articles

Positive Impact of Social Media on Disease Awareness and Management in Patients with Inherited Bleeding Disorders: Saudi Experience from a Tertiary Care Hospital

Mahsen AlSaleh, MD, Tarek Owaidah, MD, Hazzaa Alzahrani, MD, Tahani Bin Ali, MD, Huda ElFaraidi, MD, Mahmoud Abu Riash, RN, Zikra Alkhayal, MD, AbdulKareem Al Momen, MD, Viqaruddin Mohammed, MSc, CCRP, Azzah AlZahrani, MD

Blood (2017) 130 (Supplement 1): 5587.

https://doi.org/10.1182/blood.V130.Suppl_1.5587.5587

Published: 2017

Journal Articles

The Impact of a Multidisciplinary Sickle Cell and Gynecology Clinic

Vardya A Tasha, MD

Blood (2016) 128 (22): 1319.

https://doi.org/10.1182/blood.V128.22.1319.1319

Published: 2016

Journal Articles

Telehematology: Expanding Comprehensive Care for Pediatric Patients with Blood Disorders through Telemedicine at Several Delivery Sites (Medical Homes, Hospital Clinics, Home Setting and Hemophilia Treatment Centers (HTC)) and with Interdisciplinary Providers

Roshni Kulkarni, Laura Carlson, RN, Rebecca A Malouin, Ph. D.,M.S, M.P.H, Marcia L Bird, LMSW, Colleen Vallad-Hix, Michelle Witkop, DNP, FNP-BC, Ajovi Scott-Emuakpor, MDPhD, Renuka Gera, MD, Steve Gualdoni, PA

Blood (2015) 126 (23): 5576.

https://doi.org/10.1182/blood.V126.23.5576.5576

Published: 2015

Journal Articles

Disparities Between Patient and Hematology/Oncology Physician Expectations for Integrative Oncology in an Ethnically Diverse Population

Hansra Damien, MD, Ramdial Jeremy, MD, Martinez Gianni, Farooq Faheem, MS3, Alfredo Torres, MD, Saravia Diana, MD, Ashwin Mehta, MD, Eugene Ahn, MD

Blood (2014) 124 (21): 2641.

https://doi.org/10.1182/blood.V124.21.2641.2641

Published: 2014

Journal Articles

Successful Outcomes Of An Infant Sickle Cell Clinic In Luanda, Angola

Patrick T. McGann, MD, Margarida Muhongo, Elizabeth McGann, Vysolela de Oliveira, Brigida Santos, MD, Russell E. Ware, MD, PhD

Blood (2013) 122 (21): 2934.

https://doi.org/10.1182/blood.V122.21.2934.2934

Published: 2013

Journal Articles

Treatment Patterns and Outcomes Of Sickle Cell Patients With Frequent ER Visits: A Single Center Experience

Veronique Naessens, MDCM, FRCPC, Richard Ward, MBBS, MSc, MRCP, FRCPath, Kevin H.M. Kuo, MD, FRCPC

Blood (2013) 122 (21): 1010.

https://doi.org/10.1182/blood.V122.21.1010.1010

Published: 2013

Journal Articles

A Comparison of Chronic Manual and Automated Red Blood Cell Exchange Transfusion in Sickle Cell Disease Patients From Two Comprehensive Care Centres in the United Kingdom

Kevin H.M. Kuo, MD, FRCPC, Richard Ward, MBBS, MRCP, FRCPath, Jo Howard, MB, BChir, MRCP, FRCPath, Paul Telfer, MA, DM, BM, BCh, FRCP, FRCPath

Blood (2012) 120 (21): 3430.

https://doi.org/10.1182/blood.V120.21.3430.3430

Published: 2012

Journal Articles

A Comparison of Automated Red Blood Cell Depletion/Exchange to Automated Red Cell Blood Exchange in Sickle Cell Patients.

Kevin H.M. Kuo, MD, FRCPC, David Barth, MD, FRCPC

Blood (2012) 120 (21): 2281.

https://doi.org/10.1182/blood.V120.21.2281.2281

Published: 2012

Journal Articles

The Effect of Comprehensive Care and Degree of Iron Overload on Maternal and Fetal Outcomes in Pregnancies of Transfusion-Dependent Beta-Thalassemia Patients

Kevin H.M. Kuo, MD, Eiran Warner, BA, Mathew Sermer, MD, Richard Ward, MD

Blood (2011) 118 (21): 5297.

https://doi.org/10.1182/blood.V118.21.5297.5297

Published: 2011

Journal Articles

The Effect of Comprehensive Care on Maternal and Fetal Outcomes in Sickle Cell Disease Pregnancies

Kevin H.M. Kuo, MD, Eiran Warner, BA, Mathew Sermer, MD, Richard Ward, MD

Blood (2011) 118 (21): 4842.

https://doi.org/10.1182/blood.V118.21.4842.4842

Published: 2011

Journal Articles

Efficiency of the Neonatal Screening Program for Sickle Cell Disease. the Belgian Experience

Phu-Quoc Le, MD, Alina Ferster, MD, Françoise Vertongen, MD, PhD, Christiane Vermylen, MD, PhD, Anna Vanderfaeillie, MD, Catherine Heijmans, MD, Ba-Cuong Nguyen, Malou Ngalula Mijinga, nurse, Beatrice Gulbis, MD, PhD

Blood (2010) 116 (21): 4816.

https://doi.org/10.1182/blood.V116.21.4816.4816

Published: 2010

Journal Articles

Hospitalization Rate and Regional Differences in Comprehensive Care in Transfused Patients with Sickle Cell Disease Compared to Thalassemia: A Report from the Multi-Center Study of Iron Overload.

Ellen B. Fung, PhD, RD, Paul Harmatz, MD, Meredith Milet, MS, Samir K. Ballas, MD, Laura DeCastro, MD, Ward Hagar, MD, Lee Hilliard, MD, William Owen, MD, Kim Smith-Whitley, MD, Elliott Vichinsky, MD

Blood (2005) 106 (11): 3189.

https://doi.org/10.1182/blood.V106.11.3189.3189

Published: 2005

Journal Articles

Variability in Measures of Health Outcomes in Sickle Cell Disease (SCD) Patients with Access to Comprehensive Care Centers.

Sadhna M. Shankar, MD, MPH, Patrick Abrogast, Ph.D, Ed Mitchel, MS, Hua Ding, MS, Winfred Wang, MD, Marie R. Griffin, MD, MPH

Blood (2005) 106 (11): 294.

https://doi.org/10.1182/blood.V106.11.294.294

Published: 2005

Journal Articles

A Multidisciplinary Care Management Program for Patients with Sickle Cell Syndromes Significantly Reduces Health Care Resource Utilization.

William S. Jonas, MD, Matthew Hogan, MD, Allan F. Platt, PA, Melanie Jacob, MD, JoAnn A. Beasley, RN, Philip Lamson, Sheila Palmer, PA, Hanna J. Khoury, MD, James R. Eckman, MD

Blood (2005) 106 (11): 1339.

https://doi.org/10.1182/blood.V106.11.1339.1339

Published: 2005

NARROW

A Pilot Adult Sickle Cell Hematology Clinic in California's Inland Empire Improves Patient Outcome

Did the Outcome of Sicke Cell Disease Babies Screened at Birth Improved from 2000? a Single Center Experience

Follow-up and Treatment Expectancy and Compliance of Y-Generation Hemophiliacs

Positive Impact of Social Media on Disease Awareness and Management in Patients with Inherited Bleeding Disorders: Saudi Experience from a Tertiary Care Hospital

The Impact of a Multidisciplinary Sickle Cell and Gynecology Clinic

Telehematology: Expanding Comprehensive Care for Pediatric Patients with Blood Disorders through Telemedicine at Several Delivery Sites (Medical Homes, Hospital Clinics, Home Setting and Hemophilia Treatment Centers (HTC)) and with Interdisciplinary Providers

Disparities Between Patient and Hematology/Oncology Physician Expectations for Integrative Oncology in an Ethnically Diverse Population

Successful Outcomes Of An Infant Sickle Cell Clinic In Luanda, Angola

Treatment Patterns and Outcomes Of Sickle Cell Patients With Frequent ER Visits: A Single Center Experience

A Comparison of Chronic Manual and Automated Red Blood Cell Exchange Transfusion in Sickle Cell Disease Patients From Two Comprehensive Care Centres in the United Kingdom

A Comparison of Automated Red Blood Cell Depletion/Exchange to Automated Red Cell Blood Exchange in Sickle Cell Patients.

The Effect of Comprehensive Care and Degree of Iron Overload on Maternal and Fetal Outcomes in Pregnancies of Transfusion-Dependent Beta-Thalassemia Patients

The Effect of Comprehensive Care on Maternal and Fetal Outcomes in Sickle Cell Disease Pregnancies

Efficiency of the Neonatal Screening Program for Sickle Cell Disease. the Belgian Experience

Hospitalization Rate and Regional Differences in Comprehensive Care in Transfused Patients with Sickle Cell Disease Compared to Thalassemia: A Report from the Multi-Center Study of Iron Overload.

Variability in Measures of Health Outcomes in Sickle Cell Disease (SCD) Patients with Access to Comprehensive Care Centers.

A Multidisciplinary Care Management Program for Patients with Sickle Cell Syndromes Significantly Reduces Health Care Resource Utilization.

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American Society of Hematology

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American Society of Hematology

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