Literature DB >> 31990651

Sickle cell disease: A primary care update.

Grace Onimoe1, Seth Rotz2.   

Abstract

Sickle cell disease (SCD) is the most common hemoglobinopathy in the United States and causes significant disease-related morbidity including multiorgan damage, chronic anemia, and debilitating pain crises. Primary care physicians play a key role in the medical home model of care for adults with SCD. This review focuses on current recommendations for health maintenance and provides a brief summary of disease complications and current updates.
Copyright © 2020 The Cleveland Clinic Foundation. All Rights Reserved.

Entities:  

Year:  2020        PMID: 31990651     DOI: 10.3949/ccjm.87a.18051

Source DB:  PubMed          Journal:  Cleve Clin J Med        ISSN: 0891-1150            Impact factor:   2.321


  2 in total

1.  Association of sickle cell trait with β-cell dysfunction and physical activity in adults living with and without HIV in Tanzania.

Authors:  Belinda V Kweka; Cyprian Fredrick; Brenda Kitilya; Kidola Jeremiah; Eric Lyimo; Suzanne Filteau; Andrea M Rehman; Henrik Friis; Mette F Olsen; Daniel Faurholt-Jepsen; Rikke Krogh-Madsen; George PrayGod
Journal:  APMIS       Date:  2022-03-01       Impact factor: 3.428

2.  Catastrophic Neurological Complications in 2 Patients With Sickle Cell Disease and COVID-19.

Authors:  Karen Clarke; Karima Benameur; Zanthia Wiley; Yoo Mee Shin; Mohamad Moussa; Fuad El Rassi; Morgan McLemore
Journal:  J Investig Med High Impact Case Rep       Date:  2022 Jan-Dec
  2 in total

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