Treatment options for sickle cell disease (SCD) pain could be tailored to pain locations. But few epidemiologic descriptions of SCD pain location exist; these are based on few subjects over short time periods. We examined whether SCD pain locations vary by disease genotype, gender, age, frequency of pain, depression, pain crisis or healthcare utilization
The acutely painful episodes that characterize sickle-cell disease were described in 1872 by African...
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health...
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health...
Treatment options for sickle cell disease (SCD) pain could be tailored to pain locations. But few ep...
Until recent decades, sickle cell disease (SCD) was associated with recurrent, disabling pain, organ...
Until recent decades, sickle cell disease (SCD) was associated with recurrent, disabling pain, organ...
Sickle cell disease (SCD) is an inherited hematological disease marked by intense pain. Early in lif...
Sickle cell disease (SCD) is an inherited hematological disease marked by intense pain. Early in lif...
Painful vaso‐occlusive crises ( VOC s) are the hallmark of sickle cell disease ( SCD ); however, man...
Sickle cell pain includes 3 types: acute recurrent painful crises, chronic pain syndromes, and neuro...
Sickle pain is the hallmark of sickle cell disease (SCD). It could be acute, persistent/relapsing, c...
Sickle cell disease (SCD) is a highly complex inherited disorder of hemoglobin structure. Although t...
Background: Sickle cell disease (SCD) is characterized by frequent, unpredictable pain episodes and ...
OBJECTIVE: The aim of this exploratory, cross-sectional study was to evaluate pain in sickle cell di...
Acute pain is the hallmark of sickle cell disease and is the most common cause of hospital admission...
The acutely painful episodes that characterize sickle-cell disease were described in 1872 by African...
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health...
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health...
Treatment options for sickle cell disease (SCD) pain could be tailored to pain locations. But few ep...
Until recent decades, sickle cell disease (SCD) was associated with recurrent, disabling pain, organ...
Until recent decades, sickle cell disease (SCD) was associated with recurrent, disabling pain, organ...
Sickle cell disease (SCD) is an inherited hematological disease marked by intense pain. Early in lif...
Sickle cell disease (SCD) is an inherited hematological disease marked by intense pain. Early in lif...
Painful vaso‐occlusive crises ( VOC s) are the hallmark of sickle cell disease ( SCD ); however, man...
Sickle cell pain includes 3 types: acute recurrent painful crises, chronic pain syndromes, and neuro...
Sickle pain is the hallmark of sickle cell disease (SCD). It could be acute, persistent/relapsing, c...
Sickle cell disease (SCD) is a highly complex inherited disorder of hemoglobin structure. Although t...
Background: Sickle cell disease (SCD) is characterized by frequent, unpredictable pain episodes and ...
OBJECTIVE: The aim of this exploratory, cross-sectional study was to evaluate pain in sickle cell di...
Acute pain is the hallmark of sickle cell disease and is the most common cause of hospital admission...
The acutely painful episodes that characterize sickle-cell disease were described in 1872 by African...
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health...
Pain in sickle cell disease (SCD) is associated with increased morbidity, mortality, and high health...