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WHAT IS SICKLE CELL DISEASE?
PSYCHOSOCIAL RESEARCH AND SICKLE CELL
PAIN AND SICKLE CELL DISEASE
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adolescents adults with SCD affected by SCD analgesia analgesics Anionwu areas aspects of SCD assessment associated with SCD attitudes Black and Laws Brozovic cent Child Behaviour childhood children with SCD children with sickle clinical complications condition coping Davies doctors drug ethnic evidence experience extent factors functioning gene genetic haemoglobinopathy illness severity important improvements individuals infection influence inherited interventions Journal leg ulcers levels locus of control London measures Medicine ment Midence molecules numbers opiates pain crises pain management parents patients with SCD Pediatrics person potential pregnancy present priapism programmes psychosocial recessive gene red blood cells relation to SCD relationships reported risk role sample SC disease Scale SCD pain screening siblings Sickle and Thalassaemia sickle cell anaemia Sickle Cell Centre sickle cell disease sickle cell trait strategies stress studies sufferers symptoms Thalassaemia Centre tion treatment variables Varni Walco