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Article
Open AccessGlucose phosphate isomerase deficiency demasked by whole-genome sequencing: a case report
Glucose-6-phosphate isomerase deficiency is a rare genetic disorder causing hereditary nonspherocytic hemolytic anemia. It is the second most common glycolytic enzymopathy in red blood cells. About 90 cases ar...
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Article
Open AccessClinical recovery of two hip adductor longus ruptures: a case-report of a soccer player
Non-operative treatment of acute hip adductor longus ruptures in athletes has been described in the literature. However, very limited information concerning the recovery of this type of injury exists. This cas...