Acute pancreatitis as initial presentation for hereditary spherocytosis: A case report

before, to Jn exp(-ne) by somatic mutations and the babies survive to juveniles with probabil- ity Jn exp(-ne) and then give birth to new babies having a juvenile survival

Regarding controls, we have compared the currents measured from the RBCs of our patients once with their transportation control, i.e., currents measured from the RBCs of a

Here, we report the case of a pancreatic islet recipient who developed aHUS that was associated with a comple- ment component 3 (C3) gene mutation, along with sec- ondary ESRD,

L’archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des

A variety of mutations have been reported in the L-ferritin subunit gene (FTL gene) that cause the following five diseases: (1) hereditary hyperferritinemia with cataract

recently, Mirollo and Vilonen [MiV] have shown that these categories are again equivalent to module categories over certain finite dimensional

When there are no differences in initial scores between preexisting stable groups, the change score analysis, ANCOVA, and the residual change analysis would yield similar

This review shows that LHON can be a multiorgan disor- der, that involvement of organs other than the eye may be subclinical possibly depending on the heteroplasmy rates of