background pompe disease is an inherited metabolic disorder characterized by α-glycosidase deficiency, which leads to lysosomal glycogen accumulation in many different tissues. the infantile form is the most severe with a rapidly fatal outcome, while the late onset form has a greater phenotypic variability, characterized by skeletal muscle dysfunction and early respiratory involvement. bone min...

Objective: Temporal Lobe Epilepsy (TLE) can contribute to various emotional symptoms by damaging the temporal lobe. This study aimed at investigating emotion processing in patients with early- and late-onset TLE compared to a healthy group. Methods: In this causal-comparative study, 60 patients with diagnosed TLE were compared to 60 healthy controls to identify emotion processing styles. The d...

the aim of the present study was to compare the occurrence and duration of clinical mastitis in different seasons, stages of lactation period and parities in a holstein dairy farm in iran. a retrospective epidemiological survey from april 2005 to march 2008 was conducted on 884 clinical mastitis cases of 7437 lactations. data of each case including calendar-date of mastitis onset, days in milk ...