https://www.selleckchem.com/pr....oducts/bardoxolone.h
Biallelic mutations in the PTF1A enhancer are the commonest cause of isolated pancreatic agenesis. These patients do not have severe neurological features associated with loss-of-function PTF1A mutations. Their clinical phenotype and disease progression have not been well characterized. To evaluate phenotype and genotype characteristics and long-term follow-up of patients with PTF1A enhancer mutations. Twelve tertiary pediatric endocrine referral centers. Thirty patients with diabetes caused by PTF1A enhancer mutations. Median follo

https://www.selleckchem.com/pr....oducts/Aloxistatin.h
What role does the presence of facial speech play for children with dyslexia? Current literature proposes two distinctive claims. One claim states that children with dyslexia make less use of visual information from the mouth during speech processing due to a deficit in recruitment of audiovisual areas. An opposing claim suggests that children with dyslexia are in fact reliant on such information in order to compensate for auditory/phonological impairments. The current paper aims at directly testing these contrasting hypotheses (her