Abstract Purpose of Review This review highlights indications and evidence on laser
therapy in the management of diabetic retinopathy and diabetic macular edema. Particular …

Pendred syndrome is a recessively inherited disorder with the hallmark features of
congenital deafness and thyroid goitre. By some estimates, the disorder may account for …

To identify genes important for human cognitive development, we studied Williams
syndrome (WS), a developmental disorder that includes poor visuospatial constructive …

Pendrin is an anion transporter encoded by the PDS/Pds gene. In humans, mutations in
PDS cause the genetic disorder Pendred syndrome, which is associated with deafness and …

Following the positional cloning of PDS, the gene mutated in the deafness/goitre disorder
Pendred syndrome (PS), numerous studies have focused on defining the role of PDS in …

Pendred syndrome is an autosomal recessive disorder characterized by congenital
deafness and thyroid goiter. The thyroid disease typically develops around puberty and is …

Tremendous advances in human genetics have been made in recent years, as the fruits of
the Human Genome Project are facilitating the identification of genes associated with myriad …

Pendred's syndrome is an autosomal-recessive disorder characterized by deafness and
goiter. After our recent identification of the human gene mutated in Pendred's syndrome …

Pendrin is an anion exchanger expressed along the apical plasma membrane and apical
cytoplasmic vesicles of type B and of non-A, non-B intercalated cells of the distal convoluted …

Background Pendred syndrome, a common autosomal-recessive disorder characterized by
congenital deafness and goiter, is caused by mutations of SLC26A4, which codes for …