Tooth number abnormality is one of the most common dental developmental diseases,
which includes both tooth agenesis and supernumerary teeth. Tooth development is …

The study of extracellular phosphorylation was initiated in late 19th century when the
secreted milk protein, casein, and egg-yolk protein, phosvitin, were shown to be …

Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting
enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel …

Introduction The aim of this systematic review (Prospero CRD42022323188) is to investigate
whether an association exists in patients with amelogenesis imperfecta (AI) between …

Objectives To identify etiologic variants and perform deep dental phenotyping in patients
with amelogenesis imperfecta (AI). Methods Three patients of two unrelated families were …

Enamel renal syndrome (ERS) or so-called amelogenesis imperfecta type IG is a very rare
disorder characterized by the triad of amelogenesis imperfecta, gingival enlargement and …

Amelogenesis imperfecta (AI) is a heterogeneous group of genetic rare diseases disrupting
enamel development (Smith et al., Front Physiol, 2017a, 8, 333). The clinical enamel …

Objective The aim of systematic review was to describe the phenotypes and molecular
profiles of syndromes with gingival fibromatosis (GF). Methods A comprehensive search of …

Background Enamel renal syndrome is a rare genetic disorder transmitted through an
autosomal recessive mode. It is featured by a hypoplastic amelogenesis imperfecta, delayed …

Background: Physical activity alleviates chronic stress. The latest research suggests a
relationship between resilience and physical fitness. Beneficial adaptations of the …