Results 71 to 80 of about 7,605 (223)
The needle study: Machine learning as a new method for case‐finding in celiac disease
Abstract Objectives Despite a well‐defined diagnostic work‐up, uncertainties persist regarding celiac disease (CeD) detection strategies in the general population. Machine learning (ML) algorithms offer promise in aiding medical decision‐making on clinical data.
Chiara Maria Trovato +9 more
wiley +1 more source
ENAMEL HYPOPLASIA IN A MEDIEVAL POPULATION FROM SLABOSZEWO [PDF]
ENAMEL HYPOPLASIA IN A MEDIEVAL POPULATION FROM SLABOSZEWO. Enamel hypoplasia in 68 individuals from a medieval cemetery of Slaboszewo (North-Western Poland) was analysed. Individual ages at defect development were assessed.
Krem, Marta, Piontek, Janusz
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Enamel hypoplasia and stature in two historic London populations [PDF]
Enamel hypoplasia and stunted stature are non-specific indicators of stress that are often caused by nutritional stress and exposure to disease in adolescence.
Sarah M. Hawks
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Heart Transplant for Noncompaction Cardiomyopathy in NONO‐Related Syndromic Intellectual Disability
Silent NONO variant c.348G>A caused exon 4 skipping, frameshift, and nonsense‐mediated decay in a boy with neurodevelopmental delay and severe left ventricular noncompaction requiring heart transplantation in early childhood. Stable graft function at 14 years highlights favorable long‐term cardiac outcome; literature review confirms a recognizable ...
Julia S. Singer +5 more
wiley +1 more source
OBJECTIVES:The study tried to determine if malnutrition (underweight, stunting, wasting, overweight) and enamel defects (enamel hypoplasia, hypomineralized second molar, amelogenesis imperfecta, fluorosis) were associated with early childhood caries (ECC)
Morenike Oluwatoyin Folayan +5 more
doaj +1 more source
Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise +5 more
wiley +1 more source
LINEAR ENAMEL HYPOPLASIA IN ROMAN IERAPETRA [PDF]
This study focuses on the prevalence of linear enamel hypoplasia in a sample of teeth from the Roman site of Ierapetra in southeast Crete. Linear enamel hypoplasia (LEH) is a dental defect that can be caused by childhood physiological stress like ...
Smith, Susan K., McKenna, Morgan E.
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Occurrence of epidermolysis bullosa along with Amelogenesis imperfecta in female patient of India
Epidermolysis bullosa (EB) is an inherited disorder, which is characteristically presented as skin blisters developing in response to minor injury. Junctional variety of EB is also associated with enamel hypoplasia.
A P Javed +5 more
doaj +1 more source
Gingival and Periodontal Diseases and Conditions in Children and Adolescents: Consensus Report
ABSTRACT Background The objectives of this Focused Workshop were to update the epidemiology, aetiology, risk factors, diagnosis and management of gingival and periodontal diseases and conditions in children and adolescents, and to explore the applicability of the 2018 Classification in children and adolescents.
Iain Chapple +30 more
wiley +1 more source
A pilot study of the genotype and phenotype in Amelogenesis Imperfecta and Molar Incisor Hypomineralization [PDF]
Background Enamel is an external layer of the crown, and its production can be affected by genetic, systemic or environmental causes Amelogenesis Imperfecta (AI) is an inherited defect of dental enamel, and can be autosomal dominant, recessive, x-linked ...
Abdullatif, MAA
core

