Results 91 to 100 of about 4,008 (210)

Elevated platelet counts in a cohort of children with moderate-severe osteogenesis imperfecta suggest that inflammation is present [PDF]

open access: yes, 2018
BACKGROUND: Elevated platelet counts are observed in cancer, autoimmunity and inflammation with concurrent illness. Proinflammatory cytokines are elevated in murine osteogenesis imperfecta (OI) models.
Bishop, N., Offiah, A.C., Salter, L.
core   +1 more source

Regional odontodysplasia of the deciduous and permanent teeth associated with eruption disorders : a case report [PDF]

open access: yes, 2008
Regional odontodysplasia (RO) is an unusual, non-hereditary anomaly of the dental hard tissues with characteristic clinical, radiographic and histological findings.
Gunhan, Omer   +5 more
core  

The relationship between pulp calcifications and salivary gland calcifications [PDF]

open access: yes, 2014
Aim: Pulp stones are discrete calcified bodies found in the dental pulp. Sialolithasis is the most common salivary gland disease. The aim of the present study was to determine the relationship between the pulp stones and salivary gland stones.
Farzan, Rahman   +4 more
core   +1 more source

Laporan Kasus: Dentinogenesis Imperfekta [PDF]

open access: yes, 2019
Dentinogenesis imperfecta is the one of most common hereditary disorder of dentin formation, especially at histodifferentiation stage. It reported have to an incidences of 1 in 8000.
Abdurokhman, Evellyn Islami   +1 more
core   +2 more sources

Type III Osteogenesis Imperfecta With Dentinogenesis Imperfecta - A Case Report And review of Literature

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2003
Osteogenesis Imperfecta is a genetic disorder affecting approximately 20,000 U.S. population with multiple fracture of the bone. The, actual literature of the number of patients suffering from Osteogenesis Impcrfecta in Indian Population is still nor ...
Prabal Pal
doaj  

Dentinogenesis imperfecta: The Genetic Causes and Outcomes [PDF]

open access: yes, 2021
Dentinogenesis imperfecta (DI) is a genetic disorder characterized by dentin discoloration, tooth development irregularities, and decreased tooth strength. This autosomal dominant disorder is identified in individuals of all ages.
Johnson, Sydney P, Ms.
core   +1 more source

Guideline on therapeutic dentistry for the 5-th term [PDF]

open access: yes, 2016
РУКОВОДСТВАСТОМАТОЛОГИЯ ЛЕЧЕБНО-ВОССТАНОВИТЕЛЬНАЯСТОМАТОЛОГИЯ ТЕРАПЕВТИЧЕСКАЯИНОСТРАННЫЕ СТУДЕНТЫУЧЕБНО-МЕТОДИЧЕСКИЕ ПОСОБИЯПособие составлено в соответствии с учебной программой для медицинских вузов по терапевтической стоматологии.
Korenevskaya, N. A.   +2 more
core  

Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations [PDF]

open access: yes, 2014
Amelogenesis imperfecta (AI) is a genetically and clinically heterogeneous group of inherited dental enamel defects. Commonly described as an isolated trait, it may be observed concomitantly with other orodental and/or systemic features such as ...
Acevedo, A-C   +8 more
core   +1 more source

THE CONTRIBUTION OF KINETIC THERAPY IN LOBSTEIN’S DISEASE [PDF]

open access: yesAnnals of the “Ştefan cel Mare” University: Physical Education and Sport Section - The Science and Art of Movement, 2018
Osteogenesis imperfecta is a genetic disease of the connective tissue whose main clinical sign is increased bone fragility, manifested especially through fractures of the long limbs. OI presents major clinical signs and minor clinical signs.
Sergiu Danail, Danelciuc Francisc Tadeus
doaj  

Oral Health-Related Quality of Life in Dutch Adults With Osteogenesis Imperfecta. [PDF]

open access: yes
Objective: To explore the oral health-related quality of life and its possible risk factors among adults with Osteogenesis Imperfecta using the Oral Health Impact Profile (OHIP)-49 questionnaire.
Appelman-Dijkstra, Natasha   +8 more
core   +1 more source

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