Results 141 to 150 of about 15,328 (193)

Genotype and Phenotype of 198 Korean Patients With Nonlethal Osteogenesis Imperfecta: A Retrospective Cohort Study. [PDF]

Hum Mutat
Lee J, Lee HR, Ko JM, Shin CH, Lee W, Song MH, Cho TJ.   +6 more
europepmc   +1 more source

Osteogenesis Imperfecta Type 4 With COL1A2 c.1135G>A (p.Gly379Arg) Variant: Unmodified by Concurrent ALPL c.1559delT (p.Leu520ArgfsTer86) Carrier Status: A Case Report. [PDF]

Cureus
Nomura K, Oda Y, Yamaguchi S, Ito T, Namai Y.   +4 more
europepmc   +1 more source

Elevated periostin level in serum of adults with osteogenesis imperfecta is associated with disease severity.

J Clin Endocrinol Metab
Mercier-Guery A, Auroux M, Gineyts E, Borel O, Szulc P, Sornay-Rendu E, Fontanges E, Croset M, Rousseau JC, Chapurlat R.   +9 more
europepmc   +1 more source

The Inorganic Phase in Dentinogenesis imperfecta

Journal of Dental Research, 1981
High resolution TEM, X-ray diffraction analysis, infrared absorption spectroscopy, thermogravimetry, and chemical and electron microprobe analyses showed that in dentinogenesis imperfecta the mineral phase is a carbonated apatite with crystallites of normal size, but less numerous than in normal dentin.
B, Kerebel, G, Daculsi, J, Menanteau, L M, Kerebel   +3 more
openaire   +3 more sources

[Dentinogenesis imperfecta].

Pedodontie Francaise, 1981
Based on three cases(two autopsies and one biopsy) we have conducted a pathological study On dentino genesis imperfecta. Two cases were classified into type I dentinogenesis imperfecta, which were associated with congenital osteogenesis imperfecta.
이석근, 임창윤, 지제근
core   +4 more sources

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Uninherited dentinogenesis imperfecta

Oral Surgery, Oral Medicine, Oral Pathology, 1975
The rare hereditary disease, dentinogenesis imperfecta, is a disturbance of dentin formation in both the deciduous and permanent dentitions. It may be associated with osteogenesis imperfecta, though it is probably that the two diseases are carried by different genes. This association was recognized in a 19-year-old man.
R M, Orlowski, C M, Reeve
openaire   +2 more sources

Dentinogenesis imperfecta associated with short stature, hearing loss and mental retardation: a new syndrome with autosomal recessive inheritance?

Journal of Oral Pathology and Medicine, 2005
The follow-up history and oral findings in two brothers from consanguineous parents suggest that the association of dentinogenesis imperfecta (DI), delayed tooth eruption, mild mental retardation, proportionate short stature, sensorineural hearing loss ...
Rita Cauwels, Geert Mortier, L C Martens
exaly   +2 more sources

Hereditary dentinogenesis imperfecta

The Journal of Pediatrics, 1964
Summary A classic case of hereditary dentinogenesis imperfecta with its genealogy has been presented and its possible treatment discussed.
openaire   +2 more sources

The Role of Dentists in Diagnosing Osteogenesis Imperfecta in Patients With Dentinogenesis Imperfecta

Journal of the American Dental Association, 2008
Background. Osteogenesis imperfecta (OI), also known as ""brittle bone disease,"" can be difficult to diagnose in its mild form. The authors describe a clinical case of a diagnosis of dentinogenesis imperfecta (DI), In which a literature review combined ...
Cleonice S. Teixeira, Yara Terezinha Corrêa Silva-Sousa, Manoel Damião Sousa-Neto   +2 more
exaly   +1 more source

Dentinogenesis imperfecta with dens in dente

Oral Surgery, Oral Medicine, Oral Pathology, 1983
An uncommon case of dentinogenesis imperfecta with dens in dente was studied by light microscopy, microradiography, and electron-microprobe analysis. Numerous canals and cellular inclusions were found in the coronal portion of the dentin where the tubules were sparse and irregularly distributed.
B, Kerebel, L M, Kerebel, G, Daculsi, J, Doury   +3 more
openaire   +2 more sources