Results 71 to 80 of about 5,733 (168)

Management of a hopeless mandibular molar: A case report

open access: yesIranian Endodontic Journal, 2011
Intentional tooth reimplantation can be an alternative treatment option for teeth with poor or hopeless prognosis where coronal and surgical endodontic treatment(s) are not possible.
saeed asgary
doaj  

Novel ocular observations in a child with Joubert syndrome type 6 due to pathogenic variant in TMEM67 gene

open access: yesAmerican Journal of Ophthalmology Case Reports
Purpose: To describe unique ocular features in a child with Joubert syndrome type 6. Observations: A 4-year-old male patient presented with right microphthalmia and non-dilating pupil and left primary position nystagmus. Brain MRI revealed a “molar tooth
Maram EA Abdalla Elsayed   +3 more
doaj   +1 more source

Radiological features of Joubert syndrome and clinical case presentation

open access: yesRadiology Case Reports
Joubert Syndrome, manifests in a spectrum of neurological symptoms. This case describes a 7-year-old girl with perinatal complications, and subsequent neurodevelopmental challenges. An MRI confirmed the diagnosis of Joubert syndrome, with the distinctive
Jorge Ariel Montero Torres, MD   +4 more
doaj   +1 more source

Histological investigation of the effects of nano titanium dioxide on the development of the first mandibular molar bud in NMRI mouse strain in vivo

open access: yesیافته‌های نوین در علوم زیستی, 2017
Nowadays, with the applications of titanium dioxide nanoparticles (TiO2-NPs) in pharmacy, food industry, cosmetics, toothpaste and sunscreens, pregnant women are exposed to nanoparticles.
Seyedeh Sadaneh Tabatabaei Nia   +2 more
doaj  

Signs of molar incisor hypomineralization before eruption of the affected tooth: Case report [PDF]

open access: gold
Claudia Maria de Souza Peruch   +3 more
openalex   +1 more source

Molar tooth sign: A characteristic image in Joubert syndrome

open access: yesNeurología (English Edition), 2010
Hurtado, P., Pachajoa, H.
openaire   +2 more sources

Suboccipital Atretic Cephalocele as a Marker for Joubert-Plus Syndrome: An Extended Phenotype of the CPLANE1 Gene Mutation. [PDF]

open access: yesCureus
Babiker AI   +8 more
europepmc   +1 more source

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