Results 71 to 80 of about 5,733 (168)
Management of a hopeless mandibular molar: A case report
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
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
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
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
EP06.05: It is possible to diagnose Joubert syndrome with prenatal sonographic “molar tooth sign” [PDF]
Lijuan Sun +3 more
openalex +1 more source
MONITORING OF VITAL SIGNS AND HEMODYNAMIC CHANGES IN PATIENTS UNDERGOING TOOTH EXTRACTION AND THIRD MOLAR SURGERY - LITERATURE REVIEW [PDF]
Natali Tomeva, Elitsa Deliverska
openalex +1 more source
Signs of molar incisor hypomineralization before eruption of the affected tooth: Case report [PDF]
Claudia Maria de Souza Peruch +3 more
openalex +1 more source
Comprehensive Rehabilitation in a Child with Joubert Syndrome: A Case Report. [PDF]
Mathews E, Goyal V, Mhambre A, Gaur AK.
europepmc +1 more source
Molar tooth sign: A characteristic image in Joubert syndrome
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]
Babiker AI +8 more
europepmc +1 more source

