Results 51 to 60 of about 57,472 (341)

RETRACTED: CHOICE OF OSTEOFIXATION OF EPITHESIS IN TOTAL DEFECT OF THE MAXILLOFACIAL REGION

open access: yesВестник медицинского института «Реавиз»: Реабилитация, врач и здоровье, 2021
RETRACTED ARTICLERelevance. Surgical treatment of neoplasms, various genetic disorders and facial trauma often contribute to a violation of the general aesthetic perception of a person and the development of dysfunctions [1].
N. I. Tcherezova
doaj   +1 more source

Feline vestibular disorders. Part II: diagnostic approach and differential diagnosis. [PDF]

open access: yes, 1999
Results of a neurological examination usually permit localisation of a vestibular disorder to either the central or peripheral parts of the vestibular system. Many different disorders located in the same part of the vestibular system will produce similar
LeCouteur, RA, Vernau, KM
core  

A case report and genetic characterization of a massive acinic cell carcinoma of the parotid with delayed distant metastases. [PDF]

open access: yes, 2013
We describe the presentation, management, and clinical outcome of a massive acinic cell carcinoma of the parotid gland. The primary tumor and blood underwent exome sequencing which revealed deletions in CDKN2A as well as PPP1R13B, which induces p53.
Agrawal, Sumit K   +17 more
core   +3 more sources

[Treatment of facial and oral cavity neoplasms].

open access: closedCzasopismo stomatologiczne, 1981
J. Stypulkowska   +6 more
openalex   +2 more sources

Cerebrospinal Fluid Liquid Biopsy Enables Targeted Therapy Without Tissue Diagnosis in Pediatric Low‐Grade Gliomas With BRAF V600E Mutation

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT We present two pediatric cases of pediatric low‐grade gliomas (PLGG) with BRAF V600E mutations diagnosed and monitored using cerebrospinal fluid (CSF) liquid biopsy analyzed via digital droplet PCR (ddPCR), without tissue biopsy. Both patients were treated with dabrafenib and trametinib and monitored through clinical assessments, magnetic ...
Hannah Sultan   +5 more
wiley   +1 more source

Horner Syndrome Due to Intrathoracic Multinodular Goiter (Case Report)

open access: yesTürk Nöroloji Dergisi, 2013
Horner syndrome is characterized by miosis, ptosis, facial anhydrosis and enophtalmus and is caused by a lesion along the oculosymphathetic pathway from the hypothalamus to the eye. The long course of the oculosympathetic pathway predisposes it to a wide
Selda Korkmaz   +3 more
doaj   +1 more source

Laser treatment of 13 benign oral vascular lesions by three different surgical techniques [PDF]

open access: yes, 2013
Objectives: Benign Oral Vascular Lesions (BOVLs) are a group of vascular diseases characterized by congenital, inflammatory or neoplastic vascular dilations clinically evidenced as more or less wide masses of commonly dark bluish color.
DEL VECCHIO, Alessandro   +6 more
core   +1 more source

Prognostic Impact of Treatment Modalities, Including Targeted Compartmental Radio‐Immunotherapy, in a Cohort of Neuroblastoma Patients With CNS Metastases at Relapse

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction Neuroblastoma (NB) with central nervous system (CNS) metastases is rare at diagnosis, but occurs more often during relapse/progression. Patients with CNS metastases face a dismal prognosis, with no standardized curative treatment available.
Vicente Santa‐Maria Lopez   +13 more
wiley   +1 more source

Glomus Tumor of the Face: A Case Report and Literature Review

open access: yesIndian Journal of Plastic Surgery
Glomus tumors are benign mesenchymal neoplasms arising from the glomus body. The most common site of presentation of a glomus tumor is the subungual region, followed by the fingertip and foot.
Sanjay Maurya   +3 more
doaj   +1 more source

Optimum imaging for sinonasal malignancy [PDF]

open access: yes, 2002
A combination of computed tomography (CT) and magnetic resonance imaging (MRI) is now established as the optimum assessment of sinonasal malignancy.
Howard, D, Lloyd, G, Lund, VJ, Savy, L
core   +1 more source

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