Results 51 to 60 of about 6,672 (205)

Survival of dental implants in patients with oral cancer treated by surgery and radiotherapy: a retrospective study [PDF]

open access: yes, 2015
BACKGROUND: The aim of this retrospective study was to evaluate the survival of dental implants placed after ablative surgery, in patients affected by oral cancer treated with or without radiotherapy.
A Agresti   +37 more
core   +2 more sources

Juvenile ‘Perinasal’ Angiofibroma [PDF]

open access: yesIndian Journal of Otolaryngology and Head & Neck Surgery, 2017
The extranasopharyngeal angiofibroma is a separate clinical entity but those involving infratemporal fossa and cheek resemble juvenile nasopharyngeal angiofibroma (JNA) and hence have been labelled as juvenile perinasal angiofibroma (JPA) in this paper. This paper presents a 7th case of JPA and attempts to review the world literature on JPA, along with
Anupam, Mishra   +2 more
openaire   +2 more sources

A Retrospective Cross‐Sectional Study of 142 Patients in a Multidisciplinary Tuberous Sclerosis Clinic

open access: yesClinical Genetics, EarlyView.
We found key differences between tuberous sclerosis patients with TSC1 and TSC2 variants. Patients carrying TSC2 variants had more severe and earlier‐onset symptoms. We also identified two distinct clinical subgroups which follow different disease courses: one characterized by predominant renal involvement and the other by more pronounced neurological ...
Hila Weisblum Neuman   +6 more
wiley   +1 more source

A rare case of angiofibroma of the mandible: A case report

open access: yesJournal of Oral Biology and Craniofacial Research, 2016
Angiofibroma is a rare, highly vascular nonencapsulated tumor, which is locally invasive. A rare case of angiofibroma of the mandible in a 16-year-old female patient is reported here. The lesion was excised along with surgical removal of right mandibular
Mohammed Israr Ul Khaliq   +2 more
doaj   +1 more source

Identification of a novel TSC2 c.3610G > A, p.G1204R mutation contribute to aberrant splicing in a patient with classical tuberous sclerosis complex: a case report [PDF]

open access: yes, 2018
Background: Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by hamartomas in any organ systems. Mutations in the TSC1 or TSC2 gene lead to the dysfunction of hamartin or tuberin proteins, which cause tuberous sclerosis ...
Bottillo, I   +7 more
core   +2 more sources

Acral Mesenchymal Spindle Cell Neoplasm With a Novel HMGA2::NCOA2 Fusion

open access: yesJournal of Cutaneous Pathology, EarlyView.
ABSTRACT Molecular profiling has revolutionized the field of soft tissue pathology, enhancing diagnostic precision and treatment strategies. The integration of molecular analysis and immunohistochemistry has been crucial for classifying diagnostically challenging acral mesenchymal neoplasms.
Grace Z. Armstrong   +5 more
wiley   +1 more source

Robustness of a convolutional neural network trained on dermoscopic images and challenged with close‐up images

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and Objectives Deep learning‐convolutional neural networks (DL‐CNNs) have demonstrated high diagnostic accuracy within the domain of dermoscopy. However, many clinical settings lack dermoscopic devices, requiring reliance on close‐up images. This study evaluates the robustness of a DL‐CNN trained on dermoscopic images when challenged
Anastasia Sophie Vollmer   +6 more
wiley   +1 more source

Tratamiento quirúrgico del angiofibroma nasofaríngeo juvenil mediante un proceso secuencial de atención: resultados observados en 81 pacientes [PDF]

open access: yes, 2007
Se diagnosticaron y trataron 81 pacientes por angiofibroma nasofaríngeo juvenil (ANJ) en el Hospital Clínico quirúrgico "Hermanos Ameijeiras" (Ciudad Habana, Cuba), entre 1984 y 2005.
Cordero Escobar,Idoris   +6 more
core  

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

open access: yesInternational Journal of Dermatology, Volume 65, Issue 3, Page 464-488, March 2026.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla   +8 more
wiley   +1 more source

ANGIOFIBROMA NASOFARÍNGEO JUVENIL GRADO IV [PDF]

open access: yes, 2017
El angiofibroma nasofaríngeo juvenil es una neoplasia vasoformativa benigna de lento crecimiento, localmente agresiva. Este es un tumor relativamente raro y esporádico el cual representa aproximadamente el 0.5% de todos los tumores de cabeza y cuello ...
Benavides Cerros, Yolanda Marisol   +3 more
core   +1 more source

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