Results 21 to 30 of about 5,977 (216)

A Collaborative Model for Accelerating the Discovery and Translation of Cancer Therapies [PDF]

open access: yes, 2017
Preclinical studies using genetically engineered mouse models (GEMM) have the potential to expedite the development of effective new therapies; however, they are not routinely integrated into drug development pipelines. GEMMs may be particularly valuable
Braun, Benjamin S.   +13 more
core   +1 more source

Retroperitoneal Malignant Peripheral Nerve Sheath Tumour: A Rare Case Report [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2015
Malignant nerve sheath tumours (MPNST) are rare neoplasias and retroperitoneal cases are fairly rare and clinically difficult to be detected, but they are very agressive neoplasias. MPNST are frequently seen in head, neck and upper extremities.
Ayse Nur Deger   +4 more
doaj   +1 more source

Voluminous Plexiform Neurofibroma of the Foot in a Newborn - A Case Report Orthopedic-Traumatology Surgery Department - Batna Hospital Laboratory of Acquired and Constitutional Genetic Diseases (MAGECA) Faculty of Medicine -Batna 2 University

open access: yesFoot & Ankle Surgery: Techniques, Reports & Cases, 2022
Neurofibromas are the cardinal dermatological signs of neurofibromatosis type I or Von Recklinghausen disease; also, they are benign tumors of the nerve sheaths.
Prof. Nacer Khernane   +4 more
doaj   +1 more source

Plexiform neurofibroma of the submandibular gland in patient with von Recklinghausen's disease

open access: yesRare Tumors, 2011
Plexiform neurofibroma of the submandibular gland is an extremely rare tumor. Herein, we report a case of plexiform neurofibroma in a patient with a von Recklinghausen's disease (NF-1) who presented with a submandibular mass mimicking a submandibular ...
Hassan Al Bisher   +3 more
doaj   +1 more source

Features of CT and EUS in mesenteric plexiform neurofibroma with Neurofibromatosis type I: A case report

open access: yesRadiology Case Reports, 2021
Plexiform neurofibroma(PNF) is a rare benign tumor of the peripheral nerve, belonging to a subtype of neurofibroma. PNF is common in the head, neck and trunk. It is uncommonly observed in the mesentery. We report a case of mesenteric PNF in a 64-year-old
Ye-ting Li, Bachelor's degree   +8 more
doaj   +1 more source

Integrative genomic analyses of neurofibromatosis tumours identify SOX9 as a biomarker and survival gene [PDF]

open access: yes, 2013
Understanding the biological pathways critical for common neurofibromatosis type 1 (NF1) peripheral nerve tumours is essential, as there is a lack of tumour biomarkers, prognostic factors and therapeutics.
Aronow, Bruce J   +19 more
core   +1 more source

Progesterone and Estrogen Receptors in Neurofibromas of Patients with NF1

open access: yesClinical Medicine Insights: Pathology, 2008
Neurofibromatosis type 1 (NF1) or von Recklinghausen disease is a genetic disorder affecting the growth of cells in nervous system. One of the most remarkable characteristics of this disease is the development of benign tumors of the nervous system ...
Mauro Geller   +9 more
doaj   +1 more source

Massive Plexiform Neurofibroma of the Neck and Larynx

open access: yesInternational Archives of Otorhinolaryngology, 2015
Introduction Laryngeal neurofibromas are extremely rare, accounting for only 0.03 to 0.1% of benign tumors of the larynx. Objectives To report the first case of massive neck plexiform neurofibroma with intralaryngeal (supraglottic) extension
Mohammad Kamal Mobashir   +4 more
doaj   +1 more source

Giant elephantiasis neuromatosa in the setting of neurofibromatosis type 1: A case report [PDF]

open access: yes, 2016
Elephantiasis neuromatosa (EN) can arise from a plexiform neurofibroma of the superficial and deep nerves developing from a hyperproliferation of the perineural connective tissue infiltrating adjacent fat and muscles.
Dealis, Cristina   +9 more
core   +1 more source

Hypervascular neurofibromas in a case of neurofibromatosis type 1: a case report [PDF]

open access: yes, 2011
Neurofibromatosis type 1 is one of the most frequently inherited diseases affecting 1:3500 newborn. The diagnosis of Neurofibromatosis type 1 is not dilemmatic because of typical clinical features.
Gogineni, Subhas Babu   +1 more
core   +1 more source

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