Results 51 to 60 of about 19,908 (210)

The association between neural crest‐derived glia and melanocyte lineages throughout development and disease

Developmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient cell population that emerges from the dorsal neural tube during neurulation and migrates extensively throughout the embryo. Among their diverse derivatives, glial cells (such as Schwann and satellite ganglionic cells) and melanocytes represent two major lineages. In vitro studies suggested they share a common
Chaya Kalcheim
wiley   +1 more source

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

, 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, Giovannini, Marco, Hardiman, Atira, Jegga, Anil G, Jessen, Walter J, Kaiser, Sergio, Lazaro, Conxi, Li, Hua, Lopez, Eva, Mehta, Tapan, Miller, Shyra J, Muir, David, Nielsen, Gunnlaugur Petur, Page, Grier, Ratner, Nancy, Serra, Eduard, Sites, Emily, Stemmer-Rachamimov, Anat, Upadhyaya, Meena, Wallace, Margaret R   +19 more
core   +1 more source

Novel drugs approved by the EMA, the FDA and the MHRA in 2025: A year in review

British Journal of Pharmacology, EarlyView.
Abstract In the 2025 novel drug mini‐review, one can take a full measure of the ingenuity that underlies current drug design and development, despite the year's smaller harvest (46 novel drugs) compared to 2024 (53) and 2023 (70). 54% of the novel drugs are first‐in‐class (FIC).
Andreas Papapetropoulos, Stavros Topouzis, Steve P. H. Alexander, Miriam M. Cortese‐Krott, Zsuzsanna Helyes, Kirill Martemyanov, Claudio Mauro, Nithyanandan Nagercoil, Reynold A. Panettieri Jr, Hemal H. Patel, Rainer Schulz, Barbara Stefanska, Gary J. Stephens, Nathalie Vergnolle, Xin Wang, Stephen Ward, Péter Ferdinandy   +16 more
wiley   +1 more source

Arteriovenous malformation underlying a plexiform neurofibroma: An unusual presentation

Indian Dermatology Online Journal, 2017
Vascular abnormalities associated with neurofibromatosis type 1 are well described in the literature, however, arteriovenous malformation is a very rare finding in neurofibromatosis type 1.
Zaheer Abbas, Sepideh Khani, Javad Zare
doaj   +1 more source

A patient with neurofibroma (schwannoma) in peri-sacral: A case report [PDF]

, 2015
Schwannomas are benign tumors of the nerve sheath and are usually single encapsulated and slow growing in peripheral or sympathetic nervous system. In this report a 49 year-old man is presented with one year complain of abdominal pain and intermittent ...
Jouybari, L., Mojarad, F.A., Sanagoo, A., Sharifi, G.   +3 more
core  

Schwann cell hamartoma: case report [PDF]

, 2011
BACKGROUND: Colorectal polyps of mesenchymal origin represent a small percentage of gastrointestinal (GI) lesions. Nevertheless, they are encountered with increasing frequency since the widespread adoption of colonoscopy screening.
Elena Guerini Rocco, Francesca Iannuzzi, Alessandra Dell'Era, Monica Falleni, Laura Moneghini, Franca Di Nuovo, Paola Braidotti, Gaetano Bulfamante, Solange Romagnoli   +8 more
core   +3 more sources

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

Rare 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, Ravi Kant, Ahmed Aldamati, Aysha Ahmed Badar   +3 more
doaj   +1 more source

Malignant peripheral nerve sheath tumor of the cervical vagus nerve in a neurofibromatosis type 1 patient - An unusual presentation [PDF]

, 2010
Malignant peripheral nerve sheath tumors (MPNST’S) of the head and neck comprise 2% to 6% of head and neck sarcomas. These tumors may arise as sporadic variants or in patients with neurofibromatosis (NF).
Bahl, A, Bansal, S, Bhagat, S, Gupta, A
core   +1 more source

Atypical presentation of extraspinal neurofibroma presenting with acute-onset monoparesis and Horner's syndrome: Case report and review of literature

Journal of Craniovertebral Junction and Spine, 2019
The clinical presentation of spinal or extraspinal neurofibroma is radiculopathy or myelopathy, pain, and motor weakness. Extraspinal neurofibroma presenting with acute-onset monoparesis and Horner's syndrome is very rare. We report the case of a 55-year-
Lokesh S Nehete, Subhas K Konar, B N Nandeesh, Dhaval Shukla, B Indira Devi   +4 more
doaj   +1 more source

Socially oriented attention in young children with neurofibromatosis type 1: An eye‐tracking study

Developmental Medicine &Child Neurology, Volume 68, Issue 4, Page 541-548, April 2026.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.70050 Abstract Aim To examine visual engagement to social stimuli and response to joint attention in young children with neurofibromatosis type 1 (NF1) and typically developing peers (controls). Method Forty‐five preschool children were studied cross‐sectionally (mean age [SD] = 4 
Kristina M. Haebich, Darren R. Hocking, Hayley Darke, Rachel Mackenzie, Kathryn N. North, Giacomo Vivanti, Jonathan M. Payne   +6 more
wiley   +1 more source