Results 141 to 150 of about 97,471 (278)

The PERISCOPE Cohort: A Retrospective Study of Clinicopathological and TRAF7 Genetic Findings in Intraneural Perineurioma

European Journal of Neurology, Volume 33, Issue 2, February 2026.
ABSTRACT Background Intraneural perineurioma (INP) is a rare, benign peripheral nerve sheath tumour that typically presents in adolescence or early adulthood as a slowly progressive, motor‐predominant mononeuropathy or plexopathy. Although its clinicoradiological and histopathological features are well characterised, the genetic basis remains ...
Eduardo Boiteux Uchôa Cavalcanti, Alessandra de La Rocque Ferreira, Nilo Sakai Júnior, Francineide Sadala de Souza, Heveline Becker de Moura, Eni Braga Da Silveira, Graciela Maria Barbosa Lacerda Martins, Marcio de Mendonça Cardoso   +7 more
wiley   +1 more source

Pathology in Practice [PDF]

, 2017
Lofts, R, Priestnall, S L, Summers, B A, Terry, R   +3 more
core   +1 more source

Neurofibromatosis [PDF]

Proceedings of the Royal Society of Medicine, 1930
openaire   +3 more sources

Intraparotid Neurofibromatosis [PDF]

Ear, Nose & Throat Journal, 2012
Ryan F, Osborne, Jason S, Hamilton, Reena, Gupta   +2 more
openaire   +2 more sources

Molecular profile of atypical Leydig cell tumours

Histopathology, Volume 88, Issue 3, Page 628-635, February 2026.
Copy number variations by themselves are not sufficient to discriminate between benign and potential malignant Leydig cell tumours (LCTs). Genomic instability was only detected in malignant and atypical cases, and not in any benign tumours. Currently, the presence of metastasis remains the only malignant criterion for LCTs.
Muhammad F.K. Choudhry, Diogo Caires, Yaser Gamallat, Asli Yilmaz, Fadi Brimo, Bob Argiropoulos, Tarek A. Bismar   +6 more
wiley   +1 more source

Multiple gastrointestinal stromal tumors: analysis of clinicopathologic characteristics and prognosis of 20 patients

Cancer Management and Research, 2019
Kai Li, WEH Tjhoi, Chunhui Shou, Weili Yang, Qing Zhang, Xiaosun Liu, Jiren YuDepartment of Gastrointestinal Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, People’s Republic of ChinaPurpose: Multiple ...
Li K, Tjhoi WEH, Shou C, Yang W, Zhang Q, Liu X, Yu J   +6 more
doaj  

Neurofibromatosis [PDF]

Journal of Neurology, Neurosurgery & Psychiatry, 2003
openaire   +2 more sources

Healthcare Utilisation and Barriers and Facilitators of Healthcare Access for Young People With Intellectual Disability: A Systematic Review

Journal of Intellectual Disability Research, Volume 70, Issue 2, Page 130-161, February 2026.
ABSTRACT Background Young people with intellectual disability may exhibit poorer general health, higher mortality rates and greater limitations from physical or mental illnesses compared to the general population. It is important to understand how this may relate to healthcare utilisation, including factors influencing healthcare access for young ...
Felicia Kreps, Shalini Wijekulasuriya, Yvonne Zurynski, Rebecca Mitchell   +3 more
wiley   +1 more source

Two Familial Neurofibromatosis Cases With Different Phenomenic Characteristics

Türk Nöroloji Dergisi, 2008
Scientific BACKGROUND: Neurofibromatosis is an autosomal dominant genetic disease which affects skin, nervous system and eyes. Neurofibromatosis has two frequently seen subtypes which are called Type 1 (Von Recklinghausen disease: periferal ...
Ülgen Kökeş, Fazilet Hız, Suna Özlem Mutlu, Deniz Yücel, Meral Çınar   +4 more
doaj  

Activity of Selumetinib in Neurofibromatosis Type 1-Related Plexiform Neurofibromas.

New England Journal of Medicine, 2016
E. Dombi, A. Baldwin, L. Marcus, M. Fisher, B. Weiss, AeRang Kim, P. Whitcomb, Staci Martin, L. Aschbacher-Smith, T. Rizvi, Jianqiang Wu, Rachel Ershler, P. Wolters, Janet Therrien, J. Glod, J. Belasco, E. Schorry, A. Brofferio, Amy J. Starosta, A. Gillespie, A. Doyle, N. Ratner, B. Widemann   +22 more
semanticscholar   +1 more source