Results 151 to 160 of about 67,683 (260)

Treating Severe Cervical Deformity in Neurofibromatosis 1 with a Posterior Fibula Graft from Occiput to Thoracic Spine: A Case Report

Spine Surgery and Related Research
Bungo Otsuki, Shunsuke Fujibayashi, Takashi Noguchi, Takayoshi Shimizu, Shuichi Matsuda   +4 more
doaj   +1 more source

Molecular pathology of phyllodes tumours of the breast—much more than MED12

Histopathology, Volume 88, Issue 6, Page 1115-1125, May 2026.
Phyllodes tumours can develop from fibroadenomas bearing MED12 variants by the development of pTERT alterations (“MED12 pathway”) or de novo (“MED12 independent pathway”). Grade progression is associated with increasing genetic complexity including cancer driver gene aberrations. Molecular alterations can be useful in assigning grade and distinguishing
Jia‐Min B Pang, Kylie L Gorringe, Puay Hoon Tan, Stephen B Fox   +3 more
wiley   +1 more source

Diagnoses of double heterozygous NF1 variants and dual RASopathy. [PDF]

Mol Cell Pediatr
Angelova-Toshkina D, Schanze D, Vaassen P, Frühwald MC, Rosenbaum T, Zenker M, Kuhlen M.   +6 more
europepmc   +1 more source

NF1 Positive [PDF]

, 2020
openaire   +1 more source

Who can safely discontinue lifelong follow‐up among patients with sporadic pheochromocytoma and paraganglioma?

Journal of Internal Medicine, Volume 299, Issue 5, Page 615-627, May 2026.
Abstract Background Current guidelines recommend at least 10 years of follow‐up for all pheochromocytoma and paraganglioma (PPGL) patients and lifelong monitoring for high‐risk individuals. Nonetheless, data identifying patients who may not require routine lifelong follow‐up are scarce. Methods Among 999 patients with PPGL, 703 who were non‐metastatic,
Min Jeong Park, Seung Shin Park, Won Woong Kim, Su‐Jin Kim, Yu‐Mi Lee, Kyu Eun Lee, Tae‐Yon Sung, Jae‐Kyung Won, Dong Eun Song, Jung‐Min Koh, Sara Talvacchio, Tamara Prodanov, Hussam Alkaissi, Karel Pacak, Seung Hun Lee, Jung Hee Kim   +15 more
wiley   +1 more source

Everyday executive functions in children with neurofibromatosis type 1: Data from nine institutions. [PDF]

Neuropsychology
Zong X, Liu D, Wu X, Wolters PL, Payne JM, Klein-Tasman BP, Walsh KS, Janusz J, Pride N, Morris SM, Bearden CE, Stavinoha PL, Hou Y.   +12 more
europepmc   +1 more source

A case report of malignant transformation in neurofibromatosis type 1: pain and rapid growth as key indicators for early biopsy. [PDF]

Front Oncol
Zhao Y, Cao JY, Li Y, Huo JY, Zhao ZW, Xue L, Li J, Duan CZ.   +7 more
europepmc   +1 more source

NF1 gene

, 2018
Jeremy Jones, Daniel Bell
openaire   +1 more source

Progressive cervicothoracic meningocele with neurovascular compression and spinal deformity in neurofibromatosis type 1: a decade-long radiological and clinical evolution with operative repair. Illustrative case. [PDF]

J Neurosurg Case Lessons
Mousa AH, Hafiz B, Turkistani A, Alsindi T, Aref M.   +4 more
europepmc   +1 more source

DNA source and primer choice affect the reliability of metabarcoding for nematode community profiling in agricultural soils. [PDF]

PLoS One
Akanwari J, Islam MR, Liang P, Sultana T.   +3 more
europepmc   +1 more source