Results 101 to 110 of about 32,275 (267)

Association Between Sensorineural Hearing Loss and Neurocognitive Performance in Survivors of Childhood Cancer: A Systematic Review and Meta‐Analysis

open access: yesCancer Medicine, Volume 14, Issue 22, November 2025.
This systematic review and meta‐analysis found that childhood cancer survivors with severe sensorineural hearing loss (s‐SNHL) had significantly lower scores in various neurocognitive domains, including IQ, memory, and processing speed, compared to survivors without s‐SNHL.
Jennifer E. Schlak   +5 more
wiley   +1 more source

Primary dorsal spine primitive neuroectodermal tumor in an adult patient: Case report and literature review

open access: yesJournal of Craniovertebral Junction and Spine, 2017
Primary spinal primitive neuroectodermal tumor (psPNET) is a rare entity with few cases reported in literature. We report a case of a 50-year-old female who presented to us with paraplegia and was diagnosed with extradural dorsal spine psPNET.
Satyashiva Munjal   +5 more
doaj   +1 more source

Evidence of a dual histogenetic pathway of sacrococcygeal teratomas [PDF]

open access: yes, 2016
Aims Sacrococcygeal teratomas are rare tumours that occur most frequently in neonates, although adult cases also occur. The molecular pathogenesis of these tumours and their long-term prognosis is uncertain.
Cheng, Liang   +10 more
core   +1 more source

Building Immunocompetent Cerebral Organoids From a Developmental Perspective

open access: yesGlia, Volume 73, Issue 11, Page 2154-2166, November 2025.
Main Points Conventional cerebral organoids do not contain microglia, which must be added. We propose recommendations to assess microglial immunocompetence using quantitative approaches and stringent statistical analysis to help develop standardized protocols.
Xabier Cuesta‐Puente   +8 more
wiley   +1 more source

Arising Mediastinal Adenocarcinoma in A Patient With A 14 Years History of Mature Teratoma

open access: yesRespirology Case Reports, Volume 13, Issue 11, November 2025.
This case highlights the importance of long‐term follow‐up in patients with mediastinal teratomas, given the rare but significant risk of malignant transformation. Awareness of this possibility can facilitate early diagnosis and timely intervention, ultimately improving patient outcomes. ABSTRACT Mature teratomas are typically benign germ cell tumours (
Yanis Widhiya Ningrum   +2 more
wiley   +1 more source

Primitive neuroectodermal tumor transformation of testicular teratoma

open access: yesUrology Annals, 2018
Malignant transformation of teratoma develops in a small subset of testis cancer patients. Primitive neuroectodermal tumor represents a highly malignant component of testicular germ cell tumors.
Anastasios Karatzas   +5 more
doaj   +1 more source

Primary spinal extradural Ewing's sarcoma (primitive neuroectodermal tumor): Report of a case and meta-analysis of the reported cases in the literature

open access: yesSurgical neurology international, 2012
Background: Primary spinal primitive neuroectodermal tumors (PNET) and/or spinal extraskeletal Ewing's sarcoma family tumors (ESET) are rare lesions appearing in the spinal extradural space.
Saeed Saeedinia   +4 more
semanticscholar   +1 more source

Expression of stabilized β-catenin in differentiated neurons of transgenic mice does not result in tumor formation [PDF]

open access: yes, 2002
Background: Medulloblastomas, embryonal tumors arising in the cerebellum, commonly contain mutations that activate Wnt signaling. To determine whether increased Wnt signaling in the adult CNS is sufficient to induce tumor formation, we created transgenic
MD Taylor   +35 more
core   +2 more sources

Renal Primitive Neuroectodermal Tumor

open access: yesMedicine, 2015
Primitive neuroectodermal tumor (PNET) is a malignant small round cell tumor and typically arises from bone or soft tissue in adolescents and young adults. Renal PNET is extraordinarily rare and exhibits highly aggressive biological behavior with poor prognosis.We present here a new case of renal PNET in a 31-year-old female. The patients were referred
Yang, Cheng   +8 more
openaire   +2 more sources

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