Results 71 to 80 of about 14,338 (204)

Conservative multimodal management of a primitive neuroectodermal tumor of the thyroid

open access: yesRare Tumors, 2013
Primitive neuroectodermal tumors (PNET) represent 1% of sarcomas. Head and neck peripheral PNETs have an intermediate prognosis between abdominopelvic disease and extremities.
Juliette Haudebourg   +9 more
doaj   +1 more source

Ewing’s Sarcoma [PDF]

open access: yes, 2018
Ewing’s sarcoma is the second most common malignant tumor of the bone occurring in children and adolescents. Typically, patients present between the ages of 10 and 20, with the disease having a slight predilection for males.1 Tumors often arise in the ...
Fenderson, PhD, Bruce A.   +1 more
core   +1 more source

Mutations in the RB1 Gene in Argentine Retinoblastoma Patients and Uncommon Clinical Presentations [PDF]

open access: yes, 2015
Background: Retinoblastoma, the most common ocular cancer of childhood, is caused by inactivation of the RB1 tumor suppressor gene in the developing retina.
Alonso, Cristina   +6 more
core   +1 more source

Development of the neurohypophysis: A major neuroendocrine interface

open access: yesJournal of Neuroendocrinology, Volume 38, Issue 1, January 2026.
Abstract The neurohypophysis is a major central neuroendocrine interface regulating reproductive functions and water homeostasis. Distinct neurovascular cell types interact via evolutionarily conserved signaling molecules in the developing neurohypophysis, providing a model system for studying principles in neuroendocrine interface morphogenesis.
Athul R. Ramesh   +5 more
wiley   +1 more source

Primary intracranial peripheral primitive neuroectodermal tumor in an adult patient with aphasia: A rare case report

open access: yesClinical Case Reports, 2022
Primary intracranial peripheral primitive neuroectodermal tumors (pPNETs) are extremely rare malignancies that commonly affect children and adolescents. Only 10 cases over the age of 33 have been reported.
Kazem Ghaemi   +2 more
doaj   +1 more source

Ewing Family Tumors: Potential Prognostic Value of Reverse-Transcriptase Polymerase Chain Reaction Detection of Minimal Residual Disease in Peripheral Blood Samples [PDF]

open access: yes, 1998
In more than 95% of patients, the Ewing family of tumors (ET) has chimeric transcripts caused by fusion of the EWS gene to either FLI1 or ERG. The presence of specific EWS-FLI1 or EWS-ERG transcripts in peripheral blood (PB) samples of
Alava, E. (Enrique) de   +4 more
core  

Clinical, Pathological, and Surgical Outcomes for Adult Pineoblastomas [PDF]

open access: yes, 2015
Introduction Pineoblastomas are uncommon primitive neuroectodermal tumors that occur mostly in children; they are exceedingly rare in adults.
Ariai, Mohammad S.   +8 more
core   +2 more sources

Primary renal primitive neuroectodermal tumor.

open access: yesJournal of postgraduate medicine, 2015
Primitive Neuroectodermal Tumor of the kidney is a rare entity. Very few cases of primary renal PNET have been reported to date. Most literature about rPNET is isolated case reports. We report a case of rPNET in a 39-year-old male with a pre-operative diagnosis of renal cell carcinoma with renal vein thrombosis.
Goel, V   +5 more
openaire   +2 more sources

Haplótipos de diferentes SNPs no interior do gene EWS em indivíduos afetados e não-afetados pelo sarcoma de Ewing [PDF]

open access: yes, 2012
Ewing’s sarcoma was first described by James Ewing in 1921 and it is the second most common bone tumor in children and young adults. Both chromosomal breakage and translocation occur in this sarcoma.
Silva, Déborah Soares Bispo Santos
core  

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