Results 11 to 20 of about 95,175 (328)

Teratoma congênito de orofaringe: relato de caso Oropharyngeal congenital teratoma: a case report [PDF]

open access: yesRevista Brasileira de Ginecologia e Obstetrícia, 2005
O teratoma congênito de orofaringe é o tipo mais raro de teratoma, compreendendo apenas 2% desses tumores fetais. O diagnóstico deve ser realizado o mais precocemente possível, preferencialmente durante o pré-natal.
Yuri Seguchi Chaves   +6 more
doaj   +5 more sources

Teratoma of the tongue [PDF]

open access: bronzeCancer, 1966
A. Pidd Miller, Jon B. Owens
openalex   +4 more sources

Brain teratoma in a free-ranging mallard (Anas platyrhynchos) ˗ case report [PDF]

open access: yesArquivo Brasileiro de Medicina Veterinária e Zootecnia, 2021
Teratoma is a rare neoplasia with differentiation in two or three germ cell lines. Intracranial teratoma in birds has rarely been reported, especially affecting the brain.
C.H. Santana   +8 more
doaj   +1 more source

Mature Cystic Teratoma: An Integrated Review

open access: yesInternational Journal of Molecular Sciences, 2023
Ovarian dermoid cysts, also called mature cystic teratomas (MCTs), account for 69% of ovarian germ cell tumors in young women. The tumors are formed by tissues derived from three germ layers, and sebaceous materials are most commonly seen.
Luping Cong   +5 more
semanticscholar   +1 more source

Long-Term Prognosis of Patients With Anti-N-Methyl-D-Aspartate Receptor Encephalitis Who Underwent Teratoma Removal: An Observational Study

open access: yesFrontiers in Neurology, 2022
ObjectiveThis study aimed to evaluate the clinical characteristics and long-term surgical outcomes of patients with anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis with teratoma.MethodsPatients who were admitted to West China Hospital from June ...
Hesheng Zhang   +5 more
doaj   +1 more source

The Association of Ovarian Teratoma and Anti-N-Methyl-D-Aspartate Receptor Encephalitis: An Updated Integrative Review

open access: yesInternational Journal of Molecular Sciences, 2021
Ovarian teratomas are by far the most common ovarian germ cell tumor. Most teratomas are benign unless a somatic transformation occurs. The designation of teratoma refers to a neoplasm that differentiates toward somatic-type cell populations.
Cheng-Yang Wu   +2 more
semanticscholar   +1 more source

Risk of epilepsy in gonadal teratoma: a nationwide population-based study

open access: yesScientific Reports, 2023
Epilepsy is a common neurological disease. Systemic tumors are associated with an increased risk of epileptic events. Paraneoplastic encephalitis related to gonadal teratoma is frequently accompanied by seizures and life-threatening status epilepticus ...
Seonghoon Kim   +6 more
doaj   +1 more source

Metastatic Mature Teratoma and Growing Teratoma Syndrome in Patients with Testicular Non-Seminomatous Germ Cell Tumors

open access: yesKorean Journal of Radiology, 2021
Metastatic mature teratoma is a common radiologic and histopathologic finding after chemotherapy for metastatic non-seminomatous germ cell tumors. The leading theory for these residual tumors is the selective chemotherapy resistance of teratomas versus ...
Daniel B. Green   +4 more
semanticscholar   +1 more source

Serum Small RNA Sequencing and miR-375 Assay Do Not Identify the Presence of Pure Teratoma at Postchemotherapy Retroperitoneal Lymph Node Dissection

open access: yesEuropean Urology Open Science, 2021
Existing tumor markers for testicular germ cell tumor (TGCT) cannot detect the presence of pure teratoma. Serum miRNAs have strong performance detecting other subtypes of TGCT. Previous reports suggest high levels of miR-375 expression in teratoma tissue.
John T. Lafin   +22 more
doaj   +1 more source

Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome [PDF]

open access: yes, 2018
Smith-Magenis syndrome (SMS) is a complex genetic disorder characterized by developmental delay, behavioural problems and circadian rhythm dysregulation. About 90% of SMS cases are due to a 17p11.2 deletion containing retinoic acid induced1 (RAI1) gene,
Altieri, Filomena   +12 more
core   +9 more sources

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