Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Shervin Pejhan"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Primary dural Hodgkin lymphoma (PDHL) is an extremely rare subset of Hodgkin lymphoma (HL). Its existence is controversial, as Hodgkin lymphoma is not traditionally thought to arise from the central nervous system (CNS) or its meninges and o
Externí odkaz:
https://doaj.org/article/c8817d89fe654482ad266abf90922ae0
Autor:
Marjorie Buist, Nada El Tobgy, Danilo Shevkoplyas, Matthew Genung, Annan Ali Sher, Shervin Pejhan, Mojgan Rastegar
Publikováno v:
Cells, Vol 11, Iss 9, p 1442 (2022)
Eukaryotic gene expression is controlled at multiple levels, including gene transcription and protein translation initiation. One molecule with key roles in both regulatory mechanisms is methyl CpG binding protein 2 (MeCP2). MECP2 gain- and loss-of-f
Externí odkaz:
https://doaj.org/article/5bdb92bdafeb4848b4e80d2333575968
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Rett Syndrome (RTT) is a rare and progressive neurodevelopmental disorder that is caused by de novo mutations in the X-linked Methyl CpG binding protein 2 (MECP2) gene and is subjected to X-chromosome inactivation. RTT is commonly associated with neu
Externí odkaz:
https://doaj.org/article/206a236184654a22828c914682f0aecf
Autor:
Carl O. Olson, Shervin Pejhan, Daniel Kroft, Kimia Sheikholeslami, David Fuss, Marjorie Buist, Annan Ali Sher, Marc R. Del Bigio, Yehezkel Sztainberg, Victoria Mok Siu, Lee Cyn Ang, Marianne Sabourin-Felix, Tom Moss, Mojgan Rastegar
Publikováno v:
Frontiers in Genetics, Vol 9 (2018)
Rett syndrome (RTT) is a severe and rare neurological disorder that is caused by mutations in the X-linked MECP2 (methyl CpG-binding protein 2) gene. MeCP2 protein is an important epigenetic factor in the brain and in neurons. In Mecp2-deficient neur
Externí odkaz:
https://doaj.org/article/d5ec5417e1f1402e90cc3f8fa5bb1e26
Autor:
Shervin Pejhan, Mojgan Rastegar
Publikováno v:
Biomolecules, Vol 11, Iss 1, p 75 (2021)
Rett Syndrome (RTT) is a severe, rare, and progressive developmental disorder with patients displaying neurological regression and autism spectrum features. The affected individuals are primarily young females, and more than 95% of patients carry de
Externí odkaz:
https://doaj.org/article/6a8e16a883d0464d85f635bf342ad92f
Publikováno v:
Medical Journal of The Islamic Republic of Iran, Vol 22, Iss 1, Pp 52-54 (2008)
Malacoplakia is a rare chronic inflammatory disease associated with infection and immunosuppression, and very few occurrences have been reported in the bone. The authors describe the case of a 22-year-old woman with paraplegia and urinary and fecal i
Externí odkaz:
https://doaj.org/article/55c7462ba8db4d6fa833991e565c1c7b
Publikováno v:
Medical Journal of The Islamic Republic of Iran, Vol 20, Iss 3, Pp 155-157 (2006)
Malignant germ-cell tumors (MGCT) are rare tumors of childhood accounting for less than 3% of pediatric malignancies.Endodermal sinus tumor(EST)forms the most common histologic subtype of MGCT.The vagina is an extremely rare site for GCTs. An 8-month
Externí odkaz:
https://doaj.org/article/c827ce3d2dfb48acb1096980dc8175da
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 82:296-301
The COVID-19 pandemic has had a significant impact on medical services. Many countries postponed nonemergent procedures to preserve hospital resources for the unprecedented situation. Surgical backlogs caused by the COVID-19 pandemic have been evalua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac1c9b452ea1ffe84a2a4bbb97720ac0
https://doi.org/10.1093/jnen/nlad005
https://doi.org/10.1093/jnen/nlad005
We present the rare case of a 71 year old man with intracranial primary dural Hodgkin lymphoma (PDHL). He underwent subtotal resection of the mass, followed by adjuvant chemotherapy and consolidative radiotherapy, with no recurrence at 5 years follow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::093243f435e46ef2b4fc81b22ef3f4eb
https://doi.org/10.22541/au.165665564.44094402/v1
https://doi.org/10.22541/au.165665564.44094402/v1
Publikováno v:
Annals of Neurology. 90:999-1000
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b63ad62c684f96d259ac0ddb90c1cd9
https://doi.org/10.1002/ana.26234
https://doi.org/10.1002/ana.26234