Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Isa Jahanzad"'
Autor:
Farhad Shahi, Razieh Alishahi, Hossein Pashaiefar, Isa Jahanzad, Naser Kamalian, Ardeshir Ghavamzadeh, Marjan Yaghmaie
Publikováno v:
Iranian Journal of Pathology, Vol 12, Iss 3, Pp 209-217 (2017)
Background & Objective: Soft tissue sarcomas (STS) constitute an uncommon and heterogeneous group of tumors of mesenchymal origin and various cytogenetic abnormalities ranging from distinct genomic rearrangements, such as chromosomal translocations a
Externí odkaz:
https://doaj.org/article/11d39c8cb51345e5a84a4b11a28194b0
Autor:
Fereshteh Ensani, Ramesh Omranipour, Isa Jahanzad, Azadeh Jafari, Shima Nafarzadeh, Pouyan Aminishakib
Publikováno v:
Iranian Journal of Pathology, Vol 12, Iss 3, Pp 202-208 (2017)
Background &Objectives: Evaluation of estrogen receptor (ER), progesterone receptor (PR), and (human epidermal growth factor receptor-2) Her-2 on core needle biopsies (CNBs) is increasingly in use to diagnosis early breast cancer, but its concordance
Externí odkaz:
https://doaj.org/article/207599c2dab446b2ae47742c675efdd4
Autor:
Sanambar Sadighi, Mohsen Ayati, Mohammad Ali Mohagheghi, Shahriar Shahriaran, Isa Jahanzad, Somaye Safavi
Publikováno v:
Basic & Clinical Cancer Research, Vol 3, Iss 2 (2016)
Idiopathic retroperitoneal fibrosis is a rare disorder of an unknown etiology characterized by an inflammatory proliferative fibrosing process that may involve the ureters in 80-100% of cases. Â The present study was carried on a 38 years old man wh
Externí odkaz:
https://doaj.org/article/1338a837f6474b24b25280ca216e944e
Autor:
Pouyan Aminishakib, Fereshteh Ensani, Isa Jahanzad, Azadeh Jafari, Ramesh Omranipour, Shima Nafarzadeh
Publikováno v:
Iranian Journal of Pathology, Vol 12, Iss 3, Pp 202-208 (2017)
Iranian Journal of Pathology
Scopus-Elsevier
Iranian Journal of Pathology
Scopus-Elsevier
Background &Objectives: Evaluation of estrogen receptor (ER), progesterone receptor (PR), and (human epidermal growth factor receptor-2) Her-2 on core needle biopsies (CNBs) is increasingly in use to diagnosis early breast cancer, but its concordance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a1d620cf834dcb00d19b472881f4052
https://ijp.iranpath.org/article_25042_d9d52819e8185fe15f5f155b5f857544.pdf
https://ijp.iranpath.org/article_25042_d9d52819e8185fe15f5f155b5f857544.pdf
Autor:
Isa Jahanzad, Razieh Alishahi, Hossein Pashaiefar, Marjan Yaghmaie, Farhad Shahi, Ardeshir Ghavamzadeh, Naser Kamalian
Publikováno v:
Iranian Journal of Pathology, Vol 12, Iss 3, Pp 209-217 (2017)
Iranian Journal of Pathology
Iranian Journal of Pathology
Background & Objective: Soft tissue sarcomas (STS) constitute an uncommon and heterogeneous group of tumors of mesenchymal origin and various cytogenetic abnormalities ranging from distinct genomic rearrangements, such as chromosomal translocations a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6e03bb1a05e0fa48f6ffb711442e1a
https://doi.org/10.30699/ijp.2017.25043
https://doi.org/10.30699/ijp.2017.25043
Autor:
Isa Jahanzad, Sepideh Arbabi Bidgoli, Mansour Djamali Zaverhei, Bahar Yazdanmehr, Nasser Ebrahimi Daryani, Mohamadali Mohagheghi, Farid Azmoodeh Ardalan
Publikováno v:
International Journal of Cancer Research. 3:25-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff70de754baa02e56dd972821b7fedc5
https://doi.org/10.3923/ijcr.2007.25.32
https://doi.org/10.3923/ijcr.2007.25.32
Autor:
Alireza, Khoshnevisan, Sina, Abdollahzade, Isa, Jahanzad, Anoshirwan, Niknezhad, Soheil, Naderi, Masoud, Khadivi
Publikováno v:
Archives of Iranian medicine. 17(4)
Intramedullary spinal cord metastases are rare .The majority of these metastases reportedly spread from lung cancer in the cervical region; however, they have been seen to arise from a variety of other primary sources. Here, we report what is, to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dad4344722dea31ca900619d7c80d548
https://pubmed.ncbi.nlm.nih.gov/24724607
https://pubmed.ncbi.nlm.nih.gov/24724607
Autor:
Fatemeh, Mahjoub, Rana, Fereiduni, Isa, Jahanzad, Fatemeh, Farahmand, Maryam, Monajemzadeh, Mehri, Najafi
Publikováno v:
Iranian Journal of Pediatrics
Objective Wilson's disease (WD) is an autosomal recessive disease with genetic abnormality on chromosome 13 causing defect in copper metabolism and increased copper concentration in liver, central nervous system and other organs, which causes differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::069810e9a1c3b756c9a3a824b7c58bef
https://pubmed.ncbi.nlm.nih.gov/23056859
https://pubmed.ncbi.nlm.nih.gov/23056859
Publikováno v:
Iranian Journal of Pediatrics
Objective Optimum diagnosis of glomerulopathies requires light microscopy, immunofluorescence and electron microcopy. In fact electron microscopy has a confirmatory role in glomerular diseases. It provides more information for patient management and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d4362031d98b5885e3139ce5d7b1d61e
https://pubmed.ncbi.nlm.nih.gov/23056813
https://pubmed.ncbi.nlm.nih.gov/23056813
Publikováno v:
Archives of Iranian medicine. 12(2)
Familial lecithin-cholesterol acyltransferase deficiency is an uncommon autosomal recessive disorder from a heritable defect in esterification of plasma cholesterol. In 1968, the disease was described by Gjone and Norum in Norway. Our case was a 38-y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ca01a02dca5a64b7aa26c02708a3bec3
https://pubmed.ncbi.nlm.nih.gov/19249891
https://pubmed.ncbi.nlm.nih.gov/19249891