Mohammad Moshref
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Explore the profile of Mohammad Moshref including associated specialties, affiliations and a list of published articles.
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13
Citations
69
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Recent Articles
1.
Moshref M, Modarresi A, Razzaghi N
J Dent (Shiraz)
. 2022 Dec;
23(3):327-335.
PMID: 36506877
Osteoblastoma is a solitary benign bone-forming neoplasm, which comprises 1% of all primary bone tumors. Multifocal benign osteoblastoma of the jaws is very rare. Osteoblastoma must be differentiated from other...
2.
Melanotic Neuroectodermal Tumor of Infancy, a Rapidly Growing Maxillary Alveolar Mass: A Case Report
Atarbashi-Moghadam S, Lotfi A, Moshref M, Atarbashi-Moghadam F
J Dent (Shiraz)
. 2020 Mar;
21(1):77-80.
PMID: 32158789
Melanotic neuroectodermal tumor of infancy is a rare, rapidly growing, painless, pigmented neoplasm with neural crest derivation. It usually occurs during the first year of life and there is a...
3.
Atarbashi-Moghadam S, Lotfi A, Moshref M, Mokhtari S
Indian J Pathol Microbiol
. 2019 Feb;
62(1):163-164.
PMID: 30706887
Sialadenoma papilliferum (SP) is a rare benign salivary gland tumor with unclear cell origin. This report presents a new case of SP of the hard palate occurring in a 50-year-old...
4.
Lotfi A, Mokhtari S, Moshref M, Shahla M, Atarbashi Moghadam S
J Dent (Shiraz)
. 2017 Jun;
18(2):149-152.
PMID: 28620640
Solitary fibrous tumor has a wide spectrum of histopathologic features and many tumors show similar microscopic features. This similarity poses diagnostic challenges to the pathologists and immunohistochemical analysis is required...
5.
Pourdanesh F, Mohamadi M, Moshref M, Soltaninia O
J Oral Maxillofac Surg
. 2015 Jul;
73(10):2067.e1-7.
PMID: 26207695
Ameloblastic fibrosarcoma is a mixed odontogenic tumor that can originate de novo or from a transformed ameloblastic fibroma. This report describes the case of a 34-year-old woman with a recurrent,...
6.
Moshref M, Lotfi A, Mashhadi-Abbas F, Kargahi N
Iran J Cancer Prev
. 2014 Sep;
7(1):53-7.
PMID: 25250149
Granulocytic Sarcoma (GS), an unusual extramedullary tumor, is composed of immature granulocytic precursor cells. The intraoral occurrence of this tumor is extremely rare. Here, we report a case of GS...
7.
Motamedi M, Lotfi A, Azizi T, Moshref M, Farhadi S
Indian J Pathol Microbiol
. 2010 Jun;
53(2):302-4.
PMID: 20551538
Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome is a rare X-linked dominant genodermatosis related to the NF kappa B essential modulator (NEMO) gene with approximately 800 cases reported worldwide. It usually...
8.
Lotfi A, Moshref M, Varshosaz M, Jaberi-Ansari S, Ghafouri A
Arch Iran Med
. 2009 Jul;
12(4):421-3.
PMID: 19566364
Maffucci's syndrome is a rare congenital mesodermal dysplasia combined with dyschondroplasia and hemangiomatosis. About 150 cases have been reported till now. Maffucci's syndrome is often combined with other neoplasms. Herein,...
9.
Motamedi M, Lotfi A, Azizi T, Moshref M
Dent Today
. 2009 Mar;
28(2):102, 104-5.
PMID: 19275079
No abstract available.
10.
Moshref M, Khojasteh A, Kazemi B, Roudsari M, Varshowsaz M, Eslami B
Am J Med Genet A
. 2008 Feb;
146A(5):644-8.
PMID: 18247420
Here, we report a family with gigantiform cementomas, bone fractures, and autosomal dominant inheritance. Lesions are composed of benign, lobulated, calcified masses resembling cementum. Identification of a COL1A2 mutation in...