Zobrazeno 1 - 10
of 65
pro vyhledávání: '"Samin Alavi"'
Publikováno v:
Clinical Case Reports, Vol 12, Iss 5, Pp n/a-n/a (2024)
Key Clinical Message Seckel syndrome is a rare autosomal recessive disorder, characterized by growth retardation and multiple anomalies associated with CNS vasculopathy. We describe a child with Seckel syndrome who developed a stroke due to non‐moy
Externí odkaz:
https://doaj.org/article/ce9bf69eeda543f5aa264293ebd98ca8
Autor:
Mohammad Kazemian, Minoo Fallahi, Seyed Hossein Fakhraee, Samin Alavi, Naeeme Taslimi Taleghani, Sara Sani
Publikováno v:
Iranian Journal of Neonatology, Vol 9, Iss 4, Pp 84-87 (2018)
Background: Osteopetrosisis an inherited and rare bone disease, characterized by the impairment ofbone modeling and remodeling and the failure of osteoclasts to resorb bone. It also results in skeletal fragility despite increased bone mass, and may c
Externí odkaz:
https://doaj.org/article/ffed19dcc8b64e6db780f244645e03c5
Publikováno v:
Iranian Journal of Otorhinolaryngology, Vol 28, Iss 2, Pp 153-157 (2016)
Introduction: Pleomorphic adenoma is a rare benign salivary gland neoplasm in children, which can be treated by simple excision. This tumor is rarely included in the differential diagnosis of solid submandibular masses in children. In the neonates, c
Externí odkaz:
https://doaj.org/article/874cd1ea69a54b6a8a6fce33c03389b5
Autor:
Samin Alavi, Nahid Arabi, Mohammad Kaji Yazdi, Mohammad Taghi Arzanian, Farahnaz Zohrehbandian
Publikováno v:
Iranian Journal of Medical Sciences, Vol 40, Iss 5, Pp 461-464 (2015)
Human parvovirus (HPV) B19 induced aplastic crisis in a family leading to the diagnosis of hereditary spherocytosis (HS) is a very rare condition being barely reported in the literature. We herein report a 4-year-old girl, her brother, and their moth
Externí odkaz:
https://doaj.org/article/1077f002e58d4295a12146cc55f1f611
Publikováno v:
Iranian Journal of Medical Sciences, Vol 40, Iss 4, Pp 381-385 (2015)
Pyoderma vegetans (PV) is a rare inflammatory disorder characterized by vegetating pustules and plaques affecting the skin and mucosal membranes. It is believed that this entity is mostly associated with inflammatory bowel disease (IBD), chronic maln
Externí odkaz:
https://doaj.org/article/9d98dfebfd7a4780a5a7c79710ab0cd2
Autor:
Roxana Azma, Samin Alavi, Maliheh Khoddami, Mohammad Taghi Arzanian, Armin Nourmohammad, Sadaf Esteghamati
Publikováno v:
Korean Journal of Pediatrics, Vol 57, Iss 11, Pp 500-504 (2014)
Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor of intermediate malignancy with resemblance to Kaposi sarcoma. It occurs predominantly in pediatric age groups as a cutaneous lesion with focal infiltration into the a
Externí odkaz:
https://doaj.org/article/ffad2af673814cbd94867ffde893802d
Autor:
Kourosh Goudarzi Pour, Samin Alavi, Shahin Shamsian, Roxana Aghakhani, Mohammad Taghi Arzanian, Hesameddin Hoseini Tavassol, Zahra Eydian, Reyhaneh Kazemi
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 10, Iss 4 (2016)
Treatment with intensification of chemotherapy using alkylating agents and Topoisomerase II inhibitors and radiotherapy has improved the outcome of patients with solid tumors such as Ewing’s sarcoma. However, there are several reports of secondary
Externí odkaz:
https://doaj.org/article/1fd59fd692f54fc0a1ecd0895cc4deee
Autor:
Samin Alavi, Ali Kord Valeshabad, Zohreh Sharifi, Kazem Nourbakhsh, Mohammad Taghi Arzanian, Masoumeh Navidinia, Siamak Mehdizadeh Seraj
Publikováno v:
Turkish Journal of Hematology, Vol 29, Iss 2, Pp 156-161 (2012)
OBJECTIVE: Torque teno virus (TTV) infects patients at risk for parenteral exposure and chronic blood transfusion, such as those with β-thalassemic. This study aimed to assess the prevalence of TTV infection and co-infection of TTV and hepatitis C v
Externí odkaz:
https://doaj.org/article/ee8c4aa942e74eb4b5e82d3568e8f94e
Autor:
Kourosh Goudarzipour, Shahin Shamsian, Samin Alavi, Kazem Nourbakhsh, Roxana Aghakhani, Zahra Eydian, Mohammad Taghi Arzanian
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 9, Iss 2 (2015)
Introduction: Ewing’s sarcoma is the second most common primary malignant tumor of bone found in children after Osteosarcoma. It accounts for 4–9% of primary malignant bone tumors and it affects bones of the skull or face in only 1–4% of cases.
Externí odkaz:
https://doaj.org/article/77db14f782414249a9ae4dd0751753d9
Publikováno v:
Iranian Journal of Blood and Cancer, Vol 8, Iss 1, Pp 25-26 (2016)
Externí odkaz:
https://doaj.org/article/ce3503995008446c88da0dbb0370b2be