Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Kaveh Jaseb"'
Autor:
Kaveh Jaseb, Mohammad Ali Khaksar, Zahra Mansouri, Bahar Barani, Maryam Ghashghaeepour, Majid Ghanavat, Bahar Jaseb, Pedram Poorchini
Publikováno v:
Iranian Journal of Medical Sciences, Vol 47, Iss 6, Pp 612-614 (2022)
Bloodstream infections (BSIs) and subsequent development of antimicrobial resistance are life-threatening conditions in hematologic oncology patients.
Externí odkaz:
https://doaj.org/article/37665968a4b34ef893091a6f9d1b5ce8
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1279-1282 (2021)
Key Clinical Message The accurate diagnosis of Kikuchi‐Fujimoto disease can protect children from unnecessary diagnostic procedures and treatments. Also, the co‐occurrence of rare diseases with other diseases can improve or worsen the symptoms of
Externí odkaz:
https://doaj.org/article/1de113aa605d43f5a037250e8cc67642
Autor:
Kaveh Jaseb, Ehsan Ghaedi, Mohadeseh Shahin, Majid Mirmohamadkhani, Parisa Javadian, Sabahat Haghi
Publikováno v:
Journal of Nephropharmacology, Vol 7, Iss 2, Pp 74-79 (2018)
Introduction: Methotrexate (MTX) is the most generally administered antimetabolite in pediatric cancers. Renal excretion is the major route of elimination of MTX. However, renal toxicity and delayed MTX elimination is a particular concern and direct
Externí odkaz:
https://doaj.org/article/5a05cf25593a450c93eddac77144db13
Autor:
Kaveh Jaseb, Daryush Purrahman, Saeid Shahrabi, Majid Ghanavat, Hadi Rezaeean, Najmaldin Saki
Publikováno v:
Oncology Reviews, Vol 13, Iss 1 (2019)
Aberrant expression of CD5 (as a T-cell marker) is seen in some leukemia and lymphoma of B lineage origin. Given that the signaling resulting from the expression of this marker plays an essential role in the development of leukemia and lymphoma, eval
Externí odkaz:
https://doaj.org/article/1c7da14734d8448cb798d8b64a884536
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 7, Iss 3, Pp 46-53 (2013)
Objective: The use of fetal hemoglobin (HbF) inducer drugs is considered as a novel approach in treatment of β-hemoglobinopathies, especially β- thalassemia and sickle cell disease. HbF inducers including hydroxyurea, histone deacetylase (HDAC) inh
Externí odkaz:
https://doaj.org/article/ee94c8037bf341fe828390eeb22938d8
Autor:
Ali Dehghanifard, Mohammad Shahjahani, Hamid Galehdari, Fakher Rahim, Fatemeh Hamid, Kaveh Jaseb, Asnafi Ali Amin, Mohammad Ali Jalalifar, Najmaldin Saki
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 7, Iss 2, Pp 17-22 (2013)
Background: Hemoglobinopathy and thalassemia are prevalent genetic disorders throughout the world. Beta thalassemia is one of these disorders with high prevalence in Iran, especially in Khuzestan province. In this study, the rate of different mutatio
Externí odkaz:
https://doaj.org/article/166e03ed48944cb2ab0e1e95373720c8
Publikováno v:
Middle East Journal of Cancer, Vol 2, Iss 1, Pp 33-36 (2011)
Neuroblastoma is the most common extracranial solid tumor in children. The cooccurrence of neuroblastoma and acute lymphoblastic leukemia is rare. We report a rare case of advanced-stage neuroblastoma in a 3.5-year-old girl that was accompanied by ac
Externí odkaz:
https://doaj.org/article/b2734191f13d47f38c8993a5a6011268
Autor:
Sajedeh Saeidi, Kaveh Jaseb, Ali Amin Asnafi, Fakher Rahim, Fatemeh Pourmotahari, Samira Mardaniyan, Homayon Yousefi, Arash Alghasi, Mohammad Shahjahani, Najmaldin Saki
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 8, Iss 3 (2014)
Background: Immune thrombocytopenic purpura (ITP) is an autoimmune disease that can cause bleeding disorders in patients, and presents in acute and chronic forms. The acute form is frequently seen in children, but the chronic form mainly inflicts adu
Externí odkaz:
https://doaj.org/article/052185fa30f541b8b40bf3a025d8e8aa
Autor:
Ahmad Ahmadzadeh, Saeid Shahrabi, Kaveh Jaseb, Fatemeh Norozi, Mohammad Shahjahani, Tina Vosoughi, Saeideh Hajizamani, Najmaldin Saki
Publikováno v:
Oncology Reviews, Vol 8, Iss 2 (2014)
BRAF is a serine/threonine kinase with a regulatory role in the mitogen-activated protein kinase (MAPK) signaling pathway. A mutation in the RAF gene, especially in BRAF protein, leads to an increased stimulation of this cascade, causing uncontrolled
Externí odkaz:
https://doaj.org/article/01b9962c8c834f54bf8dd092c76ddfd7
Publikováno v:
Basic & Clinical Cancer Research, Vol 6, Iss 3 (2014)
Introduction: Acute leukemia is the most common malignancy in children and acute lymphoblastic leukemia (ALL) accounts for 75% of acute leukemia cases. New treatment protocols have resulted in complete remission rates up to nearly 100% in children wi
Externí odkaz:
https://doaj.org/article/8bd22e95ad1b473a90432ec01814d31c