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Duchenne muscular dystrophy: an updated review of common available therapies.
Int J Neurosci. 2018 Sep;128(9):854-864. doi: 10.1080/00207454.2018.1430694. Epub 2018 Feb 5.
Int J Neurosci. 2018.
PMID: 29351004
Review.
PD-1/PD-L1 pathway: Basic biology and role in cancer immunotherapy.
Salmaninejad A, Valilou SF, Shabgah AG, Aslani S, Alimardani M, Pasdar A, Sahebkar A.
Salmaninejad A, et al. Among authors: valilou sf.
J Cell Physiol. 2019 Aug;234(10):16824-16837. doi: 10.1002/jcp.28358. Epub 2019 Feb 19.
J Cell Physiol. 2019.
PMID: 30784085
Review.
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Tumor-associated macrophages: role in cancer development and therapeutic implications.
Salmaninejad A, Valilou SF, Soltani A, Ahmadi S, Abarghan YJ, Rosengren RJ, Sahebkar A.
Salmaninejad A, et al. Among authors: valilou sf.
Cell Oncol (Dordr). 2019 Oct;42(5):591-608. doi: 10.1007/s13402-019-00453-z. Epub 2019 May 29.
Cell Oncol (Dordr). 2019.
PMID: 31144271
Review.
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PTPN22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus.
Bahrami T, Valilou SF, Sadr M, Soltani S, Salmaninejad A, Soltaninejad E, Yekaninejad MS, Ziaee V, Rezaei N.
Bahrami T, et al. Among authors: valilou sf.
Fetal Pediatr Pathol. 2020 Feb;39(1):13-20. doi: 10.1080/15513815.2019.1630873. Epub 2019 Jun 24.
Fetal Pediatr Pathol. 2020.
PMID: 31232672
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First Report of Congenital Short Bowel Syndrome in an Iranian Patient Caused by a Mutation in the CLMP Gene.
Gharesouran J, Esfahani BS, Valilou SF, Moradi M, Mousavi MH, Rezazadeh M.
Gharesouran J, et al. Among authors: valilou sf.
J Pediatr Genet. 2019 Jun;8(2):73-80. doi: 10.1055/s-0038-1675339. Epub 2018 Oct 26.
J Pediatr Genet. 2019.
PMID: 31061750
Free PMC article.
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Eighth case of Li-Campeau syndrome in a Turkish patient caused by a novel pathogenic variant in UBR7 and expanding the phenotype.
Edizadeh M, Kaymakcalan H, Valilou SF, Şahin Y.
Edizadeh M, et al. Among authors: valilou sf.
Am J Med Genet A. 2023 May;191(5):1465-1469. doi: 10.1002/ajmg.a.63146. Epub 2023 Feb 9.
Am J Med Genet A. 2023.
PMID: 36757286
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