Vahidnezhad H - Search Results

1

Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.

Youssefian L, Vahidnezhad H, Yousefi M, Saeidian AH, Azizpour A, Touati A, Nikbakht N, Hesari KK, Adib-Sereshki MM, Zeinali S, Mansoori B, Jazayeri A, Karamzadeh R, Fortina P, Jouanguy E, Casanova JL, Uitto J. Youssefian L, et al. Among authors: vahidnezhad h. Clin Infect Dis. 2019 May 17;68(11):1938-1941. doi: 10.1093/cid/ciy942. Clin Infect Dis. 2019. PMID: 30778533 Free PMC article.

2

Modeling breast acini in tissue culture for detection of malignant phenotype reversion to non-malignant phenotype.

Vahidnezhad H, Youssefian L, Jeddi-Tehrani M, Akhondi MM, Rabbani H, Shokri F, Tabrizi M. Vahidnezhad H, et al. Iran Biomed J. 2009 Oct;13(4):191-8. Iran Biomed J. 2009. PMID: 19946344 Free article.

3

BMI1 and TWIST1 downregulated mRNA expression in basal cell carcinoma.

Rajabpour FV, Raoofian R, Youssefian L, Vahidnezhad H, Shahshahani MM, Fathi H, Noormohammadpour P, Hesari KK, Hashemzadeh-Chaleshtori M, Tabrizi M. Rajabpour FV, et al. Among authors: vahidnezhad h. Asian Pac J Cancer Prev. 2014;15(8):3797-800. doi: 10.7314/apjcp.2014.15.8.3797. Asian Pac J Cancer Prev. 2014. PMID: 24870796 Free article.

4

Lipoid proteinosis: phenotypic heterogeneity in Iranian families with c.507delT mutation in ECM1.

Youssefian L, Vahidnezhad H, Daneshpazhooh M, Abdollahzadeh S, Talari H, Khoshnevisan A, Chams-Davatchi C, Mobasher R, Li Q, Uitto J, Akhondzadeh S, Tabrizi M. Youssefian L, et al. Among authors: vahidnezhad h. Exp Dermatol. 2015 Mar;24(3):220-2. doi: 10.1111/exd.12620. Exp Dermatol. 2015. PMID: 25529926

5

The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.

Youssefian L, Vahidnezhad H, Barzegar M, Li Q, Sotoudeh S, Yazdanfar A, Ehsani AH, Kajbafzadeh AM, Mozafari N, Ebrahimi Daryani N, Agha-Hosseini F, Zeinali S, Uitto J. Youssefian L, et al. Among authors: vahidnezhad h. J Invest Dermatol. 2015 May;135(5):1447-1450. doi: 10.1038/jid.2015.9. Epub 2015 Jan 19. J Invest Dermatol. 2015. PMID: 25599393 Free article. No abstract available.

6

Fibroadipose hyperplasia versus Proteus syndrome: segmental overgrowth with a mosaic mutation in the PIK3CA gene.

Youssefian L, Vahidnezhad H, Baghdadi T, Ghaznavi A, Li Q, Tabrizi M, Uitto J. Youssefian L, et al. Among authors: vahidnezhad h. J Invest Dermatol. 2015 May;135(5):1450-1453. doi: 10.1038/jid.2015.15. Epub 2015 Jan 23. J Invest Dermatol. 2015. PMID: 25602158 Free article. No abstract available.

7

Infantile systemic hyalinosis in an Iranian family with a mutation in the CMG2/ANTXR2 gene.

Vahidnezhad H, Ziaee V, Youssefian L, Li Q, Sotoudeh S, Uitto J. Vahidnezhad H, et al. Clin Exp Dermatol. 2015 Aug;40(6):636-9. doi: 10.1111/ced.12616. Epub 2015 Mar 7. Clin Exp Dermatol. 2015. PMID: 25754064

8

Klippel-Trenaunay syndrome belongs to the PIK3CA-related overgrowth spectrum (PROS).

Vahidnezhad H, Youssefian L, Uitto J. Vahidnezhad H, et al. Exp Dermatol. 2016 Jan;25(1):17-9. doi: 10.1111/exd.12826. Epub 2015 Oct 13. Exp Dermatol. 2016. PMID: 26268729

9

Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities.

Vahidnezhad H, Yousseﬁan L, Uitto J. Vahidnezhad H, et al. J Invest Dermatol. 2016 Jan;136(1):15-23. doi: 10.1038/JID.2015.331. J Invest Dermatol. 2016. PMID: 26763419 Free article. Review.

10

Genotypic Heterogeneity and the Mode of Inheritance in Epidermolysis Bullosa.

Uitto J, Vahidnezhad H, Youssefian L. Uitto J, et al. Among authors: vahidnezhad h. JAMA Dermatol. 2016 May 1;152(5):517-20. doi: 10.1001/jamadermatol.2015.5237. JAMA Dermatol. 2016. PMID: 26817964 No abstract available.

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