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Page 1
Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients.
Momtazmanesh S, Rayzan E, Zoghi S, Shahkarami S, Molatefi R, Mohammadzadeh I, Ghaffari J, Mahmoudi H, Dmytrus J, Segarra-Roca A, Somekh I, Witzel M, Hauck F, Boztug K, Klein C, Rezaei N. Momtazmanesh S, et al. Among authors: mahmoudi h. Endocr Metab Immune Disord Drug Targets. 2022;22(1):159-168. doi: 10.2174/1871530321666210226143912. Endocr Metab Immune Disord Drug Targets. 2022. PMID: 33634762
Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency.
Youssefian L, Saeidian AH, Tavasoli AR, Kalamati E, Naghipoor K, Hozhabrpour A, Mesdaghi M, Saffarian Z, Mahmoudi H, Nabavi M, Shokri S, Zeinali S, Béziat V, Casanova JL, Jouanguy E, Uitto J, Vahidnezhad H. Youssefian L, et al. Among authors: mahmoudi h. J Invest Dermatol. 2022 Sep;142(9):2435-2445. doi: 10.1016/j.jid.2022.02.011. Epub 2022 Mar 8. J Invest Dermatol. 2022. PMID: 35276224 Free PMC article.
Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions.
Saeidian AH, Youssefian L, Huang CY, Palizban F, Naji M, Saffarian Z, Mahmoudi H, Goodarzi A, Sotoudeh S, Vahidnezhad F, Amani M, Tavakoli N, Ajami A, Mozafarpoor S, Teimoorian M, Dorgaleleh S, Shokri S, Shenagari M, Abedi N, Zeinali S, Fortina P, Béziat V, Jouanguy E, Casanova JL, Uitto J, Vahidnezhad H. Saeidian AH, et al. Among authors: mahmoudi h. JCI Insight. 2022 Apr 22;7(8):e156021. doi: 10.1172/jci.insight.156021. JCI Insight. 2022. PMID: 35316210 Free PMC article.
Neurological diseases and bullous pemphigoid: A case-control study in Iranian patients.
Daneshpazhooh M, Khorassani J, Balighi K, Ghandi N, Mahmoudi H, Tohidinik H, Hamzelou S, Chams-Davatchi C. Daneshpazhooh M, et al. Among authors: mahmoudi h. Indian J Dermatol Venereol Leprol. 2017 Mar-Apr;83(2):195-199. doi: 10.4103/0378-6323.191132. Indian J Dermatol Venereol Leprol. 2017. PMID: 27679408 Free article.
Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa.
Vahidnezhad H, Youssefian L, Saeidian AH, Zeinali S, Touati A, Abiri M, Sotoudeh S, Norouz-Zadeh S, Amirinezhad N, Mozafari N, Daneshpazhooh M, Mahmoudi H, Hamid M, Bradfield JP, Kim CE, Hakonarson H, Uitto J. Vahidnezhad H, et al. Among authors: mahmoudi h. Exp Dermatol. 2019 Oct;28(10):1118-1121. doi: 10.1111/exd.13501. Epub 2018 Feb 19. Exp Dermatol. 2019. PMID: 29364557
Iranian guideline for rituximab therapy in pemphigus patients.
Daneshpazhooh M, Balighi K, Mahmoudi H, Tavakolpour S, Abedini R, Soori T, Ehsani AH, Ghiasi M, Noormohammadpour P, Ghandi N, Lajevardi V, Sadeghinia A, Nasimi M, Azizpour A, Chams-Davatchi C. Daneshpazhooh M, et al. Among authors: mahmoudi h. Dermatol Ther. 2019 Sep;32(5):e13016. doi: 10.1111/dth.13016. Epub 2019 Jul 24. Dermatol Ther. 2019. PMID: 31269316 Review.
Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.
Youssefian L, Saeidian AH, Palizban F, Bagherieh A, Abdollahimajd F, Sotoudeh S, Mozafari N, Farahani RA, Mahmoudi H, Babashah S, Zabihi M, Zeinali S, Fortina P, Salas-Alanis JC, South AP, Vahidnezhad H, Uitto J. Youssefian L, et al. Among authors: mahmoudi h. Clin Chem. 2021 Jun 1;67(6):876-888. doi: 10.1093/clinchem/hvab042. Clin Chem. 2021. PMID: 33969388 Free PMC article.
Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.
Vahidnezhad H, Youssefian L, Saeidian AH, Ziaee V, Mahmoudi H, Parvaneh N, Ashjaei B, Shahrokh S, Kamyab Hesari K, Soltani Zangbar M, Yousefi M, Zeinali S, Uitto J. Vahidnezhad H, et al. Among authors: mahmoudi h. JAMA Dermatol. 2021 Dec 1;157(12):1466-1471. doi: 10.1001/jamadermatol.2021.3899. JAMA Dermatol. 2021. PMID: 34643647 Free PMC article.
306 results