نتائج البحث - "Vahidnezhad H."

1

Academic Journal

FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

المؤلفون: Momenilandi, M, Levy, R, Sobrino, S, Li, JW, Lagresle-Peyrou, C, Esmaeilzadeh, H, Fayand, A, Le Floc'h, C, Guerin, A, Della Mina, E, Shearer, D, Delmonte, OM, Yatim, A, Mulder, K, Mancini, M, Rinchai, D, Denis, A, Neehus, AL, Balogh, K, Brendle, S, Rokni-Zadeh, H, Changi-Ashtiani, M, Seeleuthner, Y, Deswarte, C, Bessot, B, Cremades, C, Materna, M, Cederholm, A, Ogishi, M, Philippot, Q, Beganovic, O, Ackermann, M, Wuyts, M, Khan, T, Fouere, S, Herms, F, Chanal, J, Palterer, B, Bruneau, J, Molina, TJ, Leclerc-Mercier, S, Pretet, JL, Youssefian, L, Vahidnezhad, H, Parvaneh, N, Claeys, KG, Schrijvers, R, Luka, M, Perot, P, Fourgeaud, J, Nourrisson, C, Poirier, P, Jouanguy, E, Boisson-Dupuis, S, Bustamante, J, Notarangelo, LD, Christensen, N, Landegren, N, Abel, L, Marr, N, Six, E, Langlais, D, Waterboer, T, Ginhoux, F, Ma, CS, Tangye, SG, Meyts, I, Lachmann, N, Hu, J, Shahrooei, M, Bossuyt, X, Casanova, JL, Beziat, V

المصدر: Cell. 187(11):2817

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:159710469

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2

Academic Journal

876 Loss-of-function EGFR mutation in bartter syndrome with neonatal epithelial autoinflammation

المؤلفون: Youssefian, L., Saeidian, A., Kalamati, E., Hakonarson, H., Vahidnezhad, F., Uitto, J., McGrath, J.A., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 143, issue 5, page S150 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2023.03.886
https://api.elsevier.com/content/article/PII:S0022202X23010618?httpAccept=text/xml
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3

Academic Journal

640 Treatment of recalcitrant cutaneous warts with intralesional injection of HBV vaccine

المؤلفون: Nobari, N. Najar, Keyvani, H., Goodarzi, A., Keramati, H., Nobari, M. Najar, Shahrbabaki, M. Salehi, Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 143, issue 5, page S109 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2023.03.647
https://api.elsevier.com/content/article/PII:S0022202X23008229?httpAccept=text/xml
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4

Academic Journal

044 Metatranscriptomics reveals association of α-, β-, and γ-HPVs with typical epidermodysplasia verruciformis in a large cohort of patients with CIB1, TMC6, or TMC8 mutations

المؤلفون: Saeidian, A., Youssefian, L., Béziat, V., Casanova, J., Jouanguy, E., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 12, page S188 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.09.053
https://api.elsevier.com/content/article/PII:S0022202X2201987X?httpAccept=text/xml
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5

Academic Journal

310 Metatranscriptomics detects emerging multidrug-resistant Candida auris in a family with a mild TP63-associated ectodermal dysplasia

المؤلفون: Youssefian, L., Park, J.S., Samii, R., Palizban, F., Balighi, K., Saeidian, A., Kalamati, E., Khodavaisy, S., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 12, page S233 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.09.322
https://api.elsevier.com/content/article/PII:S0022202X22022564?httpAccept=text/xml
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6

Academic Journal

055 Whole-transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

المؤلفون: Youssefian, L., Saeidian, A., Saffarian, Z., Vahidnezhad, F., Ariamanesh, M., Béziat, V., Jouanguy, E., Casanova, J., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 12, page S190 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.09.064
https://api.elsevier.com/content/article/PII:S0022202X22019984?httpAccept=text/xml
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7

Academic Journal

307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis

المؤلفون: Vahidnezhad, H., Saffarian, Z., Youssefian, L., Tavasoli, A., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 12, page S233 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.09.319
https://api.elsevier.com/content/article/PII:S0022202X22022539?httpAccept=text/xml
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8

Academic Journal

301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa

المؤلفون: Vahidnezhad, H., Youssefian, L., Tavasoli, A., Harvey, N., Mahmoudi, H., Kalamati, E., Varghaei, A., Vahidnezhad, F., Saeidian, A., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 12, page S232 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.09.313
https://api.elsevier.com/content/article/PII:S0022202X22022473?httpAccept=text/xml
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9

Academic Journal

497 Genetic variability of viral and human genomes in a large cohort of patients with typical epidermodysplasia verruciformis

المؤلفون: Saeidian, A., Youssefian, L., Mahmoudi, H., Mansouri, P., Béziat, V., Casanova, J., Jouanguy, E., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S84 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.506
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10

Academic Journal

258 Prevalence of autosomal recessive genodermatoses: Determination based on pathogenic sequence variants in publicly available exomic and genomic databases

المؤلفون: Huang, C., Saeidian, A., Youssefian, L., Vahidnezhad, H., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S44 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.265
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11

Academic Journal

489 Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S83 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.498
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12

Academic Journal

494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation

المؤلفون: Tavasoli, A., Vahidnezhad, H., Youssefian, L., Saeidian, A., Rouhani, M., Nilipour, Y., Mahmoudi, H., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S84 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.503
https://api.elsevier.com/content/article/PII:S0022202X22009447?httpAccept=text/xml
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13

Academic Journal

309 Losartan treatment improves recessive dystrophic Epidermolysis bullosa

المؤلفون: Pourani, M., Vahidnezhad, H., Youssefian, L., Rakhshan, A., Hajimoradi, B., Abdollahimajd, F., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S53 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.317
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14

Academic Journal

491 Recalcitrant cutaneous warts in a family with inherited ICOS deficiency

المؤلفون: Youssefian, L., Saeidian, A., Tavasoli, A., Kalamati, E., Naghipoor, K., Hojabrpour, A., Mesdaghi, M., Saffarian, Z., Mahmoudi, H., Nabavi, M., Shokri, S., Zeinali, S., Béziat, V., Casanova, J., Jouanguy, E., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S83 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.500
https://api.elsevier.com/content/article/PII:S0022202X22009411?httpAccept=text/xml
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15

Academic Journal

495 Mutations in different domains of bullous pemphigoid antigen-1 (BPGA1) encoded by DST result in either epidermolysis bullosa simplex or musculoskeletal and neuronal deformities-associated HSAN-VI

المؤلفون: Harvey, N., Khalesi, R., Garshasbi, M., Kalamati, E., Youssefian, L., Vahidnezhad, H., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S84 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.504
https://api.elsevier.com/content/article/PII:S0022202X22009459?httpAccept=text/xml
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16

Academic Journal

493 Chronic mucocutaneous candidiasis due to Candida auris and non-albicans Candida species in a family with a mild TP63-associated ectodermal dysplasia

المؤلفون: Park, J., Youssefian, L., Khodavaisy, S., Palizban, F., Tavasoli, A., Kalamati, E., Mahmoudi, H., Balighi, K., Mesdaghi, M., Saeidian, A., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 142, issue 8, page S84 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2022.05.502
https://api.elsevier.com/content/article/PII:S0022202X22009435?httpAccept=text/xml
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17

Academic Journal

185 GJB2 mutations in patients with ichthyosis follicularis and histopathology of porokeratotic adnexal ostial nevus

المؤلفون: Youssefian, L., Abdollahimajd, F., Naji, M., Rajabi, F., Mahmoudi, H., Kamyab Hesari, K., Ghalamkarpour, F., Zabihi, M., Teimoorian, M., Zeinali, S., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 141, issue 5, page S33 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2021.02.205
https://api.elsevier.com/content/article/PII:S0022202X21004309?httpAccept=text/xml
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18

Academic Journal

184 Whole-transcriptome analysis by RNA-Seq for genetic diagnosis of Mendelian skin disorders in the context of consanguinity

المؤلفون: Youssefian, L., Saeidian, A., Fortina, P., South, A., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 141, issue 5, page S32 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2021.02.204
https://api.elsevier.com/content/article/PII:S0022202X21004292?httpAccept=text/xml
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19

Academic Journal

186 Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation

المؤلفون: Vahidnezhad, H., Youssefian, L., Touati, A., Saeidian, A., Harvey, N., Zabihi, M., Barzegar, M., Sotoudeh, S., Liu, L., Guy, A., Kariminejad, A., Zeinali, S., Boyden, L., Choate, K., McGrath, J.A., Uitto, J.

المصدر: Journal of Investigative Dermatology ; volume 141, issue 5, page S33 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2021.02.206
https://api.elsevier.com/content/article/PII:S0022202X21004310?httpAccept=text/xml
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20

Academic Journal

172 Inherited STK4/MST1 deficiency in two unrelated families with atypical epidermodysplasia verruciformis

المؤلفون: Saeidian, A., Youssefian, L., Sotoudeh, S., Goodarzi, A., Mahmoudi, H., Yousefi, M., Zeinali, S., Casanova, J., Jouanguy, E., Uitto, J., Vahidnezhad, H.

المصدر: Journal of Investigative Dermatology ; volume 141, issue 5, page S30 ; ISSN 0022-202X

الاتاحة: http://dx.doi.org/10.1016/j.jid.2021.02.192
https://api.elsevier.com/content/article/PII:S0022202X21004176?httpAccept=text/xml
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