Works by Vahidnezhad, Hassan

Results: 66

Role of non-coding RNAs in human-papillomavirus-associated cutaneous neoplasms.

Published in:

Archives of Virology, 2025, v. 170, n. 8, p. 1, doi. 10.1007/s00705-025-06335-0

By:

Faraji, Niloofar;
Vahidnezhad, Hassan;
Eslami, Narges;
Zeinali, Tahereh;
Shenagari, Mohammad;
Shanehbandi, Dariush;
Barfejani, Arnavaz Hajizadeh

Publication type:

Article

Ichthyosis follicularis syndromes in patients with mutations in GJB2.

Published in:

Clinical & Experimental Dermatology, 2022, v. 47, n. 8, p. 1561, doi. 10.1111/ced.15217

By:

Youssefian, Leila;
Naji, Mahtab;
Park, Jason S.;
Rajabi, Fateme;
Abdollahimajd, Fahimeh;
Mahmoudi, Hamidreza;
Kamyab‐Hesari, Kambiz;
Ghalamkarpour, Fariba;
Zabihi, Masoud;
Teimoorian, Mehrdad;
Youssefian, Laya;
Zeinali, Sirous;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Integration of GWAS, QTLs and keratinocyte functional assays reveals molecular mechanisms of atopic dermatitis.

Published in:

Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-58310-7

By:

Oliva, Meritxell;
Sarkar, Mrinal K.;
March, Michael E.;
Saeidian, Amir Hossein;
Mentch, Frank D.;
Hsieh, Chen-Lin;
Tang, Fanying;
Uppala, Ranjitha;
Patrick, Matthew T.;
Li, Qinmengge;
Bogle, Rachael;
Kahlenberg, J. Michelle;
Watson, Deborah;
Glessner, Joseph T.;
Youssefian, Leila;
Vahidnezhad, Hassan;
Tsoi, Lam C.;
Hakonarson, Hakon;
Gudjonsson, Johann E.;
Smith, Kathleen M.

Publication type:

Article

Clinical Characteristics of Coronavirus Disease 2019 in a Cohort of Iranian Patients: Olfactory Dysfunction as a Frequent Clinical Presentation.

Published in:

Indian Journal of Forensic Medicine & Toxicology, 2021, v. 15, n. 2, p. 1768, doi. 10.37506/ijfmt.v15i2.14594

By:

Kamali, Alireza;
Ebadi, Mehrnoosh;
Vahidnezhad, Hassan;
Mohammadi, Alireza;
Dalvandi, Mohsen

Publication type:

Article

Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug‐induced associations.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2023, v. 37, n. 1, p. 47, doi. 10.1111/jdv.18608

By:

Park, Jason S.;
Saeidian, Amir H.;
Youssefian, Leila;
Hsu, Sylvia;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients.

Published in:

2019

By:

Guerrero-Aspizua, Sara;
Conti, Claudio J.;
Escamez, Maria Jose;
Castiglia, Daniele;
Zambruno, Giovanna;
Youssefian, Leila;
Vahidnezhad, Hassan;
Requena, Luis;
Itin, Peter;
Tadini, Gianluca;
Yordanova, Ivelina;
Martin, Ludovic;
Uitto, Jouni;
Has, Cristina;
Del Rio, Marcela

Publication type:

journal article

Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and In Silico Analysis.

Published in:

Clinical Genetics, 2025, v. 107, n. 3, p. 366, doi. 10.1111/cge.14658

By:

Biglari, Sajjad;
Nikuei, Pooneh;
Mir, Atefeh;
Vahidnezhad, Hassan;
Youssefian, Leila;
Moghaddam, Atefeh Sohanforooshan;
Tabatabaiefar, Mohammad Amin;
Saeidian, Amir Hossein;
Khorram, Erfan;
Fard, Mohammad Ali Farazi;
Farbood, Zahra;
Shahrooei, Mohammad;
Khorshid, Hamid Reza Khorram;
Esmaeilzadeh, Emran

Publication type:

Article

Correction: Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.

Published in:

Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02794-3

By:

Dehnavi, Ali Zare;
Bemanalizadeh, Maryam;
Kahani, Seyyed Mohammad;
Ashrafi, Mahmoud Reza;
Rohani, Mohammad;
Toosi, Mehran Beiraghi;
Heidari, Morteza;
Hosseinpour, Sareh;
Amini, Behnam;
Zokaei, Shaghayegh;
Rezaei, Zahra;
Aryan, Hajar;
Amanat, Man;
Vahidnezhad, Hassan;
Mohammadi, Pouria;
Garshasbi, Masoud;
Tavasoli, Ali Reza

Publication type:

Article

Phenotype and genotype heterogeneity of PLA2G6-associated neurodegeneration in a cohort of pediatric and adult patients.

Published in:

Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02780-9

By:

Dehnavi, Ali Zare;
Bemanalizadeh, Maryam;
Kahani, Seyyed Mohammad;
Ashrafi, Mahmoud Reza;
Rohani, Mohammad;
Toosi, Mehran Beiraghi;
Heidari, Morteza;
Hosseinpour, Sareh;
Amini, Behnam;
Zokaei, Shaghayegh;
Rezaei, Zahra;
Aryan, Hajar;
Amanat, Man;
Vahidnezhad, Hassan;
Mohammadi, Pouria;
Garshasbi, Masoud;
Tavasoli, Ali Reza

Publication type:

Article

A novel ITGB2 variant in a patient with severe recurrent pyoderma gangrenosum-like lesions and underlying leukocyte adhesion deficiency type I: case report and literature review.

Published in:

Archives of Dermatological Research, 2025, v. 317, n. 1, p. 1, doi. 10.1007/s00403-025-04206-x

By:

Norouzi-Barough, Leyla;
Olyaei, Nasrin Alipour;
Carapito, Raphael;
Molitor, Anne;
Biglari, Sajjad;
Poostiyan, Nazila;
Shahrooei, Mohammad;
Vahidnezhad, Hassan;
Tabatabaiefar, Mohammad Amin;
Bahram, Seiamak;
Sherkat, Roya

Publication type:

Article

The Kindler Syndrome: A Spectrum of FERMT1 Mutations in Iranian Families.

Published in:

Journal of Investigative Dermatology, 2015, v. 135, n. 5, p. 1447, doi. 10.1038/jid.2015.9

By:

Youssefian, Leila;
Vahidnezhad, Hassan;
Barzegar, Mohammadreza;
Li, Qiaoli;
Sotoudeh, Soheila;
Yazdanfar, Ameneh;
Ehsani, Amir Hooshang;
Kajbafzadeh, Abdol-Mohammad;
Mozafari, Nikoo;
Ebrahimi Daryani, Nasser;
Agha-hosseini, Farzaneh;
Zeinali, Sirous;
Uitto, Jouni

Publication type:

Article

Fibroadipose Hyperplasia versus Proteus Syndrome: Segmental Overgrowth with a Mosaic Mutation in the PIK3CA Gene.

Published in:

Journal of Investigative Dermatology, 2015, v. 135, n. 5, p. 1450, doi. 10.1038/jid.2015.15

By:

Youssefian, Leila;
Vahidnezhad, Hassan;
Baghdadi, Taghi;
Ghaznavi, Alireza;
Li, Qiaoli;
Tabrizi, Mina;
Uitto, Jouni

Publication type:

Article

The effect of family structure on the still-missing heritability and genomic prediction accuracy of type 2 diabetes.

Published in:

Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00669-7

By:

Amiri Roudbar, Mahmoud;
Vahedi, Seyed Milad;
Jin, Jin;
Jahangiri, Mina;
Lanjanian, Hossein;
Habibi, Danial;
Masjoudi, Sajedeh;
Riahi, Parisa;
Fateh, Sahand Tehrani;
Neshati, Farideh;
Zahedi, Asiyeh Sadat;
Moazzam-Jazi, Maryam;
Najd-Hassan-Bonab, Leila;
Mousavi, Seyedeh Fatemeh;
Asgarian, Sara;
Zarkesh, Maryam;
Moghaddas, Mohammad Reza;
Tenesa, Albert;
Kazemnejad, Anoshirvan;
Vahidnezhad, Hassan

Publication type:

Article

Epidermolysis bullosa and the COVID-19 pandemic: challenges and recommendations.

Published in:

Journal of Dermatological Treatment, 2022, v. 33, n. 2, p. 1178, doi. 10.1080/09546634.2020.1788701

By:

Vahidnezhad, Hassan;
Moravvej, Hamideh;
Bahmanjahromi, Ayda;
Youssefian, Leila;
Abdollahimajd, Fahimeh

Publication type:

Article

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

Published in:

Clinical Infectious Diseases, 2019, v. 68, n. 11, p. 1938, doi. 10.1093/cid/ciy942

By:

Youssefian, Leila;
Vahidnezhad, Hassan;
Yousefi, Mehdi;
Saeidian, Amir Hossein;
Azizpour, Arghavan;
Touati, Andrew;
Nikbakht, Neda;
Hesari, Kambiz Kamyab-;
Adib-Sereshki, Mohammad Mahdi;
Zeinali, Sirous;
Mansoori, Behzad;
Jazayeri, Ali;
Karamzadeh, Razieh;
Fortina, Paolo;
Jouanguy, Emmanuelle;
Casanova, Jean-Laurent;
Uitto, Jouni

Publication type:

Article

Association of MTHFR C677T polymorphism with elevated homocysteine level and disease development in vitiligo.

Published in:

International Journal of Immunogenetics, 2020, v. 47, n. 4, p. 342, doi. 10.1111/iji.12476

By:

Bagheri Hamidi, Arash;
Namazi, Nastaran;
Mohammad Amoli, Mahsa;
Amani, Maliheh;
Gholami, Morteza;
Youssefian, Leila;
Vahidnezhad, Hassan;
Abdollahimajd, Fahimeh;
Uitto, Jouni

Publication type:

Article

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Published in:

Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1159, doi. 10.1007/s10545-018-0228-6

By:

Shirzadeh, Tina;
Saeidian, Amir Hossein;
Bagherian, Hamideh;
Salehpour, Shadab;
Setoodeh, Aria;
Alaei, Mohammad Reza;
Youssefian, Leila;
Samavat, Ashraf;
Touati, Andrew;
Fallah, Mohammad‐Sadegh;
Vahidnezhad, Hassan;
Karimipoor, Morteza;
Azadmehr, Sarah;
Raeisi, Marzieh;
Bandehi Sarhadi, Ameneh;
Zafarghandi Motlagh, Fatemeh;
Jamali, Mojdeh;
Zeinali, Zahra;
Abiri, Maryam;
Zeinali, Sirous

Publication type:

Article

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Published in:

Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1159, doi. 10.1007/s10545-018-0228-6

By:

Shirzadeh, Tina;
Saeidian, Amir Hossein;
Bagherian, Hamideh;
Salehpour, Shadab;
Setoodeh, Aria;
Alaei, Mohammad Reza;
Youssefian, Leila;
Samavat, Ashraf;
Touati, Andrew;
Fallah, Mohammad-Sadegh;
Vahidnezhad, Hassan;
Karimipoor, Morteza;
Azadmehr, Sarah;
Raeisi, Marzieh;
Bandehi Sarhadi, Ameneh;
Zafarghandi Motlagh, Fatemeh;
Jamali, Mojdeh;
Zeinali, Zahra;
Abiri, Maryam;
Zeinali, Sirous

Publication type:

Article

Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA).

Published in:

2020

By:

Ziaee, Vahid;
Youssefian, Leila;
Faghankhani, Masoomeh;
Jazayeri, Ali;
Saeidian, Amir Hossein;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Letter

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification.

Published in:

PLoS Genetics, 2022, v. 18, n. 4, p. 1, doi. 10.1371/journal.pgen.1010192

By:

Ralph, Douglas;
Nitschke, Yvonne;
Levine, Michael A.;
Caffet, Matthew;
Wurst, Tamara;
Saeidian, Amir H.;
Youssefian, Leila;
Vahidnezhad, Hassan;
Terry, Sharon F.;
Rutsch, Frank;
Uitto, Jouni;
Li, Qiaoli

Publication type:

Article

Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.

Published in:

Clinical Chemistry, 2021, v. 67, n. 6, p. 876, doi. 10.1093/clinchem/hvab042

By:

Youssefian, Leila;
Saeidian, Amir Hossein;
Palizban, Fahimeh;
Bagherieh, Atefeh;
Abdollahimajd, Fahimeh;
Sotoudeh, Soheila;
Mozafari, Nikoo;
Farahani, Rahele A.;
Mahmoudi, Hamidreza;
Babashah, Sadegh;
Zabihi, Masoud;
Zeinali, Sirous;
Fortina, Paolo;
Salas-Alanis, Julio C.;
South, Andrew P.;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

A Systematic Review of Mendelian Pyoderma Gangrenosum: Clinical and Genetic Characteristics in 120 Published Patients.

Published in:

Experimental Dermatology, 2025, v. 34, n. 5, p. 1, doi. 10.1111/exd.70112

By:

Norouzi‐Barough, Leyla;
Biglari, Sajjad;
Sherkat, Roya;
Gudjonsson, Johann E.;
Hakonarson, Hakon;
Vahidnezhad, Hassan

Publication type:

Article

Pathogenic DST sequence variants result in either epidermolysis bullosa simplex (EBS) or hereditary sensory and autonomic neuropathy type 6 (HSAN‐VI).

Published in:

Experimental Dermatology, 2022, v. 31, n. 6, p. 949, doi. 10.1111/exd.14562

By:

Khalesi, Raziyeh;
Harvey, Nailah;
Garshasbi, Masoud;
Kalamati, Elnaz;
Youssefian, Leila;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Whole‐transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late‐onset segmental Darier disease.

Published in:

Experimental Dermatology, 2022, v. 31, n. 6, p. 943, doi. 10.1111/exd.14559

By:

Mohaghegh, Fatemeh;
Youssefian, Leila;
Galehdari, Hamid;
Tavakoli, Narjes;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Increased level of cathelicidin (LL‐37) in vitiligo: Possible pathway independent from vitamin D receptor gene polymorphism.

Published in:

Experimental Dermatology, 2020, v. 29, n. 12, p. 1176, doi. 10.1111/exd.14200

By:

Atazadeh, Fatemeh;
Fazeli, Zahra;
Vahidnezhad, Hassan;
Namazi, Nastaran;
Younespour, Shima;
Youssefian, Leila;
Abdollahimajd, Fahimeh;
Uitto, Jouni

Publication type:

Article

The matriptase-prostasin proteolytic cascade in dermatologic diseases.

Published in:

Experimental Dermatology, 2020, v. 29, n. 7, p. 580, doi. 10.1111/exd.14104

By:

Touati, Andrew;
Saeidian, Amir Hossein;
Youssefian, Leila;
Faghankhani, Masoomeh;
Niaziorimi, Fatemeh;
Pajouhanfar, Sara;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Linear basal cell nevus with a novel mosaic PTCH1 mutation.

Published in:

Experimental Dermatology, 2020, v. 29, n. 6, p. 531, doi. 10.1111/exd.14101

By:

Saeidian, Amir Hossein;
Cohen‐Nowak, Adam;
O'Donnell, Megan;
Shalabi, Doaa;
McGuinn, Kathleen P.;
Youssefian, Leila;
Vahidnezhad, Hassan;
Niaziorimi, Fatemeh;
Dasgeb, Bahar;
Kasper, David A.;
Lee, Jason B.;
Uitto, Jouni;
Nikbakht, Neda

Publication type:

Article

Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa.

Published in:

Experimental Dermatology, 2019, v. 28, n. 10, p. 1118, doi. 10.1111/exd.13501

By:

Vahidnezhad, Hassan;
Youssefian, Leila;
Saeidian, Amir Hossein;
Zeinali, Sirous;
Touati, Andrew;
Abiri, Maryam;
Sotoudeh, Soheila;
Norouz‐zadeh, Sara;
Amirinezhad, Niloufar;
Mozafari, Nikoo;
Daneshpazhooh, Maryam;
Mahmoudi, Hamidreza;
Hamid, Mohammad;
Bradfield, Jonathan P.;
Kim, Cecilia E.;
Hakonarson, Hakon;
Uitto, Jouni

Publication type:

Article

Advance trends in targeting homology-directed repair for accurate gene editing: An inclusive review of small molecules and modified CRISPR-Cas9 systems.

Published in:

BioImpacts, 2022, v. 12, n. 4, p. 371, doi. 10.34172/bi.2022.23871

By:

Shams, Forough;
Bayat, Hadi;
Mohammadian, Omid;
Mahboudi, Somayeh;
Vahidnezhad, Hassan;
Soosanabadi, Mohsen;
Rahimpour, Azam

Publication type:

Article

Molecular Genetics of Keratinization Disorders - What's New About Ichthyosis.

Published in:

Acta Dermato-Venereologica, 2020, v. 100, p. 177, doi. 10.2340/00015555-3431

By:

UITTO, Jouni;
YOUSSEFIAN, Leila;
SAEIDIAN, Amir Hossein;
VAHIDNEZHAD, Hassan

Publication type:

Article

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

Published in:

2017

By:

YOUSSEFIAN, Leila;
VAHIDNEZHAD, Hassan;
AGHIGHI, Yahya;
ZIAEE, Vahid;
ZEINALI, Sirous;
ABIRI, Maryam;
UITTO, Jouni

Publication type:

Case Study

Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry.

Published in:

American Journal of Medical Genetics. Part A, 2021, v. 185, n. 11, p. 3390, doi. 10.1002/ajmg.a.62456

By:

Warshauer, Emily Mira;
Brown, Adam;
Fuentes, Ignacia;
Shortt, Jonathan;
Gignoux, Chris;
Montinaro, Francesco;
Metspalu, Mait;
Youssefian, Leila;
Vahidnezhad, Hassan;
Jacków, Joanna;
Christiano, Angela M.;
Uitto, Jouni;
Fajardo‐Ramírez, Óscar R.;
Salas‐Alanis, Julio C.;
McGrath, John A.;
Consuegra, Liliana;
Rivera, Carolina;
Maier, Paul A.;
Runfeldt, Goran;
Behar, Doron M.

Publication type:

Article

Widespread aplasia cutis congenita in sibs with PLEC1 and ITGB4 variants.

Published in:

American Journal of Medical Genetics. Part A, 2019, v. 179, n. 8, p. 1547, doi. 10.1002/ajmg.a.61260

By:

Kariminejad, Ariana;
Vahidnezhad, Hassan;
Ghaderi‐Sohi, Siavash;
Ghannadan, Ali R.;
Youssefian, Leila;
Parsimehr, Elham;
Faraji Zonooz, Mehrshid;
Kariminejad, Mohammad H.;
Uitto, Jouni;
Najmabadi, Hossein;
Hennekam, Raoul C.

Publication type:

Article

Autosomal recessive cutis laxa type 1C with a homozygous LTBP4 splicing variant: a case report and update of literature.

Published in:

2022

By:

Mazaheri, Mahta;
Jahantigh, Hamid Reza;
Yavari, Mahdie;
Mirjalili, Seyed Reza;
Vahidnezhad, Hassan

Publication type:

Case Study

Successful and Sustained Treatment of Cutaneous Tumoral Lesions in Brooke–Spiegler Syndrome (BSS) Using Ablative CO<sub>2</sub> Laser: A Case Series and Literature Review.

Published in:

2025

By:

Mozafari, Nikoo;
Jafari, Mohammad Amin;
Zaresharifi, Shirin;
Vahidnezhad, Hassan;
Youssefian, Leila;
Behrangi, Elham;
Seirafianpour, Farnoosh;
Mohammad, Arash Pour;
Jafarzadeh, Alireza;
Goodarzi, Azadeh

Publication type:

Case Study

Correlation between melphalan chemotherapy with longitudinal global strain indices of the left ventricle in multiple myeloma patients: A velocity vector imaging (VVI) echocardiography study.

Published in:

2024

By:

Mirsafaee, Liaosadat;
Firouzabadi, Mohammad Dehghani;
Parkhideh, Sayeh;
Vahidnezhad, Hassan;
Firouzabadi, Fatemeh Dehghani;
Arab, Maryam;
Yousem, David M.;
Karvandi, Mersedeh

Publication type:

Letter to the Editor

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

Published in:

Experimental Dermatology, 2016, v. 25, n. 1, p. 17, doi. 10.1111/exd.12826

By:

Vahidnezhad, Hassan;
Youssefian, Leila;
Uitto, Jouni

Publication type:

Article

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

Published in:

Experimental Dermatology, 2015, v. 24, n. 3, p. 220, doi. 10.1111/exd.12620

By:

Youssefian, Leila;
Vahidnezhad, Hassan;
Daneshpazhooh, Maryam;
Abdollahzadeh, Sina;
Talari, Hamidreza;
Khoshnevisan, Alireza;
Chams‐Davatchi, Cheyda;
Mobasher, Roozbeh;
Li, Qiaoli;
Uitto, Jouni;
Akhondzadeh, Shahin;
Tabrizi, Mina

Publication type:

Article

Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-78344-9

By:

Vahidnezhad, Hassan;
Youssefian, Leila;
Faghankhani, Masoomeh;
Mozafari, Nikoo;
Saeidian, Amir Hossein;
Niaziorimi, Fatemeh;
Abdollahimajd, Fahimeh;
Sotoudeh, Soheila;
Rajabi, Fateme;
Mirsafaei, Liaosadat;
Sani, Zahra Alizadeh;
Liu, Lu;
Guy, Alyson;
Zeinali, Sirous;
Kariminejad, Ariana;
Ho, Reginald T.;
McGrath, John A.;
Uitto, Jouni

Publication type:

Article

Purpuric dermatosis and lymphocytic vasculopathy following SARS‐CoV‐2 vaccination: Report of two patients.

Published in:

Dermatologic Therapy, 2022, v. 35, n. 11, p. 1, doi. 10.1111/dth.15898

By:

Saffarian, Zahra;
Samii, Rana;
Hadizadeh, Alireza;
Ghanadan, Alireza;
Vahidnezhad, Hassan

Publication type:

Article

Losartan treatment improves recessive dystrophic epidermolysis bullosa: A case series.

Published in:

Dermatologic Therapy, 2022, v. 35, n. 7, p. 1, doi. 10.1111/dth.15515

By:

Pourani, Mohammad Reza;
Vahidnezhad, Hassan;
Mansouri, Parvin;
Youssefian, Leila;
Rakhshan, Azadeh;
Hajimoradi, Behzad;
Abdollahimajd, Fahimeh;
Uitto, Jouni

Publication type:

Article

De novo severe pemphigus vulgaris following SARS‐CoV‐2 vaccination with BBIBP‐CorV.

Published in:

Dermatologic Therapy, 2022, v. 35, n. 6, p. 1, doi. 10.1111/dth.15448

By:

Saffarian, Zahra;
Samii, Rana;
Ghanadan, Alireza;
Vahidnezhad, Hassan

Publication type:

Article

The utility of dermal fibroblasts in treatment of skin disorders: A paradigm of recessive dystrophic epidermolysis bullosa.

Published in:

Dermatologic Therapy, 2021, v. 34, n. 4, p. 1, doi. 10.1111/dth.15028

By:

Shams, Forough;
Rahimpour, Azam;
Vahidnezhad, Hassan;
Hosseinzadeh, Simzar;
Moravvej, Hamideh;
Kazemi, Bahram;
Rajabibazl, Masoumeh;
Abdollahimajd, Fahimeh;
Uitto, Jouni

Publication type:

Article

Losartan for treatment of epidermolysis bullosa: A new perspective.

Published in:

Dermatologic Therapy, 2021, v. 34, n. 1, p. 1, doi. 10.1111/dth.14638

By:

Uitto, Jouni;
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Dermatologic Therapy, 2020, v. 33, n. 6, p. 1, doi. 10.1111/dth.14493

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Asgari, Tina;
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Uitto, Jouni

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CD147 inhibitors as a treatment for melanoma: Promising agents against SARS‐CoV‐2 infection.

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Dermatologic Therapy, 2020, v. 33, n. 6, p. 1, doi. 10.1111/dth.14449

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Pourani, Mohammad Reza;
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Mycophenolate mofetil treatment of an H syndrome patient with a SLC29A3 mutation.

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Dermatologic Therapy, 2020, v. 33, n. 6, p. 1, doi. 10.1111/dth.14375

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Behrangi, Elham;
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Dermatologic Therapy, 2020, v. 33, n. 6, p. 1, doi. 10.1111/dth.14194

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Abdollahimajd, Fahimeh;
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Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran.

Published in:

International Journal of Dermatology, 2015, v. 54, n. 10, p. e416, doi. 10.1111/ijd.12804

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Barzegar, Mohammadreza;
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Article

Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.

Published in:

2021

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Vahidnezhad, Hassan;
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Kamyab Hesari, Kambiz;
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Publication type:

journal article