Works by Sotoudeh, Soheila

Results: 19

Osteomyelitis in leukocyte adhesion deficiency type 1 syndrome.

Published in:

Journal of Infection in Developing Countries, 2010, v. 4, n. 3, p. 175, doi. 10.3855/jidc.387

By:

Azad, Farahzad Jabbari;
Ardalan, Maryam;
Rafati, Ali Hoseinpoor;
Sotoudeh, Soheila;
Pourpak, Zahra

Publication type:

Article

An Unusual TEN-Like Presentation of Juvenile Bullous Pemphigoid: A Diagnostic Challenge.

Published in:

2022

By:

Nikyar, Zahra;
Hatami, Parvaneh;
Aryanian, Zeinab;
Sotoudeh, Soheila;
Ziaee, Vahid;
Goodarzi, Azadeh

Publication type:

Case Study

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

Cutaneous Granulomatosis and Class Switching Defect as a Presenting Sign in Ataxia-Telangiectasia: First Case from the National Iranian Registry and Review of the Literature.

Published in:

Immunological Investigations, 2020, v. 49, n. 6, p. 597, doi. 10.1080/08820139.2019.1692864

By:

Amirifar, Parisa;
Yazdani, Reza;
Moeini Shad, Tannaz;
Ghanadan, Alireza;
Abolhassani, Hassan;
Lavin, Martin;
Sotoudeh, Soheila;
Aghamohammadi, Asghar

Publication type:

Article

Erythropoietic protoporphyria and early onset of cholestasis.

Published in:

Turkish Journal of Pediatrics, 2012, v. 54, n. 6, p. 645

By:

Khalili, Manijeh;
Farahmand, Fatemeh;
Hirbod-Mobarakeh, Armin;
Yousefi, Azizollah;
Sotoudeh, Soheila;
Monajemzadeh, Maryam;
Razaghian, Anahita;
Rezaei, Nima

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

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

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

Onycholysis and subungual purpura of nails.

Published in:

2019

By:

Aghazadeh, Nessa;
Sotoudeh, Soheila;
Ghanadan, Alireza;
Tajalli, Mahroo;
Norton, Scott A.

Publication type:

Case Study

Filaggrin gene polymorphisms in Iranian ichthyosis vulgaris and atopic dermatitis patients.

Published in:

International Journal of Dermatology, 2018, v. 57, n. 12, p. 1485, doi. 10.1111/ijd.14213

By:

Hassani, Bita;
Isaian, Anna;
Shariat, Mansoureh;
Mollanoori, Hasan;
Sotoudeh, Soheila;
Babaei, Vahid;
Ziaali, Arghavan;
Teimourian, Shahram

Publication type:

Article

A Neonate with Indurate Dermal Papules and Nodules and Pneumonia: a Case Report.

Published in:

Acta Medica Iranica, 2014, v. 52, n. 4, p. 323

By:

Gharib, Behdad;
Almasi, Mina;
Esmaeili, Sara;
Sotoudeh, Soheila;
Monajemzadeh, Maryam;
Ramyar, Asghar;
Farshadmoghadam, Hossein;
Sabouni, Farah

Publication type:

Article

Amniotic membrane dressings for treatment of aplasia cutis in newborns.

Published in:

Pediatric Dermatology, 2024, v. 41, n. 3, p. 445, doi. 10.1111/pde.15540

By:

Kadivar, Maliheh;
Sangsari, Razieh;
Rostamli, Somayeh;
Sotoudeh, Soheila;
Mirnia, Kayvan

Publication type:

Article

Association Between Single Nucleotide Polymorphisms of the Interleukin-4 Gene and Atopic Dermatitis.

Published in:

Acta Dermatovenerologica Croatica, 2015, v. 23, n. 2, p. 96

By:

Gharagozlou, Mohammad;
Behniafard, Nasrin;
Amirzargar, Ali Akbar;
Hosseinverdi, Sima;
Sotoudeh, Soheila;
Farhadi, Elham;
Khaledi, Mojdeh;
Aryan, Zahra;
Moghaddam, Zahra Gholizadeh;
Mahmoudi, Maryam;
Aghamohammadi, Asghar;
Rezaei, Nima

Publication type:

Article

Filaggrin Single Nucleotide Polymorphisms in Atopic Dermatitis.

Published in:

Acta Dermatovenerologica Croatica, 2014, v. 22, n. 3, p. 200

By:

Khaledi, Mojdeh;
Fotouhi, Akbar;
Farhadi, Elham;
Mahdaviani, Behnaz;
Sotoudeh, Soheila;
Tavakoli, Mehdi;
Behniafard, Nasrin;
Gharagozlou, Mohammad;
Rezaei, Nima

Publication type:

Article

Mutation update: The spectra of PLEC sequence variants and related plectinopathies.

Published in:

Human Mutation, 2022, v. 43, n. 12, p. 1706, doi. 10.1002/humu.24434

By:

Vahidnezhad, Hassan;
Youssefian, Leila;
Harvey, Nailah;
Tavasoli, Ali Reza;
Saeidian, Amir Hossein;
Sotoudeh, Soheila;
Varghaei, Aida;
Mahmoudi, Hamidreza;
Mansouri, Parvin;
Mozafari, Nikoo;
Zargari, Omid;
Zeinali, Sirous;
Uitto, Jouni

Publication type:

Article

Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica.

Published in:

Human Mutation, 2020, v. 41, n. 5, p. 906, doi. 10.1002/humu.23980

By:

Vahidnezhad, Hassan;
Youssefian, Leila;
Sotoudeh, Soheila;
Liu, Lu;
Guy, Alyson;
Lovell, Patricia A.;
Kariminejad, Ariana;
Zeinali, Sirous;
McGrath, John A.;
Uitto, Jouni

Publication type:

Article

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families.

Published in:

Human Mutation, 2019, v. 40, n. 3, p. 288, doi. 10.1002/humu.23695

By:

Youssefian, Leila;
Vahidnezhad, Hassan;
Saeidian, Amir Hossein;
Touati, Andrew;
Sotoudeh, Soheila;
Mahmoudi, Hamidreza;
Mansouri, Parvin;
Daneshpazhooh, Maryam;
Aghazadeh, Nessa;
Hesari, Kambiz Kamyab;
Basiri, Mohammadreza;
Londin, Eric;
Kumar, Gaurav;
Zeinali, Sirous;
Fortina, Paolo;
Uitto, Jouni

Publication type:

Article

Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosa.

Published in:

Human Mutation, 2018, v. 39, n. 10, p. 1349, doi. 10.1002/humu.23592

By:

Vahidnezhad, Hassan;
Youssefian, Leila;
Saeidian, Amir Hossein;
Touati, Andrew;
Sotoudeh, Soheila;
Jazayeri, Ali;
Guy, Alyson;
Lovell, Patricia A.;
Liu, Lu;
Kariminejad, Ariana;
McGrath, John A.;
Zeinali, Sirous;
Uitto, Jouni

Publication type:

Article

Lupus Erythematosus and Chronic Granulomatous Disease: Report of Four Iranian Patients with AR-CGD and One XL-CGD.

Published in:

Iranian Journal of Allergy, Asthma & Immunology, 2019, v. 18, n. 4, p. 452

By:

Maddah, Marzieh;
Fazlollahi, Mohammad Reza;
Shiari, Reza;
Shahram, Farhad;
Mamishi, Setareh;
Babaie, Delara;
Monajemzadeh, Maryam;
Sotoudeh, Soheila;
Hamidieh, Amir Ali;
Badalzadeh, Mohsen;
Tajik, Shaghayegh;
Sedighipour, Leila;
Pourpak, Zahra

Publication type:

Article