Works by Parvaneh, Leila

Results: 7

The clinical significance of complete class switching defect in Ataxia telangiectasia patients.

Published in:

Expert Review of Clinical Immunology, 2017, v. 13, n. 5, p. 499, doi. 10.1080/1744666X.2017.1292131

By:

Ghiasy, Saleh;
Parvaneh, Leila;
Azizi, Gholamreza;
Sadri, Ghazal;
Zaki dizaji, Majid;
Abolhassani, Hassan;
Aghamohammadi, Asghar

Publication type:

Article

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.

Published in:

Expert Review of Clinical Immunology, 2016, v. 12, n. 4, p. 479, doi. 10.1586/1744666X.2016.1139451

By:

Abolhassani, Hassan;
Vitali, Massimiliano;
Lougaris, Vassilios;
Giliani, Silvia;
Parvaneh, Nima;
Parvaneh, Leila;
Mirminachi, Babak;
Cheraghi, Taher;
Khazaei, Hosseinali;
Mahdaviani, Seyed Alireza;
Kiaei, Fatemeh;
Tavakolinia, Naiimeh;
Mohammadi, Javad;
Negahdari, Babak;
Rezaei, Nima;
Hammarstrom, Lennart;
Plebani, Alessandro;
Aghamohammadi, Asghar

Publication type:

Article

The ENPP1 K121Q polymorphism is not associated with type 2 diabetes and related metabolic traits in an Iranian population.

Published in:

Molecular & Cellular Biochemistry, 2011, v. 350, n. 1/2, p. 113, doi. 10.1007/s11010-010-0687-z

By:

Saberi, Hamzeh;
Mohammadtaghvaei, Narges;
Gulkho, Shekufeh;
Bakhtiyari, Salar;
Mohammadi, Mohammad;
Hanachi, Parichehr;
Gerayesh-nejad, Siavash;
Zargari, Mehryar;
Ataei, Farangis;
Parvaneh, Leila;
Larijani, Bagher;
Meshkani, Reza

Publication type:

Article

Vaccine-Derived Polioviruses and Children with Primary Immunodeficiency, Iran, 1995-2014.

Published in:

2016

By:

Shaghaghi, Mohammadreza;
Shahmahmoodi, Shohreh;
Abolhassani, Hassan;
Soleyman-jahi, Saeed;
Parvaneh, Leila;
Mahmoudi, Sussan;
Chavoshzadeh, Zahra;
Yazdani, Reza;
Zahraei, Seyed Mohsen;
Ebrahimi, Mohsen;
Eslamian, Mohammad H.;
Hamideh Tabatabaie;
Yousefi, Maryam;
Kandelousi, Yaghoob M.;
Oujaghlou, Aliasghar;
Rezaei, Nima;
Aghamohammadi, Asghar;
Tabatabaie, Hamideh

Publication type:

journal article

Characterization of 11 New Cases of Leukocyte Adhesion Deficiency Type 1 with Seven Novel Mutations in the ITGB2 Gene.

Published in:

Journal of Clinical Immunology, 2010, v. 30, n. 5, p. 756, doi. 10.1007/s10875-010-9433-2

By:

Parvaneh, Nima;
Mamishi, Setareh;
Rezaei, Amir;
Rezaei, Nima;
Tamizifar, Banafshe;
Parvaneh, Leila;
Sherkat, Roya;
Ghalehbaghi, Babak;
Kashef, Sara;
Chavoshzadeh, Zahra;
Isaeian, Anna;
Ashrafi, Farzaneh;
Aghamohammadi, Asghar

Publication type:

Article

Visceral leishmaniasis in two patients with IL-12p40 and IL-12Rβ1 deficiencies.

Published in:

2017

By:

Parvaneh, Nima;
Barlogis, Vincent;
Alborzi, Abdolvahab;
Deswarte, Caroline;
Boisson‐Dupuis, Stéphanie;
Migaud, Mélanie;
Farnaria, Catherine;
Markle, Janet;
Parvaneh, Leila;
Casanova, Jean‐Laurent;
Bustamante, Jacinta;
Boisson-Dupuis, Stéphanie;
Migaud, Mélanie;
Casanova, Jean-Laurent

Publication type:

journal article

Bacillus Calmette-Guérin (BCG)-associated hemophagocytic lymphohistiocytosis in the setting of IFN-γR1 deficiency: A diagnostic dilemma.

Published in:

EJHaem, 2020, v. 1, n. 1, p. 1, doi. 10.1002/jha2.5

By:

Razaghian, Anahita;
Parvaneh, Leila;
Delkhah, Mona;
Abbasi, Arash;
Sadeghirad, Parisa;
Shahrooei, Mohammad;
Parvaneh, Nima

Publication type:

Article