OpenURL Connection Search

Select item for more details and to access through your institution.

Schimke immuno-osseous dysplasia in a boy with generalized edema; a case report.
Published in:
Journal of Nephropathology, 2024, v. 13, n. 4, p. 1, doi. 10.34172/jnp.2023.21481
By:
- Pourpashang, Paniz;
- Esfandiar, Nasrin;
- Panjeshahi, Samaneh;
- Sharafian, Samin;
- Mirbehbahani, Seyed Hamidreza
Publication type:
Article
Cernunnos defect in an Iranian patient with T− B+NK+ severe combined immunodeficiency: A case report and review of the literature.
Published in:
Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 8, p. 1, doi. 10.1002/mgg3.1990
By:
- Jamee, Mahnaz;
- Khakbazan Fard, Nasrin;
- Fallah, Shahrzad;
- Golchehre, Zahra;
- Fallahi, Mazdak;
- Shamsian, Bibi Shahin;
- Sharafian, Samin;
- Chavoshzadeh, Zahra
Publication type:
Article
Successful Hematopoietic Stem Cell Transplant in a Patient with Omenn Syndrome: A Case Report.
Published in:
Experimental & Clinical Transplantation, 2023, v. 21, n. 2, p. 189, doi. 10.6002/ect.2022.0348
By:
- Shamsian, Bibi Shahin;
- Paksaz, Amirreza;
- Chavoshzadeh, Zahra;
- Sharafian, Samin;
- Yazdi, Seyed Morteza Tabatabaee;
- Jamee, Mahnaz
Publication type:
Article
X-linked SCID with a rare mutation.
Published in:
Allergy, Asthma & Clinical Immunology, 2021, v. 17, n. 1, p. 1, doi. 10.1186/s13223-021-00605-7
By:
- Mahdavi, Fatemeh Sadat;
- Keramatipour, Mohammad;
- Ansari, Sarina;
- Sharafian, Samin;
- Karamzade, Arezou;
- Tavakol, Marzieh
Publication type:
Article
Inborn errors of immunity with kidney and urinary tract disorders: a review.
Published in:
International Urology & Nephrology, 2024, v. 56, n. 6, p. 1965, doi. 10.1007/s11255-023-03907-4
By:
- Shajari, Ahmad;
- Zare Ahmadabadi, Atefe;
- Ashrafi, Mohammad Moein;
- Mahdavi, Tolue;
- Mirzaee, Mahbubeh;
- Mohkam, Masoumeh;
- Sharafian, Samin;
- Tamiji, Mehrdad;
- Jamee, Mahnaz
Publication type:
Article
Genomic testing identifies monogenic causes in patients with very early-onset inflammatory bowel disease: a multicenter survey in an Iranian cohort.
Published in:
Clinical & Experimental Immunology, 2024, v. 217, n. 1, p. 1, doi. 10.1093/cei/uxae037
By:
- Eslamian, Golnaz;
- Jamee, Mahnaz;
- Momen, Tooba;
- Rohani, Pejman;
- Ebrahimi, Sarehossadat;
- Mesdaghi, Mehrnaz;
- Ghadimi, Soodeh;
- Mansouri, Mahboubeh;
- Mahdaviani, Seyed Alireza;
- Sadeghi-shabestari, Mahnaz;
- Fallahpour, Morteza;
- Shamsian, Bibi Shahin;
- Eslami, Narges;
- Sharafian, Samin;
- Dara, Naghi;
- Nasri, Peiman;
- Amini, Niloufar;
- Enayat, Javad;
- Fallahi, Mazdak;
- Ghasemi Hashtrodi, Leila
Publication type:
Article
Immunodeficiency due to a novel variant in PIK3CD: a case report.
Published in:
2023
By:
- Shashaani, Niloofar;
- Chavoshzadeh, Zahra;
- Ghasemi, Leila;
- Ghotbabadi, Shabnam Hajiani;
- Shiari, Sara;
- Sharafian, Samin;
- Shiari, Reza
Publication type:
Case Study
Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature.
Published in:
Journal of Clinical Immunology, 2022, v. 42, n. 8, p. 1618, doi. 10.1007/s10875-022-01337-y
By:
- Sharafian, Samin;
- Jacomelli, Gabriella;
- Tamizifar, Banafshe;
- Shahrooei, Mohammad;
- Parvaneh, Nima
Publication type:
Article
A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis.
Published in:
Journal of Clinical Immunology, 2019, v. 39, n. 1, p. 11, doi. 10.1007/s10875-018-0586-8
By:
- Sharafian, Samin;
- Ziaee, Vahid;
- Shahrooei, Mohammad;
- Ahadi, Mahsa;
- Parvaneh, Nima
Publication type:
Article
Skin manifestations in children with inborn errors of immunity in a tertiary care hospital in Iran.
Published in:
Journal of Cutaneous Immunology & Allergy, 2023, v. 6, n. 3, p. 72, doi. 10.1002/cia2.12296
By:
- Shahrbabaki, Zahra Salehi;
- Chavoshzadeh, Zahra;
- Abdollahimajd, Fahimeh;
- sharafian, Samin;
- Jamee, Mahnaz;
- Bondarenko, Anastasia;
- Mahdavi, Tolue
Publication type:
Article
Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity.
Published in:
Biology (2079-7737), 2023, v. 12, n. 5, p. 644, doi. 10.3390/biology12050644
By:
- Sharifinejad, Niusha;
- Azizi, Gholamreza;
- Rasouli, Seyed Erfan;
- Chavoshzadeh, Zahra;
- Mahdaviani, Seyed Alireza;
- Tavakol, Marzieh;
- Sadri, Homa;
- Nabavi, Mohammad;
- Ebrahimi, Sareh Sadat;
- Shirkani, Afshin;
- Vosughi Motlagh, Ahmad;
- Momen, Tooba;
- Sharafian, Samin;
- Mesdaghi, Mehrnaz;
- Eslami, Narges;
- Delavari, Samaneh;
- Bahrami, Sasan;
- Yazdani, Reza;
- Rezaei, Nima;
- Abolhassani, Hassan
Publication type:
Article
Correlation Between Anxiety Disorders and Asthma Severity Indices in Asthmatic Children.
Published in:
Shiraz E Medical Journal, 2023, v. 24, n. 6, p. 1, doi. 10.5812/semj-130199
By:
- Rekabi, Mahsa;
- Honarpisheh, Parisa;
- Karimi-Galougahi, Mahboobeh;
- Rekabi, Vahab;
- Vasheghani, Maryam;
- Eslami, Narges;
- Sharafian, Samin;
- Sharifi, Hooman;
- Mahdaviani, Alireza;
- Mansouri, Mahboubeh;
- Vasegh, Sasan;
- Shirvani, Armin;
- Pourpashang, Paniz
Publication type:
Article
Revisiting double-negative T cells in autoimmune lymphoproliferative immunodeficiencies: a case series.
Published in:
Allergologia & Immunopathologia, 2024, v. 52, n. 5, p. 1, doi. 10.15586/aei.v52i5.1115
By:
- Jamee, Mahnaz;
- Sharafian, Samin;
- Eslami, Narges;
- Bayegi, Shideh Namazi;
- Keramatipour, Mohammad;
- Nabavi, Mohamad;
- Shokri, Sima;
- Shakiba, Marjan;
- Shamsian, Bibi Shahin;
- Abolghasemi, Hassan;
- Vahidshahi, Kurosh;
- Khanbabaee, Ghamartaj;
- Armin, Shahnaz;
- Chavoshzadeh, Zahra;
- Mesdaghi, Mehrnaz
Publication type:
Article
New Presentation of CD27 Deficiency; Coronary Ectasia and COVID-19.
Published in:
2023
By:
- Golchehre, Zahra;
- Sharafian, Samin;
- Momtazmanesh, Nader;
- Chavoshzadeh, Zahra;
- Karimi, Abdollah;
- Abolhassani, Hassan;
- Aghdam, Maryam Kazemi;
- Vahidshahi, Koroush;
- Hashemimoghaddam, Seyedehatefeh;
- Kosari, Farid;
- Khafafpour, Zahra;
- Shamsian, Bibi Shahin;
- Keramatipour, Mohammad
Publication type:
Case Study
The Efficacy of a New Protocol of Oral Immunotherapy to Wheat for Desensitization and Induction of Tolerance.
Published in:
2022
By:
- Sharafian, Samin;
- Amirzargar, Aliakbar;
- Gharagozlou, Mohammad;
- Parvaneh, Nima;
- Shariat, Mansoureh;
- Tavakol, Marzieh;
- Movahedi, Masoud
Publication type:
journal article
Montelukast and Coronavirus Disease 2019: A Scoping Review.
Published in:
Iranian Journal of Allergy, Asthma & Immunology, 2021, v. 20, n. 4, p. 384, doi. 10.18502/ijaai.v20i4.6948
By:
- Sharifinejad, Niusha;
- Sharafian, Samin;
- Salekmoghadam, Sana;
- Tavakol, Marzieh;
- Qorbani, Mostafa
Publication type:
Article
Delay in Diagnosis of Two Siblings with Severe Ocular Problems and Autoimmune Polyglandular Syndrome.
Published in:
Iranian Journal of Allergy, Asthma & Immunology, 2020, v. 19, n. 3, p. 313
By:
- Sharafian, Samin;
- Tavakol, Marzieh;
- Gharagozlou, Mohammad;
- Parvaneh, Nima
Publication type:
Article
A Rare Case of Hyper IgE Syndrome with Vocal Cords Involvement.
Published in:
2019
By:
- Sharafian, Samin;
- Movahedi, Masoud;
- Kalantari, Arash;
- Parvaneh, Nima;
- Gharagozlou, Mohammad
Publication type:
journal article
A rare immunological disease, caspase 8 deficiency: case report and literature review.
Published in:
Allergy, Asthma & Clinical Immunology, 2023, v. 19, n. 1, p. 1, doi. 10.1186/s13223-023-00778-3
By:
- Bazgir, Narges;
- Tahvildari, Azin;
- Chavoshzade, Zahra;
- Jamee, Mahnaz;
- Golchehre, Zahra;
- Karimi, Abdollah;
- Dara, Naghi;
- Fallahi, Mazdak;
- Keramatipour, Mohammad;
- Karamzade, Arezou;
- Sharafian, Samin
Publication type:
Article
Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C gene.
Published in:
Allergy, Asthma & Clinical Immunology, 2023, v. 19, n. 1, p. 1, doi. 10.1186/s13223-023-00768-5
By:
- Ghadimi, Soodeh;
- Jamee, Mahnaz;
- Abolhassani, Hassan;
- Parvaneh, Nima;
- Rezaei, Nima;
- Delavari, Samaneh;
- Sadeghi-Shabestari, Mahnaz;
- Tabatabaei, Sedigheh Rafiei;
- Fahimzad, Alireza;
- Armin, Shahnaz;
- Chavoshzadeh, Zahra;
- Sharafian, Samin
Publication type:
Article
JAGN1 mutation with distinct clinical features; two case reports and literature review.
Published in:
2023
By:
- Hojabri, Mahsa;
- Farsi, Yeganeh;
- Jamee, Mahnaz;
- Abolhassani, Hassan;
- Khani, Hedieh Haji Khodaverdi;
- Karimi, Abdollah;
- Mesdaghi, Mehrnaz;
- Chavoshzadeh, Zahra;
- Sharafian, Samin
Publication type:
Case Study

Found: 21

Schimke immuno-osseous dysplasia in a boy with generalized edema; a case report.

Cernunnos defect in an Iranian patient with T<sup>−</sup> B<sup>+</sup>NK<sup>+</sup> severe combined immunodeficiency: A case report and review of the literature.

Successful Hematopoietic Stem Cell Transplant in a Patient with Omenn Syndrome: A Case Report.

X-linked SCID with a rare mutation.

Inborn errors of immunity with kidney and urinary tract disorders: a review.

Genomic testing identifies monogenic causes in patients with very early-onset inflammatory bowel disease: a multicenter survey in an Iranian cohort.

Immunodeficiency due to a novel variant in PIK3CD: a case report.

Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature.

A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis.

Skin manifestations in children with inborn errors of immunity in a tertiary care hospital in Iran.

Autoimmune versus Non-autoimmune Cutaneous Features in Monogenic Patients with Inborn Errors of Immunity.

Correlation Between Anxiety Disorders and Asthma Severity Indices in Asthmatic Children.

Revisiting double-negative T cells in autoimmune lymphoproliferative immunodeficiencies: a case series.

New Presentation of CD27 Deficiency; Coronary Ectasia and COVID-19.

The Efficacy of a New Protocol of Oral Immunotherapy to Wheat for Desensitization and Induction of Tolerance.

Montelukast and Coronavirus Disease 2019: A Scoping Review.

Delay in Diagnosis of Two Siblings with Severe Ocular Problems and Autoimmune Polyglandular Syndrome.

A Rare Case of Hyper IgE Syndrome with Vocal Cords Involvement.

A rare immunological disease, caspase 8 deficiency: case report and literature review.

Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C gene.

JAGN1 mutation with distinct clinical features; two case reports and literature review.