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AACE Clinical Case Reports|June 7, 2021
A Family With Novel X-Linked Recessive Homozygous Mutation in ANOS1 (c.628_629 del, p.1210fs∗) in Kallmann Syndrome Associated Unilateral Ptosis: Case Report and Literature ReviewShahab Noorian, Shahram Savad, Armin Khavandegar, et al.
Oxford Medical Case Reports|August 28, 2023
Food allergy masquerading as persistent proteinuria in post-infectious glomerulonephritis: a case reportMasoumeh Mohkam, Mahnaz Jamee, Nafiseh Mortazavi, et al.
Case Reports in Nephrology|May 13, 2022
Exacerbation of Congenital Hydronephrosis as the First Presentation of COVID-19 Infection in ChildrenMasoumeh Mohkam, Mahnaz Jamee, Farshid Kompani, et al.
Allergologia Et Immunopathologia|May 3, 2021
Acute pericarditis: A peculiar manifestation of common variable immune deficiencyNasim Ramzi, Shahrooz Yazdani, Hamed Talakoob, et al.
Frontiers in Medicine|September 26, 2022
Impact of incentives on COVID-19 vaccination; A systematic reviewParham Mardi, Shirin Djalalinia, Reza Kargar, et al.
Journal of Environmental and Public Health|August 30, 2021
Quality of Life and Related Paraclinical Factors in Iranian Patients with Transfusion-Dependent ThalassemiaMehran Khodashenas, Parham Mardi, Nooshin Taherzadeh-Ghahfarokhi, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation|March 15, 2023
Successful Hematopoietic Stem Cell Transplant in a Patient with Omenn Syndrome: A Case ReportBibi Shahin Shamsian, Amirreza Paksaz, Zahra Chavoshzadeh, et al.
Clinical Case Reports|September 1, 2021
Rare clinical presentations of hyper-IgE syndrome in a patient with dental abnormalities: A case reportMarzieh Heidarzadeh Arani, Atena Ramezanali Yakhchali, Mohammad Gharagozlou, et al.
Oxford Medical Case Reports|October 26, 2023
CARD9 deficiency with allergic bronchopulmonary aspergillosis (ABPA)-like presentation: a case reportMazdak Fallahi, Seyed Alireza Mahdaviani, Mohammadreza Shafiei, et al.
Immunological Investigations|October 13, 2020
Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the LiteratureNiusha Sharifinejad, Gholamreza Azizi, Nasrin Behniafard, et al.
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