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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 8
2022
Momtazmanesh, Sara; Rayzan, Elham; Zoghi, Samaneh; Shahkarami, Sepideh; Molatefi, Rasol; Mohammadzadeh, Iraj; Ghaffari, Javad; Mahmoudi, Hamidreza; Dmytrus, Jasmin; Segarra-Roca, Anna; Somekh, Ido; Witzel, Maximilian; Hauck, Fabian; Boztug, Kaan; Klein, Christoph und Rezaei, Nima
(2022):
Novel Variants of DOCK8 Deficiency in a Case Series of Iranian Patients.
In: Endocrine Metabolic & Immune Disorders - Drug Targets, Bd. 22, Nr. 1: S. 159-168
Sadeghmousavi, Shaghayegh; Shahkarami, Sepideh; Rayzan, Elham; Ahmed, Souran; Gharalari, Farzaneh Hosseini; Rohlfs, Meino; Klein, Christoph und Rezaei, Nima
(2022):
A 3-Year-Old Boy with an Xp21 Deletion Syndrome: A Case Report.
In: Endocrine Metabolic & Immune Disorders - Drug Targets, Bd. 22, Nr. 8: S. 881-887
Danandeh, Khashayar; Jabbari, Parnian; Rayzan, Elham; Zoghi, Samaneh; Shahkarami, Sepideh; Heredia, Raul Jimenez; Krolo, Ana; Shamsian, Bibi Shahin; Boztug, Kaan und Rezaei, Nima
(2022):
Case Report of a Novel NFkB Mutation in a Lymphoproliferative Disorder Patient.
In: Endocrine Metabolic & Immune Disorders - Drug Targets, Bd. 22, Nr. 10: S. 1040-1046
2021
Maroufi, Seyed F.; Shaka, Zoha; Mojtabavi, Helia; Sadeghalvad, Mona; Rayzan, Elham; Sedighi, Iraj; Shahkarami, Sepideh; Najafi, Mehri; Rohlfs, Meino; Klein, Christoph und Rezaei, Nima
(2021):
Novel G6PC3 Mutations in Patients with Congenital Neutropenia: Case Reports and Review of the Literature.
In: Endocrine Metabolic & Immune Disorders-Drug Targets, Bd. 21, Nr. 9: S. 1660-1668
Shafeghat, Melika; Esmaeilzadeh, Hossein; Sadeghalvad, Mona; Rayzan, Elham; Zoghi, Samaneh; Shahkarami, Sepideh; Heredia, Raul Jimenez; Krolo, Ana; Boztug, Kaan und Rezaei, Nima
(2021):
A novel homozygous RAG1 mutation is associated with severe combined immunodeficiency and neurological presentations.
In: Allergologia et Immunopathologia, Bd. 49, Nr. 4: S. 91-97
Shaka, Zoha; Mojtabavi, Helia; Rayzan, Elham; Zoghi, Samaneh; Shahkarami, Sepideh; Raul, Jimenez Heredia; Sedighi, Iraj; Boztug, Kaan und Rezaei, Nima
(2021):
Novel BTK mutation in X-linked agammaglobulinemia: Report of a 17-year-old male.
In: Allergologia et Immunopathologia, Bd. 49, Nr. 2: S. 80-83
2020
Rahmani, Farzaneh; Rayzan, Elham; Rahmani, Mohammad Reza; Shahkarami, Sepideh; Zoghi, Samaneh; Rezaei, Arezoo; Aryan, Zahra; Najaf, Mehri; Rohlfs, Meino; Jeske, Tim; Aflatoonian, Majid; Chavoshzadeh, Zahra; Farahnnand, Fatemeh; Motamed, Farzaneh; Rohani, Pejman; Alinnadadi, Hossein; Mandaviani, Alireza; Mansouri, Mahboubeh; Tavakol, Marzieh; Vanderberg, Mirjam; Kotlarz, Daniel; Klein, Christoph und Rezaei, Nima
(2020):
Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR).
In: Immunological Investigations, Bd. 50, Nr. 4: S. 445-459
Momtazmanesh, Sara; Rayzan, Elham; Shahkarami, Sepideh; Rohlfs, Meino; Klein, Christoph und Rezaei, Nima
(2020):
A novelVPS13Bmutation in Cohen syndrome: a case report and review of literature.
In: BMC Medical Genetics, Bd. 21, Nr. 1, 140