A. Ramyar

发表

The Clinical, Immunohematological, and Molecular Study of Iranian Patients with Severe Congenital Neutropenia

C. Klein, N. Rezaei, R. Sherkat, 2007, Journal of Clinical Immunology.

Features of Childhood Acute Myeloid Leukemia in Iran: a Report from Double Center Study.

A. Mehrvar, A. Ramyar, M. Alebouyeh, 2015, Acta medica Iranica.

Higher frequencies of chromosomal aberrations in lymphocytes of children with acute lymphoblastic leukemia after in vitro gamma irradiation

A. Aghamohammadi, K. Divsalar, A. Ramyar, 2012 .

HODGKIN LYMPHOMA IN TWO SIBLINGS WITH COMMON VARIABLE IMMUNODEFICIENCY

N. Rezaei, A. Aghamohammadi, K. Rezaei-Kalantari, 2007, Pediatric hematology and oncology.

Congenital Neutropenia and Primary Immunodeficiency Disorders: A Survey of 26 Iranian Patients

N. Rezaei, M. Mahmoudi, A. Aghamohammadi, 2005, Journal of pediatric hematology/oncology.

Study of SH2D1A gene mutation in paediatric patients with B-cell lymphoma.

N. Rezaei, A. Aghamohammadi, A. Ramyar, 2015, Allergologia et immunopathologia.

Hemophagocytic lymphohistiocytosis in a neonate with cutis marmorata telangiectatica congenita.

A. Ramyar, B. Elahi, 2006, Saudi medical journal.

Teratoid Wilms’ Tumor with Hypertension Treated with Partial Nephrectomy: Case Report with Literature Review

A. Ramyar, A. Kajbafzadeh, F. Mahjoob, 2009, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency.

N. Pouladi, N. Rezaei, K. Moazzami, 2008, Iranian journal of allergy, asthma, and immunology.

Hemophagocytic Lymphohistiocytosis in a Neonate: Case Report.

H. Dalili, A. Ramyar, Z. Mosayebi, 2017, Acta medica Iranica.

Bilateral basal ganglia involvement in a patient with Griscelli syndrome.

A. Aghamohammadi, A. Ramyar, M. Izadyar, 2006, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Spectrum of Bone Marrow Failures of Myeloid Series: New Report of Neutropenic Patients from a Referral Pediatric Center in Iran

N. Rezaei, K. Moazzami, A. Aghamohammadi, 2014, Pediatric hematology and oncology.

Severe Congenital Neutropenia or Hyper-IgM Syndrome? A Novel Mutation of CD40 Ligand in a Patient with Severe Neutropenia

Lennart Hammarstrom, N. Rezaei, A. Aghamohammadi, 2008, International Archives of Allergy and Immunology.

Cytologic phenotypes of B-cell acute lymphoblastic leukemia-a single center study.

N. Rezaei, K. Moazzami, A. Aghamohammadi, 2009, Iranian journal of allergy, asthma, and immunology.

CONGENITAL SELF HEALING CUTANEOUS LANGERHANS CELL HISTIOCYTOSIS WITH MULTIPLE HYPOPIGMENTED MACULES AFTER RECOVERY IN A NEONATE

A. Ramyar, M. Monajemzadeh, B. Yaghmaei, 2008 .

A neonate with indurate dermal papules and nodules and pneumonia: a case report.

A. Ramyar, S. Esmaeili, M. Monajemzadeh, 2014, Acta medica Iranica.

Severe valvular toxicity and pericarditis early after radiation therapy in a patient treated for Hodgkin's lymphoma.

N. Rezaei, K. Moazzami, A. Ramyar, 2010, The Turkish journal of pediatrics.

Treatment of ITP, prednisolone versus IVIG: a 12 month study in Children's Medical Center

A. Ramyar, Kalantari Najm Aldin, 2008 .

Clinical and laboratory findings in Iranian children with cyclic neutropenia.

N. Rezaei, M. Mahmoudi, A. Aghamohammadi, 2004, Iranian journal of allergy, asthma, and immunology.

In vitro chromosomal radiosensitivity in patients with common variable immunodeficiency

N. Rezaei, A. Aghamohammadi, H. Mozdarani, 2018, Central-European journal of immunology.

Assessment of in vitro chromosomal sensitivity to low doses of gamma irradiation in patients with acute lymphoblastic leukemia

N. Rezaei, A. Aghamohammadi, H. Mozdarani, 2011 .

Novel Mutation Detection of an Inflammatory Molecule Elastase ii Gene Encoding Neutrophil Elastase in Kostmann Syndrome

Z. Lari, A. Ramyar, Z. Chavoshzadeh, 2007 .

Relapse of Acute Lymphoblastic Leukemia as a Conjunctival Mass in a 9-Year-Old Girl.

A. Ramyar, M. Kanavi, M. Javadi, 2010, Journal of pediatric ophthalmology and strabismus.

UNUSUAL PRESENTATION OF RELAPSING ACUTE LYMPHOBLASTIC LEUKEMIA

A. Ramyar, M. Kanavi, M. Javadi, 2010 .

Langerhans cell histiocytosis: A case report of a three year old boy with primary oral manifestations

S. Ghadimi, A. Ramyar, B. Seraj, 2006 .

Study of SH2D1A gene mutation in paediatric patients with B-cell lymphoma.

A. Aghamohammadi, A. Ramyar, M. Izadyar, 2015, Allergologia et immunopathologia.