Nima Parvaneh

Summary

Affiliation: Tehran University of Medical Sciences
Country: Iran

Publications

  1. pmc Vaccine-associated paralytic poliomyelitis in immunodeficient children, Iran, 1995-2008
    Shohreh Shahmahmoodi
    Tehran University of Medical Sciences, 14194 Tehran, Iran
    Emerg Infect Dis 16:1133-6. 2010
  2. doi request reprint Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency
    Nima Parvaneh
    Pediatric Infectious Diseases Research Center, Children s Medical Center, Tehran University of Medical Sciences, 62 Gharib St, 14194, Tehran, Iran
    J Clin Immunol 34:123-6. 2014
  3. doi request reprint Primary immunodeficiencies predisposed to Epstein-Barr virus-driven haematological diseases
    Nima Parvaneh
    Paediatric Infectious Diseases Research Centre, Children s Medical Centre, Tehran University of Medical Sciences, Tehran, Iran
    Br J Haematol 162:573-86. 2013
  4. doi request reprint Primary immunodeficiencies: a rapidly evolving story
    Nima Parvaneh
    Pediatric Infectious Diseases Research Center, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    J Allergy Clin Immunol 131:314-23. 2013
  5. doi request reprint Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene
    Nima Parvaneh
    Infectious Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran
    J Clin Immunol 30:756-60. 2010
  6. doi request reprint Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency
    Asghar Ramyar
    Department of Pediatrics, Division of Hematology, Children Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran
    Iran J Allergy Asthma Immunol 7:169-75. 2008
  7. doi request reprint Isolation of a type 3 vaccine-derived poliovirus (VDPV) from an Iranian child with X-linked agammaglobulinemia
    Shohreh Shahmahmoodi
    National Polio Laboratory, School of Public Health and Institute of Public Health Research, Tehran University of Medical Sciences, Tehran, Iran
    Virus Res 137:168-72. 2008
  8. doi request reprint Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis
    Setareh Mamishi
    Department of Pediatrics, Infectious Disease Research Center, Children s Medical Center, Medical Sciences University of Tehran, Tehran, Iran
    Eur J Pediatr 167:1335-8. 2008
  9. doi request reprint IgA deficiency: correlation between clinical and immunological phenotypes
    Asghar Aghamohammadi
    Department of Pediatrics, Division of Immunology and Allergy, Children Medical Center Hospital, Tehran University of Medical Sciences, 62 Gharib St, Keshavarz Blvd, 14194, Tehran, Iran
    J Clin Immunol 29:130-6. 2009
  10. doi request reprint Clinical and laboratory findings in hyper-IgM syndrome with novel CD40L and AICDA mutations
    Asghar Aghamohammadi
    Center of Excellence for Pediatrics, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    J Clin Immunol 29:769-76. 2009

Collaborators

Detail Information

Publications45

  1. pmc Vaccine-associated paralytic poliomyelitis in immunodeficient children, Iran, 1995-2008
    Shohreh Shahmahmoodi
    Tehran University of Medical Sciences, 14194 Tehran, Iran
    Emerg Infect Dis 16:1133-6. 2010
    ..Changing to an inactivated polio vaccine vaccination schedule and introduction of screening of neonates for immunodeficiencies could reduce the risk for VAPP infection...
  2. doi request reprint Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency
    Nima Parvaneh
    Pediatric Infectious Diseases Research Center, Children s Medical Center, Tehran University of Medical Sciences, 62 Gharib St, 14194, Tehran, Iran
    J Clin Immunol 34:123-6. 2014
    ..Val377Ile). On demand dexamethasone resulted in a rapid amelioration of febrile episodes. The presentation of intermittent neutropenia has not been reported in HIDS and deserves more attention in large patient cohorts. ..
  3. doi request reprint Primary immunodeficiencies predisposed to Epstein-Barr virus-driven haematological diseases
    Nima Parvaneh
    Paediatric Infectious Diseases Research Centre, Children s Medical Centre, Tehran University of Medical Sciences, Tehran, Iran
    Br J Haematol 162:573-86. 2013
    ..Here, we summarize the range of PIDs that are predisposed to EBV-associated haematological diseases, describing their clinical picture and pathogenetic mechanisms. ..
  4. doi request reprint Primary immunodeficiencies: a rapidly evolving story
    Nima Parvaneh
    Pediatric Infectious Diseases Research Center, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    J Allergy Clin Immunol 131:314-23. 2013
    ..These new findings highlight the molecular pathways that are associated with clinical phenotypes and suggest potential therapies for affected patients...
  5. doi request reprint Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene
    Nima Parvaneh
    Infectious Disease Research Center, Tehran University of Medical Sciences, Tehran, Iran
    J Clin Immunol 30:756-60. 2010
    ..Severe recurrent infections, impaired wound healing, and periodontal diseases are the main features of disease...
  6. doi request reprint Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency
    Asghar Ramyar
    Department of Pediatrics, Division of Hematology, Children Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran
    Iran J Allergy Asthma Immunol 7:169-75. 2008
    ..Chronic and recurrent ITP, especially in the presence of propensity to respiratory and gastrointestinal infections mandate the evaluation for an underlying immune dysregulation such as CVID...
  7. doi request reprint Isolation of a type 3 vaccine-derived poliovirus (VDPV) from an Iranian child with X-linked agammaglobulinemia
    Shohreh Shahmahmoodi
    National Polio Laboratory, School of Public Health and Institute of Public Health Research, Tehran University of Medical Sciences, Tehran, Iran
    Virus Res 137:168-72. 2008
    ..No secondary AFP cases were found, and none of the seven tested contacts of the patient were found to be infected with poliovirus...
  8. doi request reprint Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis
    Setareh Mamishi
    Department of Pediatrics, Infectious Disease Research Center, Children s Medical Center, Medical Sciences University of Tehran, Tehran, Iran
    Eur J Pediatr 167:1335-8. 2008
    ..This suggests that a negative history for recurrent infections does not exclude the presence of a primary defect in the immune system...
  9. doi request reprint IgA deficiency: correlation between clinical and immunological phenotypes
    Asghar Aghamohammadi
    Department of Pediatrics, Division of Immunology and Allergy, Children Medical Center Hospital, Tehran University of Medical Sciences, 62 Gharib St, Keshavarz Blvd, 14194, Tehran, Iran
    J Clin Immunol 29:130-6. 2009
    ..We aimed to investigate the clinical features in relation to immune function of Iranian patients with symptomatic IGAD...
  10. doi request reprint Clinical and laboratory findings in hyper-IgM syndrome with novel CD40L and AICDA mutations
    Asghar Aghamohammadi
    Center of Excellence for Pediatrics, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    J Clin Immunol 29:769-76. 2009
    ..These patients have immunoglobulin class switch recombination defects, caused by mutations in several genes...
  11. doi request reprint Health-related quality of life in primary antibody deficiency
    Asghar Aghamohammadi
    Research Center for Immunodeficiency, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Iran J Allergy Asthma Immunol 10:47-51. 2011
    ..However, the patients with severe phenotypes and long delay in diagnosis showed lower QoL, even in medical management...
  12. ncbi request reprint Evaluation of liver diseases in Iranian patients with primary antibody deficiencies
    Farzaneh Motamed
    Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Ann Hepatol 8:196-202. 2009
    ..Patients with primary antibody deficiency (PAD) can complicate with liver disease. This study was performed in order to study the prevalence and causes of hepatobiliary diseases in Iranian patients with PAD...
  13. doi request reprint Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemia
    Asghar Aghamohammadi
    Department of Pediatrics, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Respirology 15:289-95. 2010
    ..Early diagnosis and appropriate treatment reduces the incidence of pulmonary infections in both groups of patients. However, CVID patients are prone to progressive lung disease despite optimal immunoglobulin therapy...
  14. ncbi request reprint Cutaneous granulomas in common variable immunodeficiency: case report and review of literature
    Asghar Aghamohammadi
    Department of Allergy and Clinical Immunology Children s Medical Center, No 62 Dr Gharib St, Keshavarz Blvd, Tehran, Iran
    Acta Dermatovenerol Croat 18:107-13. 2010
    ..In conclusion, taking history of recurrent infections and measuring immunoglobulin levels can be suggested in patients with granulomatous lesions instead of other expensive tests...
  15. doi request reprint Behavior abnormality following intravenous immunoglobulin treatment in patients with primary antibody deficiencies
    Sepide Saroukhani
    Research Center for Immunodeficiencies, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Hum Psychopharmacol 25:419-22. 2010
    ..Meantime behavioral disorders reactions have not been reported yet. In this study, we describe for the first time a group of patients with PADs, who were under IVIG therapy and experienced some behavioral disorders...
  16. ncbi request reprint Gastrointestinal manifestations in patients with common variable immunodeficiency
    Ahmad Khodadad
    Department of Pediatrics, Division of Gastroenterology, Children s Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran
    Dig Dis Sci 52:2977-83. 2007
    ..CVID patients are at increased risk of infectious and inflammatory conditions in the GI tract. Early diagnosis of these complications improves the quality of life and well-being of patients...
  17. ncbi request reprint Mortality and morbidity in common variable immunodeficiency
    Asghar Aghamohammadi
    Children s Medical Center, Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran
    J Trop Pediatr 53:32-8. 2007
    ..Based on our observation, it can be highlighted that all patients with CVID, even under regular immunoglobulin replacement, need close monitoring for early detection of complications and introduction of appropriate management...
  18. doi request reprint Analysis of switched memory B cells in patients with IgA deficiency
    Asghar Aghamohammadi
    Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, 62 Gharib Street, Tehran, Iran
    Int Arch Allergy Immunol 156:462-8. 2011
    ..Despite several investigations into the nature of the disease, the exact pathophysiology of SIGAD is still unknown...
  19. ncbi request reprint Severe combined immunodeficiency: a cohort of 40 patients
    Mehdi Yeganeh
    Immunology, Asthma and Allergy Research Institute, Division of Allergy and Clinical Immunology, Children s Medical Centre, Medical Sciences University of Tehran, Tehran, Iran
    Pediatr Allergy Immunol 19:303-6. 2008
    ..A complete blood count of cord blood could reveal lymphocytopenia at birth; this helps early diagnosis. Genetic consultation would help the families with affected members preventing new SCID offspring...
  20. doi request reprint Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspot
    Setareh Mamishi
    Infectious Disease Research Center, Children s Medical Center, 62 Gharib St, 14194 Tehran, Iran
    J Clin Immunol 28:384-9. 2008
    ..The disease is caused by mutations in RAB27A gene, coding a small GTPase involved in terminal phases of cytotoxic granule/melanosome exocytosis...
  21. ncbi request reprint Screening of the Bruton Tyrosine Kinase (BTK) Gene Mutations in 13 Iranian Patients with Presumed X-Linked Agammaglobulinemia
    Asghar Aghamohammadi
    Department of Clinical Pediatric Immunology of Children s Medical Center, Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran
    Iran J Allergy Asthma Immunol 3:175-9. 2004
    ..The results of this study further support the notion that molecular genetic testing represents an important tool for definitive and early diagnosis of XLA and may allow accurate carrier detection and prenatal diagnosis...
  22. ncbi request reprint A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficiencies
    Setareh Mamishi
    Department of Pediatrics, Children s Medical Center, Tehran University of Medical Sciences, Iran
    Braz J Infect Dis 14:351-5. 2010
    ..Respiratory tract infections were the prominent cause of hospitalization among studied patients, followed by gastrointestinal infections...
  23. doi request reprint Impact of delayed diagnosis in children with primary antibody deficiencies
    Asghar Aghamohammadi
    Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    J Microbiol Immunol Infect 44:229-34. 2011
    ..To evaluate the diagnostic delay in Iranian PADs in association with their infections, we scored such manifestations to find an association between such delay and the scoring system...
  24. pdf Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease
    Shahram Teimourian
    Immunology, Asthma and Allergy Research Institute, Medical Sciences of Tehran University, and Department of Cell and Molecular Biology, Khatam University, Tehran, Iran
    Br J Haematol 141:848-51. 2008
    ..373G>A); a splice site mutation in intron 5 (c.369+1G>A); a frameshift in exon 6 (c.385delGAGC); a frameshift in exon 3 (c.174delG); and a frameshift in exon 4 (c.223delC)...
  25. doi request reprint Progression of selective IgA deficiency to common variable immunodeficiency
    Asghar Aghamohammadi
    Department of Allergy and Clinical Immunology, Children s Medical Center, Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran
    Int Arch Allergy Immunol 147:87-92. 2008
    ..Early diagnosis of this conversion and institution of immunoglobulin therapy is effective in preventing severe bacterial infections and pulmonary insufficiency...
  26. ncbi request reprint Vaccine-associated paralytic poliomyelitis in a patient with MHC class II deficiency
    Nima Parvaneh
    Department of Pediatrics, Infectious Disease Research Center, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    J Clin Virol 39:145-8. 2007
    ..We describe a fatal case of VAPP in an 8-month-old boy with Major Histocompatibility Class II deficiency. The isolated poliovirus was a Sabin type 2-type 1 recombinant that showed 1.4% VP1 divergence from Sabin type 2...
  27. pmc Assessment of pubertal development in Iranian girls
    Ali Rabbani
    Growth and Development Research Center, Tehran University of Medical Sciences, Tehran, IR Iran Department of Pediatrics, Tehran University of Medical Sciences, Tehran, IR Iran Children s Medical Center, Pediatrics Center of Excellence, Tehran, IR Iran
    Iran J Pediatr 20:160-6. 2010
    ..We estimated pubertal development of 7,493 normal Iranian girls aged 6 to 20 years in a cross-sectional study...
  28. doi request reprint Evaluation of serum IgA levels in Iranian patients with type 1 diabetes mellitus
    Fatemeh Sayarifard
    Department of Pediatrics, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Acta Diabetol 49:131-5. 2012
    ..7% (1:150), which is much higher than reported prevalences in general populations. Further studies are needed for better understanding the possible etiologies of increased IgA deficiency in DM1 and its effects on diabetes control...
  29. ncbi request reprint Disseminated Bacillus Calmette-Guerin infection after BCG vaccination
    Mohammad Sadegh Rezai
    Department of Pediatrics, School of Medicine, Medical Sciences University of Tehran, Tehran, Iran
    J Trop Pediatr 54:413-6. 2008
    ..Severe immune-compromised infants are at greatest risk and they respond poorly to standard therapies...
  30. pmc Evaluation of antibody response to polysaccharide vaccine and switched memory B cells in pediatric patients with inflammatory bowel disease
    Gholamhossein Fallahi
    Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Gut Liver 8:24-8. 2014
    ..Inflammatory bowel disease (IBD) is a chronic disease of the gastrointestinal tract, whose etiologies are still unknown. This study was performed to evaluate the humoral immune response in terms of B cell functions in selected IBD patients...
  31. doi request reprint Human papillomavirus detected in esophageal squamous cell carcinoma in Iran
    Afshin Abdirad
    Tehran University of Medical Sciences, The Cancer Research Center, Tehran, Iran
    Eur J Intern Med 23:e59-62. 2012
    ....
  32. doi request reprint Combined immunodeficiency presenting with vaccine-associated paralytic poliomyelitis: a case report and narrative review of literature
    Mohammadreza Shaghaghi
    Research Center for Immunodeficiencies, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Science, Tehran, Iran
    Immunol Invest 43:292-8. 2014
    ..Herein we report a case of combined immunodeficiency with paralytic complication due to oral polio vaccine and we present a literature review on this topic. ..
  33. doi request reprint Vitamin D insufficiency among children and adolescents living in Tehran, Iran
    Ali Rabbani
    Growth and Development Research Center, Children s Medical Center, Tehran University of Medical Sciences, 62 Gharib St, Tehran 14155 6386, Iran
    J Trop Pediatr 55:189-91. 2009
    ..Encouraging girls to have more sun exposure, fortification of foods and prescription of supplemental vitamin D are recommended...
  34. pmc Timing of puberty in Iranian girls according to their living area: a national study
    Mohammad Esmaeil Motlagh
    Bureau of Family Health, Ministry of Health and Medical Education, Tehran, Iran
    J Res Med Sci 16:276-81. 2011
    ..This study aimed to compare the timing of puberty between various geographic locations and different ethnicities...
  35. ncbi request reprint Diffuse dermal melanocytosis in two patients with Sandhoff disease and mucopolysaccharidosis VI
    Mahmoud Reza Ashrafi
    Department of Pediatrics, Children s Medical Center, Tehran, Iran
    Int J Dermatol 53:736-8. 2014
    ..We describe for the first time the presence of DM in two patients with Sandhoff disease and mucopolysaccharidosis VI. ..
  36. doi request reprint Treatment of pemphigus vulgaris with mycophenolate mofetil as a steroid-sparing agent
    Nafiseh Esmaili
    Department of Dermatology, School of Medicine, Medical Sciences University of Tehran, Tehran, Iran
    Eur J Dermatol 18:159-64. 2008
    ..3%. It can be concluded that, except for generalized diseases, mycophenolate mofetil can be used safely and effectively in patients with pemphigus vulgaris as a first line, steroid sparing agent...
  37. ncbi request reprint Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemia
    Asghar Aghamohammadi
    Division of Clinical Pediatric Immunology, Children s Medical Center, Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran
    Int Arch Allergy Immunol 141:408-14. 2006
    ..Eighty-five percent of the patients with this phenotype have mutations in Bruton's tyrosine kinase (BTK) gene...
  38. ncbi request reprint Pubertal development in a random sample of 4,020 urban Iranian girls
    Ali Rabbani
    Growth and Development Research Center, Children s Medical Center, Tehran, Iran
    J Pediatr Endocrinol Metab 21:681-7. 2008
    ..Entering puberty is an important milestone of human growth and maturation associated with marked physiological and psychological changes...
  39. ncbi request reprint Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiency
    Nima Parvaneh
    Children s Hospital Center, Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran
    Brain Dev 29:124-6. 2007
    ..Neurologic abnormalities are salient features of this syndrome. We describe for the first time a patient with this rare disorder presented with progressive multifocal leukoencephalopathy...
  40. ncbi request reprint Griscelli syndrome type 2; a pediatric case with immunodeficiency
    Parviz Tabatabaie
    Department of Pediatric Infectious Disease, Children s Medical Center, School of Medicine, Medical Sciences, University of Tehran, Tehran, Iran
    Iran J Allergy Asthma Immunol 6:155-7. 2007
    ..On the basis of these clinical and laboratory findings, Griscelli syndrome was diagnosed. The child succumbed to infection during an accelerated phase of the disease...
  41. pmc Successful treatment of fungal osteomyelitis with voriconazole in a patient with chronic granulomatous disease
    Masoud Mohammadpour
    Department of Pediatrics, Tehran University of Medical Sciences, Tehran, IR Iran Children s Medical Center, Pediatrics Center of Excellence, Tehran University of Medical Sciences, Tehran, IR Iran
    Iran J Pediatr 20:487-90. 2010
    ..With the great successes in antibacterial prophylaxis and therapy, fungal infections are a persistent problem. Invasive aspergillosis is the most important cause of mortality in CGD...
  42. ncbi request reprint Autoimmune lymphoproliferative syndrome: meticulous care for diagnosis
    Nima Parvaneh
    Children s Medical Center, Department of Pediatrics, Tehran University of Medical Sciences, Tehran, Iran
    Iran J Allergy Asthma Immunol 4:197. 2005
    ..Although the clinical presentation was in favor of ALPS, a precise diagnosis needed more laboratory evaluations...
  43. ncbi request reprint Lymphoma of mucosa-associated lymphoid tissue in common variable immunodeficiency
    Asghar Aghamohammadi
    Department of Clinical Pediatric Immunology, Children s Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran
    Leuk Lymphoma 47:343-6. 2006
    ..Open lung biopsy showed a MALT lymphoma. Although a rare complication, pulmonary low grade B-cell lymphoma is a diagnosis that must be kept in mind in CVID patients with chronic pulmonary symptoms unresponsive to conventional therapies...
  44. ncbi request reprint Invasive aspergillosis in chronic granulomatous disease: report of 7 cases
    Setareh Mamishi
    Department of Pediatrics, Infectious Disease Research Center, Children s Medical Center, Tehran University of Medical Sciences, No 62, Gharib St, Tehran 14194, Iran
    Eur J Pediatr 166:83-4. 2007
  45. doi request reprint Novel UBR1 gene mutation in a patient with typical phenotype of Johanson-Blizzard syndrome
    Gholam Hossein Fallahi
    Department of Pediatrics, Pediatrics Center of Excellence, Children s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
    Eur J Pediatr 170:233-5. 2011
    ..Prompt diagnosis and exact monitoring of the patients with JBS are required to avoid further complications...