نیما پروانه

متولد 1355 تهران

 دکتر نیما پروانه

تحصیلات:

فارغ التحصیل پزشکی عمومی 1381 دانشگاه علوم پزشکی اصفهان

بورد تخصصی بیماری های کودکان 1384 دانشگاه علوم پزشکی تهران

بورد فوق تخصصی آلرژی و ایمونولوژی بالینی 1393 دانشگاه علوم پزشکی تهران

 

سمت های علمی :

-استادیار بیماری های کودکان دانشگاه علوم پزشکی تهران 1385-1393

-دانشیار آلرژی و ایمونولوژی بالینی دانشگاه علوم پزشکی تهران 1393 تا کنون

– عضو شورای پژوهشی مرکز تحقیقات نقص ایمنی دانشگاه علوم پزشکی تهران

– عضو شورای پژوهشی مرکز تحقیقات بیماری های عفونی کودکان دانشگاه علوم پزشکی تهران

 

 

موفقیت های علمی و پژوهشی

 

  • رتبه اول کشوری امتحان بورد تخصصی بیماری های کودکان در سال 1384
  • رتبه اول کشوری امتحان بورد فوق تخصصی آلرژی و ایمونولوژی بالینی سال 1393
  • رتبه اول پژوهشگر جوان در یازدهمین جشنواره علوم پزشکی سینا
  • رتبه دوم مقاله بالینی در شانزدهمین جشنواره علوم پزشکی رازی

 

 

تالیف کتاب:

  • درمان بیماری های نقص ایمنی اولیه, 1385
  • نویسنده همکار در Primary Immunodeficiency Diseases ویرایشهای اول و دوم در سالهای 2008 و 2017

 

مقالات علمی: بیش از 100 مقاله علمی در مجلات داخلی و بین المللی (https://www.ncbi.nlm.nih.gov/pubmed/?term=parvaneh+n)

 

 

Primary immunodeficiencies: a rapidly evolving story.

Parvaneh N, Casanova JL, Notarangelo LD, Conley ME.

J Allergy Clin Immunol. 2013 Feb;131(2):314-23. doi: 10.1016/j.jaci.2012.11.051. Review.

1.

Vaccine-associated paralytic poliomyelitis in immunodeficient children, Iran, 1995-2008.

Shahmahmoodi S, Mamishi S, Aghamohammadi A, Aghazadeh N, Tabatabaie H, Gooya MM, Zahraei SM, Mousavi T, Yousefi M, Farrokhi K, Mohammadpour M, Ashrafi MR, Nategh R, Parvaneh N.

Emerg Infect Dis. 2010 Jul;16(7):1133-6. doi: 10.3201/eid1607.091606.

2.

Primary immunodeficiencies predisposed to Epstein-Barr virus-driven haematological diseases.

Parvaneh N, Filipovich AH, Borkhardt A.

Br J Haematol. 2013 Sep;162(5):573-86. doi: 10.1111/bjh.12422. Epub 2013 Jun 11. Review.

 

3.
 

Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2.

Ohbayashi N, Mamishi S, Ishibashi K, Maruta Y, Pourakbari B, Tamizifar B, Mohammadpour M, Fukuda M, Parvaneh N.

Pigment Cell Melanoma Res. 2010 Jun;23(3):365-74. doi: 10.1111/j.1755-148X.2010.00705.x. Epub 2010 Apr 3.

4.
 

Inborn errors of metabolism underlying primary immunodeficiencies.

Parvaneh N, Quartier P, Rostami P, Casanova JL, de Lonlay P.

J Clin Immunol. 2014 Oct;34(7):753-71. doi: 10.1007/s10875-014-0076-6. Epub 2014 Aug

5.
Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene.

Parvaneh N, Mamishi S, Rezaei A, Rezaei N, Tamizifar B, Parvaneh L, Sherkat R, Ghalehbaghi B, Kashef S, Chavoshzadeh Z, Isaeian A, Ashrafi F, Aghamohammadi A.

J Clin Immunol. 2010 Sep;30(5):756-60. doi: 10.1007/s10875-010-9433-2. Epub 2010 Jun 12

 

6.      
Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspot.

Mamishi S, Modarressi MH, Pourakbari B, Tamizifar B, Mahjoub F, Fahimzad A, Alyasin S, Bemanian MH, Hamidiyeh AA, Fazlollahi MR, Ashrafi MR, Isaeian A, Khotaei G, Yeganeh M, Parvaneh N.

J Clin Immunol. 2008 Jul;28(4):384-9. doi: 10.1007/s10875-008-9192-5. Epub 2008 Mar 19.

 

7.
Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency.

Parvaneh N, Ziaee V, Moradinejad MH, Touitou I.

J Clin Immunol. 2014 Jan;34(1):123-6. doi: 10.1007/s10875-013-9955-5. Epub 2013 Nov 1.

 

8.
 

Vaccine-associated paralytic poliomyelitis in a patient with MHC class II deficiency.

Parvaneh N, Shahmahmoudi S, Tabatabai H, Zahraei M, Mousavi T, Esteghamati AR, Gooya MM, Mamishi S, Nategh R, Kew OM.

J Clin Virol. 2007 Jun;39(2):145-8. Epub 2007 May 16

9.
Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency.

Parvaneh N, Teimourian S, Jacomelli G, Badalzadeh M, Bertelli M, Zakharova E, Tabatabaei P, Parvaneh L, Pourakbari B, Yeganeh M, Tamizifar B, Mamishi S, Micheli V.

Clin Biochem. 2008 Mar;41(4-5):350-2. Epub 2007 Nov 21. No abstract available

 

10.
 

Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis.

Mamishi S, Shahmahmoudi S, Tabatabaie H, Teimourian S, Pourakbari B, Gheisari Y, Yeganeh M, Salavati A, Esteghamati AR, Gooya MM, Nategh R, Parvaneh N.

Eur J Pediatr. 2008 Nov;167(11):1335-8. doi: 10.1007/s00431-008-0674-5. Epub 2008 Mar 4.

 

11.
Impaired in-vitro responses to IL-12 and IFN-γ in Iranian patients with Mendelian susceptibility to mycobacterial disease.

Parvaneh N, Pourakbari B, Rezaei N, Omidvar A, Sabouni F, Mahmoudi S, Khotaei G, Mamishi S.

Allergol Immunopathol (Madr). 2015 Sep-Oct;43(5):456-60. doi: 10.1016/j.aller.2014.05.008. Epub 2014 Sep 6.

12.
Retropharyngeal abscess after BCG vaccination. Parvaneh N, Mamishi S, Monajemzadeh M. Int J Ped Otolaryngol. 2006; 1: 279-281 13.
A novel deletion mutation in the human hairless (HR) gene in an Iranian family with atrichia and papular lesions.

Balighi K, Lajevardi V, Moeineddin F, Jelani M, Tamizifar B, Nikoo A, Javed Q, Ahmad W, Parvaneh N.

Clin Exp Dermatol. 2009 Oct;34(7):e498-500. doi: 10.1111/j.1365-2230.2009.03578.x. No abstract available

14.
Autoimmune Lymphoproliferative Syndrome: Meticulous Care for Diagnosis. Parvaneh N, Yeganeh M, Aghamohammadi A. 2005; 4: 197 15.
Parvaneh, N., Teimourian, S.

Letter to the Editor [1]

(2008) Archives of Iranian Medicine, 11 (1), pp. 129-130.

16.
Mandibuloacral dysplasia in an Iranian girl. Abbasi F, Parvaneh N, Mostafavi F, Mehdizadeh M, Shiva S, Rabbani A. Iran J Radiol. 2006; 3: 241-244. 17.
Parvaneh, N., Pourakbari, B., Daneshjoo, K.H., Ashraf, H., Salavati, A., Mamishi, S.

Polymorphism in the first intron of interferon-gamma gene (+874T/A) in patients with BCG adenitis

(2009) Iranian Journal of Public Health, 38 (3), pp. 12-16.

18.
Selective antibody deficiency and its relation to the IgG2 and IgG3 subclass titers in recurrent respiratory infections.

Sherkat R, Shoaei P, Parvaneh N, Babak A, Kassaian N.

Iran J Immunol. 2013 Mar;10(1):55-60. doi: IJIv10i1A7

19.
Deficient Expression of Bruton’s Tyrosine Kinase in Monocytes from X-Linked Agammaglobulinemia as

Evaluated by a Flow Cytometric Analysis and its Clinical Application to Carrier Detection. Asghar Aghamohammadi, Ali Akbar Amirzargar, Nima Parvaneh, Paul Marjousef, Mostafa Moin, Abolhassan Farhoudi, Mehdi Yeganeh, Toshio Miyawaki. Iran J Immunol. 2005; 2: 201-207

20.
Epidermodysplasia verruciformis associated with plasmablastic lymphoma and hepatitis B virus infection.

Shayanfar N, Babaheidarian P, Rahmani H, Azadmanesh K, Sohrabi A, Mohammadpour M, Mirzaie AZ, Parvaneh N.

Acta Dermatovenerol Croat. 2012;20(4):267-71.

21.
Cutaneous granulomas in common variable immunodeficiency: case report and review of literature.

Aghamohammadi A, Abolhassani H, Rezaei N, Kalantari N, Tamizifar B, Cheraghi T, Parvaneh N, Yeganeh M, Moazzami K, Ebrahimi-Daryani N, Anaraki MR.

Acta Dermatovenerol Croat. 2010;18(2):107-13. Review

22.
The effect of positive family history of autoimmunity in juvenile idiopathic arthritis characteristics; a case control study.

Khani M, Ziaee V, Moradinejad MH, Parvaneh N.

Iran J Pediatr. 2013 Oct;23(5):569-673.

23.
Neonatal marfan syndrome: report of two cases.

Ghandi Y, Zanjani KS, Mazhari-Mousavi SE, Parvaneh N.

Iran J Pediatr. 2013 Feb;23(1):113-7.

24.
Kalantari, N., Taherikalani, M., Parvaneh, N., Mamishi, S.

Etiology and antimicrobial susceptibility of bacterial septic arthritis and osteomyelitis

(2007) Iranian Journal of Public Health, 36 (3), pp. 27-32.

25.
Rezaei, A., Aghamohammadi, A., Moradinejad, M.H., Parvaneh, N., Rezaei, N., Seyedtabaei, R., Omran, H.A., Shahrestani, T., Amirzargar, A.A.

B-cell lineage study in patients with Juvenile idiopathic arthritis

(2008) Iranian Journal of Pediatrics, 18 (4), pp. 343-350.

26.
Aghamohammadi, A., Tavassoli, M., Abolhassani, H., Parvaneh, N., Moazzami, K., Allahverdi, A., Mahdaviani, S.-A., Atarod, L., Rezaei, N.

Infectious and non-infectious complications among undiagnosed patients with common variable immunodeficiency

(2009) Iranian Journal of Pediatrics, 19 (4), pp. 367-375.

27.
Assessment of pubertal development in Iranian girls.

Rabbani A, Motlagh ME, Mohammad K, Ardalan G, Maftoon F, Shahryari S, Khodaei S, Sotoudeh A, Mohammadi MR, Gharaei JM, Zia-Aldini H, Kamali K, Motaghian M, Hosseini KM, Salavati A, Rabbani A, Parvaneh N

28.
Successful treatment of fungal osteomyelitis with voriconazole in a patient with chronic granulomatous disease.

Mohammadpour M, Mamishi S, Oaji M, Pourpak Z, Parvaneh N.

Iran J Pediatr. 2010 Dec;20(4):487-90

29.
Timing of puberty in Iranian girls according to their living area: a national study.

Motlagh ME, Rabbani A, Kelishadi R, Mirmoghtadaee P, Shahryari S, Ardalan G, Ziaodini H, Parvaneh N, Khodaei S, Poursafa P, Sotoudeh A.

J Res Med Sci. 2011 Mar;16(3):276-81

30.
Health-related quality of life in primary antibody deficiency.

Aghamohammadi A, Montazeri A, Abolhassani H, Saroukhani S, Pourjabbar S, Tavassoli M, Darabi B, Imanzadeh A, Parvaneh N, Rezaei N.

Iran J Allergy Asthma Immunol. 2011 Mar;10(1):47-51. doi: 010.01/ijaai.4751

31.
Griscelli syndrome type 2; a pediatric case with immunodeficiency.

Tabatabaie P, Mahjoub F, Cheraghi T, Parvaneh N.

Iran J Allergy Asthma Immunol. 2007 Sep;6(3):155-7.

32.
Screening of the Bruton Tyrosine Kinase (BTK) Gene Mutations in 13 Iranian Patients with Presumed X-Linked Agammaglobulinemia.

Aghamohammadi A, Parvaneh N, Kanegana H, Moin M, Amirzargar AA, Farhoudi A, Pourpak Z, Movahedi M, Gharagozlou M, Rezaei N, Futatani T, Miyawaki T.

Iran J Allergy Asthma Immunol. 2004 Dec;3(4):175-9.

33.
Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency.

 

 

Ramyar A, Aghamohammadi A, Moazzami K, Rezaei N, Yeganeh M, Cheraghi T, Pouladi N, Heydari G, Abolhassani H, Amirzargar AA, Parvaneh N, Moin M.:

34.
Pubertal development in a random sample of 4,020 urban Iranian girls.

Rabbani A, Khodai S, Mohammad K, Sotoudeh A, Karbakhsh M, Nouri K, Salavati A, Parvaneh N.

J Pediatr Endocrinol Metab. 2008 Jul;21(7):681-7.

35.
Gastrointestinal manifestations in patients with common variable immunodeficiency.

Khodadad A, Aghamohammadi A, Parvaneh N, Rezaei N, Mahjoob F, Bashashati M, Movahedi M, Fazlollahi MR, Zandieh F, Roohi Z, Abdollahzade S, Salavati A, Kouhi A, Talebpour B, Daryani NE.Daryani NE.

36.
Disseminated Bacillus Calmette-Guerin infection after BCG vaccination.

Rezai MS, Khotaei G, Mamishi S, Kheirkhah M, Parvaneh N.

J Trop Pediatr. 2008 Dec;54(6):413-6. doi: 10.1093/tropej/fmn053. Epub 2008 Jul 1.

37.
Vitamin D insufficiency among children and adolescents living in Tehran, Iran.

Rabbani A, Alavian SM, Motlagh ME, Ashtiani MT, Ardalan G, Salavati A, Rabbani B, Rabbani A, Shams S, Parvaneh N.

J Trop Pediatr. 2009 Jun;55(3):189-91. doi: 10.1093/tropej/fmn078. Epub 2008 Sep 5.

38.
Mortality and morbidity in common variable immunodeficiency.

Aghamohammadi A, Pouladi N, Parvaneh N, Yeganeh M, Movahedi M, Gharagolou M, Pourpak Z, Rezaei N, Salavati A, Abdollahzade S, Moin M.

J Trop Pediatr. 2007 Feb;53(1):32-8. Epub 2006 Dec 13

39.
A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficiencies.

Mamishi S, Eghbali AN, Rezaei N, Abolhassani H, Parvaneh N, Aghamohammadi A.

Braz J Infect Dis. 2010 Jul-Aug;14(4):351-5.

40.
Diffuse dermal melanocytosis in two patients with Sandhoff disease and mucopolysaccharidosis VI.

Ashrafi MR, Tavasoli A, Shiva S, Parvaneh N, Tamizifar B.

Int J Dermatol. 2014 Jun;53(6):736-8. doi: 10.1111/ijd.12303. Epub 2013 Oct 18.

41.
2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay.

Rashidi-Nezhad A, Parvaneh N, Farzanfar F, Azimi C, Harewood L, Akrami SM, Reymond A.

Eur J Med Genet. 2012 Mar;55(3):203-10. doi: 10.1016/j.ejmg.2012.01.012. Epub 2012 Feb 4.

42.
Evaluation of antibody response to polysaccharide vaccine and switched memory B cells in pediatric patients with inflammatory bowel disease.

Fallahi G, Aghamohammadi A, Khodadad A, Hashemi M, Mohammadinejad P, Asgarian-Omran H, Najafi M, Farhmand F, Motamed F, Soleimani K, Soheili H, Parvaneh N, Darabi B, Nasiri Kalmarzi R, Pourhamdi S, Abolhassani H, Mirminachi B, Rezaei N.

Gut Liver. 2014 Jan;8(1):24-8. doi: 10.5009/gnl.2014.8.1.24. Epub 2013 Aug 14

43.
Novel UBR1 gene mutation in a patient with typical phenotype of Johanson-Blizzard syndrome.

Fallahi GH, Sabbaghian M, Khalili M, Parvaneh N, Zenker M, Rezaei N.

Eur J Pediatr. 2011 Feb;170(2):233-5. doi: 10.1007/s00431-010-1239-y. Epub 2010 Jun 17.

44.
Invasive aspergillosis in chronic granulomatous disease: report of 7 cases.

Mamishi S, Parvaneh N, Salavati A, Abdollahzadeh S, Yeganeh M.

Eur J Pediatr. 2007 Jan;166(1):83-4. Epub 2006 Jun 28. No abstract available.

45.
Molecular diagnosis of X-linked chronic granulomatous disease in Iran.

Teimourian S, Rezvani Z, Badalzadeh M, Kannengiesser C, Mansouri D, Movahedi M, Zomorodian E, Parvaneh N, Mamishi S, Pourpak Z, Moin M.

Int J Hematol. 2008 May;87(4):398-404. doi: 10.1007/s12185-008-0060-0.

46.
Treatment of pemphigus vulgaris with mycophenolate mofetil as a steroid-sparing agent.

Esmaili N, Chams-Davatchi C, Valikhani M, Farshidfar F, Parvaneh N, Tamizifar B.

Eur J Dermatol. 2008 Mar-Apr;18(2):159-64. doi: 10.1684/ejd.2008.0354.

47.
Evaluation of liver diseases in Iranian patients with primary antibody deficiencies.

Motamed F, Aghamohammadi A, Soltani M, Mansouri M, Rezaei N, Teimourian S, Pouladi N, Abdollahzadeh S, Parvaneh N.

Ann Hepatol. 2009 Jul-Sep;8(3):196-202

48.
First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literature.

Ehmke N, Parvaneh N, Krawitz P, Ashrafi MR, Karimi P, Mehdizadeh M, Krüger U, Hecht J, Mundlos S, Robinson PN.

Am J Med Genet A. 2014 Dec;164A(12):3170-5. doi: 10.1002/ajmg.a.36772. Epub 2014 Oct 20. Review.

49.
Behavior abnormality following intravenous immunoglobulin treatment in patients with primary antibody deficiencies.

Saroukhani S, Aghamohammadi A, Mahmoudi-Gharaei J, Abolhassani H, Cheraghi T, Imanzaeh A, Moazzami K, Parvaneh N, Rezaei N.

Hum Psychopharmacol. 2010 Jul;25(5):419-22. doi: 10.1002/hup.1125.

50.
IsoIation of a type 3 vaccine-derived poliovirus (VDPV) from an Iranian child with X-linked agammaglobulinemia.

Shahmahmoodi S, Parvaneh N, Burns C, Asghar H, Mamishi S, Tabatabaie H, Chen Q, Teimourian S, Gooya MM, Esteghamati AR, Mousavi T, Yousefi M, Farrokhi K, Mashlool M, Kew O, Nategh R.

Virus Res. 2008 Oct;137(1):168-72. doi: 10.1016/j.virusres.2008.07.006. Epub 2008 Aug 15.

51.
Impact of delayed diagnosis in children with primary antibody deficiencies.

Aghamohammadi A, Bahrami A, Mamishi S, Mohammadi B, Abolhassani H, Parvaneh N, Rezaei N.

J Microbiol Immunol Infect. 2011 Jun;44(3):229-34. doi: 10.1016/j.jmii.2011.01.026. Epub 2011 Jan 18

52.
Evaluation of serum IgA levels in Iranian patients with type 1 diabetes mellitus.

Sayarifard F, Aghamohammadi A, Haghi-Ashtiani MT, Rajab A, Irani H, Ahmadian JH, Zaridoost A, Parvaneh N, Rezaei N, Rabbani A.

Acta Diabetol. 2012 Apr;49(2):131-5. doi: 10.1007/s00592-010-0183-7. Epub 2010 Apr 22.

53.
Tuberculosis: a new look at an old disease.

Rezaei N, Aghamohammadi A, Mansouri D, Parvaneh N, Casanova JL.

Expert Rev Clin Immunol. 2011 Mar;7(2):129-31. doi: 10.1586/eci.11.1. No abstract available

54.
Common variable immunodeficiency: a heterogeneous group needs further subclassification.

Aghamohammadi A, Parvaneh N, Rezaei N.

Expert Rev Clin Immunol. 2009 Nov;5(6):629-31. doi: 10.1586/eci.09.65. No abstract available.

55.
Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients.

Aghamohammadi A, Abolhassani H, Latif A, Tabassomi F, Shokuhfar T, Torabi Sagvand B, Shahinpour S, Mirminachi B, Parvaneh N, Movahedi M, Gharagozlou M, Sherkat R, Amin R, Aleyasin S, Faridhosseini R, Jabbari-Azad F, Cheraghi T, Eslamian MH, Khalili A, Kalantari N, Shafiei A, Dabbaghzade A, Khayatzadeh A, Ebrahimi M, Razavinejad D, Bazregari S, Ebrahimi M, Ghaffari J, Bemanian MH, Behniafard N, Kashef S, Mohammadzadeh I, Hammarström L, Rezaei N. Expert Rev Clin Immunol. 2014 Oct;10(10):1405-17

56.
Adverse reactions of prophylactic intravenous immunoglobulin; a 13-year experience with 3004 infusions in Iranian patients with primary immunodeficiency diseases.

Dashti-Khavidaki S, Aghamohammadi A, Farshadi F, Movahedi M, Parvaneh N, Pouladi N, Moazzami K, Cheraghi T, Mahdaviani SA, Saghafi S, Heydari G, Abdollahzade S, Rezaei N.

J Investig Allergol Clin Immunol. 2009;19(2):139-45

57.
Analysis of class-switched memory B cells in patients with common variable immunodeficiency and its clinical implications.

Vodjgani M, Aghamohammadi A, Samadi M, Moin M, Hadjati J, Mirahmadian M, Parvaneh N, Salavati A, Abdollahzade S, Rezaei N, Srrafnejad A.

J Investig Allergol Clin Immunol. 2007;17(5):321-8

58.
Severe congenital neutropenia in 2 siblings of consanguineous parents. The role of HAX1 deficiency.

Mamishi S, Esfahani SA, Parvaneh N, Diestelhorst J, Rezaei N.

J Investig Allergol Clin Immunol. 2009;19(6):500-3.

59.
A novel RAB27A mutation in a patient with Griscelli syndrome type 2.

Shamsian BS, Norbakhsh K, Rezaei N, Safari A, Gharib A, Pourpak Z, Alavi S, Parvaneh N, Arzanian MT.

J Investig Allergol Clin Immunol. 2010;20(7):612-5.

60.
Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adults.

Aghamohammadi A, Abolhassani H, Moazzami K, Parvaneh N, Rezaei N.

J Investig Allergol Clin Immunol. 2010;20(5):372-9

61.
Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome.

Aghamohammadi A, Imai K, Moazzami K, Abolhassani H, Tabatabaeiyan M, Parvaneh N, Nasiri Kalmarzi R, Nakagawa N, Oshima K, Ohara O, Nonoyama S, Rezaei N.

J Investig Allergol Clin Immunol. 2010;20(5):442-5

62.
Autoimmune phenotype in patients with common variable immunodeficiency.

Abolhassani H, Amirkashani D, Parvaneh N, Mohammadinejad P, Gharib B, Shahinpour S, Hirbod-Mobarakeh A, Mirghorbani M, Movahedi M, Gharagozlou M, Rezaei N, Aghamohammadi A.

J Investig Allergol Clin Immunol. 2013;23(5):323-9.

63.
Molecular characterization of Bruton’s tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia.

Nasseri S, Sorouri R, Pourpak Z, Yeganeh M, Aghamohammadi A, Fiorini M, Shahkarami S, Mosallaei M, Rezaei N, Parvaneh N.

J Investig Allergol Clin Immunol. 2011;21(7):572-4. No abstract available.

64.
Genetic defects in B-cell development and their clinical consequences.

Abolhassani H, Parvaneh N, Rezaei N, Hammarström L, Aghamohammadi A.

J Investig Allergol Clin Immunol. 2014;24(1):6-22; quiz 2 p following 22. Review

65.
Severe primary antibody deficiency due to a novel mutation of mu heavy chain.

Mohammadzadeh I, Yeganeh M, Aghamohammadi A, Parvaneh N, Behniafard N, Abolhassani H, Tabassomi F, Hemmat M, Kanegane H, Miyawaki T, Ohara O, Rezaei N.

J Investig Allergol Clin Immunol. 2012;22(1):78-9. No abstract available

66.
Hematologically important mutations: leukocyte adhesion deficiency (first update).

van de Vijver E, Maddalena A, Sanal Ö, Holland SM, Uzel G, Madkaikar M, de Boer M, van Leeuwen K, Köker MY, Parvaneh N, Fischer A, Law SK, Klein N, Tezcan FI, Unal E, Patiroglu T, Belohradsky BH, Schwartz K, Somech R, Kuijpers TW, Roos D.

Blood Cells Mol Dis. 2012 Jan 15;48(1):53-61. doi: 10.1016/j.bcmd.2011.10.004. Epub 2011 Nov 30. Review.

67.
Progression of selective IgA deficiency to common variable immunodeficiency.

 

 

Aghamohammadi A, Mohammadi J, Parvaneh N, Rezaei N, Moin M, Espanol T, Hammarstrom L.

Int Arch Allergy Immunol. 2008;147(2):87-92. doi: 10.1159/000135694. Epub 2008 Jun 3.

68.
Clinical, immunological and molecular characteristics of 37 Iranian patients with X-linked agammaglobulinemia.

Aghamohammadi A, Fiorini M, Moin M, Parvaneh N, Teimourian S, Yeganeh M, Goffi F, Kanegane H, Amirzargar AA, Pourpak Z, Rezaei N, Salavati A, Pouladi N, Abdollahzade S, Notarangelo LD, Miyawaki T, Plebani A.

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Leuk Lymphoma. 2006 Feb;47(2):343-6. Review.

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Eur J Intern Med. 2012 Mar;23(2):e59-62. doi: 10.1016/j.ejim.2011.06.011. Epub 2011 Nov 12.

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Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.

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IgA deficiency: correlation between clinical and immunological phenotypes.

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J Clin Immunol. 2009 Jan;29(1):130-6. doi: 10.1007/s10875-008-9229-9. Epub 2008 Aug 6.

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L-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey.

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Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemia.

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Respirology. 2010 Feb;15(2):289-95. doi: 10.1111/j.1440-1843.2009.01679.x. Epub 2009 Dec 27

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Severe combined immunodeficiency: a cohort of 40 patients.

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Pediatr Allergy Immunol. 2008 Jun;19(4):303-6. Epub 2007 Dec 18

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Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia.

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J Pediatr. 2012 Apr;160(4):679-683.e2. doi: 10.1016/j.jpeds.2011.09.019. Epub 2011 Nov 1

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Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease.

Teimourian S, Zomorodian E, Badalzadeh M, Pouya A, Kannengiesser C, Mansouri D, Cheraghi T, Parvaneh N.

Br J Haematol. 2008 Jun;141(6):848-51. doi: 10.1111/j.1365-2141.2008.07148.x. Epub 2008 Apr 18.

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Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds.

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Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.

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Clin Infect Dis. 2014 Jan;58(2):204-13. doi: 10.1093/cid/cit722. Epub 2013 Nov 1

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The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2.

Jessen B, Bode SF, Ammann S, Chakravorty S, Davies G, Diestelhorst J, Frei-Jones M, Gahl WA, Gochuico BR, Griese M, Griffiths G, Janka G, Klein C, Kögl T, Kurnik K, Lehmberg K, Maul-Pavicic A, Mumford AD, Pace D, Parvaneh N, Rezaei N, de Saint Basile G, Schmitt-Graeff A, Schwarz K, Karasu GT, Zieger B, Zur Stadt U, Aichele P, Ehl S.

Blood. 2013 Apr 11;121(15):2943-51. doi: 10.1182/blood-2012-10-463166. Epub 2013 Feb 12.

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Combined immunodeficiency presenting with vaccine-associated paralytic poliomyelitis: a case report and narrative review of literature.

Shaghaghi M, Parvaneh N, Ostad-Rahimi P, Fathi SM, Shahmahmoodi S, Abolhassani H, Aghamohammadi A.

Immunol Invest. 2014;43(3):292-8. doi: 10.3109/08820139.2013.859156. Epub 2013 Dec 2. Review.

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Periodic Fever: a review on clinical, management and guideline for Iranian patients – part I.

Ahmadinejad Z1, Mansori S1, Ziaee V2, Alijani N1, Aghighi Y3, Parvaneh N4, Mordinejad MH5. Iran J Pediatr. 2014 Feb;24(1):1-13.

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