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Volumn 1250, Issue 1, 2012, Pages 56-61

Primary immunodeficiency diseases in the Middle East

Author keywords

Middle East; Primary immunodeficiency; Saudi Arabia

Indexed keywords

CD40 ANTIGEN; INTERLEUKIN 1 RECEPTOR ASSOCIATED KINASE 4;

EID: 84857466998     PISSN: 00778923     EISSN: 17496632     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2011.06379.x     Document Type: Article
Times cited : (15)

References (37)
  • 2
    • 77954885007 scopus 로고    scopus 로고
    • Parental consanguinity and the risk of primary immunodeficiency disorders: report from the Kuwait National Primary Immunodeficiency Disorders Registry
    • Al-Herz, W., K.K. Naguib, L.D. Notarangelo, et al 2011. Parental consanguinity and the risk of primary immunodeficiency disorders: report from the Kuwait National Primary Immunodeficiency Disorders Registry. Int. Arch. Allergy Immunol. 154: 76-80.
    • (2011) Int. Arch. Allergy Immunol. , vol.154 , pp. 76-80
    • Al-Herz, W.1    Naguib, K.K.2    Notarangelo, L.D.3
  • 3
    • 84857464068 scopus 로고    scopus 로고
    • Primary Immunodeficiency Diseases: A Molecular & Cellular Approach, 2nd ed. Oxford University Press.
    • Ochs H.D., C.I.E. Smith & J. M. Puck 2006. Primary Immunodeficiency Diseases: A Molecular & Cellular Approach, 2nd ed. Oxford University Press.
    • (2006)
    • Ochs, H.D.1    Smith, C.I.E.2    Puck, J.M.3
  • 4
    • 57149144518 scopus 로고    scopus 로고
    • The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases
    • Al-Muhsen, S. & J.L. Casanova 2008. The genetic heterogeneity of mendelian susceptibility to mycobacterial diseases. J. Allergy Clin. Immunol. 122: 1043-1051.
    • (2008) J. Allergy Clin. Immunol. , vol.122 , pp. 1043-1051
    • Al-Muhsen, S.1    Casanova, J.L.2
  • 5
    • 70350367182 scopus 로고    scopus 로고
    • Consanguinity and reproductive health among Arabs
    • Tadmouri, G.O., P. Nair, T. Obeid, et al. 2009. Consanguinity and reproductive health among Arabs. Reprod. Health 6: 17.
    • (2009) Reprod. Health , vol.6 , pp. 17
    • Tadmouri, G.O.1    Nair, P.2    Obeid, T.3
  • 6
    • 0036844992 scopus 로고    scopus 로고
    • Primary immunodeficiency in Iran: first report of the National Registry of PID in children and adults
    • Aghamohammadi, A., M. Moein, A. Farhoudi, et al 2002. Primary immunodeficiency in Iran: first report of the National Registry of PID in children and adults. Clin. Immunol. 22: 375-380.
    • (2002) Clin. Immunol. , vol.22 , pp. 375-380
    • Aghamohammadi, A.1    Moein, M.2    Farhoudi, A.3
  • 7
    • 40149099628 scopus 로고    scopus 로고
    • Primary immunodeficiency disorders in Kuwait: first report from Kuwait National Primary Immunodeficiency Registry (2004-2006)
    • Epub 2007 Nov 16
    • Al-Herz, W. 2008. Primary immunodeficiency disorders in Kuwait: first report from Kuwait National Primary Immunodeficiency Registry (2004-2006). J. Clin. Immunol. 28: 186-193 [Epub 2007 Nov 16].
    • (2008) J. Clin. Immunol. , vol.28 , pp. 186-193
    • Al-Herz, W.1
  • 8
    • 33751084044 scopus 로고    scopus 로고
    • Frequency and clinical manifestations of patients with primary immunodeficiency disorders in Iran: update from the Iranian Primary Immunodeficiency Registry
    • Rezaei, N., A. Aghamohammadi, M. Moin, et al 2006. Frequency and clinical manifestations of patients with primary immunodeficiency disorders in Iran: update from the Iranian Primary Immunodeficiency Registry. J. Clin. Immunol. 26: 519-532.
    • (2006) J. Clin. Immunol. , vol.26 , pp. 519-532
    • Rezaei, N.1    Aghamohammadi, A.2    Moin, M.3
  • 9
    • 0027053748 scopus 로고
    • Chronic granulomatous disease with renal stones
    • Mohammed, S.H. & H. Vyas 1992. Chronic granulomatous disease with renal stones. Pediatr. Radiol. 22: 596-597.
    • (1992) Pediatr. Radiol. , vol.22 , pp. 596-597
    • Mohammed, S.H.1    Vyas, H.2
  • 11
    • 42949179437 scopus 로고    scopus 로고
    • Periodontal manifestation of leukocyte adhesion deficiency type I
    • Dababneh, R., A.M. Al-Wahadneh, S. Hamadneh, et al 2008. Periodontal manifestation of leukocyte adhesion deficiency type I. J. Periodontol. 79: 764-768.
    • (2008) J. Periodontol. , vol.79 , pp. 764-768
    • Dababneh, R.1    Al-Wahadneh, A.M.2    Hamadneh, S.3
  • 12
    • 39049180260 scopus 로고    scopus 로고
    • Bone marrow transplantation for leukocyte adhesion deficiency-I: case report
    • Al-wahadneh, A.M., I. Haddadin, M. Hamouri, et al 2006. Bone marrow transplantation for leukocyte adhesion deficiency-I: case report. Saudi J. Kidney Dis. Transpl. 17: 564-567.
    • (2006) Saudi J. Kidney Dis. Transpl. , vol.17 , pp. 564-567
    • Al-wahadneh, A.M.1    Haddadin, I.2    Hamouri, M.3
  • 13
    • 0036843771 scopus 로고    scopus 로고
    • Incidence of primary immunodeficiency syndromes in Israel
    • Golan, H., I. Dalal, B.Z. Garty, et al 2002. Incidence of primary immunodeficiency syndromes in Israel. Isr. Med. Assoc. J. 4(Suppl. 11): 868-871.
    • (2002) Isr. Med. Assoc. J. , vol.4 , Issue.SUPPL. 11 , pp. 868-871
    • Golan, H.1    Dalal, I.2    Garty, B.Z.3
  • 14
    • 50549084879 scopus 로고    scopus 로고
    • Stem cell transplantation for primary immunodeficiencies: King Faisal Specialist Hospital experience from 1993 to 2006
    • Al-Ghonaium, A. 2008. Stem cell transplantation for primary immunodeficiencies: King Faisal Specialist Hospital experience from 1993 to 2006. Bone Marrow Transplant. 42(Suppl. 1): S53-S56.
    • (2008) Bone Marrow Transplant , vol.42 , Issue.SUPPL. 1
    • Al-Ghonaium, A.1
  • 15
    • 79959744811 scopus 로고    scopus 로고
    • ICF syndrome in Saudi Arabia: immunological, cytogenetic and molecular analysis
    • Kaya, N., S. Al-Muhsen, B. Al-Saud, et al 2011. ICF syndrome in Saudi Arabia: immunological, cytogenetic and molecular analysis J. Clin. Immunol. 31(2): 245-252.
    • (2011) J. Clin. Immunol. , vol.31 , Issue.2 , pp. 245-252
    • Kaya, N.1    Al-Muhsen, S.2    Al-Saud, B.3
  • 16
    • 77955582316 scopus 로고    scopus 로고
    • Hematopoietic SCT in children with Griscelli syndrome: a single-center experience
    • Al-Ahmari, A., A. Al-Ghonaium, M. Al-Mansoori, et al 2010. Hematopoietic SCT in children with Griscelli syndrome: a single-center experience. Bone Marrow Transplant. 45: 1294-1299.
    • (2010) Bone Marrow Transplant , vol.45 , pp. 1294-1299
    • Al-Ahmari, A.1    Al-Ghonaium, A.2    Al-Mansoori, M.3
  • 17
    • 77952581213 scopus 로고    scopus 로고
    • Allogeneic stem cell transplantation using myeloablative and reduced-intensity conditioning in patients with major histocompatibility complex class II deficiency
    • Epub 2010 Jan 14
    • Al-Mousa, H., Z. Al-Shammari, A. Al-Ghonaium, et al 2010. Allogeneic stem cell transplantation using myeloablative and reduced-intensity conditioning in patients with major histocompatibility complex class II deficiency. Biol. Blood Marrow Transplant. 16: 818-823 [Epub 2010 Jan 14].
    • (2010) Biol. Blood Marrow Transplant , vol.16 , pp. 818-823
    • Al-Mousa, H.1    Al-Shammari, Z.2    Al-Ghonaium, A.3
  • 18
    • 79960273078 scopus 로고    scopus 로고
    • Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type 1: a single center experience
    • Al-Dhekri, H., H. Al-Mousa, M. Ayas, et al 2011. Allogeneic hematopoietic stem cell transplantation in leukocyte adhesion deficiency type 1: a single center experience. Biol. Blood Marrow Transplant. 17: 1245-1249.
    • (2011) Biol. Blood Marrow Transplant. , vol.17 , pp. 1245-1249
    • Al-Dhekri, H.1    Al-Mousa, H.2    Ayas, M.3
  • 19
    • 71049192431 scopus 로고    scopus 로고
    • Molecular analysis of T-B-NK± severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia
    • Alsmadi, O., A. Al-Ghonaium, S. Al-Muhsen, et al 2009. Molecular analysis of T-B-NK± severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia. BMC Med. Genet. 10: 116.
    • (2009) BMC Med. Genet. , vol.10 , pp. 116
    • Alsmadi, O.1    Al-Ghonaium, A.2    Al-Muhsen, S.3
  • 20
    • 67349129365 scopus 로고    scopus 로고
    • Primary immunodeficiency diseases in Egyptian children: a single-center study
    • Reda, S.M., H.M. Afifi & M.M. Amine 2009. Primary immunodeficiency diseases in Egyptian children: a single-center study. J. Clin. Immunol. 29: 343-351.
    • (2009) J. Clin. Immunol , vol.29 , pp. 343-351
    • Reda, S.M.1    Afifi, H.M.2    Amine, M.M.3
  • 21
    • 0035940417 scopus 로고    scopus 로고
    • Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM
    • Ferrari, S., S. Giliani, A. Insalaco, et al 2001. Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM. Proc. Natl. Acad. Sci. U.S.A. 98: 12614-12619.
    • (2001) Proc. Natl. Acad. Sci. U.S.A , vol.98 , pp. 12614-12619
    • Ferrari, S.1    Giliani, S.2    Insalaco, A.3
  • 22
    • 9144261081 scopus 로고    scopus 로고
    • Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity
    • Renner, E.D., J.M. Puck, S.M. Holland, et al 2004. Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity. J. Pediatr. 144: 939.
    • (2004) J. Pediatr. , vol.144 , pp. 939
    • Renner, E.D.1    Puck, J.M.2    Holland, S.M.3
  • 23
    • 70949098060 scopus 로고    scopus 로고
    • Combined immunodeficiency associated with DOCK8 mutations
    • Zhang, Q., J.C. Davis, I.T. Lamborn, et al 2009. Combined immunodeficiency associated with DOCK8 mutations. N. Engl. J. Med. 361: 2046-2055.
    • (2009) N. Engl. J. Med. , vol.361 , pp. 2046-2055
    • Zhang, Q.1    Davis, J.C.2    Lamborn, I.T.3
  • 24
    • 71149115670 scopus 로고    scopus 로고
    • Large deletions and point mutations involving DOCK8 in the autosomal recessive form of the hyper-IgE syndrome
    • Engelhardt, K.R., S. McGhee, S. Winkler, et al 2009. Large deletions and point mutations involving DOCK8 in the autosomal recessive form of the hyper-IgE syndrome. J. Allergy Clin. Immunol. 124: 1289.
    • (2009) J. Allergy Clin. Immunol. , vol.124 , pp. 1289
    • Engelhardt, K.R.1    McGhee, S.2    Winkler, S.3
  • 25
    • 70350500464 scopus 로고    scopus 로고
    • Familial hemophagocyticlymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11
    • Stadt, U., J. Rohr, W. Seifert, et al 2009. Familial hemophagocyticlymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11. Am. J. Hum. Genet. 85: 482-492.
    • (2009) Am. J. Hum. Genet. , vol.85 , pp. 482-492
    • Stadt, U.1    Rohr, J.2    Seifert, W.3
  • 26
    • 39249084392 scopus 로고    scopus 로고
    • Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases
    • Bustamante, J., S. Boisson-Dupuis, E. Jouanguy, et al 2008. Novel primary immunodeficiencies revealed by the investigation of paediatric infectious diseases. Curr. Opin. Immunol. 20: 39-48.
    • (2008) Curr. Opin. Immunol. , vol.20 , pp. 39-48
    • Bustamante, J.1    Boisson-Dupuis, S.2    Jouanguy, E.3
  • 27
    • 78649351360 scopus 로고    scopus 로고
    • Revisiting human IL-12RA1 deficiency: a survey of 141 patients from 30 countries
    • Beaucoudrey, L.D., A. Samarina, J. Bustamante, et al 2010. Revisiting human IL-12RA1 deficiency: a survey of 141 patients from 30 countries. Medicine (Baltimore) 89(6): 381-402.
    • (2010) Medicine (Baltimore) , vol.89 , Issue.6 , pp. 381-402
    • Beaucoudrey, L.D.1    Samarina, A.2    Bustamante, J.3
  • 28
    • 67651007827 scopus 로고    scopus 로고
    • A partial form of recessive STAT1 deficiency in humans
    • Chapgier, A., X.F. Kong, S. Boisson-Dupuis, et al 2009. A partial form of recessive STAT1 deficiency in humans. J. Clin. Invest. 119: 1502-1514.
    • (2009) J. Clin. Invest. , vol.119 , pp. 1502-1514
    • Chapgier, A.1    Kong, X.F.2    Boisson-Dupuis, S.3
  • 29
    • 78650633201 scopus 로고    scopus 로고
    • A novel form of human STAT1 deficiency impairing early but not late responses to interferons
    • Kong, X.F., M. Ciancanelli, S. Al-Hajjar, et al 2010. A novel form of human STAT1 deficiency impairing early but not late responses to interferons. Blood 116: 5895-5906.
    • (2010) Blood , vol.116 , pp. 5895-5906
    • Kong, X.F.1    Ciancanelli, M.2    Al-Hajjar, S.3
  • 30
    • 0037371835 scopus 로고    scopus 로고
    • Impaired response to interferon-alpha/beta and lethal viral disease in human STAT1 deficiency
    • Dupuis, S., E. Jouanguy, S. Al-Hajjar, et al 2003. Impaired response to interferon-alpha/beta and lethal viral disease in human STAT1 deficiency. Nat. Genet. 33: 388-391.
    • (2003) Nat. Genet. , vol.33 , pp. 388-391
    • Dupuis, S.1    Jouanguy, E.2    Al-Hajjar, S.3
  • 31
    • 0037471003 scopus 로고    scopus 로고
    • Pyogenic bacterial infections in humans with IRAK-4 deficiency
    • Picard, C., A. Puel, M. Bonnet, et al 2003. Pyogenic bacterial infections in humans with IRAK-4 deficiency. Science 299(5615): 2076.
    • (2003) Science , vol.299 , Issue.5615 , pp. 2076
    • Picard, C.1    Puel, A.2    Bonnet, M.3
  • 32
    • 78649358887 scopus 로고    scopus 로고
    • Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency
    • Picard, C., H. Bernuth, P. Ghandil, et al 2010. Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency. Medicine 89: 403-425.
    • (2010) Medicine , vol.89 , pp. 403-425
    • Picard, C.1    Bernuth, H.2    Ghandil, P.3
  • 33
    • 33750016788 scopus 로고    scopus 로고
    • Herpes simplex virus encephalitis in human UNC-93B deficiency
    • Casrouge, A., S.-Y. Zhang, C. Eidenschenk, et al 2006. Herpes simplex virus encephalitis in human UNC-93B deficiency. Science 314: 308-331.
    • (2006) Science , vol.314 , pp. 308-331
    • Casrouge, A.1    Zhang, S.-Y.2    Eidenschenk, C.3
  • 34
    • 34548699323 scopus 로고    scopus 로고
    • TLR3 deficiency in patients with herpes simplex encephalitis
    • Zhang, S-Y., E. Jouanguy, S. Ugolini, et al. 2007. TLR3 deficiency in patients with herpes simplex encephalitis. Science 317: 1522-1527.
    • (2007) Science , vol.317 , pp. 1522-1527
    • Zhang, S.-Y.1    Jouanguy, E.2    Ugolini, S.3
  • 35
    • 84055190795 scopus 로고    scopus 로고
    • Herpes simplex encephalitis in patients with autosomal recessive and dominant TRIF deficiency
    • Sancho-Shimizu1, V., R. Pérez de Diego, L. Lazaro Lorenzo, et al 2011. Herpes simplex encephalitis in patients with autosomal recessive and dominant TRIF deficiency. J. Clin. Invest. 121(12): 4889-4902.
    • (2011) J. Clin. Invest. , vol.121 , Issue.12 , pp. 4889-4902
    • Sancho-Shimizu1, V.1    de Pérez, D.R.2    Lorenzo, L.L.3
  • 36
    • 0017232852 scopus 로고
    • Familial hepatic venoocclusive disease with probable immune deficiency
    • Mellis, C. & P.M. Bale 1976. Familial hepatic venoocclusive disease with probable immune deficiency. J. Pediatr. 88: 236-242.
    • (1976) J. Pediatr. , vol.88 , pp. 236-242
    • Mellis, C.1    Bale, P.M.2
  • 37
    • 33745258176 scopus 로고    scopus 로고
    • Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease
    • Roscioli, T., S.T. Cliffe, D.B. Bloch, et al 2006. Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease. Nat. Genet. 38: 620-622.
    • (2006) Nat. Genet. , vol.38 , pp. 620-622
    • Roscioli, T.1    Cliffe, S.T.2    Bloch, D.B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.