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Items: 1 to 20 of 22

1.

Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients.

Ben-Mustapha I, Ben-Farhat K, Guirat-Dhouib N, Dhemaied E, Larguèche B, Ben-Ali M, Chemli J, Bouguila J, Ben-Mansour L, Mellouli F, Khemiri M, Béjaoui M, Barbouche MR.

J Clin Immunol. 2013 May;33(4):865-70. doi: 10.1007/s10875-013-9863-8. Epub 2013 Jan 13.

PMID:
23314770
2.

Combined immunodeficiency with defective expression in MHC class II genes.

Griscelli C, Lisowska-Grospierre B, Mach B.

Immunodefic Rev. 1989;1(2):135-53. Review.

PMID:
2517209
3.

C5 complement deficiency in a Saudi family, molecular characterization of mutation and literature review.

Arnaout R, Al Shorbaghi S, Al Dhekri H, Al-Mousa H, Al Ghonaium A, Al Saud B, Al Muhsen S, Al Baik L, Hawwari A.

J Clin Immunol. 2013 May;33(4):871-5. doi: 10.1007/s10875-013-9872-7. Epub 2013 Feb 1. Review.

PMID:
23371790
4.

MHC class II deficiency cured by unrelated mismatched umbilical cord blood transplantation: case report and review of 68 cases in the literature.

Siepermann M, Gudowius S, Beltz K, Strier U, Feyen O, Troeger A, Göbel U, Laws HJ, Kögler G, Meisel R, Dilloo D, Niehues T.

Pediatr Transplant. 2011 Jun;15(4):E80-6. doi: 10.1111/j.1399-3046.2010.01292.x. Epub 2010 Mar 4. Review.

PMID:
20214747
5.

The MHC in human bone marrow allotransplantation.

Yunis EJ, Awdeh Z, Raum D, Alper CA.

Clin Haematol. 1983 Oct;12(3):641-80. Review.

PMID:
6227438
6.

Bone marrow transplantation in major histocompatibility complex class II deficiency: a single-center study of 19 patients.

Klein C, Cavazzana-Calvo M, Le Deist F, Jabado N, Benkerrou M, Blanche S, Lisowska-Grospierre B, Griscelli C, Fischer A.

Blood. 1995 Jan 15;85(2):580-7. Review.

7.

[Primary immunodeficiencies. Clinical features and variant forms].

Fontán Casariego G.

Allergol Immunopathol (Madr). 2001 May-Jun;29(3):101-7. Review. Spanish.

PMID:
11434882
8.

Consanguinity and primary immunodeficiencies.

Al-Herz W, Aldhekri H, Barbouche MR, Rezaei N.

Hum Hered. 2014;77(1-4):138-43. doi: 10.1159/000357710. Epub 2014 Jul 29. Review.

PMID:
25060276
9.

Report of the Tunisian Registry of Primary Immunodeficiencies: 25-Years of Experience (1988-2012).

Mellouli F, Mustapha IB, Khaled MB, Besbes H, Ouederni M, Mekki N, Ali MB, Larguèche B, Hachicha M, Sfar T, Gueddiche N, Barsaoui S, Sammoud A, Boussetta K, Becher SB, Meherzi A, Guandoura N, Boughammoura L, Harbi A, Amri F, Bayoudh F, Jaballah NB, Tebib N, Bouaziz A, Mahfoudh A, Aloulou H, Mansour LB, Chabchoub I, Boussoffara R, Chemli J, Bouguila J, Hassayoun S, Hammami S, Habboul Z, Hamzaoui A, Ammar J, Barbouche MR, Bejaoui M.

J Clin Immunol. 2015 Nov;35(8):745-53. doi: 10.1007/s10875-015-0206-9. Epub 2015 Oct 13. Review.

PMID:
26464197
10.

Major histocompatibility complex class II deficiency: a clinical review.

Elhasid R, Etzioni A.

Blood Rev. 1996 Dec;10(4):242-8. Review.

PMID:
9012922
11.

Clinical, immunological, and molecular characterization of hyper-IgM syndrome due to CD40 deficiency in eleven patients.

Al-Saud BK, Al-Sum Z, Alassiri H, Al-Ghonaium A, Al-Muhsen S, Al-Dhekri H, Arnaout R, Alsmadi O, Borrero E, Abu-Staiteh A, Rawas F, Al-Mousa H, Hawwari A.

J Clin Immunol. 2013 Nov;33(8):1325-35. Review.

PMID:
24122029
12.

Primary immune deficiency disorders in the South Pacific: the clinical utility of a customized genetic testing program in New Zealand.

Ameratunga R, Woon ST, Brewerton M, Koopmans W, Jordan A, Brothers S, Singh R.

Ann N Y Acad Sci. 2011 Nov;1238:53-64. doi: 10.1111/j.1749-6632.2011.06238.x. Review.

PMID:
22129053
13.

Flow cytometric immunophenotyping in the diagnosis and follow-up of immunodeficient children.

de Vries E, Noordzij JG, Kuijpers TW, van Dongen JJ.

Eur J Pediatr. 2001 Oct;160(10):583-91. Review.

PMID:
11686500
15.

[A major histocompatibility complex class Ⅱ deficiency case report and literature review].

Wu WC, Wang W, Song HM, Ma MS, Tang XY, Jian S, Zhang MQ, Xiao J, Qiu ZQ, Liu YL.

Zhonghua Er Ke Za Zhi. 2016 Aug;54(8):614-8. doi: 10.3760/cma.j.issn.0578-1310.2016.08.013. Review. Chinese.

PMID:
27510876
16.

MHC class II deficiency: Report of a novel mutation and special review.

Farrokhi S, Shabani M, Aryan Z, Zoghi S, Krolo A, Boztug K, Rezaei N.

Allergol Immunopathol (Madr). 2017 Jul 1. pii: S0301-0546(17)30077-0. doi: 10.1016/j.aller.2017.04.006. [Epub ahead of print] Review.

PMID:
28676232
17.

Molecular diagnosis of primary immunodeficiency diseases in a developing country: Iran as an example.

Latif AH, Tabassomi F, Abolhassani H, Hammarström L.

Expert Rev Clin Immunol. 2014 Mar;10(3):385-96. doi: 10.1586/1744666X.2014.880654. Epub 2014 Jan 22. Review.

PMID:
24450304
18.

Specific aspects of consanguinity: some examples from the Tunisian population.

Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, Abdelhak S.

Hum Hered. 2014;77(1-4):167-74. doi: 10.1159/000362167. Epub 2014 Jul 29. Review.

PMID:
25060280
19.

Important differences in the diagnostic spectrum of primary immunodeficiency in adults versus children.

Abolhassani H, Rezaei N, Mohammadinejad P, Mirminachi B, Hammarstrom L, Aghamohammadi A.

Expert Rev Clin Immunol. 2015 Feb;11(2):289-302. doi: 10.1586/1744666X.2015.990440. Epub 2015 Jan 5. Review.

PMID:
25556968
20.

Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population.

Barbouche MR, Mekki N, Ben-Ali M, Ben-Mustapha I.

Front Immunol. 2017 Jun 27;8:737. doi: 10.3389/fimmu.2017.00737. eCollection 2017. Review.

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