(Q37962987)

26 August 2017

title

Primary immunodeficiencies in highly consanguineous North African populations (English)

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26 August 2017

author name string

Mohamed-Ridha Barbouche

1

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26 August 2017

Nermeen Galal

2

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26 August 2017

Imen Ben-Mustapha

3

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26 August 2017

Leïla Jeddane

4

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26 August 2017

Fethi Mellouli

5

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26 August 2017

Fatima Ailal

6

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26 August 2017

Mohamed Bejaoui

7

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26 August 2017

Jeanette Boutros

8

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26 August 2017

Aisha Marsafy

9

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26 August 2017

Ahmed Aziz Bousfiha

10

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26 August 2017

language of work or name

English

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publication date

1 November 2011

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Annals of the New York Academy of Sciences

26 August 2017

published in

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26 August 2017

volume

1238

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26 August 2017

page(s)

42-52

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Human primary immunodeficiency diseases

26 August 2017

cites work

1 reference

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21 January 2018

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21 January 2018

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Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain

21 January 2018

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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

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Study of regions of extended homozygosity provides a powerful method to explore haplotype structure of human populations.

21 January 2018

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Genome-wide autozygosity mapping in human populations

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Endogamy, consanguinity and community disease profiles.

21 January 2018

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Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B.

21 January 2018

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The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population

21 January 2018

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21 January 2018

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Consanguineous marriages and their effects on common adult diseases: studies from an endogamous population

21 January 2018

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The prevalence of consanguineous marriages in an underserved area in Lebanon and its association with congenital anomalies.

21 January 2018

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21 January 2018

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Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guérin infection

21 January 2018

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Inherited interleukin 12 deficiency in a child with bacille Calmette-Guérin and Salmonella enteritidis disseminated infection

21 January 2018

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Clinical and genetic heterogeneity of inherited autosomal recessive susceptibility to disseminated Mycobacterium bovis bacille calmette-guérin infection

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Impaired response to interferon-alpha/beta and lethal viral disease in human STAT1 deficiency

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Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immunological implications

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Critical issues and needs in management of primary immunodeficiency diseases in Latin America.

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis.

21 January 2018

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Community-acquired poliovirus infection in children with primary immunodeficiencies in Tunisia

21 January 2018

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Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

21 January 2018

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10.1111/J.1749-6632.2011.06260.X

21 January 2018

Identifiers

DOI

1 reference

26 August 2017

1 reference