Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients.
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Primary immunodeficiencies associated with eosinophiliaFirst report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012)Lessons from Genetic Studies of Primary Immunodeficiencies in a Highly Consanguineous Population.Primary immunodeficiencies underlying fungal infectionsOral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome).IMMUNODEFICIENCIES. Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations.Disseminated Bacillus Calmette-Guérin (BCG) infection following allogeneic hematopoietic stem cell transplant in a patient with Bare Lymphocyte Syndrome type II.Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait.FOXN1 deficient nude severe combined immunodeficiency.Primary immunodeficiencies in highly consanguineous North African populations.New genetic discoveries and primary immune deficiencies.Host genetics of invasive Aspergillus and Candida infections.Primary Immunodeficiency Diseases in Saudi Arabia: a Tertiary Care Hospital Experience over a Period of Three Years (2010-2013).A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients.Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients.Human immunity against EBV-lessons from the clinic.Family History of Early Infant Death Correlates with Earlier Age at Diagnosis But Not Shorter Time to Diagnosis for Severe Combined Immunodeficiency.Clinical, immunological and genetic features in eleven Algerian patients with major histocompatibility complex class II expression deficiency.Alternative donor SCT for the treatment of MHC class II deficiency.Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India.Sigmoid colon mucosal gene expression supports alterations of neuronal signaling in irritable bowel syndrome with constipation.Cutaneous Manifestations of Primary Immunodeficiency Diseases in Tunisian Children
P2860
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P2860
Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients.
description
2011 nî lūn-bûn
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2011年の論文
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name
Major histocompatibility compl ...... tion: a survey of 35 patients.
@en
Major histocompatibility compl ...... tion: a survey of 35 patients.
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type
label
Major histocompatibility compl ...... tion: a survey of 35 patients.
@en
Major histocompatibility compl ...... tion: a survey of 35 patients.
@nl
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Major histocompatibility compl ...... tion: a survey of 35 patients.
@en
Major histocompatibility compl ...... tion: a survey of 35 patients.
@nl
P2093
P50
P1433
P1476
Major histocompatibility compl ...... tion: a survey of 35 patients.
@en
P2093
Alain Fischer
Aziz Bousfiha
Barbara Lisowska-Grospierre
Danielle Canioni
Mohamed Bejaoui
Monia Ouederni
Pierre Frange
Sami Scerra
Stéphane Blanche
P304
P356
10.1182/BLOOD-2011-05-352716
P407
P50
P577
2011-09-08T00:00:00Z