Profound Reversible Hypogammaglobulinemia Caused by Celiac Disease in the Absence of Protein Losing Enteropathy.

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Application of diagnostic and treatment criteria for common variable immunodeficiency disorder.Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.

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P2860

Profound Reversible Hypogammaglobulinemia Caused by Celiac Disease in the Absence of Protein Losing Enteropathy.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年论文

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2015年论文

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Profound Reversible Hypogammag ...... of Protein Losing Enteropathy.

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Profound Reversible Hypogammag ...... of Protein Losing Enteropathy.

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Profound Reversible Hypogammag ...... of Protein Losing Enteropathy.

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Profound Reversible Hypogammag ...... of Protein Losing Enteropathy.

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Maneka Deo

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Mee Ling Yeong

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Richard Henderson Steele

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Russell William Barker

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See-Tarn Woon

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Wikke Koopmans

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P2860

Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions

Inflammatory and autoimmune complications of common variable immune deficiency.

Nodular regenerative hyperplasia in common variable immunodeficiency.

ACG clinical guidelines: diagnosis and management of celiac disease

Sarcoidosis and common variable immunodeficiency. Report of 8 cases and review of the literature.

Safety and antibody response, including antibody persistence for 5 years, after primary vaccination or revaccination with pneumococcal polysaccharide vaccine in middle-aged and older adults.

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.

Infections in 252 patients with common variable immunodeficiency.

Common variable immunodeficiency and the gastrointestinal tract.

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

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s10875-015-0189-6

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scholarly article

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10.1007/S10875-015-0189-6

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Rohan Ameratunga

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2015-08-29T00:00:00Z

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Profound Reversible Hypogammaglobulinemia Caused by Celiac Disease in the Absence of Protein Losing Enteropathy.

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P2860

P2860

Profound Reversible Hypogammaglobulinemia Caused by Celiac Disease in the Absence of Protein Losing Enteropathy.

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P1433

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P2093

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P478

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P698