Combined Immunodeficiency With Inflammatory Bowel Disease in a Patient With TTC7A Deficiency
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Heather Torbic | F. Rieder | M. Rizk | David T. Broome | I. Gordon | S. Krishnan | Keith K. Lai | Andrew Young | Maged Rizk
[1] S. Tsai,et al. Novel Mutations of the Tetratricopeptide Repeat Domain 7A Gene and Phenotype/Genotype Comparison , 2017, Front. Immunol..
[2] N. Sebire,et al. Phenotypic and Genotypic Characterisation of Inflammatory Bowel Disease Presenting Before the Age of 2 years , 2017, Journal of Crohn's & colitis.
[3] G. Lucchini,et al. Stem cell transplantation for tetratricopeptide repeat domain 7A deficiency: long-term follow-up. , 2016, Blood.
[4] Y. Lau,et al. Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency , 2015, Clinical genetics.
[5] L. Notarangelo. Multiple intestinal atresia with combined immune deficiency , 2014, Current opinion in pediatrics.
[6] F. Rieux-Laucat,et al. Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency. , 2014, The Journal of allergy and clinical immunology.
[7] E. Haddad,et al. Multiple Intestinal Atresia With Combined Immune Deficiency Related to TTC7A Defect Is a Multiorgan Pathology , 2014, Medicine.
[8] E. Schadt,et al. Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease. , 2014, Gastroenterology.
[9] A. Fischer,et al. TTC7A mutations disrupt intestinal epithelial apicobasal polarity. , 2014, The Journal of clinical investigation.
[10] Michael P. Snyder,et al. Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias. , 2013, The Journal of allergy and clinical immunology.
[11] P. Awadalla,et al. Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia , 2013, Journal of Medical Genetics.
[12] R. Fehon,et al. Ezrin, Radixin and Moesin: key regulators of membrane-cortex interactions and signaling. , 2011, Current opinion in cell biology.
[13] M. Kirschfink,et al. Recurrent infections in partial complement factor I deficiency: evaluation of three generations of a Brazilian family , 2006, Clinical and experimental immunology.