about
Multidisciplinary surgical management of Cowden syndrome: Report of a case.PI3Kδ and primary immunodeficiencies.Immune dysregulation in patients with PTEN hamartoma tumor syndrome: Analysis of FOXP3 regulatory T cells.De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis.Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis.Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism.Phosphoinositide-3-Kinase Signaling in Human Natural Killer Cells: New Insights from Primary Immunodeficiency.Respiratory Manifestations of the Activated Phosphoinositide 3-Kinase Delta Syndrome."Immune TOR-opathies," a Novel Disease Entity in Clinical Immunology.PI3Kδ hyper-activation promotes development of B cells that exacerbate Streptococcus pneumoniae infection in an antibody-independent manner
P2860
Q37302554-C1574DE0-E897-4C1D-8989-717963C70FAFQ37623828-6E0000B6-A866-421C-9210-C402C793BDF8Q37626146-C11D9CD3-EECD-445E-8355-4071E583F525Q38775751-CB3AD21F-1FE7-479D-A684-520494F6DE13Q41153268-145469F7-ADBE-40BB-BC2A-21C0F1E225CBQ47102025-FD68C695-5F72-49E1-8652-345BF68D8F61Q52643680-3F955A14-8406-41D2-A72F-6EAFBE0CA6E1Q54964512-7F44FD03-8215-4635-8F0C-38FDE2079A39Q54977058-449C863A-ABF0-4666-907A-DF99AA4CBED6Q58793836-EEF10258-C87C-4BB0-8081-59C4095A4101
P2860
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Cowden's syndrome with immunodeficiency.
@en
type
label
Cowden's syndrome with immunodeficiency.
@en
prefLabel
Cowden's syndrome with immunodeficiency.
@en
P2093
P2860
P1476
Cowden's syndrome with immunodeficiency.
@en
P2093
Anita Chandra
Julian Barwell
Michael J Browning
Valentina Carbonaro
P2860
P304
P356
10.1136/JMEDGENET-2015-103266
P407
P577
2015-08-05T00:00:00Z