Research
Type:LetterClear
- Fatal capillary leak syndrome in a child with acute lymphoblastic leukemia treated with moxetumomab pasudotox for pre-transplant minimal residual disease reduction Letter,Academic ArticlePublication Date: 2020Local Authors (Claimed):
- Familial Chylomicronemia Syndrome With a Novel Homozygous LPL Mutation Identified in Three Siblings in Their 50s Letter,Academic ArticlePublication Date: 2020Local Authors (Claimed):
- Forced migration and foot care in people with diabetes Letter,Academic ArticlePublication Date: 2020Local Authors (Claimed):
- F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects Letter,Academic ArticlePublication Date: 2019Local Authors (Claimed):
- Failed Attempt With Paired Associative Stimulation to Separate Functional and Organic Dystonia Letter,Academic ArticlePublication Date: 2018Local Authors (Claimed):
- Formaldehyde, Hematotoxicity, and Chromosomal Changes-Response Letter,Academic ArticlePublication Date: 2018Local Authors (Claimed):
- Frequency and consequence of the recurrent YY1 p.T372R mutation in sporadic insulinomas Letter,Academic ArticlePublication Date: 2018Local Authors (Claimed):
- Foreign antigen-independent memory-phenotype CD4(+) T cells: a new player in innate immunity? Letter,Academic ArticlePublication Date: 2018Local Authors (Claimed):
- First Identification of an Inherited TPSAB1 Quintuplication in a Patient with Clonal Mast Cell Disease Letter,Academic ArticlePublication Date: 2018Local Authors (Claimed):
- FGFR2 amplification in metastatic hormone-positive breast cancer and response to an mTOR inhibitor Letter,Academic ArticlePublication Date: 2017Local Authors (Claimed):