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1.
Partial Response to Sorafenib in a Child With a Myeloid/Lymphoid Neoplasm, Eosinophilia, and a ZMYM2-FLT3 Fusion.
J Pediatr Hematol Oncol
; 43(4): e508-e511, 2021 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32852395
2.
Clinical symptoms and markers of disease mechanisms in adolescent chronic fatigue following Epstein-Barr virus infection: An exploratory cross-sectional study.
Brain Behav Immun
; 80: 551-563, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31039432
3.
Predictors of chronic fatigue in adolescents six months after acute Epstein-Barr virus infection: A prospective cohort study.
Brain Behav Immun
; 75: 94-100, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30261303
4.
Lifestyle factors during acute Epstein-Barr virus infection in adolescents predict physical activity six months later.
Acta Paediatr
; 108(8): 1521-1526, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-30685875
5.
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.
J Allergy Clin Immunol
; 139(1): 232-245, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27577878
6.
Targeting Integrin α4ß7 in Steroid-Refractory Intestinal Graft-versus-Host Disease.
Biol Blood Marrow Transplant
; 23(1): 172-175, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27777142
7.
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia.
Am J Hum Genet
; 95(1): 96-107, 2014 Jul 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-24931394
8.
A Cross-Sectional Study of the Prevalence of Gastrointestinal Symptoms and Pathology in Patients With Common Variable Immunodeficiency.
Am J Gastroenterol
; 111(10): 1467-1475, 2016 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-27527747
9.
Neonatal Levels of T-cell Receptor Excision Circles (TREC) in Patients with 22q11.2 Deletion Syndrome and Later Disease Features.
J Clin Immunol
; 35(4): 408-15, 2015 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-25814142
10.
Retinoic acid improves defective TLR9/RP105-induced immune responses in common variable immunodeficiency-derived B cells.
J Immunol
; 191(7): 3624-33, 2013 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-24006462
11.
NUP214 fusion genes in acute leukemias: genetic characterization of rare cases.
Front Oncol
; 14: 1371980, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38571499
12.
Extracorporeal Photopheresis as Graft-versus-Host Disease Prophylaxis: A Randomized Controlled Trial.
Transplant Cell Ther
; 29(6): 364.e1-364.e11, 2023 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-36878428
13.
Intensifying treatment in PET-positive multiple myeloma patients after upfront autologous stem cell transplantation.
Leukemia
; 37(10): 2107-2114, 2023 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37568010
14.
Markers of extracellular matrix remodeling and systemic inflammation in patients with heritable thoracic aortic diseases.
Front Cardiovasc Med
; 9: 1073069, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36606286
15.
Interleukin-6 inhibition in ST-elevation myocardial infarction: Immune cell profile in the randomised ASSAIL-MI trial.
EBioMedicine
; 80: 104013, 2022 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-35504178
16.
T cells targeted to TdT kill leukemic lymphoblasts while sparing normal lymphocytes.
Nat Biotechnol
; 40(4): 488-498, 2022 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-34873326
17.
Thymectomy in Juvenile Myasthenia Gravis Is Safe Regarding Long Term Immunological Effects.
Front Neurol
; 12: 596859, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33716918
18.
Therapy-induced Deletion in 11q23 Leading to Fusion of KMT2A With ARHGEF12 and Development of B Lineage Acute Lymphoplastic Leukemia in a Child Treated for Acute Myeloid Leukemia Caused by t(9;11)(p21;q23)/KMT2A-MLLT3.
Cancer Genomics Proteomics
; 18(1): 67-81, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33419897
19.
Striking decrease in the total precursor B-cell compartment during early childhood as evidenced by flow cytometry and gene expression changes.
Pediatr Hematol Oncol
; 27(1): 31-45, 2010 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-20121553
20.
Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency.
Front Immunol
; 11: 1417, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32754152