Detalhe da pesquisa
1.
Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD).
J Transl Med
; 21(1): 410, 2023 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37353797
2.
Rechallenge With Switching Immune Checkpoint Inhibitors Following Autoimmune Myocarditis in a Patient With Lynch Syndrome.
J Natl Compr Canc Netw
; 21(9): 894-899, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37673116
3.
NCCN Guidelines® Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 1.2021.
J Natl Compr Canc Netw
; 19(10): 1122-1132, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34666312
4.
Case report expanding the germline AXIN2- related phenotype to include olfactory neuroblastoma and gastric adenoma.
BMC Med Genet
; 21(1): 161, 2020 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32807118
5.
Correction: Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD).
J Transl Med
; 22(1): 400, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38689323
6.
NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Colorectal, Version 3.2017.
J Natl Compr Canc Netw
; 15(12): 1465-1475, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29223984
7.
Feasibility of Large-Scale Identification of Sessile Serrated Polyp Patients Using Electronic Records: A Utah Study.
Dig Dis Sci
; 62(6): 1455-1463, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28315031
8.
Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology.
J Natl Compr Canc Netw
; 14(8): 1010-30, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27496117
9.
Utility of Genetic Testing in Persons With Multiple Colorectal Polyps.
Clin Gastroenterol Hepatol
; 17(10): 1942-1944, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30876960
10.
Cronkhite-Canada Syndrome: A Rare Cause of Gastrointestinal Polyposis With Response to Emerging Therapy.
ACG Case Rep J
; 11(4): e01331, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38586820
11.
Rare hereditary cause of chronic pancreatitis in a young male: SPINK1 mutation.
Pan Afr Med J
; 28: 110, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29515728
12.
Associations between Environmental Exposures and Incident Colorectal Cancer by ESR2 Protein Expression Level in a Population-Based Cohort of Older Women.
Cancer Epidemiol Biomarkers Prev
; 24(4): 713-9, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25650184