Detalles de la búsqueda
1.
ATOR-1017 (evunzekibart), an Fc-gamma receptor conditional 4-1BB agonist designed for optimal safety and efficacy, activates exhausted T cells in combination with anti-PD-1.
Cancer Immunol Immunother
; 72(12): 4145-4159, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-37796298
2.
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer.
BMC Cancer
; 23(1): 738, 2023 Aug 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37563628
3.
Prophylactic Mastectomy: Postoperative Skin Flap Thickness Evaluated by MRT, Ultrasound and Clinical Examination.
Ann Surg Oncol
; 27(7): 2221-2228, 2020 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-31907748
4.
Delirium and Developmental Disability: Improving Specificity of a Pediatric Delirium Screen.
Pediatr Crit Care Med
; 21(5): 409-414, 2020 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-32106184
5.
Healthcare professionals' responsibility for informing relatives at risk of hereditary disease.
J Med Ethics
; 2020 Nov 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-33246998
6.
Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.
Hered Cancer Clin Pract
; 18: 18, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32944097
7.
A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortality.
Genet Med
; 21(2): 471-476, 2019 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29915381
8.
Administration of low-dose combination anti-CTLA4, anti-CD137, and anti-OX40 into murine tumor or proximal to the tumor draining lymph node induces systemic tumor regression.
Cancer Immunol Immunother
; 67(1): 47-60, 2018 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28905118
9.
Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.
Genet Med
; 19(1): 62-68, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27228464
10.
Novel findings of left ventricular non-compaction cardiomyopathy, microform cleft lip and poor vision in patient with SMC1A-associated Cornelia de Lange syndrome.
Am J Med Genet A
; 173(2): 414-420, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-28102598
11.
High adherence to a gluten-free diet in adolescents with screening-detected celiac disease.
J Pediatr Gastroenterol Nutr
; 60(1): 54-9, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25238121
12.
Celiac disease can be predicted by high levels of anti-tissue transglutaminase antibodies in population-based screening.
J Pediatr Gastroenterol Nutr
; 60(6): 787-91, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25564816
13.
Meeting the Mental Health Needs of the Homebound: A Psychiatric Consult Service Within a Home-Based Primary Care Program.
Care Manag J
; 16(3): 122-8, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26414814
14.
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants.
Gut
; 63(3): 415-22, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-23704318
15.
Iroquois homeodomain transcription factors in heart development and function.
Circ Res
; 110(11): 1513-24, 2012 May 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-22628575
16.
Internalizing the threat of risk--a qualitative study about adolescents' experience living with screening-detected celiac disease 5 years after diagnosis.
Health Qual Life Outcomes
; 12: 91, 2014 Jun 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-24915870
17.
Body mass index is not a reliable tool in predicting celiac disease in children.
BMC Pediatr
; 14: 165, 2014 Jun 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-24981433
18.
Iroquois homeobox gene 3 establishes fast conduction in the cardiac His-Purkinje network.
Proc Natl Acad Sci U S A
; 108(33): 13576-81, 2011 Aug 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-21825130
19.
How hereditary cancer risk disclosure to relatives is handled in practice - Patient perspectives from a Swedish cancer genetics clinic.
Patient Educ Couns
; 126: 108319, 2024 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-38788311
20.
The experience of receiving a letter from a cancer genetics clinic about risk for hereditary cancer.
Eur J Hum Genet
; 32(5): 539-544, 2024 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-38355958