Detalhe da pesquisa
1.
Nicolaides-Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion.
Cardiol Young
; 32(5): 821-823, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-34521483
2.
Barriers and facilitators to the use of e-health by older adults: a scoping review.
BMC Public Health
; 21(1): 1556, 2021 08 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34399716
3.
Association of unbalanced translocation der(1;7) with germline GATA2 mutations.
Blood
; 138(23): 2441-2445, 2021 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34469508
4.
Bicoronal and metopic craniosynostosis in association with a de novo unbalanced t(2;7) chromosomal translocation.
Am J Med Genet A
; 173(1): 274-279, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27774767
5.
Proof-of-Concept of Polymeric Sol-Gels in Multi-Drug Delivery and Intraoperative Image-Guided Surgery for Peritoneal Ovarian Cancer.
Pharm Res
; 33(9): 2298-306, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27283829
6.
A case report of primary ciliary dyskinesia, laterality defects and developmental delay caused by the co-existence of a single gene and chromosome disorder.
BMC Med Genet
; 16: 45, 2015 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-26123568
7.
De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay.
Am J Med Genet A
; 167A(5): 1134-41, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25810372
8.
Hydrogel-Based Drug Delivery Systems for Poorly Water-Soluble Drugs.
Molecules
; 20(11): 20397-408, 2015 Nov 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-26580588
9.
A systematic review of research on empathy in health care.
Health Serv Res
; 58(2): 250-263, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35765156
10.
Similar but different: identical pathology with differing outcome in 'Not-so-identical' twins.
Br J Haematol
; 178(1): 152-153, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27102370
11.
Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome.
Blood
; 116(19): 3766-9, 2010 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20802024
12.
An Australian Regional Response to Marriage Equality: Newcastle and the Hunter.
J Homosex
; 69(11): 1980-2001, 2022 Sep 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34085901
13.
Generation of an epigenetic signature by chronic hypoxia in prostate cells.
Hum Mol Genet
; 18(19): 3594-604, 2009 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19584087
14.
The early impact of COVID-19 on primary care psychological therapy services: A descriptive time series of electronic healthcare records.
EClinicalMedicine
; 37: 100939, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34386738
15.
Frequency and Prognostic Impact of ALK Amplifications and Mutations in the European Neuroblastoma Study Group (SIOPEN) High-Risk Neuroblastoma Trial (HR-NBL1).
J Clin Oncol
; 39(30): 3377-3390, 2021 10 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34115544
16.
Heterogeneity of the MYCN oncogene in neuroblastoma.
Clin Cancer Res
; 15(6): 2085-90, 2009 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19276282
17.
Predicting patient engagement in IAPT services: a statistical analysis of electronic health records.
Evid Based Ment Health
; 23(1): 8-14, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32046987
18.
A retrospective study of myeloid leukaemia in children with Down syndrome in Ireland.
Ir J Med Sci
; 189(3): 979-984, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32006388
19.
A chromosomal 5q31.1 gain involving PITX1 causes Liebenberg syndrome.
Am J Med Genet A
; 164A(11): 2958-60, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25124102
20.
Cytogenetic characterization of childhood acute lymphoblastic leukemia in Nicaragua.
Pediatr Blood Cancer
; 53(7): 1238-41, 2009 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19672974