Detalhe da pesquisa
1.
Development and application of a weighted change score to evaluate interventions for vasomotor symptoms in patients with breast cancer using regression trees: a cohort study.
Breast Cancer Res Treat
; 2024 May 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38763972
2.
Evaluation of a nurse-led glaucoma assessment clinic for non-complex patients.
J Clin Nurs
; 32(17-18): 6743-6750, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869616
3.
Delivery of cancer care via an outpatient telephone support line: a cross-sectional study of oncology nursing perspectives on quality and challenges.
Support Care Cancer
; 30(11): 9079-9091, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-35980464
4.
Using machine learning to predict individual patient toxicities from cancer treatments.
Support Care Cancer
; 30(9): 7397-7406, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35614153
5.
Vasomotor symptoms in early breast cancer-a "real world" exploration of the patient experience.
Support Care Cancer
; 30(5): 4437-4446, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35112212
6.
Legal Privilege Legislation: Consequences for Patient Safety.
Healthc Q
; 25(1): 21-27, 2022 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-35596760
7.
Developing patient-centred strategies to optimize the management of vasomotor symptoms in breast cancer patients: a survey of health care providers.
Breast Cancer Res Treat
; 188(2): 343-350, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34159473
8.
A randomized trial comparing vascular access strategies for patients receiving chemotherapy with trastuzumab for early-stage breast cancer.
Support Care Cancer
; 28(10): 4891-4899, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32002617
9.
A multicentre, randomized pilot trial comparing vascular access strategies for early stage breast cancer patients receiving non-trastuzumab containing chemotherapy.
Breast Cancer Res Treat
; 178(2): 337-345, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31392518
10.
Athena: Specialty Certificate Examination case for cutaneous allergy.
Clin Exp Dermatol
; 48(7): 817-818, 2023 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37012683
11.
Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage.
Prenat Diagn
; 36(4): 312-20, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26824862
12.
Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.
J Med Genet
; 50(9): 635-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23812911
13.
Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome.
Hum Mutat
; 34(5): 686-96, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23420520
14.
Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma.
Clin Endocrinol (Oxf)
; 78(6): 898-906, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23072324
15.
CHRNG genotype-phenotype correlations in the multiple pterygium syndromes.
J Med Genet
; 49(1): 21-6, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22167768
16.
The Genetics of Inherited Cholestatic Disorders in Neonates and Infants: Evolving Challenges.
Genes (Basel)
; 12(11)2021 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34828443
17.
Design and validation of a metabolic disorder resequencing microarray (BRUM1).
Hum Mutat
; 31(7): 858-65, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20578233
18.
A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene.
Hum Mutat
; 31(1): E1043-51, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19802896
19.
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.
Hum Mutat
; 31(1): 41-51, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19802898
20.
Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: implications for molecular diagnosis.
Mol Genet Metab
; 100(2): 207-12, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20226704