Detalhe da pesquisa
1.
Health-related quality of life in women with primary ovarian insufficiency: a scoping review of the literature and implications for targeted interventions.
Hum Reprod
; 37(12): 2817-2830, 2022 11 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36102839
2.
Coping response and family communication of cancer risk in men harboring a BRCA mutation: A mixed methods study.
Psychooncology
; 31(3): 486-495, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34582073
3.
Latinx individuals' knowledge of, preferences for, and experiences with prenatal genetic testing: a scoping review.
Reprod Health
; 19(1): 134, 2022 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35668466
4.
Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome.
Neuroendocrinology
; 111(1-2): 99-114, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-32074614
5.
Decision coaching for people making healthcare decisions.
Cochrane Database Syst Rev
; 11: CD013385, 2021 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34749427
6.
Evaluating co-created patient-facing materials to increase understanding of genetic test results.
J Genet Couns
; 30(2): 598-605, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33098367
7.
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Hum Mol Genet
; 27(2): 359-372, 2018 01 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29202173
8.
GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty.
Hum Reprod
; 35(10): 2312-2322, 2020 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32862222
9.
Parent of origin differences in psychosocial burden and approach to BRCA risk management.
Breast J
; 26(4): 734-738, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31659791
10.
Thigh and abdominal adipose tissue depot associations with testosterone levels in postmenopausal females.
Clin Endocrinol (Oxf)
; 90(3): 433-439, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30575083
11.
Developing a rare disease chronic care model: Management of systemic sclerosis (MANOSS) study protocol.
J Adv Nurs
; 75(12): 3774-3791, 2019 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-31452216
12.
Clinical challenge: When is delayed puberty more than a "late bloomer"?
J Pediatr Nurs
; 74: 135-137, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38155018
13.
Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.
Genet Med
; 20(8): 872-881, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29144511
14.
Fertility induction in hypogonadotropic hypogonadal men.
Clin Endocrinol (Oxf)
; 89(6): 712-718, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30194850
15.
Accuracy, satisfaction and usability of a flash glucose monitoring system among children and adolescents with type 1 diabetes attending a summer camp.
Pediatr Diabetes
; 19(7): 1276-1284, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30014625
16.
Acceptance of the Advanced Practice Nurse in Lung Cancer Role by Healthcare Professionals and Patients: A Qualitative Exploration.
J Nurs Scholarsh
; 50(5): 540-548, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30033614
17.
Patient Perspectives on Nurse-led Consultations Within a Pilot Structured Transition Program for Young Adults Moving From an Academic Tertiary Setting to Community-based Type 1 Diabetes Care.
J Pediatr Nurs
; 38: 99-105, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29357987
18.
Correspondence on "Ensuring best practice in genomics education and evaluation: Reporting item standards for education and its evaluation in genomics (RISE2 Genomics)" by Nisselle et al.
Genet Med
; 24(4): 962-963, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34930661
19.
Adherence to treatment in men with hypogonadotrophic hypogonadism.
Clin Endocrinol (Oxf)
; 86(3): 377-383, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27647266
20.
What's missing in sex chromosome aneuploidies? Representation and inclusion.
J Pediatr Nurs
; 62: 202-204, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35125170