Andrew Dwyer

Publications | Mémoires et thèses

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55 publications

2019 | 2018 | 2017 | 2016 | 2015 | 2014 | 2013 | 2012 | 2011 | 2010 | 2000 |
 
Functional Hypogonadotropic Hypogonadism in Men: Underlying Neuroendocrine Mechanisms and Natural History.
Dwyer A.A., Chavan N.R., Lewkowitz-Shpuntoff H., Plummer L., Hayes F.J., Seminara S.B., Crowley W.F., Pitteloud N., Balasubramanian R., 2019/08/01. The Journal of clinical endocrinology and metabolism, 104 (8) pp. 3403-3414. Peer-reviewed.
[DOI] [Pmid] [serval:BIB_BFD303671FD6]
A novel CHD7 mutation in an adolescent presenting with growth and pubertal delay.
Antoniou M.C., Bouthors T., Xu C., Phan-Hug F., Elowe-Gruau E., Stoppa-Vaucher S., Sloot A.V., Acierno J., Cassatella D., Richard C. et al., 2019/03. Annals of pediatric endocrinology & metabolism, 24 (1) pp. 49-54. Peer-reviewed.
 
Thigh and abdominal adipose tissue depot associations with testosterone levels in postmenopausal females.
Ofori E.K., Conde Alonso S., Correas-Gomez L., Carnero E.A., Zwygart K., Hugues H., Bardy D., Hans D., Dwyer A.A., Amati F., 2019/03. Clinical endocrinology, 90 (3) pp. 433-439. Peer-reviewed.
[DOI] [WoS] [Pmid] [serval:BIB_7EA748B2CAF8]
 
Accuracy, satisfaction and usability of a flash glucose monitoring system among children and adolescents with type 1 diabetes attending a summer camp.
Hansen E.A., Klee P., Dirlewanger M., Bouthors T., Elowe-Gruau E., Stoppa-Vaucher S., Phan-Hug F., Antoniou M.C., Pasquier J., Dwyer A.A. et al., 2018/11. Pediatric diabetes, 19 (7) pp. 1276-1284. Peer-reviewed.
 
Erratum to: Multidisciplinary management of diabetic kidney disease: a systematic review and meta-analysis.
Helou N., Dwyer A., Shaha M., Zanchi A., 2018/09..
 
Evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants.
Xu C., Cassatella D., van der Sloot A.M., Quinton R., Hauschild M., De Geyter C., Flück C., Feller K., Bartholdi D., Nemeth A. et al., 2018/08. Genetics in medicine, 20 (8) pp. 872-881. Peer-reviewed.
 
Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures.
Cassatella D., Howard S.R., Acierno J.S., Xu C., Papadakis G.E., Santoni F.A., Dwyer A.A., Santini S., Sykiotis G.P., Chambion C. et al., 2018/04. European journal of endocrinology, 178 (4) pp. 377-388. Peer-reviewed.
 
Meta-analysis of the effectiveness of nursing discharge planning interventions for older inpatients discharged home.
Mabire C., Dwyer A., Garnier A., Pellet J., 2018/04. Journal of advanced nursing, 74 (4) pp. 788-799. Peer-reviewed.
International practice settings, interventions and outcomes of nurse practitioners in geriatric care: A scoping review.
Chavez K.S., Dwyer A.A., Ramelet A.S., 2018/02. International journal of nursing studies, 78 pp. 61-75. Peer-reviewed.
 
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Bouilly J., Messina A., Papadakis G., Cassatella D., Xu C., Acierno J.S., Tata B., Sykiotis G., Santini S., Sidis Y. et al., 2018/01/15. Human molecular genetics, 27 (2) pp. 359-372. Peer-reviewed.
 
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.
Zoni S., Verga M.E., Hauschild M., Aquarone-Vaucher M.P., Gyuriga T., Ramelet A.S., Dwyer A.A., 2018. Journal of pediatric nursing, 38 pp. 99-105. Peer-reviewed.
Beyond hormone replacement: quality of life in women with congenital hypogonadotropic hypogonadism.
Dzemaili S., Tiemensma J., Quinton R., Pitteloud N., Morin D., Dwyer A.A., 2017/08. Endocrine connections, 6 (6) pp. 404-412. Peer-reviewed.
 
Feasibility of advanced practice nursing in lung cancer consultations during early treatment: A phase II study.
Serena A., Dwyer A., Peters S., Eicher M., 2017/08. European journal of oncology nursing, 29 pp. 106-114. Peer-reviewed.
 
Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism.
Xu C., Lang-Muritano M., Phan-Hug F., Dwyer A.A., Sykiotis G.P., Cassatella D., Acierno J., Mohammadi M., Pitteloud N., 2017/08. Clinical genetics, 92 (2) pp. 213-216. Peer-reviewed.
β-Klotho deficiency protects against obesity through a crosstalk between liver, microbiota, and brown adipose tissue.
Somm E., Henry H., Bruce S.J., Aeby S., Rosikiewicz M., Sykiotis G.P., Asrih M., Jornayvaz F.R., Denechaud P.D., Albrecht U. et al., 2017/04/20. JCI insight, 2 (8). Peer-reviewed.
[DOI] [WoS] [Pmid] [serval:BIB_94A6C8A6A9EA]
Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism.
COST Action BM1105, Badiu C., Bonomi M., Borshchevsky I., Cools M., Craen M., Ghervan C., Hauschild M., Hershkovitz E., Hrabovszky E. et al., 2017/03/20. Orphanet journal of rare diseases, 12 (1) p. 57. Peer-reviewed.
 
Adherence to treatment in men with hypogonadotrophic hypogonadism.
Dwyer A.A., Tiemensma J., Quinton R., Pitteloud N., Morin D., 2017/03. Clinical endocrinology, 86 (3) pp. 377-383. Peer-reviewed.
 
Feasibility of advanced practice nurse in lung cancer consultations during early treatment: a phase II study
Serena A., Dwyer A., Peters S., Eicher M., 2017/02. European Journal of Cancer, 72 pp. S160.
 
Society for Endocrinology UK guidance on the evaluation of suspected disorders of sexual development: emphasizing the opportunity to predict adolescent pubertal failure through a neonatal diagnosis of absent minipuberty.
Quinton R., Mamoojee Y., Jayasena C.N., Young J., Howard S., Dunkel L., Cheetham T., Smith N., Dwyer A.A., 2017/02. Clinical endocrinology, 86 (2) pp. 305-306. Peer-reviewed.
 
Effectiveness of nursing discharge planning interventions on health-related outcomes in elderly inpatients discharged home: A systematic review
Mabire C., Dwyer A., Garnier A., Pellet J., 2016/09/14. JBI database of systematic reviews and implementation reports, 9 pp. 217-260. Peer-reviewed.
 
Effectiveness of nursing discharge planning interventions on health-related outcomes in discharged elderly inpatients: a systematic review.
Mabire Cedric, Dwyer Andrew, Garnier Antoine, Pellet Joannie, 2016/09. JBI Database of Systematic Reviews and Implementation Reports, 14 (9) pp. 217-260. Peer-reviewed.
[DOI] [serval:BIB_4F0BDFFAE9F1]
 
Multidisciplinary management of diabetic kidney disease: a systematic review and meta-analysis.
Helou N., Dwyer A., Shaha M., Zanchi A., 2016/07. JBI database of systematic reviews and implementation reports, 14 (7) pp. 169-207. Peer-reviewed.
 
Congenital hypogonadotropic hypogonadism: implications of absent mini-puberty.
Dwyer A.A., Jayasena C.N., Quinton R., 2016/06. Minerva endocrinologica, 41 (2) pp. 188-195. Peer-reviewed.
 
MANAGEMENT OF ENDOCRINE DISEASE: Reversible hypogonadotropic hypogonadism.
Dwyer A.A., Raivio T., Pitteloud N., 2016/06. European journal of endocrinology, 174 (6) pp. R267-74. Peer-reviewed.
Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations.
Villanueva C., Jacobson-Dickman E., Xu C., Manouvrier S., Dwyer A.A., Sykiotis G.P., Beenken A., Liu Y., Tommiska J., Hu Y. et al., 2015/11. Genetics In Medicine : Official Journal of the American College of Medical Genetics, 17 (8) pp. 651-659. Peer-reviewed.
Comment on reversal of hypogonadotropic hypogonadism in a Chinese cohort.
Dwyer A., Raivio T., 2015. Asian Journal of Andrology, 17 (3) p. 508.
 
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism-pathogenesis, diagnosis and treatment.
Boehm U., Bouloux P.M., Dattani M.T., de Roux N., Dodé C., Dunkel L., Dwyer A.A., Giacobini P., Hardelin J.P., Juul A. et al., 2015. Nature Reviews. Endocrinology, 11 (9) pp. 547-564. Peer-reviewed.
 
Gonadotrophin replacement for induction of fertility in hypogonadal men.
Dwyer A.A., Raivio T., Pitteloud N., 2015. Best Practice and Research. Clinical Endocrinology and Metabolism, 29 (1) pp. 91-103. Peer-reviewed.
 
Natural history of growth hormone deficiency in a pediatric cohort.
Deillon E., Hauschild M., Faouzi M., Stoppa-Vaucher S., Elowe-Gruau E., Dwyer A., Theintz G.E., Dubuis J.M., Mullis P.E., Pitteloud N. et al., 2015. Hormone Research In Pædiatrics, 83 (4) pp. 252-261. Peer-reviewed.
Psychosexual development in men with congenital hypogonadotropic hypogonadism on long-term treatment: a mixed methods study.
Dwyer A.A., Quinton R., Pitteloud N., Morin D., 2015. Sexual Medicine, 3 (1) pp. 32-41. Peer-reviewed.
 
TRANSITION IN ENDOCRINOLOGY: Hypogonadism in adolescence.
Dwyer A.A., Phan-Hug F., Hauschild M., Elowe-Gruau E., Pitteloud N., 2015. European Journal of Endocrinology, 173 (1) pp. R15-R24. Peer-reviewed.
Identifying the unmet health needs of patients with congenital hypogonadotropic hypogonadism using a web-based needs assessment: implications for online interventions and peer-to-peer support.
Dwyer A.A., Quinton R., Morin D., Pitteloud N., 2014/06. Orphanet Journal of Rare Diseases, 9 (83) p. 83. Peer-reviewed.
 
Adherence to treatment for chronic hypogonadism: the role of illness perceptions and depressive symptoms.
Dwyer A., Tiemensma J., Quinton R., Morin D., Pitteloud N., 2014. dans 16th European Congress of Endocrinology, Endocrine Abstracts. Peer-reviewed.
 
Hormonal control of spermatogenesis in men: therapeutic aspects in hypogonadotropic hypogonadism.
Pitteloud N., Dwyer A., 2014. Annales d'endocrinologie, 75 (2) pp. 98-100. Peer-reviewed.
 
Multidisciplinary management of diabetic kidney disease: a sistematic review protocol
Helou N. Dwyer A. Burnier M. Shaha M. Zanchi A. , 2014. The JBI Database of Systematic Reviews and Implementation Reports, 12 (7) pp. 192-203. Peer-reviewed.
Skeletal muscle mitochondria in the elderly: effects of physical fitness and exercise training.
Broskey N.T., Greggio C., Boss A., Boutant M., Dwyer A., Schlueter L., Hans D., Gremion G., Kreis R., Boesch C. et al., 2014. Journal of Clinical Endocrinology and Metabolism, 99 (5) pp. 1852-1861.
Abrupt decrease in serum testosterone levels after an oral glucose load in men: implications for screening for hypogonadism.
Caronia L.M., Dwyer A.A., Hayden D., Amati F., Pitteloud N., Hayes F.J., 2013. Clinical Endocrinology, 78 (2) pp. 291-296.
 
Effectiveness of nursing discharge planning interventions on health-related outcomes in elderly inpatients discharged home: a systematic review protocol
Mabire C., Monod S., Dwyer A., Pellet J., 2013. JBI Database of Systematic Reviews and Implementation Reports, 11 (8) pp. 1-12. Peer-reviewed.
 
Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism.
Miraoui H., Dwyer A.A., Sykiotis G.P., Plummer L., Chung W., Feng B., Beenken A., Clarke J., Pers T.H., Dworzynski P. et al., 2013. American Journal of Human Genetics, 92 (5) pp. 725-743.
 
Prioritizing genetic testing in patients with kallmann syndrome using clinical phenotypes.
Costa-Barbosa F.A., Balasubramanian R., Keefe K.W., Shaw N.D., Al-Tassan N., Plummer L., Dwyer A.A., Buck C.L., Choi J.H., Seminara S.B. et al., 2013. Journal of Clinical Endocrinology and Metabolism, 98 (5) pp. E943-E953.
 
Short stature, complex cardiac defects, and developmental delay associated with a de novo microduplication of chromosome 15q13.2q13
Hauschild M, Martinet D, Phan Hug F, Stoppa S, Cassatella D, Dwyer A, Pitteloud N, Addor MC, 2013. dans Congrès de la Société Suisse d'endocrinologie pédiatrique, Septembre 2013.
Testosterone Restoration by Enclomiphene Citrate in Men with Secondary Hypogonadism: a pharmacodynamic and Pharmacokinetic study.
Wiehle R., Cunningham G.R., Pitteloud N., Wike J., Hsu K., Fontenot G.K., Rosner M., Dwyer A., Podolski J., 2013. Bju International, 112 (8) pp. 1188-1200. Peer-reviewed.
 
Trial of recombinant follicle-stimulating hormone pretreatment for gnrh-induced fertility in patients with congenital hypogonadotropic hypogonadism.
Dwyer A.A., Sykiotis G.P., Hayes F.J., Boepple P.A., Lee H., Loughlin K.R., Dym M., Sluss P.M., Crowley W.F., Pitteloud N., 2013. Journal of Clinical Endocrinology and Metabolism, 98 (11) pp. E1790-E1795.
 
An ancient founder mutation in PROKR2 impairs human reproduction.
Avbelj Stefanija M., Jeanpierre M., Sykiotis G.P., Young J., Quinton R., Abreu A.P., Plummer L., Au M.G., Balasubramanian R., Dwyer A.A. et al., 2012. Human Molecular Genetics, 21 (19) pp. 4314-4324.
 
Genetic overlap in kallmann syndrome, combined pituitary hormone deficiency, and septo-optic dysplasia.
Raivio T., Avbelj M., McCabe M.J., Romero C.J., Dwyer A.A., Tommiska J., Sykiotis G.P., Gregory L.C., Diaczok D., Tziaferi V. et al., 2012. Journal of Clinical Endocrinology and Metabolism, 97 (4) pp. E694-E699.
 
The lack of effect of insulin on luteinizing hormone pulsatility in healthy male volunteers provides evidence of a sexual dimorphism in the metabolic regulation of reproductive hormones.
Pesant M.H., Dwyer A., Marques Vidal P., Schneiter P., Giusti V., Tappy L., Pralong F.P., 2012. American Journal of Clinical Nutrition, 96 (2) pp. 283-288. Peer-reviewed.
 
Expanding the phenotype and genotype of female GnRH deficiency.
Shaw N.D., Seminara S.B., Welt C.K., Au M.G., Plummer L., Hughes V.A., Dwyer A.A., Martin K.A., Quinton R., Mericq V. et al., 2011. Journal of Clinical Endocrinology and Metabolism, 96 (3) pp. E566-E576.
 
Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory.
Mitchell A.L., Dwyer A., Pitteloud N., Quinton R., 2011. Trends In Endocrinology and Metabolism, 22 (7) pp. 249-258.
 
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1.
Chan Y.M., Broder-Fingert S., Paraschos S., Lapatto R., Au M., Hughes V., Bianco S.D., Min L., Plummer L., Cerrato F. et al., 2011. Journal of Clinical Endocrinology and Metabolism, 96 (11) pp. E1771-E1781.
Role of fibroblast growth factor (FGF) signaling in the neuroendocrine control of human reproduction.
Miraoui H., Dwyer A., Pitteloud N., 2011. Molecular and Cellular Endocrinology, 346 (1-2) pp. 37-43.
 
The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations.
Martin C., Balasubramanian R., Dwyer A.A., Au M.G., Sidis Y., Kaiser U.B., Seminara S.B., Pitteloud N., Zhou Q.Y., Crowley W.F., 2011. Endocrine Reviews, 32 (2) pp. 225-246.
 
Congenital idiopathic hypogonadotropic hypogonadism: evidence of defects in the hypothalamus, pituitary, and testes.
Sykiotis G.P., Hoang X.H., Avbelj M., Hayes F.J., Thambundit A., Dwyer A., Au M., Plummer L., Crowley W.F., Pitteloud N., 2010. Journal of Clinical Endocrinology and Metabolism, 95 (6) pp. 3019-3027. Peer-reviewed.
 
Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons.
Balasubramanian R., Dwyer A., Seminara S.B., Pitteloud N., Kaiser U.B., Crowley W.F., 2010. Neuroendocrinology, 92 (2) pp. 81-99.
 
The long-term clinical follow-up and natural history of men with adult-onset idiopathic hypogonadotropic hypogonadism.
Dwyer A.A., Hayes F.J., Plummer L., Pitteloud N., Crowley W.F., 2010. Journal of Clinical Endocrinology and Metabolism, 95 (9) pp. 4235-4243.
 
Hypogonadotropic Hypogonadism (Hh) and Gonadotropin Therapy
Hayes F., Dwyer A., Pitteloud N., 2000. Endotext pp. 1-25. Peer-reviewed.
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