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Items: 1 to 20 of 21

1.

Orthodontic correction of severe Class II malocclusion in a patient with Prader-Willi syndrome.

Ishihara Y, Sugawara Y, Ei Hsu Hlaing E, Nasu M, Kataoka T, Odagaki N, Takano-Yamamoto T, Yamashiro T, Kamioka H.

Am J Orthod Dentofacial Orthop. 2018 Nov;154(5):718-732. doi: 10.1016/j.ajodo.2017.05.040.

PMID:
30384943
2.

No central adrenal insufficiency found in patients with Prader-Willi syndrome with an overnight metyrapone test.

Obrynba KS, Hoffman RP, Repaske DR, Anglin K, Kamboj MK.

J Pediatr Endocrinol Metab. 2018 Jul 26;31(7):809-814. doi: 10.1515/jpem-2017-0487.

PMID:
29959886
3.

High levels of caregiver burden in Prader-Willi syndrome.

Kayadjanian N, Schwartz L, Farrar E, Comtois KA, Strong TV.

PLoS One. 2018 Mar 26;13(3):e0194655. doi: 10.1371/journal.pone.0194655. eCollection 2018.

4.

Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

Çizmecioğlu FM, Jones JH, Paterson WF, Kherra S, Kourime M, McGowan R, Shaikh MG, Donaldson M.

J Clin Res Pediatr Endocrinol. 2018 Jul 31;10(3):264-273. doi: 10.4274/jcrpe.0029. Epub 2018 Mar 19.

5.

Autistic, Aberrant, and Food-Related Behaviors in Adolescents and Young Adults with Prader-Willi Syndrome: The Effects of Age and Genotype.

Ishii A, Ihara H, Ogata H, Sayama M, Gito M, Murakami N, Ayabe T, Oto Y, Takahashi A, Nagai T.

Behav Neurol. 2017;2017:4615451. doi: 10.1155/2017/4615451. Epub 2017 Dec 26.

6.

Prader-Willi syndrome: a nest for premature coronary artery disease?

Brás DR, Semedo P, Piçarra BC, Fernandes R.

BMJ Case Rep. 2018 Feb 7;2018. pii: bcr-2017-222828. doi: 10.1136/bcr-2017-222828.

PMID:
29437709
7.

Eye Tracking as a Marker of Hyperphagia in Prader-Willi Syndrome.

Key AP, Dykens EM.

Dev Neuropsychol. 2018;43(2):152-161. doi: 10.1080/87565641.2017.1367395. Epub 2018 Feb 7.

PMID:
29412007
8.

Silent aspiration in infants with Prader-Willi syndrome identified by videofluoroscopic swallow study.

Salehi P, Stafford HJ, Glass RP, Leavitt A, Beck AE, McAfee A, Ambartsumyan L, Chen M.

Medicine (Baltimore). 2017 Dec;96(50):e9256. doi: 10.1097/MD.0000000000009256.

9.

Aberrant, autistic, and food-related behaviors in adults with Prader-Willi syndrome. The comparison between young adults and adults.

Ogata H, Ihara H, Gito M, Sayama M, Murakami N, Ayabe T, Oto Y, Nagai T, Shimoda K.

Res Dev Disabil. 2018 Feb;73:126-134. doi: 10.1016/j.ridd.2017.12.020. Epub 2018 Jan 8.

PMID:
29324255
10.

AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial.

Allas S, Caixàs A, Poitou C, Coupaye M, Thuilleaux D, Lorenzini F, Diene G, Crinò A, Illouz F, Grugni G, Potvin D, Bocchini S, Delale T, Abribat T, Tauber M.

PLoS One. 2018 Jan 10;13(1):e0190849. doi: 10.1371/journal.pone.0190849. eCollection 2018.

11.

Severe obstructive sleep disorders in Prader-Willi syndrome patients in southern Italy.

Canora A, Franzese A, Mozzillo E, Fattorusso V, Bocchino M, Sanduzzi A.

Eur J Pediatr. 2018 Sep;177(9):1367-1370. doi: 10.1007/s00431-017-3083-9. Epub 2018 Jan 9.

PMID:
29318372
12.

The Prevalence and Treatment of Hip Dysplasia in Prader-Willi Syndrome (PWS).

Trizno AA, Jones AS, Carry PM, Georgopoulos G.

J Pediatr Orthop. 2018 Mar;38(3):e151-e156. doi: 10.1097/BPO.0000000000001118.

PMID:
29309382
13.

Growth hormone receptor (GHR) gene polymorphism and scoliosis in Prader-Willi syndrome.

Butler MG, Hossain W, Hassan M, Manzardo AM.

Growth Horm IGF Res. 2018 Apr;39:29-33. doi: 10.1016/j.ghir.2017.12.001. Epub 2017 Dec 6.

PMID:
29273483
14.

GHRH plus arginine and arginine administration evokes the same ratio of GH isoforms levels in young patients with Prader-Willi syndrome.

Rigamonti AE, Crinò A, Bocchini S, Convertino A, Bidlingmaier M, Haenelt M, Tamini S, Cella SG, Grugni G, Sartorio A.

Growth Horm IGF Res. 2018 Apr;39:13-18. doi: 10.1016/j.ghir.2017.11.005. Epub 2017 Nov 27.

PMID:
29217318
15.

Temple syndrome as a differential diagnosis to Prader-Willi syndrome: Identifying three new patients.

Lande A, Kroken M, Rabben K, Retterstøl L.

Am J Med Genet A. 2018 Jan;176(1):175-180. doi: 10.1002/ajmg.a.38533. Epub 2017 Nov 21.

PMID:
29159982
16.

A model to characterize psychopathological features in adults with Prader-Willi syndrome.

Thuilleaux D, Laurier V, Copet P, Tricot J, Demeer G, Mourre F, Tauber M, Jauregi J.

Am J Med Genet A. 2018 Jan;176(1):41-47. doi: 10.1002/ajmg.a.38525. Epub 2017 Nov 17.

PMID:
29150898
17.

25OH vitamin D levels in pediatric patients affected by Prader-Willi syndrome.

Fintini D, Pedicelli S, Bocchini S, Bizzarri C, Grugni G, Cappa M, Crinò A.

J Endocrinol Invest. 2018 Jun;41(6):739-742. doi: 10.1007/s40618-017-0781-0. Epub 2017 Nov 3.

PMID:
29101669
18.

Oxytocin and Prader-Willi Syndrome.

Kabasakalian A, Ferretti CJ, Hollander E.

Curr Top Behav Neurosci. 2018;35:529-557. doi: 10.1007/7854_2017_28. Review.

PMID:
28956320
19.

Survival trends from the Prader-Willi Syndrome Association (USA) 40-year mortality survey.

Manzardo AM, Loker J, Heinemann J, Loker C, Butler MG.

Genet Med. 2018 Jan;20(1):24-30. doi: 10.1038/gim.2017.92. Epub 2017 Jul 6.

20.

Effects of MetAP2 inhibition on hyperphagia and body weight in Prader-Willi syndrome: A randomized, double-blind, placebo-controlled trial.

McCandless SE, Yanovski JA, Miller J, Fu C, Bird LM, Salehi P, Chan CL, Stafford D, Abuzzahab MJ, Viskochil D, Barlow SE, Angulo M, Myers SE, Whitman BY, Styne D, Roof E, Dykens EM, Scheimann AO, Malloy J, Zhuang D, Taylor K, Hughes TE, Kim DD, Butler MG.

Diabetes Obes Metab. 2017 Dec;19(12):1751-1761. doi: 10.1111/dom.13021. Epub 2017 Jul 13.

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