32815268 30904443 29273483 26592417 27854358 32121146 31333129 32375863 28682308 29184809 36339399 29492297 36458449 31698873 30575291 28933395 29271568 36750945 32411831 32630716 - Search Results

Year	Number of Results
2016	4
2017	5
2018	4
2019	3
2020	5
2022	2
2023	2

1

Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.

Muthusamy K, Macke EL, Klee EW, Tebben PJ, Hand JL, Hasadsri L, Marcou CA, Schimmenti LA. Muthusamy K, et al. Am J Med Genet A. 2020 Oct;182(10):2442-2449. doi: 10.1002/ajmg.a.61792. Epub 2020 Aug 20. Am J Med Genet A. 2020. PMID: 32815268

2

Epigenetic therapy of Prader-Willi syndrome.

Kim Y, Wang SE, Jiang YH. Kim Y, et al. Transl Res. 2019 Jun;208:105-118. doi: 10.1016/j.trsl.2019.02.012. Epub 2019 Mar 5. Transl Res. 2019. PMID: 30904443 Free PMC article. Review.

3

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

Butler MG, Hossain W, Hassan M, Manzardo AM. Butler MG, et al. Growth Horm IGF Res. 2018 Apr;39:29-33. doi: 10.1016/j.ghir.2017.12.001. Epub 2017 Dec 6. Growth Horm IGF Res. 2018. PMID: 29273483 Free PMC article.

4

Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.

Butler MG, Manzardo AM, Forster JL. Butler MG, et al. Curr Pediatr Rev. 2016;12(2):136-66. doi: 10.2174/1573396312666151123115250. Curr Pediatr Rev. 2016. PMID: 26592417 Free PMC article. Review.

5

Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey.

Butler MG, Manzardo AM, Heinemann J, Loker C, Loker J. Butler MG, et al. Genet Med. 2017 Jun;19(6):635-642. doi: 10.1038/gim.2016.178. Epub 2016 Nov 17. Genet Med. 2017. PMID: 27854358 Free PMC article.

6

Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi Syndrome.

van Bosse HJP, Butler MG. van Bosse HJP, et al. Genes (Basel). 2020 Feb 28;11(3):260. doi: 10.3390/genes11030260. Genes (Basel). 2020. PMID: 32121146 Free PMC article. Review.

7

Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.

Butler MG, Miller JL, Forster JL. Butler MG, et al. Curr Pediatr Rev. 2019;15(4):207-244. doi: 10.2174/1573396315666190716120925. Curr Pediatr Rev. 2019. PMID: 31333129 Free PMC article. Review.

8

Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years.

Mongkollarp N, Tim-Aroon T, Okascharoen C, Wichajarn K, Phosuwattanakul J, Chongviriyaphan N, Wattanasirichaigoon D. Mongkollarp N, et al. Orphanet J Rare Dis. 2020 May 6;15(1):111. doi: 10.1186/s13023-020-01388-7. Orphanet J Rare Dis. 2020. PMID: 32375863 Free PMC article.

9

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

Manzardo AM, Loker J, Heinemann J, Loker C, Butler MG. Manzardo AM, et al. Genet Med. 2018 Jan;20(1):24-30. doi: 10.1038/gim.2017.92. Epub 2017 Jul 6. Genet Med. 2018. PMID: 28682308 Free PMC article.

10

Review of Prader-Willi syndrome: the endocrine approach.

Heksch R, Kamboj M, Anglin K, Obrynba K. Heksch R, et al. Transl Pediatr. 2017 Oct;6(4):274-285. doi: 10.21037/tp.2017.09.04. Transl Pediatr. 2017. PMID: 29184809 Free PMC article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

Search Page

Search Results