Osann K - Search Results

1

Molecular subtype and growth hormone effects on dysmorphology in Prader-Willi syndrome.

Oldzej J, Manazir J, Gold JA, Mahmoud R, Osann K, Flodman P, Cassidy SB, Kimonis VE. Oldzej J, et al. Among authors: osann k. Am J Med Genet A. 2020 Jan;182(1):169-175. doi: 10.1002/ajmg.a.61408. Epub 2019 Nov 29. Am J Med Genet A. 2020. PMID: 31782896

2

Genetic Subtype-Phenotype Analysis of Growth Hormone Treatment on Psychiatric Behavior in Prader-Willi Syndrome.

Montes AS, Osann KE, Gold JA, Tamura RN, Driscoll DJ, Butler MG, Kimonis VE. Montes AS, et al. Genes (Basel). 2020 Oct 23;11(11):1250. doi: 10.3390/genes11111250. Genes (Basel). 2020. PMID: 33114160 Free PMC article.

3

Contributing factors of mortality in Prader-Willi syndrome.

Proffitt J, Osann K, McManus B, Kimonis VE, Heinemann J, Butler MG, Stevenson DA, Gold JA. Proffitt J, et al. Among authors: osann k. Am J Med Genet A. 2019 Feb;179(2):196-205. doi: 10.1002/ajmg.a.60688. Epub 2018 Dec 19. Am J Med Genet A. 2019. PMID: 30569567 Free PMC article.

4

Molecular Classes and Growth Hormone Treatment Effects on Behavior and Emotion in Patients with Prader-Willi Syndrome.

Mahmoud R, Swanson HD, Butler MG, Flodman P, Gold JA, Miller JL, Roof E, Osann K, Dykens E, Driscoll DJ, Kimonis V. Mahmoud R, et al. Among authors: osann k. J Clin Med. 2022 May 4;11(9):2572. doi: 10.3390/jcm11092572. J Clin Med. 2022. PMID: 35566699 Free PMC article.

5

Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.

Gold JA, Ruth C, Osann K, Flodman P, McManus B, Lee HS, Donkervoort S, Khare M, Roof E, Dykens E, Miller JL, Driscoll DJ, Butler MG, Heinemann J, Cassidy S, Kimonis VE. Gold JA, et al. Among authors: osann k. Genet Med. 2014 Feb;16(2):164-9. doi: 10.1038/gim.2013.97. Epub 2013 Aug 8. Genet Med. 2014. PMID: 23928912 Free PMC article.

6

Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis.

Greenwood J, Flodman P, Osann K, Boyadjiev SA, Kimonis V. Greenwood J, et al. Among authors: osann k. Genet Med. 2014 Apr;16(4):302-10. doi: 10.1038/gim.2013.134. Epub 2013 Sep 26. Genet Med. 2014. PMID: 24071792 Free PMC article.

7

Meta-analysis of genotype-phenotype analysis of OPA1 mutations in autosomal dominant optic atrophy.

Ham M, Han J, Osann K, Smith M, Kimonis V. Ham M, et al. Among authors: osann k. Mitochondrion. 2019 May;46:262-269. doi: 10.1016/j.mito.2018.07.006. Epub 2018 Aug 27. Mitochondrion. 2019. PMID: 30165240

8

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia.

Mehta SG, Khare M, Ramani R, Watts GD, Simon M, Osann KE, Donkervoort S, Dec E, Nalbandian A, Platt J, Pasquali M, Wang A, Mozaffar T, Smith CD, Kimonis VE. Mehta SG, et al. Among authors: osann ke. Clin Genet. 2013 May;83(5):422-31. doi: 10.1111/cge.12000. Epub 2012 Oct 4. Clin Genet. 2013. PMID: 22909335 Free PMC article.

9

Co-occurrence of celiac disease and other autoimmune diseases in celiacs and their first-degree relatives.

Neuhausen SL, Steele L, Ryan S, Mousavi M, Pinto M, Osann KE, Flodman P, Zone JJ. Neuhausen SL, et al. J Autoimmun. 2008 Sep;31(2):160-5. doi: 10.1016/j.jaut.2008.06.001. Epub 2008 Aug 8. J Autoimmun. 2008. PMID: 18692362 Free PMC article.

10

Radiological features of Paget disease of bone associated with VCP myopathy.

Farpour F, Tehranzadeh J, Donkervoort S, Smith C, Martin B, Vanjara P, Osann K, Kimonis VE. Farpour F, et al. Among authors: osann k. Skeletal Radiol. 2012 Mar;41(3):329-37. doi: 10.1007/s00256-011-1193-4. Epub 2011 Jun 4. Skeletal Radiol. 2012. PMID: 21643886

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