Whitehead KJ - Search Results

1

The effects of nasal closure on quality of life in patients with hereditary hemorrhagic telangiectasia.

Thomson RS, Molin NL, Whitehead KJ, Ashby S, Johnson L, Ward PD, McRae BR, Wilson KF, McDonald J. Thomson RS, et al. Among authors: whitehead kj. Laryngoscope Investig Otolaryngol. 2018 Apr 19;3(3):178-181. doi: 10.1002/lio2.157. eCollection 2018 Jun. Laryngoscope Investig Otolaryngol. 2018. PMID: 30062132 Free PMC article.

2

Hereditary hemorrhagic telangiectasia: genetics and molecular diagnostics in a new era.

McDonald J, Wooderchak-Donahue W, VanSant Webb C, Whitehead K, Stevenson DA, Bayrak-Toydemir P. McDonald J, et al. Front Genet. 2015 Jan 26;6:1. doi: 10.3389/fgene.2015.00001. eCollection 2015. Front Genet. 2015. PMID: 25674101 Free PMC article. Review.

3

An evaluation of the severity and progression of epistaxis in hereditary hemorrhagic telangiectasia 1 versus hereditary hemorrhagic telangiectasia 2.

Hunter BN, Timmins BH, McDonald J, Whitehead KJ, Ward PD, Wilson KF. Hunter BN, et al. Among authors: whitehead kj. Laryngoscope. 2016 Apr;126(4):786-90. doi: 10.1002/lary.25604. Epub 2015 Sep 15. Laryngoscope. 2016. PMID: 26372311 Free PMC article.

4

Effect of Topical Intranasal Therapy on Epistaxis Frequency in Patients With Hereditary Hemorrhagic Telangiectasia: A Randomized Clinical Trial.

Whitehead KJ, Sautter NB, McWilliams JP, Chakinala MM, Merlo CA, Johnson MH, James M, Everett EM, Clancy MS, Faughnan ME, Oh SP, Olitsky SE, Pyeritz RE, Gossage JR. Whitehead KJ, et al. JAMA. 2016 Sep 6;316(9):943-51. doi: 10.1001/jama.2016.11724. JAMA. 2016. PMID: 27599329 Clinical Trial.

5

Epistaxis in children and adolescents with hereditary hemorrhagic telangiectasia.

Gonzalez CD, Mcdonald J, Stevenson DA, Whitehead KJ, Petersen MG, Presson AP, Ding Q, Wilson KF. Gonzalez CD, et al. Among authors: whitehead kj. Laryngoscope. 2018 Jul;128(7):1714-1719. doi: 10.1002/lary.27015. Epub 2017 Nov 24. Laryngoscope. 2018. PMID: 29171658

6

Clinical presentation and treatment paradigms in patients with hereditary hemorrhagic telangiectasia and spinal vascular malformations.

Eli I, Gamboa NT, Joyce EJ, Park MS, Taussky P, Schmidt RH, Couldwell WT, McDonald J, Whitehead KJ, Kalani MYS. Eli I, et al. Among authors: whitehead kj. J Clin Neurosci. 2018 Apr;50:51-57. doi: 10.1016/j.jocn.2018.01.010. Epub 2018 Feb 3. J Clin Neurosci. 2018. PMID: 29398197

7

Clinical presentation and treatment paradigms of brain arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia.

Gamboa NT, Joyce EJ, Eli I, Park MS, Taussky P, Schmidt RH, McDonald J, Whitehead KJ, Kalani MYS. Gamboa NT, et al. Among authors: whitehead kj. J Clin Neurosci. 2018 May;51:22-28. doi: 10.1016/j.jocn.2018.01.019. Epub 2018 Feb 23. J Clin Neurosci. 2018. PMID: 29483005

8

Vitamin D levels are associated with epistaxis severity and bleeding duration in hereditary hemorrhagic telangiectasia.

Weber LM, McDonald J, Whitehead K. Weber LM, et al. Biomark Med. 2018 Apr;12(4):365-371. doi: 10.2217/bmm-2017-0229. Epub 2018 Mar 14. Biomark Med. 2018. PMID: 29537299 Free PMC article.

9

Genome sequencing reveals a deep intronic splicing ACVRL1 mutation hotspot in Hereditary Haemorrhagic Telangiectasia.

Wooderchak-Donahue WL, McDonald J, Farrell A, Akay G, Velinder M, Johnson P, VanSant-Webb C, Margraf R, Briggs E, Whitehead KJ, Thomson J, Lin AE, Pyeritz RE, Marth G, Bayrak-Toydemir P. Wooderchak-Donahue WL, et al. Among authors: whitehead kj. J Med Genet. 2018 Dec;55(12):824-830. doi: 10.1136/jmedgenet-2018-105561. Epub 2018 Sep 22. J Med Genet. 2018. PMID: 30244195

10

Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?

Wooderchak-Donahue WL, Akay G, Whitehead K, Briggs E, Stevenson DA, O'Fallon B, Velinder M, Farrell A, Shen W, Bedoukian E, Skrabann CM, Antaya RJ, Henderson K, Pollak J, Treat J, Day R, Jacher JE, Hannibal M, Bontempo K, Marth G, Bayrak-Toydemir P, McDonald J. Wooderchak-Donahue WL, et al. Genet Med. 2019 Sep;21(9):2007-2014. doi: 10.1038/s41436-019-0443-z. Epub 2019 Feb 14. Genet Med. 2019. PMID: 30760892 Free article.

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