Marchuk DA - Search Results

1

Genetic considerations relevant to intracranial hemorrhage and brain arteriovenous malformations.

Kim H, Marchuk DA, Pawlikowska L, Chen Y, Su H, Yang GY, Young WL. Kim H, et al. Among authors: marchuk da. Acta Neurochir Suppl. 2008;105:199-206. doi: 10.1007/978-3-211-09469-3_38. Acta Neurochir Suppl. 2008. PMID: 19066109 Free PMC article. Review.

2

Cyclo-oxygenase 2, a putative mediator of vessel remodeling, is expressed in the brain AVM vessels and associates with inflammation.

Keränen S, Suutarinen S, Mallick R, Laakkonen JP, Guo D, Pawlikowska L, Jahromi BR, Rauramaa T, Ylä-Herttuala S, Marchuk D, Krings T, Koivisto T, Lawton M, Radovanovic I, Kim H, Faughnan ME, Frösen J. Keränen S, et al. Acta Neurochir (Wien). 2021 Sep;163(9):2503-2514. doi: 10.1007/s00701-021-04895-z. Epub 2021 Jun 29. Acta Neurochir (Wien). 2021. PMID: 34185176 Free PMC article.

3

Utility of modified Rankin Scale for brain vascular malformations in hereditary hemorrhagic telangiectasia.

Thompson KP, Nelson J, Kim H, Weinsheimer SM, Marchuk DA, Lawton MT, Krings T, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Thompson KP, et al. Among authors: marchuk da. Orphanet J Rare Dis. 2021 Sep 19;16(1):390. doi: 10.1186/s13023-021-02012-y. Orphanet J Rare Dis. 2021. PMID: 34538258 Free PMC article.

4

Abnormal pattern of Tie-2 and vascular endothelial growth factor receptor expression in human cerebral arteriovenous malformations.

Hashimoto T, Emala CW, Joshi S, Mesa-Tejada R, Quick CM, Feng L, Libow A, Marchuk DA, Young WL. Hashimoto T, et al. Among authors: marchuk da. Neurosurgery. 2000 Oct;47(4):910-8; discussion 918-9. doi: 10.1097/00006123-200010000-00022. Neurosurgery. 2000. PMID: 11014431

5

Predictors of mortality in patients with hereditary hemorrhagic telangiectasia.

Thompson KP, Nelson J, Kim H, Pawlikowska L, Marchuk DA, Lawton MT, Faughnan ME; Brain Vascular Malformation Consortium HHT Investigator Group. Thompson KP, et al. Among authors: marchuk da. Orphanet J Rare Dis. 2021 Jan 6;16(1):12. doi: 10.1186/s13023-020-01579-2. Orphanet J Rare Dis. 2021. PMID: 33407668 Free PMC article.

6

Endoglin, an ancillary TGFbeta receptor, is required for extraembryonic angiogenesis and plays a key role in heart development.

Arthur HM, Ure J, Smith AJ, Renforth G, Wilson DI, Torsney E, Charlton R, Parums DV, Jowett T, Marchuk DA, Burn J, Diamond AG. Arthur HM, et al. Among authors: marchuk da. Dev Biol. 2000 Jan 1;217(1):42-53. doi: 10.1006/dbio.1999.9534. Dev Biol. 2000. PMID: 10625534 Free article.

7

Genetic abnormalities in hereditary hemorrhagic telangiectasia.

Marchuk DA. Marchuk DA. Curr Opin Hematol. 1998 Sep;5(5):332-8. doi: 10.1097/00062752-199809000-00005. Curr Opin Hematol. 1998. PMID: 9776212 Review.

8

Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred.

McDonald JE, Miller FJ, Hallam SE, Nelson L, Marchuk DA, Ward KJ. McDonald JE, et al. Among authors: marchuk da. Am J Med Genet. 2000 Aug 14;93(4):320-7. doi: 10.1002/1096-8628(20000814)93:4<320::aid-ajmg12>3.0.co;2-r. Am J Med Genet. 2000. PMID: 10946360 Review.

9

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.

Berg JN, Gallione CJ, Stenzel TT, Johnson DW, Allen WP, Schwartz CE, Jackson CE, Porteous ME, Marchuk DA. Berg JN, et al. Among authors: marchuk da. Am J Hum Genet. 1997 Jul;61(1):60-7. doi: 10.1086/513903. Am J Hum Genet. 1997. PMID: 9245985 Free PMC article.

10

Novel missense and frameshift mutations in the activin receptor-like kinase-1 gene in hereditary hemorrhagic telangiectasia. Mutations in brief no. 164. Online.

Klaus DJ, Gallione CJ, Anthony K, Yeh EY, Yu J, Lux A, Johnson DW, Marchuk DA. Klaus DJ, et al. Among authors: marchuk da. Hum Mutat. 1998;12(2):137. doi: 10.1002/(SICI)1098-1004(1998)12:2<137::AID-HUMU16>3.0.CO;2-J. Hum Mutat. 1998. PMID: 10694922

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