Blakemore K - Search Results

1

Germline mutations in the alternative pathway of complement predispose to HELLP syndrome.

Vaught AJ, Braunstein EM, Jasem J, Yuan X, Makhlin I, Eloundou S, Baines AC, Merrill SA, Chaturvedi S, Blakemore K, Sperati CJ, Brodsky RA. Vaught AJ, et al. Among authors: blakemore k. JCI Insight. 2018 Mar 22;3(6):e99128. doi: 10.1172/jci.insight.99128. JCI Insight. 2018. PMID: 29563339 Free PMC article.

2

Vein of galen aneurysmal malformation: prognostic markers depicted on fetal MRI.

Wagner MW, Vaught AJ, Poretti A, Blakemore KJ, Huisman TA. Wagner MW, et al. Neuroradiol J. 2015 Feb;28(1):72-5. doi: 10.15274/NRJ-2014-10106. Neuroradiol J. 2015. PMID: 25924177 Free PMC article.

3

Direct evidence of complement activation in HELLP syndrome: A link to atypical hemolytic uremic syndrome.

Vaught AJ, Gavriilaki E, Hueppchen N, Blakemore K, Yuan X, Seifert SM, York S, Brodsky RA. Vaught AJ, et al. Among authors: blakemore k. Exp Hematol. 2016 May;44(5):390-8. doi: 10.1016/j.exphem.2016.01.005. Epub 2016 Feb 26. Exp Hematol. 2016. PMID: 26921648 Free PMC article.

4

A review of the alternative pathway of complement and its relation to HELLP syndrome: is it time to consider HELLP syndrome a disease of the alternative pathway.

Vaught AJ, Braunstein E, Chaturvedi S, Blakemore K, Brodsky RA. Vaught AJ, et al. Among authors: blakemore k. J Matern Fetal Neonatal Med. 2022 Apr;35(7):1392-1400. doi: 10.1080/14767058.2020.1755650. Epub 2020 Apr 26. J Matern Fetal Neonatal Med. 2022. PMID: 32338085 Review.

5

Prenatal diagnosis of Desbuquois dysplasia Type 1: Utilization of high-density SNP array to map homozygosity and identify the gene.

Forster KR, Hooper JE, Blakemore KJ, Baschat AA, Hoover-Fong J. Forster KR, et al. Am J Med Genet A. 2019 Dec;179(12):2490-2493. doi: 10.1002/ajmg.a.61372. Epub 2019 Oct 6. Am J Med Genet A. 2019. PMID: 31587486

6

Gestational Alloimmune Liver Disease: A Devastating Condition Preventable With Maternal Intravenous Immunoglobulin.

Anastasio HB, Grundy M, Birsner ML, Blakemore KJ. Anastasio HB, et al. Obstet Gynecol. 2016 Nov;128(5):1092-1094. doi: 10.1097/AOG.0000000000001569. Obstet Gynecol. 2016. PMID: 27741190

7

The Double Bubble Sign: Duodenal Atresia and Associated Genetic Etiologies.

Bishop JC, McCormick B, Johnson CT, Miller J, Jelin E, Blakemore K, Jelin AC. Bishop JC, et al. Among authors: blakemore k. Fetal Diagn Ther. 2020;47(2):98-103. doi: 10.1159/000500471. Epub 2019 Jun 5. Fetal Diagn Ther. 2020. PMID: 31167209 Free PMC article.

8

Alagille syndrome: prenatal diagnosis and pregnancy outcome.

Albayram F, Stone K, Nagey D, Schwarz KB, Blakemore K. Albayram F, et al. Among authors: blakemore k. Fetal Diagn Ther. 2002 May-Jun;17(3):182-4. doi: 10.1159/000048035. Fetal Diagn Ther. 2002. PMID: 11914573

9

Leiomyomata uteri, genetic amniocentesis, and the risk of second-trimester spontaneous abortion.

Salvador E, Bienstock J, Blakemore KJ, Pressman E. Salvador E, et al. Am J Obstet Gynecol. 2002 May;186(5):913-5. doi: 10.1067/mob.2002.123988. Am J Obstet Gynecol. 2002. PMID: 12015511

10

Fetomaternal alloimmune thrombocytopenia: the questions that still remain.

Althaus J, Blakemore KJ. Althaus J, et al. J Matern Fetal Neonatal Med. 2007 Sep;20(9):633-7. doi: 10.1080/14767050701490517. J Matern Fetal Neonatal Med. 2007. PMID: 17701662 Review.

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