Ernst LM - Search Results

1

Interlobular bile duct loss in pediatric cholestatic disease is associated with aberrant cytokeratin 7 expression by hepatocytes.

Ernst LM, Spinner NB, Piccoli DA, Mauger J, Russo P. Ernst LM, et al. Pediatr Dev Pathol. 2007 Sep-Oct;10(5):383-90. doi: 10.2350/06-09-0171.1. Pediatr Dev Pathol. 2007. PMID: 17929991

2

Bacterial etiology for chronic villitis is not supported by polymerase chain reaction for 16S rRNA DNA.

Ernst LM, Crouch J, Rinder H, Howe JG. Ernst LM, et al. Pediatr Dev Pathol. 2005 Nov-Dec;8(6):647-53. doi: 10.1007/s10024-005-0412-1. Epub 2005 Jul 14. Pediatr Dev Pathol. 2005. PMID: 16010482

3

A potential screening tool for IPEX syndrome.

Heltzer ML, Choi JK, Ochs HD, Sullivan KE, Torgerson TR, Ernst LM. Heltzer ML, et al. Among authors: ernst lm. Pediatr Dev Pathol. 2007 Mar-Apr;10(2):98-105. doi: 10.2350/06-07-0130.1. Pediatr Dev Pathol. 2007. PMID: 17378693

4

Hamartomatous tongue lesions in children.

Kreiger PA, Ernst LM, Elden LM, Kazahaya K, Alawi F, Russo PA. Kreiger PA, et al. Among authors: ernst lm. Am J Surg Pathol. 2007 Aug;31(8):1186-90. doi: 10.1097/PAS.0b013e3180674dd7. Am J Surg Pathol. 2007. PMID: 17667541

5

Familial perinatal liver disease and fetal thrombotic vasculopathy.

Ernst LM, Grossman AB, Ruchelli ED. Ernst LM, et al. Pediatr Dev Pathol. 2008 Mar-Apr;11(2):160-3. doi: 10.2350/07-06-0301.1. Epub 2007 Jul 2. Pediatr Dev Pathol. 2008. PMID: 17990937

6

Fetal thrombotic vasculopathy in twin placentas with complete hydatidiform mole.

Ernst LM, Chou D, Parry S. Ernst LM, et al. Pediatr Dev Pathol. 2009 Jan-Feb;12(1):63-7. doi: 10.2350/08-04-0446.1. Pediatr Dev Pathol. 2009. PMID: 18702565

7

Inflammation-induced preterm birth in a murine model is associated with increases in fetal macrophages and circulating erythroid precursors.

Ernst LM, Gonzalez J, Ofori E, Elovitz M. Ernst LM, et al. Pediatr Dev Pathol. 2010 Jul-Aug;13(4):273-81. doi: 10.2350/09-05-0649-OA.1. Pediatr Dev Pathol. 2010. PMID: 19863449

8

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis.

Conlin LK, Thiel BD, Bonnemann CG, Medne L, Ernst LM, Zackai EH, Deardorff MA, Krantz ID, Hakonarson H, Spinner NB. Conlin LK, et al. Among authors: ernst lm. Hum Mol Genet. 2010 Apr 1;19(7):1263-75. doi: 10.1093/hmg/ddq003. Epub 2010 Jan 6. Hum Mol Genet. 2010. PMID: 20053666 Free PMC article.

9

Neonatal diabetes and congenital malabsorptive diarrhea attributable to a novel mutation in the human neurogenin-3 gene coding sequence.

Pinney SE, Oliver-Krasinski J, Ernst L, Hughes N, Patel P, Stoffers DA, Russo P, De León DD. Pinney SE, et al. J Clin Endocrinol Metab. 2011 Jul;96(7):1960-5. doi: 10.1210/jc.2011-0029. Epub 2011 Apr 13. J Clin Endocrinol Metab. 2011. PMID: 21490072 Free PMC article.

10

Mutations in long-chain 3-hydroxyacyl coenzyme a dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition.

Griffin AC, Strauss AW, Bennett MJ, Ernst LM. Griffin AC, et al. Among authors: ernst lm. Pediatr Dev Pathol. 2012 Sep-Oct;15(5):368-74. doi: 10.2350/12-05-1198-OA.1. Epub 2012 Jul 2. Pediatr Dev Pathol. 2012. PMID: 22746996

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