Morton DH - Search Results

1

Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities.

Ferkol TW, Puffenberger EG, Lie H, Helms C, Strauss KA, Bowcock A, Carson JL, Hazucha M, Morton DH, Patel AC, Leigh MW, Knowles MR, Zariwala MA. Ferkol TW, et al. Among authors: morton dh. J Pediatr. 2013 Aug;163(2):383-7. doi: 10.1016/j.jpeds.2013.01.061. Epub 2013 Mar 7. J Pediatr. 2013. PMID: 23477994 Free PMC article.

2

Diagnosis and treatment of maple syrup disease: a study of 36 patients.

Morton DH, Strauss KA, Robinson DL, Puffenberger EG, Kelley RI. Morton DH, et al. Pediatrics. 2002 Jun;109(6):999-1008. doi: 10.1542/peds.109.6.999. Pediatrics. 2002. PMID: 12042535

3

Pediatric medicine and the genetic disorders of the Amish and Mennonite people of Pennsylvania.

Morton DH, Morton CS, Strauss KA, Robinson DL, Puffenberger EG, Hendrickson C, Kelley RI. Morton DH, et al. Among authors: morton cs. Am J Med Genet C Semin Med Genet. 2003 Aug 15;121C(1):5-17. doi: 10.1002/ajmg.c.20002. Am J Med Genet C Semin Med Genet. 2003. PMID: 12888982

4

One community's effort to control genetic disease.

Strauss KA, Puffenberger EG, Morton DH. Strauss KA, et al. Among authors: morton dh. Am J Public Health. 2012 Jul;102(7):1300-6. doi: 10.2105/AJPH.2011.300569. Epub 2012 May 17. Am J Public Health. 2012. PMID: 22594747 Free PMC article.

5

Amish lethal microcephaly: a new metabolic disorder with severe congenital microcephaly and 2-ketoglutaric aciduria.

Kelley RI, Robinson D, Puffenberger EG, Strauss KA, Morton DH. Kelley RI, et al. Among authors: morton dh. Am J Med Genet. 2002 Nov 1;112(4):318-26. doi: 10.1002/ajmg.10529. Am J Med Genet. 2002. PMID: 12376931

6

Management of hyperbilirubinemia and prevention of kernicterus in 20 patients with Crigler-Najjar disease.

Strauss KA, Robinson DL, Vreman HJ, Puffenberger EG, Hart G, Morton DH. Strauss KA, et al. Among authors: morton dh. Eur J Pediatr. 2006 May;165(5):306-19. doi: 10.1007/s00431-005-0055-2. Epub 2006 Jan 25. Eur J Pediatr. 2006. PMID: 16435131

7

A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.

Mohney BG, Pulido JS, Lindor NM, Hogan MC, Consugar MB, Peters J, Pankratz VS, Nasr SH, Smith SJ, Gloor J, Kubly V, Spencer D, Nielson R, Puffenberger EG, Strauss KA, Morton DH, Eldahdah L, Harris PC. Mohney BG, et al. Among authors: morton dh. Ophthalmology. 2011 Jun;118(6):1137-44. doi: 10.1016/j.ophtha.2010.10.009. Epub 2011 Jan 13. Ophthalmology. 2011. PMID: 21236492 Free PMC article.

8

Erythrocyte pyruvate kinase deficiency in an old-order Amish cohort: longitudinal risk and disease management.

Rider NL, Strauss KA, Brown K, Finkenstedt A, Puffenberger EG, Hendrickson CL, Robinson DL, Muenke N, Tselepis C, Saunders L, Zoller H, Morton DH. Rider NL, et al. Among authors: morton dh. Am J Hematol. 2011 Oct;86(10):827-34. doi: 10.1002/ajh.22118. Epub 2011 Aug 3. Am J Hematol. 2011. PMID: 21815188 Free article.

9

Genome-wide SNP arrays as a diagnostic tool: clinical description, genetic mapping, and molecular characterization of Salla disease in an Old Order Mennonite population.

Strauss KA, Puffenberger EG, Craig DW, Panganiban CB, Lee AM, Hu-Lince D, Stephan DA, Morton DH. Strauss KA, et al. Among authors: morton dh. Am J Med Genet A. 2005 Oct 15;138A(3):262-7. doi: 10.1002/ajmg.a.30961. Am J Med Genet A. 2005. PMID: 16158439

10

Clinical application of DNA microarrays: molecular diagnosis and HLA matching of an Amish child with severe combined immune deficiency.

Strauss KA, Puffenberger EG, Bunin N, Rider NL, Morton MC, Eastman JT 3rd, Morton DH. Strauss KA, et al. Among authors: morton dh, morton mc. Clin Immunol. 2008 Jul;128(1):31-8. doi: 10.1016/j.clim.2008.02.016. Epub 2008 Apr 28. Clin Immunol. 2008. PMID: 18442948

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