Morton DH - Search Results

1

Type I glutaric aciduria, part 2: a model of acute striatal necrosis.

Strauss KA, Morton DH. Strauss KA, et al. Among authors: morton dh. Am J Med Genet C Semin Med Genet. 2003 Aug 15;121C(1):53-70. doi: 10.1002/ajmg.c.20008. Am J Med Genet C Semin Med Genet. 2003. PMID: 12888986

2

Glutaric aciduria type I: a common cause of episodic encephalopathy and spastic paralysis in the Amish of Lancaster County, Pennsylvania.

Morton DH, Bennett MJ, Seargeant LE, Nichter CA, Kelley RI. Morton DH, et al. Am J Med Genet. 1991 Oct 1;41(1):89-95. doi: 10.1002/ajmg.1320410122. Am J Med Genet. 1991. PMID: 1951469

3

Branched-chain Ketoacyl Dehydrogenase Deficiency: Maple Syrup Disease.

Strauss KA, Morton DH. Strauss KA, et al. Among authors: morton dh. Curr Treat Options Neurol. 2003 Jul;5(4):329-341. doi: 10.1007/s11940-003-0039-3. Curr Treat Options Neurol. 2003. PMID: 12791200

4

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

5

Type I glutaric aciduria, part 1: natural history of 77 patients.

Strauss KA, Puffenberger EG, Robinson DL, Morton DH. Strauss KA, et al. Among authors: morton dh. Am J Med Genet C Semin Med Genet. 2003 Aug 15;121C(1):38-52. doi: 10.1002/ajmg.c.20007. Am J Med Genet C Semin Med Genet. 2003. PMID: 12888985

6

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

7

Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2.

Strauss KA, Puffenberger EG, Huentelman MJ, Gottlieb S, Dobrin SE, Parod JM, Stephan DA, Morton DH. Strauss KA, et al. Among authors: morton dh. N Engl J Med. 2006 Mar 30;354(13):1370-7. doi: 10.1056/NEJMoa052773. N Engl J Med. 2006. PMID: 16571880 Free article.

8

Prevention of brain disease from severe 5,10-methylenetetrahydrofolate reductase deficiency.

Strauss KA, Morton DH, Puffenberger EG, Hendrickson C, Robinson DL, Wagner C, Stabler SP, Allen RH, Chwatko G, Jakubowski H, Niculescu MD, Mudd SH. Strauss KA, et al. Among authors: morton dh. Mol Genet Metab. 2007 Jun;91(2):165-75. doi: 10.1016/j.ymgme.2007.02.012. Epub 2007 Apr 3. Mol Genet Metab. 2007. PMID: 17409006

9

Multimodal imaging of striatal degeneration in Amish patients with glutaryl-CoA dehydrogenase deficiency.

Strauss KA, Lazovic J, Wintermark M, Morton DH. Strauss KA, et al. Among authors: morton dh. Brain. 2007 Jul;130(Pt 7):1905-20. doi: 10.1093/brain/awm058. Epub 2007 May 3. Brain. 2007. PMID: 17478444

10

Polyhydramnios, megalencephaly and symptomatic epilepsy caused by a homozygous 7-kilobase deletion in LYK5.

Puffenberger EG, Strauss KA, Ramsey KE, Craig DW, Stephan DA, Robinson DL, Hendrickson CL, Gottlieb S, Ramsay DA, Siu VM, Heuer GG, Crino PB, Morton DH. Puffenberger EG, et al. Among authors: morton dh. Brain. 2007 Jul;130(Pt 7):1929-41. doi: 10.1093/brain/awm100. Epub 2007 May 23. Brain. 2007. PMID: 17522105

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