Gropman AL - Search Results

1

New developments in Smith-Magenis syndrome (del 17p11.2).

Gropman AL, Elsea S, Duncan WC Jr, Smith AC. Gropman AL, et al. Curr Opin Neurol. 2007 Apr;20(2):125-34. doi: 10.1097/WCO.0b013e3280895dba. Curr Opin Neurol. 2007. PMID: 17351481 Review.

2

Hypercholesterolemia in children with Smith-Magenis syndrome: del (17) (p11.2p11.2).

Smith AC, Gropman AL, Bailey-Wilson JE, Goker-Alpan O, Elsea SH, Blancato J, Lupski JR, Potocki L. Smith AC, et al. Among authors: gropman al. Genet Med. 2002 May-Jun;4(3):118-25. doi: 10.1097/00125817-200205000-00004. Genet Med. 2002. PMID: 12180145 Free article.

3

Neurologic and developmental features of the Smith-Magenis syndrome (del 17p11.2).

Gropman AL, Duncan WC, Smith AC. Gropman AL, et al. Pediatr Neurol. 2006 May;34(5):337-50. doi: 10.1016/j.pediatrneurol.2005.08.018. Pediatr Neurol. 2006. PMID: 16647992 Review.

4

Neurodevelopment of children under 3 years of age with Smith-Magenis syndrome.

Wolters PL, Gropman AL, Martin SC, Smith MR, Hildenbrand HL, Brewer CC, Smith AC. Wolters PL, et al. Among authors: gropman al. Pediatr Neurol. 2009 Oct;41(4):250-8. doi: 10.1016/j.pediatrneurol.2009.04.015. Pediatr Neurol. 2009. PMID: 19748044 Free PMC article.

5

Variations in EEG discharges predict ADHD severity within individual Smith-Lemli-Opitz patients.

Schreiber JM, Lanham DC, Trescher WH, Sparks SE, Wassif CA, Caffo BS, Porter FD, Tierney E, Gropman AL, Ewen JB. Schreiber JM, et al. Among authors: gropman al. Neurology. 2014 Jul 8;83(2):151-9. doi: 10.1212/WNL.0000000000000565. Epub 2014 Jun 11. Neurology. 2014. PMID: 24920862 Free PMC article. Clinical Trial.

6

MR Imaging Findings in Xp21.2 Duplication Syndrome.

Whitehead MT, Helman G, Gropman AL. Whitehead MT, et al. Among authors: gropman al. J Radiol Case Rep. 2016 May 31;10(5):9-14. doi: 10.3941/jrcr.v10i5.2563. eCollection 2016 May. J Radiol Case Rep. 2016. PMID: 27761175 Free PMC article.

7

Cognitive outcome in urea cycle disorders.

Gropman AL, Batshaw ML. Gropman AL, et al. Mol Genet Metab. 2004 Apr;81 Suppl 1:S58-62. doi: 10.1016/j.ymgme.2003.11.016. Mol Genet Metab. 2004. PMID: 15050975 Review.

8

Atypical patterns of inheritance.

Gropman AL, Adams DR. Gropman AL, et al. Semin Pediatr Neurol. 2007 Mar;14(1):34-45. doi: 10.1016/j.spen.2006.11.007. Semin Pediatr Neurol. 2007. PMID: 17331882 Review.

9

Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome.

Gropman AL, Rogol A, Fennoy I, Sadeghin T, Sinn S, Jameson R, Mitchell F, Clabaugh J, Lutz-Armstrong M, Samango-Sprouse CA. Gropman AL, et al. Am J Med Genet A. 2010 Jun;152A(6):1523-30. doi: 10.1002/ajmg.a.33307. Am J Med Genet A. 2010. PMID: 20503329

10

Epigenetics, copy number variation, and other molecular mechanisms underlying neurodevelopmental disabilities: new insights and diagnostic approaches.

Gropman AL, Batshaw ML. Gropman AL, et al. J Dev Behav Pediatr. 2010 Sep;31(7):582-91. doi: 10.1097/DBP.0b013e3181ee384e. J Dev Behav Pediatr. 2010. PMID: 20814257 Review.

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