Coleman K - Search Results

1

Severe aortopathy due to fibulin-4 deficiency: molecular insights, surgical strategy, and a review of the literature.

Hebson C, Coleman K, Clabby M, Sallee D, Shankar S, Loeys B, Van Laer L, Kogon B. Hebson C, et al. Among authors: coleman k. Eur J Pediatr. 2014 May;173(5):671-5. doi: 10.1007/s00431-013-2217-y. Epub 2013 Nov 26. Eur J Pediatr. 2014. PMID: 24276535 Review.

2

The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome.

Muldoon M, Ousley OY, Kobrynski LJ, Patel S, Oster ME, Fernandez-Carriba S, Cubells JF, Coleman K, Pearce BD. Muldoon M, et al. Among authors: coleman k. Eur Arch Psychiatry Clin Neurosci. 2015 Sep;265(6):519-24. doi: 10.1007/s00406-014-0546-0. Epub 2014 Sep 30. Eur Arch Psychiatry Clin Neurosci. 2015. PMID: 25267002 Free PMC article.

3

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population.

Botto LD, May K, Fernhoff PM, Correa A, Coleman K, Rasmussen SA, Merritt RK, O'Leary LA, Wong LY, Elixson EM, Mahle WT, Campbell RM. Botto LD, et al. Among authors: coleman k. Pediatrics. 2003 Jul;112(1 Pt 1):101-7. doi: 10.1542/peds.112.1.101. Pediatrics. 2003. PMID: 12837874

4

A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment.

Ousley O, Rockers K, Dell ML, Coleman K, Cubells JF. Ousley O, et al. Among authors: coleman k. Curr Psychiatry Rep. 2007 Apr;9(2):148-58. doi: 10.1007/s11920-007-0085-8. Curr Psychiatry Rep. 2007. PMID: 17389127 Review.

5

Performance on the Modified Card Sorting Test and its relation to psychopathology in adolescents and young adults with 22q11.2 deletion syndrome.

Rockers K, Ousley O, Sutton T, Schoenberg E, Coleman K, Walker E, Cubells JF. Rockers K, et al. Among authors: coleman k. J Intellect Disabil Res. 2009 Jul;53(7):665-76. doi: 10.1111/j.1365-2788.2009.01178.x. Epub 2009 May 12. J Intellect Disabil Res. 2009. PMID: 19460069

6

Chromosome 22q11.2 deletion syndrome in African-American patients: a diagnostic challenge.

Veerapandiyan A, Abdul-Rahman OA, Adam MP, Lyons MJ, Manning M, Coleman K, Kobrynski L, Taneja D, Schoch K, Zimmerman HH, Shashi V. Veerapandiyan A, et al. Among authors: coleman k. Am J Med Genet A. 2011 Sep;155A(9):2186-95. doi: 10.1002/ajmg.a.34226. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834039

7

Association of IL-12p70 and IL-6:IL-10 ratio with autism-related behaviors in 22q11.2 deletion syndrome: a preliminary report.

Ross HE, Guo Y, Coleman K, Ousley O, Miller AH. Ross HE, et al. Among authors: coleman k. Brain Behav Immun. 2013 Jul;31:76-81. doi: 10.1016/j.bbi.2012.12.021. Epub 2013 Jan 24. Brain Behav Immun. 2013. PMID: 23353117 Free PMC article.

8

Axis I psychiatric diagnoses in adolescents and young adults with 22q11 deletion syndrome.

Ousley OY, Smearman E, Fernandez-Carriba S, Rockers KA, Coleman K, Walker EF, Cubells JF. Ousley OY, et al. Among authors: coleman k. Eur Psychiatry. 2013 Sep;28(7):417-22. doi: 10.1016/j.eurpsy.2013.06.002. Epub 2013 Aug 2. Eur Psychiatry. 2013. PMID: 23916466 Free PMC article.

9

Examining the Overlap between Autism Spectrum Disorder and 22q11.2 Deletion Syndrome.

Ousley O, Evans AN, Fernandez-Carriba S, Smearman EL, Rockers K, Morrier MJ, Evans DW, Coleman K, Cubells J. Ousley O, et al. Among authors: coleman k. Int J Mol Sci. 2017 May 18;18(5):1071. doi: 10.3390/ijms18051071. Int J Mol Sci. 2017. PMID: 28524075 Free PMC article.

10

Unique mosaicism of tetraploidy and trisomy 8: clinical, cytogenetic, and molecular findings in a live-born infant.

Roberts HE, Saxe DF, Muralidharan K, Coleman KB, Zacharias JF, Fernhoff PM. Roberts HE, et al. Among authors: coleman kb. Am J Med Genet. 1996 Mar 29;62(3):243-6. doi: 10.1002/(SICI)1096-8628(19960329)62:3<243::AID-AJMG8>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8882781

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