Whitley CB - Search Results

1

Acquired autistic behaviors in children with mucopolysaccharidosis type IIIA.

Rumsey RK, Rudser K, Delaney K, Potegal M, Whitley CB, Shapiro E. Rumsey RK, et al. Among authors: whitley cb. J Pediatr. 2014 May;164(5):1147-1151.e1. doi: 10.1016/j.jpeds.2014.01.007. Epub 2014 Feb 25. J Pediatr. 2014. PMID: 24582005 Free PMC article. Clinical Trial.

2

Lysinuric protein intolerance masquerading as celiac disease: a case report.

Reinoso MA, Whitley C, Jessurun J, Schwarzenberg SJ. Reinoso MA, et al. J Pediatr. 1998 Jan;132(1):153-5. doi: 10.1016/s0022-3476(98)70502-5. J Pediatr. 1998. PMID: 9470018

3

Combination of enzyme replacement and hematopoietic stem cell transplantation as therapy for Hurler syndrome.

Tolar J, Grewal SS, Bjoraker KJ, Whitley CB, Shapiro EG, Charnas L, Orchard PJ. Tolar J, et al. Among authors: whitley cb. Bone Marrow Transplant. 2008 Mar;41(6):531-5. doi: 10.1038/sj.bmt.1705934. Epub 2007 Nov 26. Bone Marrow Transplant. 2008. PMID: 18037941 Clinical Trial.

4

START, a double blind, placebo-controlled pharmacogenetic test of responsiveness to sapropterin dihydrochloride in phenylketonuria patients.

Utz JR, Lorentz CP, Markowitz D, Rudser KD, Diethelm-Okita B, Erickson D, Whitley CB. Utz JR, et al. Among authors: whitley cb. Mol Genet Metab. 2012 Feb;105(2):193-7. doi: 10.1016/j.ymgme.2011.10.014. Epub 2011 Oct 29. Mol Genet Metab. 2012. PMID: 22112818 Clinical Trial.

5

An exploratory study of brain function and structure in mucopolysaccharidosis type I: long term observations following hematopoietic cell transplantation (HCT).

Shapiro E, Guler OE, Rudser K, Delaney K, Bjoraker K, Whitley C, Tolar J, Orchard P, Provenzale J, Thomas KM. Shapiro E, et al. Mol Genet Metab. 2012 Sep;107(1-2):116-21. doi: 10.1016/j.ymgme.2012.07.016. Epub 2012 Jul 20. Mol Genet Metab. 2012. PMID: 22867884 Free PMC article.

6

Enzyme replacement is associated with better cognitive outcomes after transplant in Hurler syndrome.

Eisengart JB, Rudser KD, Tolar J, Orchard PJ, Kivisto T, Ziegler RS, Whitley CB, Shapiro EG. Eisengart JB, et al. Among authors: whitley cb. J Pediatr. 2013 Feb;162(2):375-80.e1. doi: 10.1016/j.jpeds.2012.07.052. Epub 2012 Sep 10. J Pediatr. 2013. PMID: 22974573 Free PMC article.

7

Mucopolysaccharidosis Type IIIA presents as a variant of Klüver-Bucy syndrome.

Potegal M, Yund B, Rudser K, Ahmed A, Delaney K, Nestrasil I, Whitley CB, Shapiro EG. Potegal M, et al. Among authors: whitley cb. J Clin Exp Neuropsychol. 2013;35(6):608-16. doi: 10.1080/13803395.2013.804035. Epub 2013 Jun 8. J Clin Exp Neuropsychol. 2013. PMID: 23745734 Free PMC article.

8

Methods of neurodevelopmental assessment in children with neurodegenerative disease: Sanfilippo syndrome.

Delaney KA, Rudser KR, Yund BD, Whitley CB, Haslett PA, Shapiro EG. Delaney KA, et al. Among authors: whitley cb. JIMD Rep. 2014;13:129-37. doi: 10.1007/8904_2013_269. Epub 2013 Nov 5. JIMD Rep. 2014. PMID: 24190801 Free PMC article.

9

Neurocognitive and neuropsychiatric phenotypes associated with the mutation L238Q of the α-L-iduronidase gene in Hurler-Scheie syndrome.

Ahmed A, Whitley CB, Cooksley R, Rudser K, Cagle S, Ali N, Delaney K, Yund B, Shapiro E. Ahmed A, et al. Among authors: whitley cb. Mol Genet Metab. 2014 Feb;111(2):123-7. doi: 10.1016/j.ymgme.2013.11.014. Epub 2013 Dec 12. Mol Genet Metab. 2014. PMID: 24368159 Free PMC article.

10

Biomarkers of bone remodeling in children with mucopolysaccharidosis types I, II, and VI.

Stevenson DA, Rudser K, Kunin-Batson A, Fung EB, Viskochil D, Shapiro E, Orchard PJ, Whitley CB, Polgreen LE. Stevenson DA, et al. Among authors: whitley cb. J Pediatr Rehabil Med. 2014;7(2):159-65. doi: 10.3233/PRM-140285. J Pediatr Rehabil Med. 2014. PMID: 25096868 Free PMC article.

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