Boue D - Search Results

1

Long-term enhancement of skeletal muscle mass and strength by single gene administration of myostatin inhibitors.

Haidet AM, Rizo L, Handy C, Umapathi P, Eagle A, Shilling C, Boue D, Martin PT, Sahenk Z, Mendell JR, Kaspar BK. Haidet AM, et al. Among authors: boue d. Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4318-22. doi: 10.1073/pnas.0709144105. Epub 2008 Mar 11. Proc Natl Acad Sci U S A. 2008. PMID: 18334646 Free PMC article.

2

The congenital muscular dystrophies: recent advances and molecular insights.

Mendell JR, Boué DR, Martin PT. Mendell JR, et al. Pediatr Dev Pathol. 2006 Nov-Dec;9(6):427-43. doi: 10.2350/06-07-0127.1. Pediatr Dev Pathol. 2006. PMID: 17163796 Free PMC article. Review.

3

Hypotonia, weakness, and pontocerebellar hypoplasia in siblings.

Tsao CY, Mendell J, Sahenk Z, Rusin J, Boue D. Tsao CY, et al. Among authors: boue d. Semin Pediatr Neurol. 2008 Dec;15(4):151-3. doi: 10.1016/j.spen.2008.09.001. Semin Pediatr Neurol. 2008. PMID: 19073313

4

Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene.

Chanprasert S, Wang J, Weng SW, Enns GM, Boué DR, Wong BL, Mendell JR, Perry DA, Sahenk Z, Craigen WJ, Alcala FJ, Pascual JM, Melancon S, Zhang VW, Scaglia F, Wong LJ. Chanprasert S, et al. Mol Genet Metab. 2013 Sep-Oct;110(1-2):153-61. doi: 10.1016/j.ymgme.2013.07.009. Epub 2013 Jul 17. Mol Genet Metab. 2013. PMID: 23932787

5

A Novel De Novo Heterozygous SCN4a Mutation Causing Congenital Myopathy, Myotonia and Multiple Congenital Anomalies.

Waldrop M, Amornvit J, Pierson CR, Boue DR, Sahenk Z. Waldrop M, et al. J Neuromuscul Dis. 2019;6(4):467-473. doi: 10.3233/JND-190425. J Neuromuscul Dis. 2019. PMID: 31609695

6

Danon disease: an unusual presentation of autism.

Burusnukul P, de Los Reyes EC, Yinger J, Boué DR. Burusnukul P, et al. Pediatr Neurol. 2008 Jul;39(1):52-4. doi: 10.1016/j.pediatrneurol.2008.03.011. Pediatr Neurol. 2008. PMID: 18555174

7

Lytic skull metastasis from a follicular thyroid carcinoma in a child.

Kim SH, Kosnik E, Madden C, Morran S, Rusin J, Gordon T, Boue D. Kim SH, et al. Among authors: boue d. Pediatr Neurosurg. 1998 Feb;28(2):84-8. doi: 10.1159/000028626. Pediatr Neurosurg. 1998. PMID: 9693337

8

Clinicopathologic study of ectomesenchymomas from Intergroup Rhabdomyosarcoma Study Groups III and IV.

Boué DR, Parham DM, Webber B, Crist WM, Qualman SJ. Boué DR, et al. Pediatr Dev Pathol. 2000 May-Jun;3(3):290-300. doi: 10.1007/s100249910039. Pediatr Dev Pathol. 2000. PMID: 10742419

9

Importance of hypoxic/ischemic conditions in the development of cerebral lenticulostriate vasculopathy.

Coley BD, Rusin JA, Boue DR. Coley BD, et al. Among authors: boue dr. Pediatr Radiol. 2000 Dec;30(12):846-55. doi: 10.1007/s002470000322. Pediatr Radiol. 2000. PMID: 11149094

10

Leigh disease with mitochondrial DNA A8344G mutation: case report and brief review.

Tsao CY, Herman G, Boué DR, Prior TW, Lo WD, Atkin JF, Rusin J. Tsao CY, et al. Among authors: boue dr. J Child Neurol. 2003 Jan;18(1):62-4. doi: 10.1177/08830738030180011401. J Child Neurol. 2003. PMID: 12661941

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