Adesina AM - Search Results

1

Ablation of steroid receptor coactivator-3 resembles the human CACT metabolic myopathy.

York B, Reineke EL, Sagen JV, Nikolai BC, Zhou S, Louet JF, Chopra AR, Chen X, Reed G, Noebels J, Adesina AM, Yu H, Wong LJ, Tsimelzon A, Hilsenbeck S, Stevens RD, Wenner BR, Ilkayeva O, Xu J, Newgard CB, O'Malley BW. York B, et al. Among authors: adesina am. Cell Metab. 2012 May 2;15(5):752-63. doi: 10.1016/j.cmet.2012.03.020. Cell Metab. 2012. PMID: 22560224 Free PMC article.

2

Atypical presentation of Leigh syndrome associated with a Leber hereditary optic neuropathy primary mitochondrial DNA mutation.

Fruhman G, Landsverk ML, Lotze TE, Hunter JV, Wangler MF, Adesina AM, Wong LJ, Scaglia F. Fruhman G, et al. Among authors: adesina am. Mol Genet Metab. 2011 Jun;103(2):153-60. doi: 10.1016/j.ymgme.2011.02.014. Epub 2011 Feb 26. Mol Genet Metab. 2011. PMID: 21414825

3

Ankyrin-G isoform imbalance and interneuronopathy link epilepsy and bipolar disorder.

Lopez AY, Wang X, Xu M, Maheshwari A, Curry D, Lam S, Adesina AM, Noebels JL, Sun QQ, Cooper EC. Lopez AY, et al. Among authors: adesina am. Mol Psychiatry. 2017 Oct;22(10):1464-1472. doi: 10.1038/mp.2016.233. Epub 2016 Dec 13. Mol Psychiatry. 2017. PMID: 27956739 Free PMC article.

4

MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.

El-Hattab AW, Adesina AM, Jones J, Scaglia F. El-Hattab AW, et al. Among authors: adesina am. Mol Genet Metab. 2015 Sep-Oct;116(1-2):4-12. doi: 10.1016/j.ymgme.2015.06.004. Epub 2015 Jun 15. Mol Genet Metab. 2015. PMID: 26095523 Review.

5

Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid Tumors.

Parsons DW, Roy A, Yang Y, Wang T, Scollon S, Bergstrom K, Kerstein RA, Gutierrez S, Petersen AK, Bavle A, Lin FY, López-Terrada DH, Monzon FA, Hicks MJ, Eldin KW, Quintanilla NM, Adesina AM, Mohila CA, Whitehead W, Jea A, Vasudevan SA, Nuchtern JG, Ramamurthy U, McGuire AL, Hilsenbeck SG, Reid JG, Muzny DM, Wheeler DA, Berg SL, Chintagumpala MM, Eng CM, Gibbs RA, Plon SE. Parsons DW, et al. Among authors: adesina am. JAMA Oncol. 2016 May 1;2(5):616-624. doi: 10.1001/jamaoncol.2015.5699. JAMA Oncol. 2016. PMID: 26822237 Free PMC article.

6

Hypothyroidism after craniospinal irradiation with proton or photon therapy in patients with medulloblastoma.

Bielamowicz K, Okcu MF, Sonabend R, Paulino AC, Hilsenbeck SG, Dreyer Z, Suzawa H, Bryant R, Adesina A, Dauser R, Mahajan A, Chintagumpala M. Bielamowicz K, et al. Pediatr Hematol Oncol. 2018 May;35(4):257-267. doi: 10.1080/08880018.2018.1471111. Epub 2018 Dec 11. Pediatr Hematol Oncol. 2018. PMID: 30537887

7

Isolated mitochondrial myopathy associated with muscle coenzyme Q10 deficiency.

Lalani SR, Vladutiu GD, Plunkett K, Lotze TE, Adesina AM, Scaglia F. Lalani SR, et al. Among authors: adesina am. Arch Neurol. 2005 Feb;62(2):317-20. doi: 10.1001/archneur.62.2.317. Arch Neurol. 2005. PMID: 15710863

8

The antimicrobial protein, CAP37, is upregulated in pyramidal neurons during Alzheimer's disease.

Brock AJ, Kasus-Jacobi A, Lerner M, Logan S, Adesina AM, Anne Pereira H. Brock AJ, et al. Among authors: adesina am. Histochem Cell Biol. 2015 Oct;144(4):293-308. doi: 10.1007/s00418-015-1347-x. Epub 2015 Jul 14. Histochem Cell Biol. 2015. PMID: 26170148 Free PMC article.

9

Danon disease as an underrecognized cause of hypertrophic cardiomyopathy in children.

Yang Z, McMahon CJ, Smith LR, Bersola J, Adesina AM, Breinholt JP, Kearney DL, Dreyer WJ, Denfield SW, Price JF, Grenier M, Kertesz NJ, Clunie SK, Fernbach SD, Southern JF, Berger S, Towbin JA, Bowles KR, Bowles NE. Yang Z, et al. Among authors: adesina am. Circulation. 2005 Sep 13;112(11):1612-7. doi: 10.1161/CIRCULATIONAHA.105.546481. Epub 2005 Sep 6. Circulation. 2005. PMID: 16144992

10

Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child.

Streff H, Bi W, Colón AG, Adesina AM, Miyake CY, Lalani SR. Streff H, et al. Among authors: adesina am. Eur J Med Genet. 2019 Nov;62(11):103567. doi: 10.1016/j.ejmg.2018.11.001. Epub 2018 Nov 3. Eur J Med Genet. 2019. PMID: 30395933 Free PMC article.

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