Matheus MG - Search Results

1

Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation.

Zarate YA, Lichty AW, Champion KJ, Clarkson LK, Holden KR, Matheus MG. Zarate YA, et al. Among authors: matheus mg. J Child Neurol. 2014 Aug;29(8):NP13-7. doi: 10.1177/0883073813492384. Epub 2013 Jul 21. J Child Neurol. 2014. PMID: 23877478

2

LIS1 duplication: expanding the phenotype.

Lockrow JP, Holden KR, Dwivedi A, Matheus MG, Lyons MJ. Lockrow JP, et al. Among authors: matheus mg. J Child Neurol. 2012 Jun;27(6):791-5. doi: 10.1177/0883073811425972. Epub 2011 Dec 21. J Child Neurol. 2012. PMID: 22190508

3

Novel mutation in Sjogren-Larsson syndrome is associated with divergent neurologic phenotypes.

Davis K, Holden KR, S'Aulis D, Amador C, Matheus MG, Rizzo WB. Davis K, et al. Among authors: matheus mg. J Child Neurol. 2013 Oct;28(10):1259-65. doi: 10.1177/0883073812460581. Epub 2012 Oct 3. J Child Neurol. 2013. PMID: 23034980 Free PMC article.

4

Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.

Matheus MG, Lehman RK, Bonilha L, Holden KR. Matheus MG, et al. J Child Neurol. 2015 Oct;30(12):1664-8. doi: 10.1177/0883073815578524. Epub 2015 Apr 21. J Child Neurol. 2015. PMID: 25900139

5

Importance of genetic testing in global health during the evaluation of familial microcephaly.

Molinero I, Broman-Fulks J, Lyons MJ, Matheus MG, Chaubey A, DuPont BR, Friez MJ, Skinner SA, Holden KR. Molinero I, et al. Among authors: matheus mg. Clin Case Rep. 2016 Aug 26;4(10):968-971. doi: 10.1002/ccr3.669. eCollection 2016 Oct. Clin Case Rep. 2016. PMID: 27761248 Free PMC article.

6

ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration.

Hirose T, Cabrera-Socorro A, Chitayat D, Lemonnier T, Féraud O, Cifuentes-Diaz C, Gervasi N, Mombereau C, Ghosh T, Stoica L, Bacha JDA, Yamada H, Lauterbach MA, Guillon M, Kaneko K, Norris JW, Siriwardena K, Blasér S, Teillon J, Mendoza-Londono R, Russeau M, Hadoux J, Ito S, Corvol P, Matheus MG, Holden KR, Takei K, Emiliani V, Bennaceur-Griscelli A, Schwartz CE, Nguyen G, Groszer M. Hirose T, et al. Among authors: matheus mg. J Clin Invest. 2019 Apr 15;129(5):2145-2162. doi: 10.1172/JCI79990. eCollection 2019 Apr 15. J Clin Invest. 2019. PMID: 30985297 Free PMC article.

7

Effect of chronic transfusion therapy on progression of neurovascular pathology in pediatric patients with sickle cell anemia.

Bishop S, Matheus MG, Abboud MR, Cane ID, Adams RJ, Jackson SM, Kalpatthi R. Bishop S, et al. Among authors: matheus mg. Blood Cells Mol Dis. 2011 Aug 15;47(2):125-8. doi: 10.1016/j.bcmd.2011.06.002. Epub 2011 Jul 2. Blood Cells Mol Dis. 2011. PMID: 21724428

8

Ascending and plunging ranula in a pediatric patient.

Clyburn VL 3rd, Smith JE, Rumboldt T, Matheus MG, Day TA. Clyburn VL 3rd, et al. Among authors: matheus mg. Otolaryngol Head Neck Surg. 2009 Jun;140(6):948-9. doi: 10.1016/j.otohns.2008.12.041. Epub 2009 Apr 1. Otolaryngol Head Neck Surg. 2009. PMID: 19467424

9

Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.

Refetoff S, Pappa T, Williams MK, Matheus MG, Liao XH, Hansen K, Nicol L, Pierce M, Blasco PA, Wiebers Jensen M, Bernal J, Weiss RE, Dumitrescu AM, LaFranchi S. Refetoff S, et al. Among authors: matheus mg. Thyroid. 2021 May;31(5):713-720. doi: 10.1089/thy.2020.0306. Epub 2020 Sep 25. Thyroid. 2021. PMID: 32746752 Free PMC article.

10

Comparison of Dural Venous Sinus Volumes Before and After Flight in Astronauts With and Without Spaceflight-Associated Neuro-Ocular Syndrome.

Rosenberg MJ, Coker MA, Taylor JA, Yazdani M, Matheus MG, Blouin CK, Al Kasab S, Collins HR, Roberts DR. Rosenberg MJ, et al. Among authors: matheus mg. JAMA Netw Open. 2021 Oct 1;4(10):e2131465. doi: 10.1001/jamanetworkopen.2021.31465. JAMA Netw Open. 2021. PMID: 34705011 Free PMC article.

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