Muñoz Rojas MV - Search Results

1

Multidisciplinary management of Hunter syndrome.

Muenzer J, Beck M, Eng CM, Escolar ML, Giugliani R, Guffon NH, Harmatz P, Kamin W, Kampmann C, Koseoglu ST, Link B, Martin RA, Molter DW, Muñoz Rojas MV, Ogilvie JW, Parini R, Ramaswami U, Scarpa M, Schwartz IV, Wood RE, Wraith E. Muenzer J, et al. Among authors: munoz rojas mv. Pediatrics. 2009 Dec;124(6):e1228-39. doi: 10.1542/peds.2008-0999. Epub 2009 Nov 9. Pediatrics. 2009. PMID: 19901005 Review.

2

Carpal tunnel syndrome in mucopolysaccharidosis I: a registry-based cohort study.

Viskochil D, Muenzer J, Guffon N, Garin C, Munoz-Rojas MV, Moy KA, Hutchinson DT. Viskochil D, et al. Among authors: munoz rojas mv. Dev Med Child Neurol. 2017 Dec;59(12):1269-1275. doi: 10.1111/dmcn.13545. Epub 2017 Sep 11. Dev Med Child Neurol. 2017. PMID: 28892147 Free article. Clinical Trial.

3

Genotype-phenotype relationships in mucopolysaccharidosis type I (MPS I): Insights from the International MPS I Registry.

Clarke LA, Giugliani R, Guffon N, Jones SA, Keenan HA, Munoz-Rojas MV, Okuyama T, Viskochil D, Whitley CB, Wijburg FA, Muenzer J. Clarke LA, et al. Among authors: munoz rojas mv. Clin Genet. 2019 Oct;96(4):281-289. doi: 10.1111/cge.13583. Epub 2019 Jul 2. Clin Genet. 2019. PMID: 31194252 Free PMC article.

4

Intrathecal administration of recombinant human N-acetylgalactosamine 4-sulfatase to a MPS VI patient with pachymeningitis cervicalis.

Muñoz-Rojas MV, Horovitz DD, Jardim LB, Raymundo M, Llerena JC Jr, de Magalhães Tde S, Vieira TA, Costa R, Kakkis E, Giugliani R. Muñoz-Rojas MV, et al. Mol Genet Metab. 2010 Apr;99(4):346-50. doi: 10.1016/j.ymgme.2009.11.008. Epub 2009 Dec 5. Mol Genet Metab. 2010. PMID: 20036175

5

Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression.

Munoz-Rojas MV, Vieira T, Costa R, Fagondes S, John A, Jardim LB, Vedolin LM, Raymundo M, Dickson PI, Kakkis E, Giugliani R. Munoz-Rojas MV, et al. Am J Med Genet A. 2008 Oct 1;146A(19):2538-44. doi: 10.1002/ajmg.a.32294. Am J Med Genet A. 2008. PMID: 18792977

6

Clinical relevance of endpoints in clinical trials for acid sphingomyelinase deficiency enzyme replacement therapy.

Jones SA, McGovern M, Lidove O, Giugliani R, Mistry PK, Dionisi-Vici C, Munoz-Rojas MV, Nalysnyk L, Schecter AD, Wasserstein M. Jones SA, et al. Among authors: munoz rojas mv. Mol Genet Metab. 2020 Sep-Oct;131(1-2):116-123. doi: 10.1016/j.ymgme.2020.06.008. Epub 2020 Jun 24. Mol Genet Metab. 2020. PMID: 32616389 Free article. Review.

7

Immune tolerance induction for laronidase treatment in mucopolysaccharidosis I.

Giugliani R, Vieira TA, Carvalho CG, Muñoz-Rojas MV, Semyachkina AN, Voinova VY, Richards S, Cox GF, Xue Y. Giugliani R, et al. Among authors: munoz rojas mv. Mol Genet Metab Rep. 2017 Jan 13;10:61-66. doi: 10.1016/j.ymgmr.2017.01.004. eCollection 2017 Mar. Mol Genet Metab Rep. 2017. PMID: 28119821 Free PMC article.

8

Short stature as a presenting symptom of attenuated Mucopolysaccharidosis type I: case report and clinical insights.

Martins AM, Lindstrom K, Kyosen SO, Munoz-Rojas MV, Thibault N, Polgreen LE. Martins AM, et al. Among authors: munoz rojas mv. BMC Endocr Disord. 2018 Nov 12;18(1):83. doi: 10.1186/s12902-018-0311-x. BMC Endocr Disord. 2018. PMID: 30419879 Free PMC article.

9

Clinical manifestations and treatment of mucopolysaccharidosis type I patients in Latin America as compared with the rest of the world.

Muñoz-Rojas MV, Bay L, Sanchez L, van Kuijck M, Ospina S, Cabello JF, Martins AM. Muñoz-Rojas MV, et al. J Inherit Metab Dis. 2011 Oct;34(5):1029-37. doi: 10.1007/s10545-011-9336-2. Epub 2011 May 4. J Inherit Metab Dis. 2011. PMID: 21541721 Free PMC article.

10

Inclusion of medical genetics in primary health care: report of a pilot project in Brazil.

Vieira TA, Giugliani C, da Silva LP, Faccini LS, Loguercio Leite JC, Artigalás OA, Medeiros Lenz ML, Muñoz-Rojas MV, Giugliani R. Vieira TA, et al. Among authors: munoz rojas mv. J Community Genet. 2013 Jan;4(1):137-45. doi: 10.1007/s12687-012-0110-4. Epub 2012 Jul 25. J Community Genet. 2013. PMID: 22829114 Free PMC article. No abstract available.

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