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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1972 1
1988 1
1992 1
1995 5
1997 1
1999 2
2004 2
2005 1
2006 1
2007 3
2008 2
2009 7
2010 3
2011 4
2012 8
2013 6
2014 6
2015 3
2016 5
2017 10
2018 4
2019 6
2020 6
2021 8
2023 0
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84 results
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Page 1
Mucopolysaccharidosis Type I.
Kubaski F, de Oliveira Poswar F, Michelin-Tirelli K, Matte UDS, Horovitz DD, Barth AL, Baldo G, Vairo F, Giugliani R. Kubaski F, et al. Among authors: horovitz dd. Diagnostics (Basel). 2020 Mar 16;10(3):161. doi: 10.3390/diagnostics10030161. Diagnostics (Basel). 2020. PMID: 32188113 Free PMC article. Review.
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies.
Masnada S, Hedrich UBS, Gardella E, Schubert J, Kaiwar C, Klee EW, Lanpher BC, Gavrilova RH, Synofzik M, Bast T, Gorman K, King MD, Allen NM, Conroy J, Ben Zeev B, Tzadok M, Korff C, Dubois F, Ramsey K, Narayanan V, Serratosa JM, Giraldez BG, Helbig I, Marsh E, O'Brien M, Bergqvist CA, Binelli A, Porter B, Zaeyen E, Horovitz DD, Wolff M, Marjanovic D, Caglayan HS, Arslan M, Pena SDJ, Sisodiya SM, Balestrini S, Syrbe S, Veggiotti P, Lemke JR, Møller RS, Lerche H, Rubboli G. Masnada S, et al. Among authors: horovitz dd. Brain. 2017 Sep 1;140(9):2337-2354. doi: 10.1093/brain/awx184. Brain. 2017. PMID: 29050392 Free article.
Venous anomalies in hypoplastic posterior fossa: unsolved questions.
Protzenko T, Bellas A, Ribeiro CMC, Gonzalez SMC, Horovitz DDG. Protzenko T, et al. Among authors: horovitz ddg. Childs Nerv Syst. 2021 Oct;37(10):3177-3187. doi: 10.1007/s00381-021-05315-4. Epub 2021 Aug 18. Childs Nerv Syst. 2021. PMID: 34406451 Review.
Mucopolysaccharidosis VII in Brazil: natural history and clinical findings.
Giugliani R, Barth AL, Dumas MRC, da Silva Franco JF, de Rosso Giuliani L, Grangeiro CHP, Horovitz DDG, Kim CA, de Araújo Leão EKE, de Medeiros PFV, Miguel DSCG, Moreira MESA, Dos Santos HMGP, da Silva LCS, da Silva LR, de Souza IN, Nalin T, Garcia D. Giugliani R, et al. Among authors: horovitz ddg. Orphanet J Rare Dis. 2021 May 22;16(1):238. doi: 10.1186/s13023-021-01870-w. Orphanet J Rare Dis. 2021. PMID: 34022924 Free PMC article. Review.
Hematopoietic Stem Cell Transplantation for Mucopolysaccharidoses: Past, Present, and Future.
Taylor M, Khan S, Stapleton M, Wang J, Chen J, Wynn R, Yabe H, Chinen Y, Boelens JJ, Mason RW, Kubaski F, Horovitz DDG, Barth AL, Serafini M, Bernardo ME, Kobayashi H, Orii KE, Suzuki Y, Orii T, Tomatsu S. Taylor M, et al. Among authors: horovitz ddg. Biol Blood Marrow Transplant. 2019 Jul;25(7):e226-e246. doi: 10.1016/j.bbmt.2019.02.012. Epub 2019 Feb 14. Biol Blood Marrow Transplant. 2019. PMID: 30772512 Free PMC article. Review.
The Brazilian consensus on the management of Pompe disease.
Llerena JC Jr, Horovitz DM, Marie SK, Porta G, Giugliani R, Rojas MV, Martins AM; Brazilian Network for Studies in Pompe Disease (ReBrPOM). Llerena JC Jr, et al. Among authors: horovitz dm. J Pediatr. 2009 Oct;155(4 Suppl):S47-56. doi: 10.1016/j.jpeds.2009.07.006. J Pediatr. 2009. PMID: 19765410 Review. No abstract available.
Genetic services and testing in Brazil.
Horovitz DD, de Faria Ferraz VE, Dain S, Marques-de-Faria AP. Horovitz DD, et al. J Community Genet. 2013 Jul;4(3):355-75. doi: 10.1007/s12687-012-0096-y. Epub 2012 May 5. J Community Genet. 2013. PMID: 22565417 Free PMC article. No abstract available.
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.
Zin OA, Neves LM, Motta FL, Horovitz DDG, Guida L, Gomes LHF, Cunha DP, Rodrigues APS, Zin AA, Sallum JMF, Vasconcelos ZFM. Zin OA, et al. Among authors: horovitz ddg. Genes (Basel). 2021 Jul 13;12(7):1069. doi: 10.3390/genes12071069. Genes (Basel). 2021. PMID: 34356085 Free PMC article.
84 results