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Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's disease.
Miltenberger-Miltenyi G, Ortega RA, Domingo A, Yadav R, Nishiyama A, Raymond D, Katsnelson V, Urval N, Swan M, Shanker V, Miravite J, Walker RH, Bressman SB, Ozelius LJ, Cabassa JC, Saunders-Pullman R. Miltenberger-Miltenyi G, et al. NPJ Parkinsons Dis. 2023 Dec 7;9(1):160. doi: 10.1038/s41531-023-00599-6. NPJ Parkinsons Dis. 2023. PMID: 38062033 Free PMC article.
An Autopsy Series of Seven Cases of VPS13A Disease (Chorea-Acanthocytosis).
Ditzel RM Jr, Walker RH, Nirenberg MJ, Tetlow AM, Farrell K, Lind-Watson KJ, Thorn EL, Dangoor DK, Gordon R, De Sanctis C, Barton B, Karp BI, Kirby A, Lett DJ, Mente K, Simon DK, Velayos-Baeza A, Miltenberger-Miltenyi G, Humphrey J, Crary JF. Ditzel RM Jr, et al. Among authors: miltenberger miltenyi g. Mov Disord. 2023 Dec;38(12):2163-2172. doi: 10.1002/mds.29589. Epub 2023 Sep 5. Mov Disord. 2023. PMID: 37670483
Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea-Acanthocytosis.
Miltenberger-Miltenyi G, Jones A, Tetlow AM, Conceição VA, Crary JF, Ditzel RM Jr, Farrell K, Nandakumar R, Barton B, Karp BI, Kirby A, Lett DJ, Mente K, Morgello S, Simon DK, Walker RH. Miltenberger-Miltenyi G, et al. Mov Disord. 2023 Aug;38(8):1535-1541. doi: 10.1002/mds.29445. Epub 2023 Jun 12. Mov Disord. 2023. PMID: 37307400
VPS13A Disease.
Peikert K, Dobson-Stone C, Rampoldi L, Miltenberger-Miltenyi G, Neiman A, De Camilli P, Hermann A, Walker RH, Monaco AP, Danek A. Peikert K, et al. Among authors: miltenberger miltenyi g. 2002 Jun 14 [updated 2023 Mar 30]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2002 Jun 14 [updated 2023 Mar 30]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301561 Free Books & Documents. Review.
Serum Phospholipid Profile Changes in Gaucher Disease and Parkinson's Disease.
López de Frutos L, Almeida F, Murillo-Saich J, Conceição VA, Guma M, Queheberger O, Giraldo P, Miltenberger-Miltenyi G. López de Frutos L, et al. Among authors: miltenberger miltenyi g. Int J Mol Sci. 2022 Sep 8;23(18):10387. doi: 10.3390/ijms231810387. Int J Mol Sci. 2022. PMID: 36142296 Free PMC article.
Left ventricular noncompaction associated with a pathogenic mutation in the MYH7 gene: Known mutation, different phenotype.
Oliveira M, Azevedo O, Faria B, von Hafe P, Dias G, Faria R, Sanfins V, Lourenço M, Miltenberger-Miltenyi G, Lourenço A. Oliveira M, et al. Among authors: miltenberger miltenyi g. Rev Port Cardiol. 2022 Mar;41(3):253-259. doi: 10.1016/j.repc.2018.09.018. Epub 2022 Feb 25. Rev Port Cardiol. 2022. PMID: 36062655 Free article. English, Portuguese.
Fabry Disease and the Heart: A Comprehensive Review.
Azevedo O, Cordeiro F, Gago MF, Miltenberger-Miltenyi G, Ferreira C, Sousa N, Cunha D. Azevedo O, et al. Among authors: miltenberger miltenyi g. Int J Mol Sci. 2021 Apr 23;22(9):4434. doi: 10.3390/ijms22094434. Int J Mol Sci. 2021. PMID: 33922740 Free PMC article. Review.
Fabry Disease Therapy: State-of-the-Art and Current Challenges.
Azevedo O, Gago MF, Miltenberger-Miltenyi G, Sousa N, Cunha D. Azevedo O, et al. Among authors: miltenberger miltenyi g. Int J Mol Sci. 2020 Dec 28;22(1):206. doi: 10.3390/ijms22010206. Int J Mol Sci. 2020. PMID: 33379210 Free PMC article. Review.
Predictors of Fabry disease in patients with hypertrophic cardiomyopathy: How to guide the diagnostic strategy?
Azevedo O, Marques N, Reis L, Cruz I, Craveiro N, Antunes H, Lourenço C, Gomes R, Guerreiro RA, Faria R, Sá F, Lima R, Gaspar P, Faria R, Miltenberger-Miltenyi G, Sousa N, Cunha D; group of investigators. Azevedo O, et al. Among authors: miltenberger miltenyi g. Am Heart J. 2020 Aug;226:114-126. doi: 10.1016/j.ahj.2020.04.006. Epub 2020 Apr 18. Am Heart J. 2020. PMID: 32531501 Free article.
59 results