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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2011 | 1 |
2019 | 1 |
2020 | 2 |
2021 | 2 |
2022 | 1 |
2024 | 0 |
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Page 1
Current and Future Treatments for Classic Galactosemia.
J Pers Med. 2021 Jan 28;11(2):75. doi: 10.3390/jpm11020075.
J Pers Med. 2021.
PMID: 33525536
Free PMC article.
Review.
Hip Morphology in Mucolipidosis Type II.
Ammer LS, Oussoren E, Muschol NM, Pohl S, Rubio-Gozalbo ME, Santer R, Stuecker R, Vettorazzi E, Breyer SR.
Ammer LS, et al. Among authors: rubio gozalbo me.
J Clin Med. 2020 Mar 8;9(3):728. doi: 10.3390/jcm9030728.
J Clin Med. 2020.
PMID: 32182687
Free PMC article.
Item in Clipboard
Novel mRNA therapy restores GALT protein and enzyme activity in a zebrafish model of classic galactosemia.
Delnoy B, Haskovic M, Vanoevelen J, Steinbusch LKM, Vos EN, Knoops K, Zimmermann LJI, Noga M, Lefeber DJ, Martini PGV, Coelho AI, Rubio-Gozalbo ME.
Delnoy B, et al. Among authors: rubio gozalbo me.
J Inherit Metab Dis. 2022 Jul;45(4):748-758. doi: 10.1002/jimd.12512. Epub 2022 May 27.
J Inherit Metab Dis. 2022.
PMID: 35527402
Free PMC article.
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[13C]-galactose breath test in a patient with galactokinase deficiency and spastic diparesis.
Ficicioglu C, Demirbas D, Derks B, Pai GS, Timson DJ, Rubio-Gozalbo ME, Berry GT.
Ficicioglu C, et al. Among authors: rubio gozalbo me.
JIMD Rep. 2021 Feb 3;59(1):104-109. doi: 10.1002/jmd2.12205. eCollection 2021 May.
JIMD Rep. 2021.
PMID: 33977035
Free PMC article.
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Research activity and capability in the European reference network MetabERN.
Heard JM, Bellettato C, van Lingen C, Scarpa M; MetabERN collaboration group.
Heard JM, et al.
Orphanet J Rare Dis. 2019 May 29;14(1):119. doi: 10.1186/s13023-019-1091-8.
Orphanet J Rare Dis. 2019.
PMID: 31142374
Free PMC article.
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Psychosocial developmental milestones in men with classic galactosemia.
Gubbels CS, Maurice-Stam H, Berry GT, Bosch AM, Waisbren S, Rubio-Gozalbo ME, Grootenhuis MA.
Gubbels CS, et al. Among authors: rubio gozalbo me.
J Inherit Metab Dis. 2011 Apr;34(2):415-9. doi: 10.1007/s10545-011-9290-z. Epub 2011 Feb 25.
J Inherit Metab Dis. 2011.
PMID: 21350966
Free PMC article.
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Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network.
Heard JM, Vrinten C, Schlander M, Bellettato CM, van Lingen C, Scarpa M; MetabERN collaboration group.
Heard JM, et al.
Orphanet J Rare Dis. 2020 Jan 6;15(1):3. doi: 10.1186/s13023-019-1280-5.
Orphanet J Rare Dis. 2020.
PMID: 31907071
Free PMC article.
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