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Page 1
Ophthalmological Manifestations of Hereditary Myopathies.
J Binocul Vis Ocul Motil. 2022 Jan-Mar;72(1):4-17. Epub 2022 Jan 20.
J Binocul Vis Ocul Motil. 2022.
PMID: 35049410
Review.
Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases.
Bullich G, Matalonga L, Pujadas M, Papakonstantinou A, Piscia D, Tonda R, Artuch R, Gallano P, Garrabou G, González JR, Grinberg D, Guitart M, Laurie S, Lázaro C, Luengo C, Martí R, Milà M, Ovelleiro D, Parra G, Pujol A, Tizzano E, Macaya A, Palau F, Ribes A, Pérez-Jurado LA, Beltran S; Undiagnosed Rare Disease Program of Catalonia (URD-Cat) Consortium.
Bullich G, et al.
J Mol Diagn. 2022 May;24(5):529-542. doi: 10.1016/j.jmoldx.2022.02.003.
J Mol Diagn. 2022.
PMID: 35569879
Free article.
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A Photosynthesis-Specific Rubredoxin-Like Protein Is Required for Efficient Association of the D1 and D2 Proteins during the Initial Steps of Photosystem II Assembly.
Kiss É, Knoppová J, Aznar GP, Pilný J, Yu J, Halada P, Nixon PJ, Sobotka R, Komenda J.
Kiss É, et al. Among authors: aznar gp.
Plant Cell. 2019 Sep;31(9):2241-2258. doi: 10.1105/tpc.19.00155. Epub 2019 Jul 18.
Plant Cell. 2019.
PMID: 31320483
Free PMC article.
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Development and validation of a liquid chromatography-tandem mass spectrometry assay for hair analysis of atomoxetine and its metabolites: Application in clinical practice.
Papaseit E, Marchei E, Mortali C, Aznar G, Garcia-Algar O, Farrè M, Pacifici R, Pichini S.
Papaseit E, et al. Among authors: aznar g.
Forensic Sci Int. 2012 May 10;218(1-3):62-7. doi: 10.1016/j.forsciint.2011.10.012. Epub 2011 Oct 22.
Forensic Sci Int. 2012.
PMID: 22024657
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Adams-Oliver syndrome with unusual central nervous system alterations.
Romaní J, Puig L, Aznar G, Demestre X, Altirriba O, Alomar A.
Romaní J, et al. Among authors: aznar g.
Pediatr Dermatol. 1998 Jan-Feb;15(1):48-50. doi: 10.1046/j.1525-1470.1998.1998015048.x.
Pediatr Dermatol. 1998.
PMID: 9496805
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