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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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1987 | 2 |
1990 | 1 |
2020 | 1 |
2021 | 2 |
2022 | 1 |
2024 | 0 |
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Page 1
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications.
Sci Rep. 2021 Jan 15;11(1):1526. doi: 10.1038/s41598-021-81093-y.
Sci Rep. 2021.
PMID: 33452396
Free PMC article.
Clinical and genetical diagnosis of a case of Meretoja syndrome and frontotemporal lifting procedure.
Galindo-Bocero J, García-Martínez I, Portillo M, Hernando Acero I, García-González N.
Galindo-Bocero J, et al. Among authors: hernando acero i.
Arch Soc Esp Oftalmol (Engl Ed). 2022 Oct;97(10):583-586. doi: 10.1016/j.oftale.2022.08.004. Epub 2022 Sep 13.
Arch Soc Esp Oftalmol (Engl Ed). 2022.
PMID: 36114141
Item in Clipboard
[Prenatal diagnosis].
Hernando Acero I, Plasencia Amela A, Benavides Benavides A, Fernández Cuesta M, Fernández Toral J.
Hernando Acero I, et al.
An Esp Pediatr. 1987 Sep;27(3):183-9.
An Esp Pediatr. 1987.
PMID: 3322120
Spanish.
No abstract available.
Item in Clipboard
[Genetic counseling].
Plasencia Amela A, Hernando Acero I, Benavides Benavides A, Fernández Toral L, Fernández Cuesta M.
Plasencia Amela A, et al. Among authors: hernando acero i.
An Esp Pediatr. 1987 Aug;27(2):130-4.
An Esp Pediatr. 1987.
PMID: 3662268
Spanish.
No abstract available.
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Diagnosis of an X-linked type 2 congenital stationary night blindness using electroretinography and CACNA1F sequencing.
Galindo-Bocero J, Macías-Franco S, García-González N, Valles-Antuña C, Hernando Acero I, Rozas-Reyes P.
Galindo-Bocero J, et al. Among authors: hernando acero i.
Arch Soc Esp Oftalmol (Engl Ed). 2020 Dec;95(12):607-610. doi: 10.1016/j.oftal.2020.06.004. Epub 2020 Jul 15.
Arch Soc Esp Oftalmol (Engl Ed). 2020.
PMID: 32680768
English, Spanish.
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Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications.
Perea-Romero I, Gordo G, Iancu IF, Del Pozo-Valero M, Almoguera B, Blanco-Kelly F, Carreño E, Jimenez-Rolando B, Lopez-Rodriguez R, Lorda-Sanchez I, Martin-Merida I, Pérez de Ayala L, Riveiro-Alvarez R, Rodriguez-Pinilla E, Tahsin-Swafiri S, Trujillo-Tiebas MJ; ESRETNET Study Group; ERDC Study Group; Associated Clinical Study Group; Garcia-Sandoval B, Minguez P, Avila-Fernandez A, Corton M, Ayuso C.
Perea-Romero I, et al.
Sci Rep. 2021 May 10;11(1):10340. doi: 10.1038/s41598-021-89275-4.
Sci Rep. 2021.
PMID: 33972629
Free PMC article.
No abstract available.
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[A case of familial paracentric inversion associated with Down's syndrome. 47, XX, +21, inv (1) (p22p36)].
Alonso Villa MJ, Plasencia Amela A, Hernando Acero I, Benavides Benavides A, Fernández Cuesta M, Fernández Toral J.
Alonso Villa MJ, et al. Among authors: hernando acero i.
An Esp Pediatr. 1990 Mar;32(3):257-8.
An Esp Pediatr. 1990.
PMID: 2140666
Spanish.
No abstract available.
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