Hernando C - Search Results

1

Development of a Novel NGS Methodology for Ultrasensitive Circulating Tumor DNA Detection as a Tool for Early-Stage Breast Cancer Diagnosis.

Jiménez-Rodríguez B, Alba-Bernal A, López-López E, Quirós-Ortega ME, Carbajosa G, Garrido-Aranda A, Álvarez M, Godoy-Ortiz A, Queipo-Ortuño MI, Vicioso L, Díaz-Córdoba G, Roldán-Díaz MD, Velasco-Suelto J, Hernando C, Bermejo B, Julve-Parreño A, Lluch A, Pascual J, Comino-Méndez I, Alba E. Jiménez-Rodríguez B, et al. Among authors: hernando c. Int J Mol Sci. 2022 Dec 21;24(1):146. doi: 10.3390/ijms24010146. Int J Mol Sci. 2022. PMID: 36613590 Free PMC article.

2

Intrachromosomal 3p insertion as a cause of reciprocal pure interstitial deletion and duplication in two siblings: further delineation of the emerging proximal 3p deletion syndrome.

Lloveras E, Vendrell T, Fernández A, Castells N, Cueto A, del Campo M, Hernando C, Villa O, Plaja A. Lloveras E, et al. Among authors: hernando c. Cytogenet Genome Res. 2014;144(4):290-3. doi: 10.1159/000375184. Epub 2015 Feb 14. Cytogenet Genome Res. 2014. PMID: 25720458

3

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations.

Hernando C, Plaja A, Rigola MA, Pérez MM, Vendrell T, Egocue J, Fuster C. Hernando C, et al. J Med Genet. 2002 May;39(5):E24. doi: 10.1136/jmg.39.5.e24. J Med Genet. 2002. PMID: 12011165 Free PMC article. No abstract available.

4

Primary amenorrhea in a woman with a cryptic complex chromosome rearrangement involving the critical regions Xp11.2 and Xq24.

Hernando C, Plaja A, Català V, Sarret E, Egozcue J, Fuster C. Hernando C, et al. Fertil Steril. 2004 Dec;82(6):1666-71. doi: 10.1016/j.fertnstert.2004.05.085. Fertil Steril. 2004. PMID: 15589876 Free article.

5

Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.

Hernando C, Carrera M, Ribas I, Parear N, Baraibar R, Egocue J, Fuster C. Hernando C, et al. Prenat Diagn. 2002 Sep;22(9):802-5. doi: 10.1002/pd.415. Prenat Diagn. 2002. PMID: 12224075

6

[Cytidine diphosphate cholinne -- a new drug in the treatment of spasticity].

Hernando C, De Blas A, Cubells JM. Hernando C, et al. Rev Clin Esp. 1978 Nov 30;151(4):313-7. Rev Clin Esp. 1978. PMID: 741011 Spanish. No abstract available.

7

[Bovine cerebral cortex gangliosides in the treatment of radicular lesions (author's transl)].

Cubells JM, de Blas A, Hernando C, Rodríguez del Barrio E. Cubells JM, et al. Among authors: hernando c. Med Clin (Barc). 1980 Sep 10;75(4):156-60. Med Clin (Barc). 1980. PMID: 7412438 Spanish.

8

Clinical trial on the use of cytidine diphosphate choline in Parkinson's disease.

Cubells JM, Hernando C. Cubells JM, et al. Among authors: hernando c. Clin Ther. 1988;10(6):664-71. Clin Ther. 1988. PMID: 3064905 Clinical Trial.

9

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.

Kasher PR, Schertz KE, Thomas M, Jackson A, Annunziata S, Ballesta-Martinez MJ, Campeau PM, Clayton PE, Eaton JL, Granata T, Guillén-Navarro E, Hernando C, Laverriere CE, Liedén A, Villa-Marcos O, McEntagart M, Nordgren A, Pantaleoni C, Pebrel-Richard C, Sarret C, Sciacca FL, Wright R, Kerr B, Glasgow E, Banka S. Kasher PR, et al. Among authors: hernando c. Am J Hum Genet. 2016 Feb 4;98(2):363-72. doi: 10.1016/j.ajhg.2015.12.014. Epub 2016 Jan 28. Am J Hum Genet. 2016. PMID: 26833329 Free PMC article.

10

Three-Year Follow-Up of a Prenatally Ascertained Apparently Non-Mosaic sSMC(10): Delineation of a Non-Critical Region.

Barranco L, Costa M, Lloveras E, Ordóñez E, Maiz N, Hernando C, Villa O, Cirigliano V, Plaja A. Barranco L, et al. Among authors: hernando c. Cytogenet Genome Res. 2015;147(4):209-11. doi: 10.1159/000444600. Epub 2016 Mar 15. Cytogenet Genome Res. 2015. PMID: 26974471

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