Ramos-Arroyo M - Search Results

1

Discrepancies in reporting the CAG repeat lengths for Huntington's disease.

Quarrell OW, Handley O, O'Donovan K, Dumoulin C, Ramos-Arroyo M, Biunno I, Bauer P, Kline M, Landwehrmeyer GB; European Huntington’s Disease Network. Quarrell OW, et al. Eur J Hum Genet. 2012 Jan;20(1):20-6. doi: 10.1038/ejhg.2011.136. Epub 2011 Aug 3. Eur J Hum Genet. 2012. PMID: 21811303 Free PMC article.

2

Clinical manifestations of intermediate allele carriers in Huntington disease.

Cubo E, Ramos-Arroyo MA, Martinez-Horta S, Martínez-Descalls A, Calvo S, Gil-Polo C; European HD Network. Cubo E, et al. Neurology. 2016 Aug 9;87(6):571-8. doi: 10.1212/WNL.0000000000002944. Epub 2016 Jul 8. Neurology. 2016. PMID: 27402890

3

Study of cerebral cavernous malformation in Spain and Portugal: high prevalence of a 14 bp deletion in exon 5 of MGC4607 (CCM2 gene).

Ortiz L, Costa AF, Bellido ML, Solano F, García-Moreno JM, Gamero MA, Izquierdo G, Chadli A, Falcao F, Ferro J, Salas J, Alvarez-Cermeño JC, Montori M, Ramos-Arroyo MA, Palomino A, Pintado E, Lucas M. Ortiz L, et al. J Neurol. 2007 Mar;254(3):322-6. doi: 10.1007/s00415-006-0359-9. Epub 2007 Mar 7. J Neurol. 2007. PMID: 17345049

4

Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome.

Tejada MI, García-Alegría E, Bilbao A, Martínez-Bouzas C, Beristain E, Poch M, Ramos-Arroyo MA, López B, Fernandez Carvajal I, Ribate MP, Ramos F. Tejada MI, et al. Menopause. 2008 Sep-Oct;15(5):945-9. doi: 10.1097/gme.0b013e3181647762. Menopause. 2008. PMID: 18427356

5

Somatic CAG repeat instability in intermediate alleles of the HTT gene and its potential association with a clinical phenotype.

Ruiz de Sabando A, Ciosi M, Galbete A, Cumming SA; Spanish HD Collaborative Group; Monckton DG, Ramos-Arroyo MA. Ruiz de Sabando A, et al. Among authors: ramos arroyo ma. Eur J Hum Genet. 2024 Mar 4. doi: 10.1038/s41431-024-01546-6. Online ahead of print. Eur J Hum Genet. 2024. PMID: 38433266

6

Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease.

Ruiz de Sabando A, Urrutia Lafuente E, Galbete A, Ciosi M, García Amigot F, García Solaesa V; Spanish HD Collaborative group; Monckton DG, Ramos-Arroyo MA. Ruiz de Sabando A, et al. Among authors: ramos arroyo ma. Hum Mol Genet. 2023 Mar 6;32(6):897-906. doi: 10.1093/hmg/ddac224. Hum Mol Genet. 2023. PMID: 36130218 Free PMC article.

7

Validation of diagnostic codes and epidemiologic trends of Huntington disease: a population-based study in Navarre, Spain.

Vicente E, Ruiz de Sabando A, García F, Gastón I, Ardanaz E, Ramos-Arroyo MA. Vicente E, et al. Among authors: ramos arroyo ma. Orphanet J Rare Dis. 2021 Feb 10;16(1):77. doi: 10.1186/s13023-021-01699-3. Orphanet J Rare Dis. 2021. PMID: 33568143 Free PMC article.

8

Author response: Clinical manifestations of homozygote allele carriers in Huntington disease.

Ramos-Arroyo MA, Cubo E. Ramos-Arroyo MA, et al. Neurology. 2020 Apr 21;94(16):723-724. doi: 10.1212/WNL.0000000000009308. Neurology. 2020. PMID: 32312883 No abstract available.

9

Correction to: Genetic and clinical characterization of BRCA-associated hereditary breast and ovarian cancer in Navarra (Spain).

de Sabando AR, Lafuente EU, García-Amigot F, Sánchez AA, Garofalo LM, Moreno S, Ardanaz E, Ramos-Arroyo MA. de Sabando AR, et al. Among authors: ramos arroyo ma. BMC Cancer. 2019 Dec 17;19(1):1227. doi: 10.1186/s12885-019-6458-7. BMC Cancer. 2019. PMID: 31847820 Free PMC article.

10

Genetic and clinical characterization of BRCA-associated hereditary breast and ovarian cancer in Navarra (Spain).

Ruiz de Sabando A, Urrutia Lafuente E, García-Amigot F, Alonso Sánchez A, Morales Garofalo L, Moreno S, Ardanaz E, Ramos-Arroyo MA. Ruiz de Sabando A, et al. Among authors: ramos arroyo ma. BMC Cancer. 2019 Nov 27;19(1):1145. doi: 10.1186/s12885-019-6277-x. BMC Cancer. 2019. PMID: 31771539 Free PMC article.

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