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Sarasola, Esther
23  Ergebnisse:
Personensuche X
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1

Germline heterozygous exons 8–11 pathogenic BARD1 gene dele..:

Carrera, Sergio ; Rodríguez-Martínez, Ana Belén ; Garin, Intza...
Hereditary Cancer in Clinical Practice.  21 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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2

Gertsmann syndrome and ideomotor apraxia as the first sympt..:

Gomez-Beldarrain, Marian ; Sarasola, Esther ; Rabano, Alberto.
Neurology.  88 (2017)  16_supplement - p. , 2017
Link: https://doi.org/10.1212/..
 
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3

RNAseq based transcriptomics study of SMCs from carotid ath..:

Alloza, Iraide ; Goikuria, Haize ; Idro, Juan Luis...
Scientific Reports.  7 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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4

Mutations in TrkA Causing Congenital Insensitivity to Pain ..:

Franco, María Luisa ; Melero, Cristina ; Sarasola, Esther...
Journal of Biological Chemistry.  291 (2016)  41 - p. 21363-21374 , 2016
Link: https://doi.org/10.1074/..
 
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5

Analysis of theC9orf72Gene in Patients with Amyotrophic Lat..:

García-Redondo, Alberto ; Dols-Icardo, Oriol ; Rojas-García, Ricard...
Human Mutation.  34 (2012)  1 - p. 79-82 , 2012
Link: https://doi.org/10.1002/..
 
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6

A short in-frame deletion in NTRK1 tyrosine kinase domain c..:

Sarasola, Esther ; Rodríguez, Jose A ; Garrote, Elisa..
BMC Medical Genetics.  12 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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7

Absence of COCH gene mutations in patients with superior se..:

Crovetto, Miguel A. ; Whyte, Jaime ; Sarasola, Esther..
American Journal of Medical Genetics Part A.  158A (2011)  1 - p. 251-253 , 2011
Link: https://doi.org/10.1002/..
 
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8

Calcificación arterial generalizada idiopática de la infanc..:

Arbide del Río, Nagore ; Solano Iturri, Jon Danel ; García Barcina, María.
Revista Española de Patología.  53 (2020)  3 - p. 193-196 , 2020
Link: https://doi.org/10.1016/..
 
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9

Holt-Oram Syndrome: Family Affected Without TBX5 Mutation a..:

Murga-Eizagaechevarria, Nekane ; Garcia-Barcina, Maria ; Sarasola Diez, Esther
Revista Española de Cardiología (English Edition).  64 (2011)  12 - p. 1225-1226 , 2011
Link: https://doi.org/10.1016/..
 
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10

Germline heterozygous exons 8–11 pathogenic BARD1 gene dele..:

Carrera, Sergio ; Rodríguez-Martínez, Ana Belén ; Garin, Intza...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9883939/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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11

RNAseq based transcriptomics study of SMCs from carotid ath..:

Alloza, Iraide ; Goikuria, Haize ; Idro, Juan Luis...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471186/.  , 2017
Link: http://www.ncbi.nlm.nih...
 
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12

Mutations in TrkA Causing Congenital Insensitivity to Pain ..:

Franco, María Luisa ; Melero, Cristina ; Sarasola, Esther...
#PLACEHOLDER_PARENT_METADATA_VALUE#.  , 2016
Link: http://hdl.handle.net/10..
 
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13

Mutations in TrkA Causing Congenital Insensitivity to Pain ..:

Franco, María Luisa ; Melero, Cristina ; Sarasola, Esther...
https://doi.org/10.1074/jbc.M116.722587.  , 2016
Link: https://hdl.handle.net/2..
 
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14

A short in-frame deletion in NTRK1 tyrosine kinase domain c..:

Arístegui Javier ; Garrote Elisa ; Rodríguez Jose A..
http://www.biomedcentral.com/1471-2350/12/86.  , 2011
Link: https://doi.org/10.1186/..
 
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15

A short in-frame deletion in NTRK1 tyrosine kinase domain c..:

Sarasola, Esther ; Rodríguez, Jose A ; Garrote, Elisa..
http://www.biomedcentral.com/1471-2350/12/86.  , 2011
Link: http://www.biomedcentral..
 
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