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Servián-Morilla, Emilia
39
results:
Search for persons
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Format
Online (39)
Mediatypes
Articles (Online) (18)
OpenAccess-fulltext (21)
Languages
english (38)
spanish (1)
Sorted by: Relevance
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?
1
A splice-altering homozygous variant in COX18 causes severe..:
Mavillard, Fabiola
;
Guerra-Castellano, Alejandra
;
Guerrero-Gómez, David
...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870 (2024) 7 - p. 167330 , 2024
Link:
https://doi.org/10.1016/..
?
2
Ablation of the carboxy-terminal end of MAMDC2 causes a dis..:
Mavillard, Fabiola
;
Servian-Morilla, Emilia
;
Dofash, Lein
...
Brain. 146 (2023) 12 - p. 5235-5248 , 2023
Link:
https://doi.org/10.1093/..
?
3
Muscle MRI characteristic pattern for late-onset TK2 defici..:
Domínguez-González, Cristina
;
Fernández-Torrón, Roberto
;
Moore, Ursula
...
Journal of Neurology. 269 (2022) 7 - p. 3550-3562 , 2022
Link:
https://doi.org/10.1007/..
?
4
AKLHL403' UTR splice-altering variant causes milder NEM8, a..:
Dofash, Lein N H
;
Monahan, Gavin V
;
Servián-Morilla, Emilia
...
Human Molecular Genetics. 32 (2022) 7 - p. 1127-1136 , 2022
Link:
https://doi.org/10.1093/..
?
5
Core-rod myopathy due to a novel mutation in BTB/POZ domain..:
Garibaldi, Matteo
;
Fattori, Fabiana
;
Bortolotti, Carlo Augusto
...
Acta Neuropathologica Communications. 6 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
6
Proteolytic Processing of Neurexins by Presenilins Sustains..:
Servián-Morilla, Emilia
;
Robles-Lanuza, Estefanía
;
Sánchez-Hidalgo, Ana C.
...
The Journal of Neuroscience. 38 (2017) 4 - p. 901-917 , 2017
Link:
https://doi.org/10.1523/..
?
7
Generation of an induced pluripotent stem cell line (CSCRMi..:
Wu, Jianbo
;
Hunt, Samuel D.
;
Matthias, Nadine
...
Stem Cell Research. 24 (2017) - p. 102-105 , 2017
Link:
https://doi.org/10.1016/..
?
8
Presenilin/γ-Secretase Regulates Neurexin Processing at Syn..:
Saura, Carlos A.
;
Servián-Morilla, Emilia
;
Scholl, Francisco G.
.
PLoS ONE. 6 (2011) 4 - p. e19430 , 2011
Link:
https://doi.org/10.1371/..
?
9
Muscle MRI characteristic pattern for late-onset TK2 defici..:
Domínguez-González, Cristina
;
Fernández-Torrón, Roberto
;
Moore, Ursula
...
Instituto de Salud Carlos III PI18/01374. , 2022
Link:
https://ddd.uab.cat/reco..
?
10
Muscle MRI characteristic pattern for late-onset TK2 defici..:
Domínguez-González, Cristina
;
Fernández-Torrón, Roberto
;
Moore, Ursula
...
http://hdl.handle.net/10668/20008. , 2022
Link:
http://hdl.handle.net/10..
?
11
Muscle MRI characteristic pattern for late-onset TK2 defici..:
Domínguez-González, Cristina
;
Fernández-Torrón, Roberto
;
Moore, Ursula
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9217784/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
12
NOVEL intronic CAPN3 Roma mutation alters splicing causing ..:
Mavillard, Fabiola
;
Madruga-Garrido, Marcos
;
Rivas, Eloy
...
http://hdl.handle.net/10668/14778. , 2019
Link:
http://hdl.handle.net/10..
?
13
Core-rod myopathy due to a novel mutation in BTB/POZ domain..:
Garibaldi, Matteo
;
Fattori, Fabiana
;
Bortolotti, Carlo Augusto
...
http://hdl.handle.net/10668/12938. , 2018
Link:
http://hdl.handle.net/10..
?
14
Proteolytic Processing of Neurexins by Presenilins Sustains..:
Servián-Morilla, Emilia
;
Robles-Lanuza, Estefanía
;
Sánchez-Hidalgo, Ana C
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6596238/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
15
Core-rod myopathy due to a novel mutation in BTB/POZ domain..:
Garibaldi Matteo
;
Fattori Fabiana
;
Bortolotti Carlo Augusto
...
info:eu-repo/semantics/altIdentifier/pmid/30208948. , 2018
Link:
http://hdl.handle.net/11..
1-15