Espinós, J. C.
296  Ergebnisse:
Personensuche X
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1

Clinical spectrum of BICD2 mutations:

Frasquet, M. ; Camacho, A. ; Vílchez, R....
European Journal of Neurology.  27 (2020)  7 - p. 1327-1335 , 2020
 
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2

Bi‐allelic mutations in EGR2 cause autosomal recessive demy..:

Lupo, V. ; Won, S. ; Frasquet, M....
European Journal of Neurology.  27 (2020)  12 - p. 2662-2667 , 2020
 
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3

Clinical, radiological and genetic characterization of PLA2..:

Darling, A. ; Aguilera Albesa, S. ; Tomás Vila, M....
European Journal of Paediatric Neurology.  21 (2017)  - p. e176-e177 , 2017
 
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8

OP61 – 2294: Pantotenate kinase associated neurodegeneratio..:

Darling, A. ; Decio, A. ; Serrano, M....
European Journal of Paediatric Neurology.  19 (2015)  - p. S19-S20 , 2015
 
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12

Letter: the role of stent in the treatment of Crohn's disea..:

Loras, C. ; Pérez Roldan, F. ; Gornals, J. B....
Alimentary Pharmacology & Therapeutics.  37 (2013)  4 - p. 503-504 , 2013
 
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14

Endoscopic treatment with self‐expanding metal stents for C..:

Loras, C. ; Pérez‐Roldan, F. ; Gornals, J. B....
Alimentary Pharmacology & Therapeutics.  36 (2012)  9 - p. 833-839 , 2012
 
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