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Castro-Gago, Manuel
355  Ergebnisse:
Personensuche X
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1

Copy number variation analysis of patients with intellectua..:

Quintela, Inés ; Eirís, Jesús ; Gómez-Lado, Carmen...
Gene.  626 (2017)  - p. 189-199 , 2017
Link: https://doi.org/10.1016/..
 
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2

Articular Manifestations in Patients With Lyme Disease:

Vázquez-López, María Esther ; Díez-Morrondo, Carolina ; Sánchez-Andrade, Amalia...
Reumatología Clínica (English Edition).  12 (2016)  6 - p. 327-330 , 2016
Link: https://doi.org/10.1016/..
 
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3

Corrigendum to "Congenital neurogenic muscular atrophy in m..:

Castro-Gago, Manuel ; Dacruz-Alvarez, David ; Pintos-Martínez, Elena...
Brain and Development.  38 (2016)  8 - p. 783 , 2016
Link: https://doi.org/10.1016/..
 
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4

Congenital neurogenic muscular atrophy in megaconial myopat..:

Castro-Gago, Manuel ; Dacruz-Alvarez, David ; Pintos-Martínez, Elena...
Brain and Development.  38 (2016)  1 - p. 167-172 , 2016
Link: https://doi.org/10.1016/..
 
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5

Epidemiología de la enfermedad de Lyme en un área sanitaria..:

Vázquez-López, María Esther ; Pego-Reigosa, Robustiano ; Díez-Morrondo, Carolina...
Gaceta Sanitaria.  29 (2015)  3 - p. 213-216 , 2015
Link: https://doi.org/10.1016/..
 
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6

Milder course in Duchenne patients with nonsense mutations ..:

Castro-Gago, Manuel
Neuromuscular Disorders.  25 (2015)  5 - p. 443 , 2015
Link: https://doi.org/10.1016/..
 
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7

Assessment of a targeted resequencing assay as a support to..:

Fernández-Marmiesse, Ana ; Morey, Marcos ; Pineda, Merce...
Orphanet Journal of Rare Diseases.  9 (2014)  1 - p. 59 , 2014
Link: https://doi.org/10.1186/..
 
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8

Exome sequencing identifies a CHKB mutation in Spanish pati..:

Castro-Gago, Manuel ; Dacruz-Alvarez, David ; Pintos-Martínez, Elena...
European Journal of Paediatric Neurology.  18 (2014)  6 - p. 796-800 , 2014
Link: https://doi.org/10.1016/..
 
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9

Intrathecal baclofen for progressive neurological disease i..:

Castro-Gago, Manuel ; Pérez-Gay, Laura ; Gómez-Lado, Carmen
European Journal of Paediatric Neurology.  17 (2013)  1 - p. 116 , 2013
Link: https://doi.org/10.1016/..
 
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10

Glutaric aciduria type I: Outcome of patients with early- v..:

Couce, Ma Luz ; López-Suárez, Olalla ; Bóveda, Ma Dolores...
European Journal of Paediatric Neurology.  17 (2013)  4 - p. 383-389 , 2013
Link: https://doi.org/10.1016/..
 
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11

Mutations in the RNA exosome component gene EXOSC3 cause po..:

Wan, Jijun ; Yourshaw, Michael ; Mamsa, Hafsa...
Nature Genetics.  44 (2012)  6 - p. 704-708 , 2012
Link: https://doi.org/10.1038/..
 
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12

A Xq21.31 duplication without features of Prader–Willi synd..:

Castro-Gago, Manuel ; Pérez-Gay, Laura ; Gómez-Lado, Carmen.
Endocrine.  43 (2012)  1 - p. 238-238 , 2012
Link: https://doi.org/10.1007/..
 
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13

Dravet Syndrome and Mitochondrial Dysfunction:

Castro-Gago, Manuel ; Pérez-Gay, Laura ; Eirís-Puñal, Jesús
Journal of Child Neurology.  26 (2011)  10 - p. 1331-1332 , 2011
Link: https://doi.org/10.1177/..
 
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14

Ohtahara syndrome and respiratory chain complex I deficienc:

Castro-Gago, Manuel ; Eirís-Puñal, Jesús
Brain and Development.  33 (2011)  2 - p. 177 , 2011
Link: https://doi.org/10.1016/..
 
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15

Primary Adenosine Monophosphate (AMP) Deaminase Deficiency ..:

Castro-Gago, Manuel ; Gómez-Lado, Carmen ; Pérez-Gay, Laura...
Journal of Child Neurology.  26 (2011)  6 - p. 734-737 , 2011
Link: https://doi.org/10.1177/..
 
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