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Brain & Development
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October 22, 2008
Cardiac troponin I for accurate evaluation of cardiac status in myopathic patients
Manuel Castro-Gago, Carmen Gómez-Lado, Jesús Eirís-Puñal
American Journal of Medical Genetics. Part A
|
April 23, 2015
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome
Ines Quintela, Francisco Barros, Manuel Castro-Gago, et al.
Pediatric Neurology
|
January 13, 2009
Juvenile xanthogranuloma of the cauda equina
Manuel Castro-Gago, Carmen Gómez-Lado, Fernando Alvez, et al.
Endocrine
|
July 6, 2012
A Xq21.31 duplication without features of Prader-Willi syndrome
Manuel Castro-Gago, Laura Pérez-Gay, Carmen Gómez-Lado, et al.
Journal of Child Neurology
|
May 25, 2002
Epileptic disorder as the first neurologic manifestation of blue rubber bleb nevus syndrome
Jesús Eirís-Puñal, Mónica Picón-Cotos, Augusto Viso-Lorenzo, et al.
Journal of Child Neurology
|
May 3, 2011
Chromosomopathy manifesting as mitochondrial disease
Manuel Castro-Gago, Manuel Oscar Blanco-Barca, Laura Pérez-Gay, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 2, 2009
Abnormal myelination in Angelman syndrome
Manuel Castro-Gago, Carmen Gómez-Lado, Jesús Eirís-Puñal, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
October 26, 2006
Duane's syndrome and 22 marker chromosome: a possible cat-eye syndrome
Carmen Gómez-Lado, Jesús Eirís, José Manuel Martínez-Yriarte, et al.
Revista De Neurologia
|
January 12, 2013
[16p11.2 microdeletion associated to early onset benign childhood seizures]
Manuel Castro-Gago, Laura Pérez-Gay, Carmen Gómez-Lado, et al.
American Journal of Medical Genetics. Part A
|
April 8, 2015
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features
Ines Quintela, Francisco Barros, Ramon Lago-Leston, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
Brain & Development
|
October 22, 2008
Cardiac troponin I for accurate evaluation of cardiac status in myopathic patients
Manuel Castro-Gago, Carmen Gómez-Lado, Jesús Eirís-Puñal
American Journal of Medical Genetics. Part A
|
April 23, 2015
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome
Ines Quintela, Francisco Barros, Manuel Castro-Gago, et al.
Pediatric Neurology
|
January 13, 2009
Juvenile xanthogranuloma of the cauda equina
Manuel Castro-Gago, Carmen Gómez-Lado, Fernando Alvez, et al.
Endocrine
|
July 6, 2012
A Xq21.31 duplication without features of Prader-Willi syndrome
Manuel Castro-Gago, Laura Pérez-Gay, Carmen Gómez-Lado, et al.
Journal of Child Neurology
|
May 25, 2002
Epileptic disorder as the first neurologic manifestation of blue rubber bleb nevus syndrome
Jesús Eirís-Puñal, Mónica Picón-Cotos, Augusto Viso-Lorenzo, et al.
Journal of Child Neurology
|
May 3, 2011
Chromosomopathy manifesting as mitochondrial disease
Manuel Castro-Gago, Manuel Oscar Blanco-Barca, Laura Pérez-Gay, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 2, 2009
Abnormal myelination in Angelman syndrome
Manuel Castro-Gago, Carmen Gómez-Lado, Jesús Eirís-Puñal, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
October 26, 2006
Duane's syndrome and 22 marker chromosome: a possible cat-eye syndrome
Carmen Gómez-Lado, Jesús Eirís, José Manuel Martínez-Yriarte, et al.
Revista De Neurologia
|
January 12, 2013
[16p11.2 microdeletion associated to early onset benign childhood seizures]
Manuel Castro-Gago, Laura Pérez-Gay, Carmen Gómez-Lado, et al.
American Journal of Medical Genetics. Part A
|
April 8, 2015
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features
Ines Quintela, Francisco Barros, Ramon Lago-Leston, et al.
Page
of 5