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Pilar Poo

Showing results (1-10 of 14) with videos related to

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Epilepsy & Behavior : E&B|September 6, 2011
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role?Mireia Tondo, Pilar Poo, Montserrat Naudó, et al.
Journal of Human Genetics|May 19, 2004
Hydrocephalus and Hirschsprung's disease with a mutation of L1CAMNobuhiko Okamoto, Rolando Del Maestro, Rebeca Valero, et al.
Clinical Rheumatology|August 21, 2012
Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgiaLoreto Martorell, Mireia Tondo, Ferrán Garcia-Fructuoso, et al.
Revista De Neurologia|July 26, 2014
[Diploid/triploid mosaicism: a variable but characteristic phenotype]Daniel Natera-De Benito, Pilar Poo, Esther Gean, et al.
Early Human Development|March 1, 2011
Impact of histological chorioamnionitis, funisitis and clinical chorioamnionitis on neurodevelopmental outcome of preterm infantsNuria Rovira, Ana Alarcon, Marti Iriondo, et al.
Developmental Medicine and Child Neurology|March 5, 2004
White matter alterations associated with chromosomal disordersAngels García-Cazorla, Anna Sans, Miguel Baquero, et al.
Archives of Dermatology|May 20, 2009
Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entityM Antonia González-Enseñat, Asunción Vicente, Pilar Poo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 11, 2008
Syndrome of fixed dystonia in adolescents--short term outcome in 4 casesAnirban Majumdar, Jesús López-Casas, Pilar Poo, et al.
Pediatric Neurology|May 13, 2009
Seizures versus dystonia in encephalopathic crisis of glutaric aciduria type IAlfredo Cerisola, Jaume Campistol, Belén Pérez-Dueñas, et al.
Medicina Clinica|November 7, 2009
[Cerebral creatine deficiency: first Spanish patients harbouring mutations in GAMT gene]Angela Sempere, Carmen Fons, Angela Arias, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Epilepsy & Behavior : E&B|September 6, 2011
Predisposition to epilepsy in fragile X syndrome: does the Val66Met polymorphism in the BDNF gene play a role?Mireia Tondo, Pilar Poo, Montserrat Naudó, et al.
Journal of Human Genetics|May 19, 2004
Hydrocephalus and Hirschsprung's disease with a mutation of L1CAMNobuhiko Okamoto, Rolando Del Maestro, Rebeca Valero, et al.
Clinical Rheumatology|August 21, 2012
Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgiaLoreto Martorell, Mireia Tondo, Ferrán Garcia-Fructuoso, et al.
Revista De Neurologia|July 26, 2014
[Diploid/triploid mosaicism: a variable but characteristic phenotype]Daniel Natera-De Benito, Pilar Poo, Esther Gean, et al.
Early Human Development|March 1, 2011
Impact of histological chorioamnionitis, funisitis and clinical chorioamnionitis on neurodevelopmental outcome of preterm infantsNuria Rovira, Ana Alarcon, Marti Iriondo, et al.
Developmental Medicine and Child Neurology|March 5, 2004
White matter alterations associated with chromosomal disordersAngels García-Cazorla, Anna Sans, Miguel Baquero, et al.
Archives of Dermatology|May 20, 2009
Phylloid hypomelanosis and mosaic partial trisomy 13: two cases that provide further evidence of a distinct clinicogenetic entityM Antonia González-Enseñat, Asunción Vicente, Pilar Poo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 11, 2008
Syndrome of fixed dystonia in adolescents--short term outcome in 4 casesAnirban Majumdar, Jesús López-Casas, Pilar Poo, et al.
Pediatric Neurology|May 13, 2009
Seizures versus dystonia in encephalopathic crisis of glutaric aciduria type IAlfredo Cerisola, Jaume Campistol, Belén Pérez-Dueñas, et al.
Medicina Clinica|November 7, 2009
[Cerebral creatine deficiency: first Spanish patients harbouring mutations in GAMT gene]Angela Sempere, Carmen Fons, Angela Arias, et al.
Pageof 2