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M R Delgado

Showing results (41-50 of 51) with videos related to

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Journal of Child Neurology|May 6, 1998
Early diagnosis of subependymal giant cell astrocytoma in patients with tuberous sclerosisO A Torres, E S Roach, M R Delgado, et al.
Neurology|December 25, 2002
Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtypeA J Lewis, E M Simon, A J Barkovich, et al.
American Journal of Human Genetics|April 16, 1998
Germ-line mutational analysis of the TSC2 gene in 90 tuberous-sclerosis patientsK S Au, J A Rodriguez, J L Finch, et al.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica|July 7, 2018
[Is there a difference in the postoperative follow up of ureteropelvic junction obstruction according to age?]Y González Ruiz, P Bragagnini Rodríguez, A Siles Hinojosa, et al.
Neurology|January 27, 2010
Practice parameter: pharmacologic treatment of spasticity in children and adolescents with cerebral palsy (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society, M R Delgado, D Hirtz, et al.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica|April 29, 2022
What urethrogram sees and a surgeon does notP Salcedo Arroyo, C Domínguez García, M R Delgado Alvira, et al.
Neurology|October 9, 2002
Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brainL L Plawner, M R Delgado, V S Miller, et al.
Gait & Posture|February 9, 2000
Recommendations for the use of botulinum toxin type A in the management of cerebral palsyH K Graham, K R Aoki, I Autti-Rämö, et al.
Molecular Syndromology|November 30, 2011
TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and PhenotypeA A Keaton, B D Solomon, E F Kauvar, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Journal of Child Neurology|May 6, 1998
Early diagnosis of subependymal giant cell astrocytoma in patients with tuberous sclerosisO A Torres, E S Roach, M R Delgado, et al.
Neurology|December 25, 2002
Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtypeA J Lewis, E M Simon, A J Barkovich, et al.
American Journal of Human Genetics|April 16, 1998
Germ-line mutational analysis of the TSC2 gene in 90 tuberous-sclerosis patientsK S Au, J A Rodriguez, J L Finch, et al.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica|July 7, 2018
[Is there a difference in the postoperative follow up of ureteropelvic junction obstruction according to age?]Y González Ruiz, P Bragagnini Rodríguez, A Siles Hinojosa, et al.
Neurology|January 27, 2010
Practice parameter: pharmacologic treatment of spasticity in children and adolescents with cerebral palsy (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society, M R Delgado, D Hirtz, et al.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica|April 29, 2022
What urethrogram sees and a surgeon does notP Salcedo Arroyo, C Domínguez García, M R Delgado Alvira, et al.
Neurology|October 9, 2002
Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brainL L Plawner, M R Delgado, V S Miller, et al.
Gait & Posture|February 9, 2000
Recommendations for the use of botulinum toxin type A in the management of cerebral palsyH K Graham, K R Aoki, I Autti-Rämö, et al.
Molecular Syndromology|November 30, 2011
TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and PhenotypeA A Keaton, B D Solomon, E F Kauvar, et al.
Molecular Psychiatry|August 24, 2016
De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and femalesE E Palmer, T Stuhlmann, S Weinert, et al.
Pageof 6