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I Ferrer

Showing results (531-540 of 642) with videos related to

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Revista De Neurologia|December 17, 2008
[ARX mutations and mental retardation of unknown etiology: three new cases in Spain]M T Romero-Rubio, M Andrés-Celma, M L Castelló-Pomares, et al.
Cancer|October 15, 1983
Angiogenic activity in fluid samples from tumoral patientsS Lopez Pousa, J M Vich i Pascuchi, I Ferrer, et al.
Acta Neuropathologica|January 1, 1992
Abnormal local-circuit neurons in epilepsia partialis continua associated with focal cortical dysplasiaI Ferrer, M Pineda, M Tallada, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|December 19, 2009
[Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin]G Iglesias Escalera, I Ferrer, Ll Carrasco Marina, et al.
Human Genetics|August 11, 2004
Gene symbol: NOTCH3. Disease: CADASILI Rojas-Marcos, M Encarnacion, S Martinez-Yelamos, et al.
Journal of Medical Genetics|April 17, 2008
Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genesS Monfort, M Roselló, C Orellana, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 10, 2007
Late-onset frontotemporal dementia associated with a novel PGRN mutationA Lladó, R Sánchez-Valle, R Reñé, et al.
The Journal of Pediatrics|February 9, 2019
Thoracic Aortic Intima-Media Thickness in Preschool Children Born Small for Gestational AgeManoel Muñiz Fontán, Ignacio Oulego Erroz, Daniela Revilla Orias, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 4, 2000
Renal tubular acidosis and vasculitis associated with IgE deposits in the kidney and small vesselsL I Juncos, J C Muiño, N H García, et al.
BMJ Case Reports|July 7, 2011
Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrumC Orellana, J Bernabeu, S Monfort, et al.
Pageof 65

Showing results (531-540 of 642) with videos related to

Sort By:
Pageof 65
Revista De Neurologia|December 17, 2008
[ARX mutations and mental retardation of unknown etiology: three new cases in Spain]M T Romero-Rubio, M Andrés-Celma, M L Castelló-Pomares, et al.
Cancer|October 15, 1983
Angiogenic activity in fluid samples from tumoral patientsS Lopez Pousa, J M Vich i Pascuchi, I Ferrer, et al.
Acta Neuropathologica|January 1, 1992
Abnormal local-circuit neurons in epilepsia partialis continua associated with focal cortical dysplasiaI Ferrer, M Pineda, M Tallada, et al.
Anales De Pediatria (Barcelona, Spain : 2003)|December 19, 2009
[Succinic semialdehyde dehydrogenase deficiency: decrease in 4-OH-butyric acid levels with low doses of vigabatrin]G Iglesias Escalera, I Ferrer, Ll Carrasco Marina, et al.
Human Genetics|August 11, 2004
Gene symbol: NOTCH3. Disease: CADASILI Rojas-Marcos, M Encarnacion, S Martinez-Yelamos, et al.
Journal of Medical Genetics|April 17, 2008
Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genesS Monfort, M Roselló, C Orellana, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|April 10, 2007
Late-onset frontotemporal dementia associated with a novel PGRN mutationA Lladó, R Sánchez-Valle, R Reñé, et al.
The Journal of Pediatrics|February 9, 2019
Thoracic Aortic Intima-Media Thickness in Preschool Children Born Small for Gestational AgeManoel Muñiz Fontán, Ignacio Oulego Erroz, Daniela Revilla Orias, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|May 4, 2000
Renal tubular acidosis and vasculitis associated with IgE deposits in the kidney and small vesselsL I Juncos, J C Muiño, N H García, et al.
BMJ Case Reports|July 7, 2011
Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrumC Orellana, J Bernabeu, S Monfort, et al.
Pageof 65