Search research articles
Contact Us
Filters
Showing results (531-540 of 642) with videos related to
Page
of 65
Sort By:
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 patients
S 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 dysplasia
I 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: CADASIL
I 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 genes
S 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 mutation
A 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 Age
Manoel 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 vessels
L 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 spectrum
C Orellana, J Bernabeu, S Monfort, et al.
Page
of 65
Search research articles
Search
Showing results (531-540 of 642) with videos related to
Sort By:
Page
of 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 patients
S 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 dysplasia
I 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: CADASIL
I 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 genes
S 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 mutation
A 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 Age
Manoel 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 vessels
L 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 spectrum
C Orellana, J Bernabeu, S Monfort, et al.
Page
of 65