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World Journal of Urology
|
March 13, 2024
Nadir prostate-specific antigen after salvage cryotherapy as a potential prognostic factor for oncologic outcomes
E Carbonell, C Mercader, J Sureda, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 25, 2008
Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations
B Pérez-Dueñas, A García-Cazorla, M Pineda, et al.
Molecular Genetics and Metabolism
|
January 20, 2010
The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC)
Furhan Iqbal, Chike B Item, Maria A Vilaseca, et al.
Molecular Genetics and Metabolism
|
December 4, 2009
Response to creatine analogs in fibroblasts and patients with creatine transporter deficiency
C Fons, A Arias, A Sempere, et al.
Clinical Biochemistry
|
April 21, 2006
Oral phenylalanine loading test for the diagnosis of dominant guanosine triphosphate cyclohydrolase 1 deficiency
Eduardo López-Laso, Aida Ormazabal, Rafael Camino, et al.
Revista Espanola De Medicina Nuclear E Imagen Molecular
|
January 24, 2025
"Utility of PET/CT with [<sup>18</sup>F] F-fluorocholine in assessing the response to antiandrogenic therapy in patients with prostate cancer."
K Quintero, E Vila, L Ferrer-Mileo, et al.
Scientific Reports
|
February 27, 2013
Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas
P Sarrión, A Sangorrin, R Urreizti, et al.
Human Mutation
|
May 20, 2008
A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1)
María D Herrero-Martín, Mercedes Pineda, Paz Briones, et al.
Revista De Neurologia
|
June 18, 2004
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin]
M Pineda, A Playán-Ariso, M J Alcaine-Villarroya, et al.
Revista De Neurologia
|
December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]
L Coelho-Miranda, A Playan, R Artuch, et al.
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Search research articles
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Showing results (111-120 of 133) with videos related to
Sort By:
Page
of 14
World Journal of Urology
|
March 13, 2024
Nadir prostate-specific antigen after salvage cryotherapy as a potential prognostic factor for oncologic outcomes
E Carbonell, C Mercader, J Sureda, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 25, 2008
Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations
B Pérez-Dueñas, A García-Cazorla, M Pineda, et al.
Molecular Genetics and Metabolism
|
January 20, 2010
The identification of novel mutations in the biotinidase gene using denaturing high pressure liquid chromatography (dHPLC)
Furhan Iqbal, Chike B Item, Maria A Vilaseca, et al.
Molecular Genetics and Metabolism
|
December 4, 2009
Response to creatine analogs in fibroblasts and patients with creatine transporter deficiency
C Fons, A Arias, A Sempere, et al.
Clinical Biochemistry
|
April 21, 2006
Oral phenylalanine loading test for the diagnosis of dominant guanosine triphosphate cyclohydrolase 1 deficiency
Eduardo López-Laso, Aida Ormazabal, Rafael Camino, et al.
Revista Espanola De Medicina Nuclear E Imagen Molecular
|
January 24, 2025
"Utility of PET/CT with [<sup>18</sup>F] F-fluorocholine in assessing the response to antiandrogenic therapy in patients with prostate cancer."
K Quintero, E Vila, L Ferrer-Mileo, et al.
Scientific Reports
|
February 27, 2013
Mutations in the EXT1 and EXT2 genes in Spanish patients with multiple osteochondromas
P Sarrión, A Sangorrin, R Urreizti, et al.
Human Mutation
|
May 20, 2008
A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1)
María D Herrero-Martín, Mercedes Pineda, Paz Briones, et al.
Revista De Neurologia
|
June 18, 2004
[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin]
M Pineda, A Playán-Ariso, M J Alcaine-Villarroya, et al.
Revista De Neurologia
|
December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]
L Coelho-Miranda, A Playan, R Artuch, et al.
Page
of 14