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Farmacia Hospitalaria : Organo Oficial De Expresion Cientifica De La Sociedad Espanola De Farmacia Hospitalaria
|
June 25, 2013
[Risk prescription associated to treatment at home of the elderly patient when admitted to the hospital]
C Iniesta-Navalón, E Urbieta-Sanz, J J Gascón-Cánovas, et al.
AIDS Research and Human Retroviruses
|
September 1, 1995
Analysis of the V3 loop sequences from 10 HIV type 1-infected AIDS patients from Paraguay
A Cabello, M Cabral, M E Vera, et al.
Clinical Genetics
|
June 13, 2009
A double homozygous mutation in the POMT1 gene involving exon skipping gives rise to Walker-Warburg syndrome in two Spanish Gypsy families
R P Cotarelo, O Fano, M Raducu, et al.
Medicina Clinica
|
January 26, 1985
[Neurological manifestations of pellagra: description of 2 cases]
J A Molina Arjona, S Gomara López, F Bermejo Pareja, et al.
Histopathology
|
February 8, 2005
HDM2 overexpression and focal loss of p14/ARF expression may deregulate the p53 tumour suppressor pathway in meningeal haemangiopericytomas. Study by double immunofluorescence and laser scanning confocal microscopy
J-C Martínez, J-C Palomino, A Cabello, et al.
The Journal of Pediatrics
|
November 1, 1994
Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiency
M T García-Silva, Y Campos, A Ribes, et al.
Molecular Biology of the Cell
|
November 6, 2001
Cell cycle-dependent expression and nucleolar localization of hCAP-H
O A Cabello, E Eliseeva, W G He, et al.
Anales Espanoles De Pediatria
|
December 1, 1991
[Dysgenesis of the anterior horns and nuclei of the brain stem in multiple congenital arthrogryposis. Presentation of a case]
M Mollejo Villanueva, J Torres Mohedas, A Cabello Fernández, et al.
Revista De Neurologia
|
December 1, 2001
[Infantile neuroaxonal dystrophy. A report of two new cases and a review of the literature published over the past ten years]
T Rodríguez-Costa, A Cabello, E Recuero-Fernández, et al.
Muscle & Nerve
|
July 1, 1993
Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy
Y Campos, R Huertas, J Bautista, et al.
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of 24
Search research articles
Search
Showing results (161-170 of 239) with videos related to
Sort By:
Page
of 24
Farmacia Hospitalaria : Organo Oficial De Expresion Cientifica De La Sociedad Espanola De Farmacia Hospitalaria
|
June 25, 2013
[Risk prescription associated to treatment at home of the elderly patient when admitted to the hospital]
C Iniesta-Navalón, E Urbieta-Sanz, J J Gascón-Cánovas, et al.
AIDS Research and Human Retroviruses
|
September 1, 1995
Analysis of the V3 loop sequences from 10 HIV type 1-infected AIDS patients from Paraguay
A Cabello, M Cabral, M E Vera, et al.
Clinical Genetics
|
June 13, 2009
A double homozygous mutation in the POMT1 gene involving exon skipping gives rise to Walker-Warburg syndrome in two Spanish Gypsy families
R P Cotarelo, O Fano, M Raducu, et al.
Medicina Clinica
|
January 26, 1985
[Neurological manifestations of pellagra: description of 2 cases]
J A Molina Arjona, S Gomara López, F Bermejo Pareja, et al.
Histopathology
|
February 8, 2005
HDM2 overexpression and focal loss of p14/ARF expression may deregulate the p53 tumour suppressor pathway in meningeal haemangiopericytomas. Study by double immunofluorescence and laser scanning confocal microscopy
J-C Martínez, J-C Palomino, A Cabello, et al.
The Journal of Pediatrics
|
November 1, 1994
Encephalopathy, petechiae, and acrocyanosis with ethylmalonic aciduria associated with muscle cytochrome c oxidase deficiency
M T García-Silva, Y Campos, A Ribes, et al.
Molecular Biology of the Cell
|
November 6, 2001
Cell cycle-dependent expression and nucleolar localization of hCAP-H
O A Cabello, E Eliseeva, W G He, et al.
Anales Espanoles De Pediatria
|
December 1, 1991
[Dysgenesis of the anterior horns and nuclei of the brain stem in multiple congenital arthrogryposis. Presentation of a case]
M Mollejo Villanueva, J Torres Mohedas, A Cabello Fernández, et al.
Revista De Neurologia
|
December 1, 2001
[Infantile neuroaxonal dystrophy. A report of two new cases and a review of the literature published over the past ten years]
T Rodríguez-Costa, A Cabello, E Recuero-Fernández, et al.
Muscle & Nerve
|
July 1, 1993
Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy
Y Campos, R Huertas, J Bautista, et al.
Page
of 24