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Radiologia
|
April 20, 2024
Prevalence and prognostic meaning of interstitial lung abnormalities in remote CT scans of patients with interstitial lung disease treated with antifibrotic therapy
M M García Mullor, J J Arenas-Jiménez, A Ureña Vacas, et al.
Muscle & Nerve
|
March 1, 2002
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy
Y Campos, A García, A López, et al.
Journal of Inherited Metabolic Disease
|
March 30, 2018
Non-osteogenic muscle hypertrophy in children with McArdle disease
I Rodríguez-Gómez, A Santalla, J Díez-Bermejo, et al.
Journal of the Neurological Sciences
|
September 10, 1997
Decreased cerebrospinal fluid levels of neutral and basic amino acids in patients with Parkinson's disease
J A Molina, F J Jiménez-Jiménez, P Gomez, et al.
Journal of the Neurological Sciences
|
September 15, 1996
Neurotransmitter amino acids in cerebrospinal fluid of patients with Parkinson's disease
F J Jiménez-Jiménez, J A Molina, C Vargas, et al.
Transplantation Proceedings
|
November 22, 2005
Benefits of early biopsy on the outcome of kidney transplantation
J Dominguez, A Kompatzki, R Norambuena, et al.
International Journal of Sports Medicine
|
June 13, 2006
Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?
M Pérez, M A Martin, S Cañete, et al.
Revista De Neurologia
|
January 19, 2000
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]
M Castro-Gago, V González-Conde, M J Fernández-Seara, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
December 22, 1999
Matrix metalloproteinases expressed in squamous cell carcinoma of the oral cavity: correlation with clinicopathologic features and neo-adjuvant chemotherapy response
F J Arenas-Huertero, R Herrera-Goepfert, R Delgado-Chavez, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy
Y Campos, J Gámez, A García, et al.
Page
of 38
Search research articles
Search
Showing results (281-290 of 378) with videos related to
Sort By:
Page
of 38
Radiologia
|
April 20, 2024
Prevalence and prognostic meaning of interstitial lung abnormalities in remote CT scans of patients with interstitial lung disease treated with antifibrotic therapy
M M García Mullor, J J Arenas-Jiménez, A Ureña Vacas, et al.
Muscle & Nerve
|
March 1, 2002
Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy
Y Campos, A García, A López, et al.
Journal of Inherited Metabolic Disease
|
March 30, 2018
Non-osteogenic muscle hypertrophy in children with McArdle disease
I Rodríguez-Gómez, A Santalla, J Díez-Bermejo, et al.
Journal of the Neurological Sciences
|
September 10, 1997
Decreased cerebrospinal fluid levels of neutral and basic amino acids in patients with Parkinson's disease
J A Molina, F J Jiménez-Jiménez, P Gomez, et al.
Journal of the Neurological Sciences
|
September 15, 1996
Neurotransmitter amino acids in cerebrospinal fluid of patients with Parkinson's disease
F J Jiménez-Jiménez, J A Molina, C Vargas, et al.
Transplantation Proceedings
|
November 22, 2005
Benefits of early biopsy on the outcome of kidney transplantation
J Dominguez, A Kompatzki, R Norambuena, et al.
International Journal of Sports Medicine
|
June 13, 2006
Does the C34T mutation in AMPD1 alter exercise capacity in the elderly?
M Pérez, M A Martin, S Cañete, et al.
Revista De Neurologia
|
January 19, 2000
[Early mitochondrial encephalomyopathy due to complex IV deficiency consistent with Alpers-Huttenlocher syndrome: report of two cases]
M Castro-Gago, V González-Conde, M J Fernández-Seara, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
December 22, 1999
Matrix metalloproteinases expressed in squamous cell carcinoma of the oral cavity: correlation with clinicopathologic features and neo-adjuvant chemotherapy response
F J Arenas-Huertero, R Herrera-Goepfert, R Delgado-Chavez, et al.
Neuromuscular Disorders : NMD
|
June 19, 2001
A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with ocular myopathy
Y Campos, J Gámez, A García, et al.
Page
of 38