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Human Genetics
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March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease
Ines Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
The Journal of Rheumatology
|
October 21, 1999
Muscle dysfunction in elderly individuals with hip fracture
M R Gonzalez-Crespo, J Arenas, J J Gomez-Reino, et al.
Journal of Medical Genetics
|
March 3, 2009
Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNA
I García-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Brain : a Journal of Neurology
|
August 1, 1994
Autosomal recessive hereditary sensory neuropathy with spastic paraplegia
P K Thomas, V P Misra, R H King, 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.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica
|
November 22, 2011
[Mandibular distraction osteogenesis in patients with craniofacial malformation]
C Marañés Gálvez, A Martínez Plaza, R Fernández Valadés, et al.
International Journal of Pharmaceutics
|
March 31, 2025
Self-assembled PAMAM-G4 dendrimer nanoparticles with Phloxine B as photosensitizer for antimicrobial photodynamic therapy
David E Ybarra, Camila Quezada, Yuly A Guarín, et al.
Leukemia Research
|
January 21, 2006
Classification and scoring systems in myelodysplastic syndromes: a retrospective analysis of 311 patients
I Navarro, M A Ruiz, A Cabello, et al.
International Microbiology : the Official Journal of the Spanish Society for Microbiology
|
January 5, 2002
Screening of antimicrobial activities in red, green and brown macroalgae from Gran Canaria (Canary Islands, Spain)
A González del Val, G Platas, A Basilio, et al.
Revista De Neurologia
|
May 30, 2008
[Lymphomatosis cerebri as the cause of leukoencephalopathy]
M de Toledo, E López-Valdés, M Ferreiro, et al.
Page
of 24
Search research articles
Search
Showing results (201-210 of 239) with videos related to
Sort By:
Page
of 24
Human Genetics
|
March 26, 2009
Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease
Ines Garcia-Consuegra, J C Rubio, G Nogales-Gadea, et al.
The Journal of Rheumatology
|
October 21, 1999
Muscle dysfunction in elderly individuals with hip fracture
M R Gonzalez-Crespo, J Arenas, J J Gomez-Reino, et al.
Journal of Medical Genetics
|
March 3, 2009
Novel mutations in patients with McArdle disease by analysis of skeletal muscle mRNA
I García-Consuegra, J C Rubio, G Nogales-Gadea, et al.
Brain : a Journal of Neurology
|
August 1, 1994
Autosomal recessive hereditary sensory neuropathy with spastic paraplegia
P K Thomas, V P Misra, R H King, 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.
Cirugia Pediatrica : Organo Oficial De La Sociedad Espanola De Cirugia Pediatrica
|
November 22, 2011
[Mandibular distraction osteogenesis in patients with craniofacial malformation]
C Marañés Gálvez, A Martínez Plaza, R Fernández Valadés, et al.
International Journal of Pharmaceutics
|
March 31, 2025
Self-assembled PAMAM-G4 dendrimer nanoparticles with Phloxine B as photosensitizer for antimicrobial photodynamic therapy
David E Ybarra, Camila Quezada, Yuly A Guarín, et al.
Leukemia Research
|
January 21, 2006
Classification and scoring systems in myelodysplastic syndromes: a retrospective analysis of 311 patients
I Navarro, M A Ruiz, A Cabello, et al.
International Microbiology : the Official Journal of the Spanish Society for Microbiology
|
January 5, 2002
Screening of antimicrobial activities in red, green and brown macroalgae from Gran Canaria (Canary Islands, Spain)
A González del Val, G Platas, A Basilio, et al.
Revista De Neurologia
|
May 30, 2008
[Lymphomatosis cerebri as the cause of leukoencephalopathy]
M de Toledo, E López-Valdés, M Ferreiro, et al.
Page
of 24