Search research articles
Contact Us
Filters
Showing results (51-60 of 65) with videos related to
Page
of 7
Sort By:
Hormone Research
|
August 14, 1998
Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome
R Artuch, C Pavía, A Playán, et al.
Journal of Inherited Metabolic Disease
|
April 23, 2003
Biochemical and molecular studies in 26 Spanish patients with congenital disorder of glycosylation type Ia
P Briones, M A Vilaseca, E Schollen, et al.
Human Mutation
|
January 1, 1996
Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiency
W Lissens, L De Meirleir, S Seneca, et al.
Journal of Experimental Therapeutics & Oncology
|
May 14, 2008
Analysis of human serum from women affected by cervical lesions
Ana P Barba de la Rosa, Ofelia Y Lugo-Melchor, Erika P Briones-Cerecero, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Congenital disorder of glycosylation (CDG) type Ie. A new patient
M T García-Silva, G Matthijs, E Schollen, et al.
Protein and Peptide Letters
|
February 23, 2005
Efficient immobilization of enzymes on microchannel surface through His-tag and application for microreactor
Masaya Miyazaki, Jun Kaneno, Susumu Yamaori, 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.
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.
Journal of Inherited Metabolic Disease
|
November 20, 2009
PDH E1β deficiency with novel mutations in two patients with Leigh syndrome
E Quintana, J A Mayr, M T García Silva, 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 7
Search research articles
Search
Showing results (51-60 of 65) with videos related to
Sort By:
Page
of 7
Hormone Research
|
August 14, 1998
Multiple endocrine involvement in two pediatric patients with Kearns-Sayre syndrome
R Artuch, C Pavía, A Playán, et al.
Journal of Inherited Metabolic Disease
|
April 23, 2003
Biochemical and molecular studies in 26 Spanish patients with congenital disorder of glycosylation type Ia
P Briones, M A Vilaseca, E Schollen, et al.
Human Mutation
|
January 1, 1996
Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiency
W Lissens, L De Meirleir, S Seneca, et al.
Journal of Experimental Therapeutics & Oncology
|
May 14, 2008
Analysis of human serum from women affected by cervical lesions
Ana P Barba de la Rosa, Ofelia Y Lugo-Melchor, Erika P Briones-Cerecero, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Congenital disorder of glycosylation (CDG) type Ie. A new patient
M T García-Silva, G Matthijs, E Schollen, et al.
Protein and Peptide Letters
|
February 23, 2005
Efficient immobilization of enzymes on microchannel surface through His-tag and application for microreactor
Masaya Miyazaki, Jun Kaneno, Susumu Yamaori, 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.
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.
Journal of Inherited Metabolic Disease
|
November 20, 2009
PDH E1β deficiency with novel mutations in two patients with Leigh syndrome
E Quintana, J A Mayr, M T García Silva, 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 7