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European Journal of Medical Genetics
|
July 28, 2011
LMNA mutation in progeroid syndrome in association with strokes
L Gonzalez-Quereda, V Delgadillo, J Juan-Mateu, et al.
Clinical Rheumatology
|
December 1, 1992
Renal excretion of urate by hyperuricaemic-hyperlipidemic patients
E Collantes Estevéz, F J Tinahones Madueño, A González Ruiz, et al.
Journal of the Neurological Sciences
|
February 20, 2007
A distinct subgroup of chronic inflammatory demyelinating polyneuropathy with CNS demyelination and a favorable response to immunotherapy
Arnold Angelo M Pineda, Katsuya Ogata, Manabu Osoegawa, et al.
Molecules (Basel, Switzerland)
|
August 31, 2018
Pumilacidins from the Octocoral-Associated <i>Bacillus</i> sp. DT001 Display Anti-Proliferative Effects in <i>Plasmodium falciparum</i>
Daniel Torres-Mendoza, Lorena M Coronado, Laura M Pineda, et al.
Journal of Medical Genetics
|
July 5, 2003
Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA
A Solano, J Gámez, F J Carod, et al.
Vascular and Endovascular Surgery
|
March 22, 2022
An Enhanced Recovery After Surgery Protocol Decreases the Use of Narcotics in Infrainguinal Bypass Patients
Lili Sadri, Deepak Shan, Luis Mejia-Sierra, et al.
Pflugers Archiv : European Journal of Physiology
|
June 22, 2001
Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc-
M T Bassi, E Gasol, M Manzoni, et al.
Genes, Chromosomes & Cancer
|
January 9, 2008
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 gene
M Pineda, E Castellsagué, E Musulén, et al.
British Journal of Rheumatology
|
October 1, 1995
Increased VLDL levels and diminished renal excretion of uric acid in hyperuricaemic-hypertriglyceridaemic patients
F J Tinahones, E Collantes, F J C-Soriguer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 21, 2019
The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome
S Vidal, N Brandi, P Pacheco, et al.
Page
of 40
Search research articles
Search
Showing results (221-230 of 395) with videos related to
Sort By:
Page
of 40
European Journal of Medical Genetics
|
July 28, 2011
LMNA mutation in progeroid syndrome in association with strokes
L Gonzalez-Quereda, V Delgadillo, J Juan-Mateu, et al.
Clinical Rheumatology
|
December 1, 1992
Renal excretion of urate by hyperuricaemic-hyperlipidemic patients
E Collantes Estevéz, F J Tinahones Madueño, A González Ruiz, et al.
Journal of the Neurological Sciences
|
February 20, 2007
A distinct subgroup of chronic inflammatory demyelinating polyneuropathy with CNS demyelination and a favorable response to immunotherapy
Arnold Angelo M Pineda, Katsuya Ogata, Manabu Osoegawa, et al.
Molecules (Basel, Switzerland)
|
August 31, 2018
Pumilacidins from the Octocoral-Associated <i>Bacillus</i> sp. DT001 Display Anti-Proliferative Effects in <i>Plasmodium falciparum</i>
Daniel Torres-Mendoza, Lorena M Coronado, Laura M Pineda, et al.
Journal of Medical Genetics
|
July 5, 2003
Characterisation of repeat and palindrome elements in patients harbouring single deletions of mitochondrial DNA
A Solano, J Gámez, F J Carod, et al.
Vascular and Endovascular Surgery
|
March 22, 2022
An Enhanced Recovery After Surgery Protocol Decreases the Use of Narcotics in Infrainguinal Bypass Patients
Lili Sadri, Deepak Shan, Luis Mejia-Sierra, et al.
Pflugers Archiv : European Journal of Physiology
|
June 22, 2001
Identification and characterisation of human xCT that co-expresses, with 4F2 heavy chain, the amino acid transport activity system xc-
M T Bassi, E Gasol, M Manzoni, et al.
Genes, Chromosomes & Cancer
|
January 9, 2008
Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in the MSH2 gene
M Pineda, E Castellsagué, E Musulén, et al.
British Journal of Rheumatology
|
October 1, 1995
Increased VLDL levels and diminished renal excretion of uric acid in hyperuricaemic-hypertriglyceridaemic patients
F J Tinahones, E Collantes, F J C-Soriguer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 21, 2019
The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome
S Vidal, N Brandi, P Pacheco, et al.
Page
of 40