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Parasitology
|
October 31, 2002
Chromosome number, genome size and polymorphism of European and South African isolates of large Babesia parasites that infect dogs
D Depoix, B Carcy, E Jumas-Bilak, et al.
Journal De Radiologie
|
August 1, 1990
[MRI in subacromial pathology. Report of 20 cases]
C Poey, P Fajadet, M Pages, et al.
The Journal of Biological Chemistry
|
November 15, 1988
Phospholipid transfer protein: full-length cDNA and amino acid sequence in maize. Amino acid sequence homologies between plant phospholipid transfer proteins
F Tchang, P This, V Stiefel, et al.
Soins; La Revue De Reference Infirmiere
|
February 28, 2001
[Isolation of patients with infection caused by multi-resistant bacteria]
J Lamory, G Vidal-Trécan, M de Prittwitz, et al.
Revue Neurologique
|
February 1, 1997
[Symptomatic aneurysms of the postero-inferior cerebellar artery. A multicenter retrospective study of 29 cases]
J M Blard, P J Finiels, A Combalbert, et al.
International Journal of Antimicrobial Agents
|
September 8, 2009
An AcrAB-mediated multidrug-resistant phenotype is maintained following restoration of wild-type activities by efflux pump genes and their regulators
A Martins, C Iversen, L Rodrigues, et al.
Cancer Research
|
July 1, 1986
Distribution of the Mr 52,000 estrogen-regulated protein in benign breast diseases and other tissues by immunohistochemistry
M Garcia, G Salazar-Retana, A Pages, et al.
Medecine Et Maladies Infectieuses
|
December 29, 2018
A practical approach to tuberculosis diagnosis and treatment in liver transplant recipients in a low-prevalence area
A Bosch, F Valour, O Dumitrescu, et al.
Mitochondrion
|
December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy
S Bannwarth, V Procaccio, C Rouzier, et al.
Revue Neurologique
|
August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]
V Humbertclaude, D Hamroun, M-C Picot, et al.
Page
of 12
Search research articles
Search
Showing results (111-120 of 120) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 120 results.
Parasitology
|
October 31, 2002
Chromosome number, genome size and polymorphism of European and South African isolates of large Babesia parasites that infect dogs
D Depoix, B Carcy, E Jumas-Bilak, et al.
Journal De Radiologie
|
August 1, 1990
[MRI in subacromial pathology. Report of 20 cases]
C Poey, P Fajadet, M Pages, et al.
The Journal of Biological Chemistry
|
November 15, 1988
Phospholipid transfer protein: full-length cDNA and amino acid sequence in maize. Amino acid sequence homologies between plant phospholipid transfer proteins
F Tchang, P This, V Stiefel, et al.
Soins; La Revue De Reference Infirmiere
|
February 28, 2001
[Isolation of patients with infection caused by multi-resistant bacteria]
J Lamory, G Vidal-Trécan, M de Prittwitz, et al.
Revue Neurologique
|
February 1, 1997
[Symptomatic aneurysms of the postero-inferior cerebellar artery. A multicenter retrospective study of 29 cases]
J M Blard, P J Finiels, A Combalbert, et al.
International Journal of Antimicrobial Agents
|
September 8, 2009
An AcrAB-mediated multidrug-resistant phenotype is maintained following restoration of wild-type activities by efflux pump genes and their regulators
A Martins, C Iversen, L Rodrigues, et al.
Cancer Research
|
July 1, 1986
Distribution of the Mr 52,000 estrogen-regulated protein in benign breast diseases and other tissues by immunohistochemistry
M Garcia, G Salazar-Retana, A Pages, et al.
Medecine Et Maladies Infectieuses
|
December 29, 2018
A practical approach to tuberculosis diagnosis and treatment in liver transplant recipients in a low-prevalence area
A Bosch, F Valour, O Dumitrescu, et al.
Mitochondrion
|
December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy
S Bannwarth, V Procaccio, C Rouzier, et al.
Revue Neurologique
|
August 20, 2013
[Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]
V Humbertclaude, D Hamroun, M-C Picot, et al.
Page
of 12