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Revista De Biologia Tropical
|
January 16, 2010
[Distribution of potentially nitrogen-fixing bacteria and its relationship with physicochemical parameters in soils with three vegetation types in the southern Colombian Amazon region]
Andrea J Mantilla-Paredes, Gladys I Cardona, Clara P Peña-Venegas, et al.
Microbiology (Reading, England)
|
September 28, 2014
Klebsiella pneumoniae yfiRNB operon affects biofilm formation, polysaccharide production and drug susceptibility
Mónica G Huertas, Lina Zárate, Iván C Acosta, et al.
Boletin Medico Del Hospital Infantil De Mexico
|
November 22, 2024
Graft-versus-host disease variety toxic epidermal necrolysis. Case report
Elsa M Zúñiga-Lara, César M Zambrano-Virgen, José F Gaytán-Morales, et al.
European Journal of Medical Genetics
|
February 9, 2016
Neonatal severe hyperparathyroidism caused by homozygous mutation in CASR: A rare cause of life-threatening hypercalcemia
Heidi Murphy, Jessica Patrick, Eileen Báez-Irizarry, et al.
Gynecologic Oncology
|
May 24, 2024
ACO leakage among gynecologic cancer patients: Incidence, predictors, and impact on annual Medicare expenditure
Oyomoare L Osazuwa-Peters, Melissa A Greiner, Brystana G Kaufman, et al.
Clinical Genetics
|
September 1, 1996
Neuroradiology and clinical aspects of Usher syndrome
M L Tamayo, C Maldonado, S L Plaza, et al.
Experimental Neurology
|
November 27, 2015
TrkB gene therapy by adeno-associated virus enhances recovery after cervical spinal cord injury
Gabriel Martínez-Gálvez, Juan M Zambrano, Juan C Diaz Soto, et al.
Cardiovascular Research
|
November 21, 2014
Physiological activation of Akt by PHLPP1 deletion protects against pathological hypertrophy
Courtney Moc, Amy E Taylor, Gino P Chesini, et al.
Clinical Case Reports
|
April 12, 2017
Neonatal mucolipidosis type II alpha/beta due to compound heterozygosity for a known and novel <i>GNPTAB</i> mutation, and a concomitant heterozygous change in <i>SERPINF1</i> inherited from the mother
Kirsten A Wood, Regina M Zambrano, Bradley J Cheek, et al.
American Journal of Medical Genetics. Part A
|
April 26, 2017
Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
Andrea C Yu, Regina M Zambrano, Ingrid Cristian, et al.
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Search research articles
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Showing results (31-40 of 60) with videos related to
Sort By:
Page
of 6
Revista De Biologia Tropical
|
January 16, 2010
[Distribution of potentially nitrogen-fixing bacteria and its relationship with physicochemical parameters in soils with three vegetation types in the southern Colombian Amazon region]
Andrea J Mantilla-Paredes, Gladys I Cardona, Clara P Peña-Venegas, et al.
Microbiology (Reading, England)
|
September 28, 2014
Klebsiella pneumoniae yfiRNB operon affects biofilm formation, polysaccharide production and drug susceptibility
Mónica G Huertas, Lina Zárate, Iván C Acosta, et al.
Boletin Medico Del Hospital Infantil De Mexico
|
November 22, 2024
Graft-versus-host disease variety toxic epidermal necrolysis. Case report
Elsa M Zúñiga-Lara, César M Zambrano-Virgen, José F Gaytán-Morales, et al.
European Journal of Medical Genetics
|
February 9, 2016
Neonatal severe hyperparathyroidism caused by homozygous mutation in CASR: A rare cause of life-threatening hypercalcemia
Heidi Murphy, Jessica Patrick, Eileen Báez-Irizarry, et al.
Gynecologic Oncology
|
May 24, 2024
ACO leakage among gynecologic cancer patients: Incidence, predictors, and impact on annual Medicare expenditure
Oyomoare L Osazuwa-Peters, Melissa A Greiner, Brystana G Kaufman, et al.
Clinical Genetics
|
September 1, 1996
Neuroradiology and clinical aspects of Usher syndrome
M L Tamayo, C Maldonado, S L Plaza, et al.
Experimental Neurology
|
November 27, 2015
TrkB gene therapy by adeno-associated virus enhances recovery after cervical spinal cord injury
Gabriel Martínez-Gálvez, Juan M Zambrano, Juan C Diaz Soto, et al.
Cardiovascular Research
|
November 21, 2014
Physiological activation of Akt by PHLPP1 deletion protects against pathological hypertrophy
Courtney Moc, Amy E Taylor, Gino P Chesini, et al.
Clinical Case Reports
|
April 12, 2017
Neonatal mucolipidosis type II alpha/beta due to compound heterozygosity for a known and novel <i>GNPTAB</i> mutation, and a concomitant heterozygous change in <i>SERPINF1</i> inherited from the mother
Kirsten A Wood, Regina M Zambrano, Bradley J Cheek, et al.
American Journal of Medical Genetics. Part A
|
April 26, 2017
Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?
Andrea C Yu, Regina M Zambrano, Ingrid Cristian, et al.
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of 6