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Neuromuscular Disorders : NMD
|
March 1, 1994
Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy
G Piccolo, G Azan, P Tonin, et al.
Boletin Medico Del Hospital Infantil De Mexico
|
June 9, 2021
Raoultella ornithinolytica urinary tract infection in a pediatric patient with T-cell precursor acute lymphoblastic leukemia
Ma Camila Prada-Avella, Miguel A Luengas-Monroy, Amaranto Suárez, et al.
Journal of Fungi (Basel, Switzerland)
|
April 25, 2025
Resilience in Resistance: The Role of Cell Wall Integrity in Multidrug-Resistant Candida
Iván A Banda-Flores, David Torres-Tirado, Héctor M Mora-Montes, et al.
Actas Urologicas Espanolas
|
March 1, 1990
[Retrovesical pelvic masses: diagnosis]
P Paniagua, J Extramiana, M Mora, et al.
The Journal of Clinical Investigation
|
August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine
P Bernasconi, E Torchiana, P Confalonieri, et al.
Case Reports in Gastroenterology
|
November 24, 2011
Gastric marginal zone B cell lymphoma of the duodenum
A Ndzengue, R Khurana, M Mora, et al.
Life Sciences in Space Research
|
April 25, 2025
Non-DNA radiosensitive targets that initiate persistent behavioral deficits in rats exposed to space radiation
Tore Straume, Ana M Mora, James B Brown, et al.
Current Medicinal Chemistry
|
March 17, 2012
An artificial neural network model for predicting the subcellular localization of photosensitisers for photodynamic therapy of solid tumours
R Tejedor-Estrada, S Nonell, J Teixido, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
December 3, 2014
[Non-Hodgkin lymphoma: Excellent results at the expense of the high toxicity of the treatment]
M A Baena-Gómez, M Mora Matilla, A Lassaletta Atienza, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth Disease
D Pareyson, D Menichella, S Botti, et al.
Page
of 68
Search research articles
Search
Showing results (311-320 of 679) with videos related to
Sort By:
Page
of 68
Neuromuscular Disorders : NMD
|
March 1, 1994
Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy
G Piccolo, G Azan, P Tonin, et al.
Boletin Medico Del Hospital Infantil De Mexico
|
June 9, 2021
Raoultella ornithinolytica urinary tract infection in a pediatric patient with T-cell precursor acute lymphoblastic leukemia
Ma Camila Prada-Avella, Miguel A Luengas-Monroy, Amaranto Suárez, et al.
Journal of Fungi (Basel, Switzerland)
|
April 25, 2025
Resilience in Resistance: The Role of Cell Wall Integrity in Multidrug-Resistant Candida
Iván A Banda-Flores, David Torres-Tirado, Héctor M Mora-Montes, et al.
Actas Urologicas Espanolas
|
March 1, 1990
[Retrovesical pelvic masses: diagnosis]
P Paniagua, J Extramiana, M Mora, et al.
The Journal of Clinical Investigation
|
August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine
P Bernasconi, E Torchiana, P Confalonieri, et al.
Case Reports in Gastroenterology
|
November 24, 2011
Gastric marginal zone B cell lymphoma of the duodenum
A Ndzengue, R Khurana, M Mora, et al.
Life Sciences in Space Research
|
April 25, 2025
Non-DNA radiosensitive targets that initiate persistent behavioral deficits in rats exposed to space radiation
Tore Straume, Ana M Mora, James B Brown, et al.
Current Medicinal Chemistry
|
March 17, 2012
An artificial neural network model for predicting the subcellular localization of photosensitisers for photodynamic therapy of solid tumours
R Tejedor-Estrada, S Nonell, J Teixido, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
December 3, 2014
[Non-Hodgkin lymphoma: Excellent results at the expense of the high toxicity of the treatment]
M A Baena-Gómez, M Mora Matilla, A Lassaletta Atienza, et al.
Annals of the New York Academy of Sciences
|
November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth Disease
D Pareyson, D Menichella, S Botti, et al.
Page
of 68