Search Results - "Araque, D"

An alternative method for the synthesis of functional Au/WO3 materials and their use in the photocatalytic production of hydrogen by Durán-Álvarez, J.C., Del Angel, R., Ramírez-Ortega, D., Guerrero-Araque, D., Zanella, R.

“…[Display omitted] •Cationic adsorption of the [Au(en)2]Cl3 complex was successfully performed on WO3.•pH = 10 and 16 h of reaction time were the optimal…”
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Ag2O/TiO2 nanostructures for the photocatalytic mineralization of the highly recalcitrant pollutant iopromide in pure and tap water by Durán-Álvarez, J.C., Hernández-Morales, V.A., Rodríguez-Varela, M., Guerrero-Araque, D., Ramirez-Ortega, D., Castillón, F., Acevedo-Peña, P., Zanella, R.

“…[Display omitted] •Several loadings of Ag2O nanoparticles deposited on TiO2 by deposition-precipitation.•High mineralization of iopromide using Ag2O/TiO2…”
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Synthesis and Characterization of the All Solid Z-Scheme Bi2WO6/Ag/AgBr for the Photocatalytic Degradation of Ciprofloxacin in Water by Durán-Álvarez, J. C., Méndez-Galván, M., Lartundo-Rojas, L., Rodríguez-Varela, M., Ramírez-Ortega, D., Guerrero-Araque, D., Zanella, R.

“…The continuous release of antibiotics to the environment via wastewater is becoming a priority. Since conventional depuration systems are unable to remove…”
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Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex by Cammarata‐Scalisi, F., Vidales Moreno, C., Stock, F., Avendaño, A., Araque, D., Lacruz‐Rengel, M.A., Diociaiuti, A., Bellacchio, E., Callea, M.

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Early severe pachyonychia congenita subtype PC‐K6a with a novel mutation in the KRT6A gene by Cammarata‐Scalisi, F., Natsuga, K., Toyonaga, E., Nishie, W., Shimizu, H., Avendaño, A., Araque, D., Da Silva, G., Bellacchio, E., Callea, M.

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Mosaic trisomy 13 by Cammarata-Scalisi, F, Araque, D, Lacruz-Rengel, M A, Valera-Ruíz, B

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Trisomía 13 en mosaico by Cammarata-Scalisi, F, Araque, D, Lacruz-Rengel, M.A, Valera-Ruíz, B

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660 CONDYLE FRACTURE DURING THE CHILDBIRTH by Araque, D.

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Two novel mutations in the TSC 2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex by Cammarata‐Scalisi, F., Vidales Moreno, C., Stock, F., Avendaño, A., Araque, D., Lacruz‐Rengel, M.A., Diociaiuti, A., Bellacchio, E., Callea, M.

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Early severe pachyonychia congenita subtype PC ‐K6a with a novel mutation in the KRT 6A gene by Cammarata‐Scalisi, F., Natsuga, K., Toyonaga, E., Nishie, W., Shimizu, H., Avendaño, A., Araque, D., Da Silva, G., Bellacchio, E., Callea, M.

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Historical perspective and new developments regarding conversion coatings and seals for zinc deposits by Cornelious, Sean E., Araque, Juan D.

“…Producing quality parts that meet a customer's aesthetic and corrosion protection demands is what every zinc metal finisher strives for. Ongoing changes in…”
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Augmented reality motion-based robotics off-line programming by Araque, D, Diaz, R, Perez-Gutierrez, B, Uribe, A J

“…Augmented reality allows simulating, designing, projecting and validating robotic workcells in industrial environments that are not equipped with real…”
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Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex by Cammarata-Scalisi, F, Vidales Moreno, C, Stock, F, Avendaño, A, Araque, D, Lacruz-Rengel, M A, Diociaiuti, A, Bellacchio, E, Callea, M

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PRIMARY ADRENAL INSUFFICIENCY SECONDARY TO CHRONIC POSACONAZOLE USE by Araque, Daniela Pirela, Zuniga, Gabriela, Ayala, Alejandro R

“…Posaconazole (PSO) is commonly used in the treatment of invasive fungal infections. PSO-induced primary adrenal insufficiency (PAI) is rare, and we present…”
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Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene by Cammarata-Scalisi, F, Natsuga, K, Toyonaga, E, Nishie, W, Shimizu, H, Avendaño, A, Araque, D, Da Silva, G, Bellacchio, E, Callea, M

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Mosaic trisomy 13 by Cammarata-Scalisi, F, Araque, D, Lacruz-Rengel, M A, Valera-Ruíz, B

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Amyloid Goiter in a Patient with Cystic Fibrosis by Omiste, Antonio, Maldonado-Araque, Cristina, Olveira, Casilda, Mellado, Jose, Olveira, Gabriel

“…Objective: Amyloidosis (AA) is a disorder characterized by the local or systemic deposition of amorphous fibrous material. The most commonly affected organs…”
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