Publications by authors named "Soledad Rodriguez"

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Identification of a novel SACS gene mutation leading to spastic ataxia Charlevoix-Saguenay type: a case report.
Víctor Raggio, Andrea Rey, Camila Simoes, Florencia Birriel, Soledad Rodriguez

J Med Case Rep· August 2025

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[Educational intervention as a prevention strategy for intestinal parasitosis, and assessment of the enteroparasitological status in child development centers in the city of Santa Fe, Argentina].
César Ernesto Gutiérrez, María Agustina Jaras Horno, Carolina Aro, Andrea Florencia Gómez Colussi, María Belén Cheirano

Rev Argent Microbiol· April 2025

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Effects of Fermentation Temperature, Drying Temperature, Caliber Size, Starter Culture, and Sodium Lactate on Listeria monocytogenes Inactivation During Salami Production.
Giannina Brugnini, Jesica Rodríguez, Soledad Rodríguez, Inés Martínez, Ronny Pelaggio

J Food Prot· June 2024

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Two compound heterozygous variants in the gene are responsible for neuronal cereidolipofuscinoses disorder in a child: a case report.
Federico Baltar, Camila Simoes, Francisco Garagorry, Martín Graña, Soledad Rodríguez

Front Pediatr· May 2024

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Exome Sequencing Reveals Biallelic Mutations in Gene in a Girl with a Very Rare Skeletal Dysplasia.
Víctor Raggio, Soledad Rodríguez, Sandra Feder, Rosario Gueçaimburú, Lucía Spangenberg

Diagnostics (Basel)· January 2024

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Fibrodysplasia ossificans progressiva in a 3-year-old female patient.
Cecilia Moreira, Gabriel Dapueto, Gabriel Peluffo, Alejandra Vomero, Alejandra Tapié

Bol Med Hosp Infant Mex· March 2023

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Computational and mitochondrial functional studies of novel compound heterozygous variants in SPATA5 gene support a causal link with epileptogenic encephalopathy.
Víctor Raggio, Martín Graña, Erik Winiarski, Santiago Mansilla, Camila Simoes

Hum Genomics· February 2023

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Suspected adverse events following immunization against SARS-CoV2 in a university hospital in 2021: Observational study.
Dolores Rodríguez, Pilar Ordoñez, Roser Llop, Sebastián Videla, Aurema Otero, Soledad Rodriguez

Medicine (Baltimore)· October 2022

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Novel frameshift mutation in LIS1 gene is a probable cause of lissencephaly: a case report.
Camila Simoes, Martín Graña, Soledad Rodriguez, Federico Baltar Yanes, Alejandra Tapié

BMC Pediatr· September 2022

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Novel frameshift mutation in PURA gene causes severe encephalopathy of unclear cause.
Lucía Spangenberg, Rosario Guecaimburú, Alejandra Tapié, Susana Vivas, Soledad Rodríguez

Mol Genet Genomic Med· May 2021

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Whole genome sequencing reveals a frameshift mutation and a large deletion in YY1AP1 in a girl with a panvascular artery disease.
Víctor Raggio, Nicolas Dell'Oca, Camila Simoes, Alejandra Tapié, Conrado Medici, Soledad Rodriguez

Hum Genomics· May 2021

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Effect of UV-C Irradiation and Lactic Acid Application on the Inactivation of and Lactic Acid Bacteria in Vacuum-Packaged Beef.
Giannina Brugnini, Soledad Rodríguez, Jesica Rodríguez, Caterina Rufo

Foods· May 2021

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Perceived Social Support from Significant Others among Binge Drinking and Polyconsuming Spanish University Students.
Carolina Tinajero, Fernando Cadaveira, M Soledad Rodríguez, M Fernanda Páramo

Int J Environ Res Public Health· November 2019

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Effective determination of ampicillin in cow milk using a molecularly imprinted polymer as sorbent for sample preconcentration.
B Soledad-Rodríguez, P Fernández-Hernando, R M Garcinuño-Martínez, J S Durand-Alegría

Food Chem· June 2017

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[Guidelines for the prevention and control of tuberculosis in health care workers].
Irma Casas, Jose Dominguez, Soledad Rodríguez, Joan Matllo, Neus Altet

Med Clin (Barc)· December 2015

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Occurrence of erythromycin residues in sheep milk. Validation of an analytical method.
M A García-Mayor, G Paniagua-González, B Soledad-Rodríguez, R M Garcinuño-Martínez, P Fernández-Hernando

Food Chem Toxicol· April 2015

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Digits backward and the children's embedded figures test among school-age Spanish children.
M Adelina Guisande, M Soledad Rodríguez, Leandro S Almeida, Carolina Tinajero, M Fernanda Páramo

Percept Mot Skills· December 2008

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Thrombin generation in platelet-poor plasma is normal in patients with hereditary mucocutaneous haemorrhages.
Teresa Quiroga, Manuela Goycoolea, Peter L A Giesen, María Morales, Blanca Muñoz

Pathophysiol Haemost Thromb· April 2004

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[Hemolytic-uremic syndrome].
S Figueroa, A Bidegain, M Soledad Rodríguez, W Rodríguez, J Valenzuela

Rev Chil Pediatr· April 1988

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