Mario Matos

Hydrocephalus in children - A rare case of pineal cavernoma and literature review.

Authors:

Ricardo Malcata Nogueira Luis Santos Cardoso Lino Fonseca Miguel Correia Amets Iraneta Pedro Roque Mario Matos Manuela Mafra

Surg Neurol Int 2020 18;11:294. Epub 2020 Sep 18.

Department of Pathological Anatomy, Centro Hospitalar Universitario Lisboa Central, R. Jose Antonio Serrano, Lisbon, Lisbon, Portugal.

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September 2020

BRAF V600E mutation and 9p21: CDKN2A/B and MTAP co-deletions - Markers in the clinical stratification of pediatric gliomas.

Authors:

Laura Frazão Maria do Carmo Martins Vasco Moura Nunes José Pimentel Claudia Faria José Miguéns Amets Sagarribay Mário Matos Duarte Salgado Sofia Nunes Manuela Mafra Lúcia Roque

BMC Cancer 2018 Dec 17;18(1):1259. Epub 2018 Dec 17.

Unidade de Investigação em Patobiologia Molecular (UIPM) - IPOFG Cytogenetic Laboratory, Portuguese Cancer Institute, R. Professor Lima Basto, 1099-023, Lisbon, Portugal.

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December 2018

Mutations in ATP6V1B1 and ATP6V0A4 genes cause recessive distal renal tubular acidosis in Mexican families.

Authors:

Laura I Escobar Christopher Simian Cyrielle Treard Donia Hayek Carolina Salvador Norma Guerra Mario Matos Mara Medeiros Sandra Enciso María Dolores Camargo Rosa Vargas-Poussou

Mol Genet Genomic Med 2016 May 14;4(3):303-11. Epub 2016 Feb 14.

Département de Génetique Hôpital Européen Georges Pompidou Paris France.

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May 2016

Intraventricular colistin in Gram-negative ventriculoperitoneal shunt infection in two pediatric patients.

Authors:

Ana Sofia Santos Amets Iraneta Mário Matos Maria Joao Brito

Acta Neurochir (Wien) 2015 Dec 22;157(12):2219-20. Epub 2015 Sep 22.

Pediatric Infectious Diseases Unit, Hospital Dona Estefânia, CHLC, Lisbon, Portugal.

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December 2015

Serum markers of low-turnover bone disease in Mexican children with chronic kidney disease undergoing dialysis.

Authors:

Marcela Avila-Díaz Mario Matos Elvia García-López María-del-Carmen Prado Florencia Castro-Vázquez María-de-Jesús Ventura Elia González Dante Amato Ramón Paniagua

Perit Dial Int 2006 Jan-Feb;26(1):78-84

Unidad de Investigación Médica en Enfermedades Nefrológicas, Hospital de Especialidades, Centro Médico Nacional Siglo XXI, México DF, México.

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June 2006

Publications by authors named "Mario Matos"

Hydrocephalus in children - A rare case of pineal cavernoma and literature review.

Authors:

BRAF V600E mutation and 9p21: CDKN2A/B and MTAP co-deletions - Markers in the clinical stratification of pediatric gliomas.

Authors:

Mutations in ATP6V1B1 and ATP6V0A4 genes cause recessive distal renal tubular acidosis in Mexican families.

Authors:

Intraventricular colistin in Gram-negative ventriculoperitoneal shunt infection in two pediatric patients.

Authors:

Serum markers of low-turnover bone disease in Mexican children with chronic kidney disease undergoing dialysis.

Authors: