Publications by authors named "Yolanda Martin"

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Women from rural Guatemala who speak Mayan languages have reduced odds of diabetes, hypertension and obesity.
Stephen Alajajian, Anahí Venzor Strader, Yolanda Juarez Martin, Caitlin Scott, Peter Rohloff

Front Public Health· July 2025

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Prevalence of diabetes among Indigenous women in Guatemala: a retrospective chart review.
Stephen Alajajian, Jenny Bartolimin, Yolanda Juarez Martin, Caitlin Scott, Peter Rohloff

BMC Res Notes· July 2024

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Prevalence of diabetes among Indigenous women in Guatemala: A retrospective chart review study of 13 643 patients between 2015-2022.
Stephen Alajajian, Jenny Bartolimin, Yolanda Juarez Martin, Caitlin Scott, Peter Rohloff

medRxiv· January 2024

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Successful Pregnancy and Cancer Outcomes With Ipilimumab and Nivolumab for Metastatic Renal Cell Carcinoma: Case Report and Review of the Literature.
Francisco Zambrana, Carmen Barbancho, Miriam Huelves, Belén García de Santiago, Yolanda Martín

J Immunother· January 2023

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Neurofibromatosis type 1 families with first-degree relatives harbouring distinct pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?
Belen Garcia, Nuria Catasus, Andrea Ros, Inma Rosas, Alejandro Negro, Yolanda Martin

J Med Genet· October 2022

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Prognostic value of somatosensory-evoked potentials in the newborn with hypoxic-ischemic encephalopathy after the introduction of therapeutic hypothermia.
María Arriaga-Redondo, Dorotea Blanco Bravo, Alejandra Aguado Del Hoyo, Ana Polo Arrondo, Yolanda Ruiz Martín

Eur J Pediatr· April 2022

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National protocol led to significant improvements in follow-up programmes for very low birth weight or very preterm infants.
Begoña Loureiro, Javier De la Cruz Bértolo, Dorotea Blanco, Gemma Ginovart, Ana Jiménez

Acta Paediatr· August 2021

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Co-occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2.
Ramón Peces, Rocío Mena, Yolanda Martín, Concepción Hernández, Carlos Peces

Mol Genet Genomic Med· August 2020

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Molecular characterization of Latin American invasive Streptococcus pneumoniae serotype 19A isolates.
Jaime Moreno, Carolina Duarte, Ana Paula Cassiolato, Grettel Chanto Chacón, Pedro Alarcon

Vaccine· April 2020

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Polyvinyl alcohol cryogel phantoms of biological tissues for wideband operation at microwave frequencies.
Natalia Arteaga-Marrero, Enrique Villa, Javier González-Fernández, Yolanda Martín, Juan Ruiz-Alzola

PLoS One· March 2020

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Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1.
Magdalena Koczkowska, Tom Callens, Yunjia Chen, Alicia Gomes, Alesha D Hicks, Martin B Delatycki, Mayra Martinez Ojeda, Yolanda Martin

Hum Mutat· January 2020

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Spanish survey on follow-up programmes for children born very preterm.
Carmen Rosa Pallás-Alonso, Begoña Loureiro, Javier De la Cruz Bértolo, Pilar García, Gemma Ginovart

Acta Paediatr· June 2019

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Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.
Magdalena Koczkowska, Tom Callens, Alicia Gomes, Angela Sharp, Yunjia Chen, Mayra Martinez Ojeda, Yolanda Martin

Genet Med· April 2019

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Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.
Magdalena Koczkowska, Tom Callens, Alicia Gomes, Angela Sharp, Yunjia Chen, Mayra Martinez Ojeda, Yolanda Martin

Genet Med· March 2019

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Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.
Magdalena Koczkowska, Yunjia Chen, Tom Callens, Alicia Gomes, Angela Sharp, Yolanda Martin

Am J Hum Genet· January 2018

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Obstetric care navigation: a new approach to promote respectful maternity care and overcome barriers to safe motherhood.
Kirsten Austad, Anita Chary, Boris Martinez, Michel Juarez, Yolanda Juarez Martin

Reprod Health· November 2017

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Agreement between a simple dyspnea-guided treatment algorithm for stable COPD and the GOLD guidelines: a pilot study.
Carlos Cabrera, Ciro Casanova, Yolanda Martín, Virginia Mirabal, María Del Carmen Sánchez

Int J Chron Obstruct Pulmon Dis· August 2017

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Adams-Oliver Syndrome with Unusual Central Nervous System Findings and an Extrahepatic Portosystemic Shunt.
Carlos Pérez-García, Yolanda Ruíz Martín, Alejandra Aguado Del Hoyo, Carlos Marín Rodríguez, Minia Campos Domínguez

Pediatr Rep· June 2017

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Functional PTGS2 polymorphism-based models as novel predictive markers in metastatic renal cell carcinoma patients receiving first-line sunitinib.
Arancha Cebrián, Teresa Gómez Del Pulgar, María José Méndez-Vidal, María Luisa Gonzálvez, Nuria Lainez, Yolanda Martin

Sci Rep· January 2017

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Functional Analysis of Mutations in Exon 9 of NF1 Reveals the Presence of Several Elements Regulating Splicing.
Elisabete Hernández-Imaz, Yolanda Martín, Laura de Conti, German Melean, Ana Valero

PLoS One· June 2016

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High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phenotype Correlation.
Kitiwan Rojnueangnit, Jing Xie, Alicia Gomes, Angela Sharp, Tom Callens, Martin G Bialer, Yolanda Martin

Hum Mutat· November 2015

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Two-weekly dose-adjusted (DA)-EPOCH-like chemotherapy with high-dose dexamethasone plus rituximab (DA-EDOCH14-R) in poor-prognostic untreated diffuse large B-cell lymphoma.
Julio García-Suárez, Elena Flores, Marta Callejas, Ignacio Arribas, Juan-José Gil-Fernández

Br J Haematol· February 2013

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RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomas.
German Melean, Ana Velasco, Elisabete Hernández-Imaz, Francisco Javier Rodríguez-Álvarez, Yolanda Martín

Neurogenetics· August 2012

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Progress and challenges in developing a molecular diagnostic test for neurofibromatosis type 1.
Yolanda Martín, Ana Dopazo, Concepción Hernández-Chico

Expert Rev Mol Diagn· September 2011

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A highly sensitive genetic protocol to detect NF1 mutations.
María Carmen Valero, Yolanda Martín, Elisabete Hernández-Imaz, Alba Marina Hernández, Germán Meleán

J Mol Diagn· March 2011

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