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Dose volume histogram constraints in patients with head and neck cancer treated with surgery and adjuvant HDR brachytherapy: A proposal of the head and neck and skin GEC ESTRO Working group

Radiotherapy and oncology, 2021-01, Vol.154, p.128-134

2021

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Neoadjuvant chemotherapy without radiotherapy for patients with locally advanced rectal cancer. Oncologic outcomes

Revista española de enfermedades digestivas, 2020-01, Vol.112 (1), p.16

2020

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Missense mutations have unexpected consequences: The McArdle disease paradigm

Human mutation, 2018-10, Vol.39 (10), p.1338-1343

2018

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Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis

International journal of molecular sciences, 2022-04, Vol.23 (9), p.4650

2022

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Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report

Genes, 2020-07, Vol.11 (8), p.855

2020

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A transcriptomic approach to search for novel phenotypic regulators in McArdle disease

PloS one, 2012-02, Vol.7 (2), p.e31718-e31718

2012

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Expression of glycogen phosphorylase isoforms in cultured muscle from patients with McArdle's disease carrying the p.R771PfsX33 PYGM mutation

PloS one, 2010-10, Vol.5 (10), p.e13164

2010

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Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry

Journal of neurology, neurosurgery and psychiatry, 2012-03, Vol.83 (3), p.322-328

2012

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Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update

BMC genomics, 2017-11, Vol.18 (Suppl 8), p.819-819, Article 819

2017

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Alternative treatments for oral bisphosphonate-related osteonecrosis of the jaws: a pilot study comparing fibrin rich in growth factors and teriparatide

Medicina oral, patología oral y cirugía bucal, 2014-07, Vol.19 (4), p.e320-e326

2014

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Bisphosphonate-related osteonecrosis associated with dental implants: a microcomputed tomography study

Implant dentistry, 2014-06, Vol.23 (3), p.258-263

2014

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Epidemiology, pharmacology and clinical characterization of bisphosphonate-related osteonecrosis of the jaw. A retrospective study of 70 cases

Acta otorrinolaringologica espanola, 2015-05, Vol.66 (3), p.139

2015

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Genotype modulators of clinical severity in McArdle disease

Neuroscience letters, 2007-07, Vol.422 (3), p.217-222

2007

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A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patients

Human mutation, 2007-02, Vol.28 (2), p.203-204

2007

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Expression of the muscle glycogen phosphorylase gene in patients with McArdle disease: the role of nonsense-mediated mRNA decay

Human mutation, 2008-02, Vol.29 (2), p.277-283

2008

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Sinus Mucosal Thickening in Bisphosphonate-Related Osteonecrosis of the Jaws: A Case-Control Study

O.R.L. Journal for oto-rhino-laryngology and its related specialties, 2014-01, Vol.76 (4), p.199-206

2014

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A "man-in-the-middle" approach for enhancing legacy safety-critical Avionics systems

2023 IEEE/AIAA 42nd Digital Avionics Systems Conference (DASC), 2023, p.1-6

2023

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IEEE_Xplore

AMPD1 Genotypes and Exercise Capacity in McArdle Patients

International journal of sports medicine, 2008-04, Vol.29 (4), p.331-335

2008

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Epidemiología, farmacología y caracterización clínica de la osteonecrosis de los maxilares. Un estudio retrospectivo de 70 casos

Acta otorrinolaringológica española, 2015-05, Vol.66 (3), p.139-147

2015

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Epidemiology, Pharmacology and Clinical Characterization of Bisphosphonate-related Osteonecrosis of the Jaw. A Retrospective Study of 70 Cases

Acta otorrinolaringológica española (English), 2015-05, Vol.66 (3), p.139-147

2015

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Expression of Glycogen Phosphorylase Isoforms in Cultured Muscle from Patients with McArdle´s Disease Carrying the p.R771PfsX33 PYGM Mutation

PloS one, 2010-10

2010

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Taking advantage of an old concept, “illegitimate transcription”, for a proposed novel method of genetic diagnosis of McArdle disease

Genetics in medicine, 2016-11, Vol.18 (11), p.1128-1135

2016

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PP113: Sinus mucosal involvement in patients with bisphosphonate-related osteonecrosis of the jaw

Oral oncology, 2013-05, Vol.49, p.S132-S132

2013

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PP113

Oral oncology, 2013-05, Vol.49, p.S132-S132

2013

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Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report

Genes, 2020, Vol.11 (8)

2020

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Dose volume histogram constraints in patients with head and neck cancer treated with surgery and adjuvant HDR brachytherapy: A proposal of the head and neck and skin GEC ESTRO Working group

Neoadjuvant chemotherapy without radiotherapy for patients with locally advanced rectal cancer. Oncologic outcomes

Missense mutations have unexpected consequences: The McArdle disease paradigm

Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis

Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report

A transcriptomic approach to search for novel phenotypic regulators in McArdle disease

Expression of glycogen phosphorylase isoforms in cultured muscle from patients with McArdle's disease carrying the p.R771PfsX33 PYGM mutation

Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry

Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update

Alternative treatments for oral bisphosphonate-related osteonecrosis of the jaws: a pilot study comparing fibrin rich in growth factors and teriparatide

Bisphosphonate-related osteonecrosis associated with dental implants: a microcomputed tomography study

Epidemiology, pharmacology and clinical characterization of bisphosphonate-related osteonecrosis of the jaw. A retrospective study of 70 cases

Genotype modulators of clinical severity in McArdle disease

A proposed molecular diagnostic flowchart for myophosphorylase deficiency (McArdle disease) in blood samples from Spanish patients

Expression of the muscle glycogen phosphorylase gene in patients with McArdle disease: the role of nonsense-mediated mRNA decay

Sinus Mucosal Thickening in Bisphosphonate-Related Osteonecrosis of the Jaws: A Case-Control Study

A "man-in-the-middle" approach for enhancing legacy safety-critical Avionics systems

AMPD1 Genotypes and Exercise Capacity in McArdle Patients

Epidemiología, farmacología y caracterización clínica de la osteonecrosis de los maxilares. Un estudio retrospectivo de 70 casos

Epidemiology, Pharmacology and Clinical Characterization of Bisphosphonate-related Osteonecrosis of the Jaw. A Retrospective Study of 70 Cases

Expression of Glycogen Phosphorylase Isoforms in Cultured Muscle from Patients with McArdle´s Disease Carrying the p.R771PfsX33 PYGM Mutation

Taking advantage of an old concept, “illegitimate transcription”, for a proposed novel method of genetic diagnosis of McArdle disease

PP113: Sinus mucosal involvement in patients with bisphosphonate-related osteonecrosis of the jaw

PP113

Novel NDUFA13 Mutations Associated with OXPHOS Deficiency and Leigh Syndrome: A Second Family Report

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