Author details

Full Name

David G??mez-Andr??s

Affiliation

Vall d'Hebron University Hospital and VHIR (Euro-NMD

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37503136	The Medical Action Ontology: A Tool for Annotating and Analyzing Treatments and Clinical Management of Human Disease.	medRxiv	2023
37963467	The Medical Action Ontology: A tool for annotating and analyzing treatments and clinical management of human disease.	Med	2023
37521501	Internet of medical things. Measurement of respiratory dynamics using wearable sensors in post-COVID-19 patients.	Enfoque UTE	2023
34559299	Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort.	J Neurol	2022
35782747	Gait analysis under the lens of statistical physics.	Comput Struct Biotechnol J	2022
36365918	Toward an Automatic Assessment of Cognitive Dysfunction in Relapsing-Remitting Multiple Sclerosis Patients Using Eye Movement Analysis.	Sensors (Basel)	2022
35214383	Eye Movement Alterations in Post-COVID-19 Condition: A Proof-of-Concept Study.	Sensors (Basel)	2022
35241415	Delphi consensus on recommendations for the treatment of spinal muscular atrophy in Spain (RET-AME consensus).	Neurologia (Engl Ed)	2022
35030636	"Leukodystrophy-Like" Phenotype in Anti-MOG Antibody-Associated Disorders.	Neuropediatrics	2022
34238719	Treatment of patients with spinal muscular atrophy 5q: towards a new protocol.	Neurologia (Engl Ed)	2021
33597769	DLG4-related synaptopathy: a new rare brain disorder.	Genet Med	2021
33752678	Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome.	Orphanet J Rare Dis	2021
34736625	Two decades of advances in muscle imaging in children: from pattern recognition of muscle diseases to quantification and machine learning approaches.	Neuromuscul Disord	2021
34240052	International retrospective natural history study of <i>LMNA</i>-related congenital muscular dystrophy.	Brain Commun	2021
32380746	Consumption of Goat Cheese Naturally Rich in Omega-3 and Conjugated Linoleic Acid Improves the Cardiovascular and Inflammatory Biomarkers of Overweight and Obese Subjects: A Randomized Controlled Trial.	Nutrients	2020
32770013	Retinal and brain damage during multiple sclerosis course: inflammatory activity is a key factor in the first 5 years.	Sci Rep	2020
32875335	New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy.	Brain	2020
32787960	A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome.	Orphanet J Rare Dis	2020
32410949	MCT8 Deficiency: The Road to Therapies for a Rare Disease.	Front Neurosci	2020
30476213	Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources.	Nucleic Acids Res	2019
31727541	MYO-MRI diagnostic protocols in genetic myopathies.	Neuromuscul Disord	2019
30578674	Disease duration and disability in dysfeRlinopathy can be described by muscle imaging using heatmaps and random forests.	Muscle Nerve	2019
29624713	Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvement.	Muscle Nerve	2018
33265160	Characterizing Normal and Pathological Gait through Permutation Entropy.	Entropy (Basel)	2018
30066418	Muscle imaging in laminopathies: Synthesis study identifies meaningful muscles for follow-up.	Muscle Nerve	2018
29518090	Gait phenotypes in paediatric hereditary spastic paraplegia revealed by dynamic time warping analysis and random forests.	PLoS One	2018
26909158	Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit.	Cerebellum Ataxias	2016
26573435	Muscle imaging in muscle dystrophies produced by mutations in the EMD and LMNA genes.	Neuromuscul Disord	2016
26670690	Pediatric laminopathies: Whole-body magnetic resonance imaging fingerprint and comparison with Sepn1 myopathy.	Muscle Nerve	2016
24529924	'SARAgraph': a proposed graphic system for representing ataxia progression.	Neurologia	2015
25808192	Whole-body muscle magnetic resonance imaging in SEPN1-related myopathy shows a homogeneous and recognizable pattern.	Muscle Nerve	2015
24610691	[External evaluation of gait and functional changes after a single-session multiple myofibrotenotomy in school-aged children with spastic diplegia].	Rev Neurol	2014
25083788	Abnormal motor phenotype at adult stages in mice lacking type 2 deiodinase.	PLoS One	2014
22703633	Gait parameters in a reference sample of healthy Spanish schoolchildren: multivariate descriptive statistics and asymmetries observed in left and right cycles.	Neurologia	2013

1 - 34 of 34

Hernan Gonorazky

The Hospital for Sick Children, University of Toronto

Career Start Year 2014

Number of shared co-authors 5

Jonathan D Santoro

Children's Hospital Los Angeles

Career Start Year 2013

Number of shared co-authors 0

William T Triplett

College of Public Health and Health Professions, University of Florida

Career Start Year 2013

Number of shared co-authors 0

Vamshi K Rao

Lurie Children's Hospital of Chicago

Career Start Year 2010

Number of shared co-authors 0

Susan Byrne

Royal College of Surgeons in Ireland

Career Start Year 2010

Number of shared co-authors 1

Timothy Feyma

200 University Ave E

Career Start Year 2008

Number of shared co-authors 3

Kush Kapur

Boston Children's Hospital, Harvard Medical School

Career Start Year 2008

Number of shared co-authors 0

Erika Molteni

King's College London

Career Start Year 2007

Number of shared co-authors 0

Michael Scheel

Charite School of Medicine and University Hospital Berlin

Career Start Year 2007

Number of shared co-authors 1

Mohammad Salajegheh

VA Boston Healthcare System

Career Start Year 2005

Number of shared co-authors 0

Athina Papadopoulou

University Hospital Basel

Career Start Year 2003

Number of shared co-authors 2

Francisco A Perez

Seattle Children's Hospital

Career Start Year 2000

Number of shared co-authors 0

Hugh J McMillan

Montreal Children's Hospital, McGill University

Career Start Year 1997

Number of shared co-authors 4

Kathryn J Swoboda

Center for Genomic Medicine, Massachusetts General Hospital

Career Start Year 1994

Number of shared co-authors 5

Petra Kaufmann

Novartis Gene Therapies

Career Start Year 1994

Number of shared co-authors 15

Yuko Shimizu

Tokyo Women's Medical University School of Medicine

Career Start Year 1992

Number of shared co-authors 0

Ros Quinlivan

The Institute of Neurology, National Hospital for Neurology and Neurosurgery

Career Start Year 1992

Number of shared co-authors 12

Peter Hedera

University of Louisville

Career Start Year 1992

Number of shared co-authors 1

Kate Bushby

Institute of Genetic Medicine, International Centre for Life

Career Start Year 1991

Number of shared co-authors 16

Isabella Moroni

Fondazione IRCCS Istituto Neurologico Carlo Besta

Career Start Year 1990

Number of shared co-authors 5

Lefkos T Middleton

Ageing Epidemiology Research Unit, School of Public Health, Imperial College London

Career Start Year 1988

Number of shared co-authors 0

Camilo Toro

National Human Genome Research Institute, National Institutes of Health

Career Start Year 1986

Number of shared co-authors 20

Kathryn N North

Murdoch Children's Research Institute

Career Start Year 1984

Number of shared co-authors 10

Andrea Martinuzzi

Scientific Institute, IRCCS Eugenio Medea, Conegliano-Pieve di Soligo Research Centre

Career Start Year 1984

Number of shared co-authors 2

Basil T Darras

Boston Children's Hospital, Harvard Medical School

Career Start Year 1983

Number of shared co-authors 5

Nancy L Kuntz

Lurie Children's Hospital

Career Start Year 1982

Number of shared co-authors 4

Jonathan W Mink

University of Rochester Medical Center

Career Start Year 1981

Number of shared co-authors 1

Richard S Finkel

Center for Experimental Neurotherapeutics, St. Jude Children's Research Hospital

Career Start Year 1979

Number of shared co-authors 4

Alexandra Durr

Sorbonne University, Paris Brain Institute - ICM, Inserm, CNRS

Career Start Year 1975

Number of shared co-authors 5

David J Burn

Population Health Sciences Institute, Newcastle University

Career Start Year 1975

Number of shared co-authors 10

row(s) 1 - 30 of 30

Hanns Lochm??ller

Children's Hospital of Eastern Ontario Research Institute

Co-authored papers 5

Leigh C Carmody

Center for the Science of Therapeutics, Broad Institute of MIT and Harvard

Co-authored papers 5

Rachel Thompson

Children's Hospital of Eastern Ontario Research Institute

Co-authored papers 5

Hannah Blau

Co-authored papers 3

Morgan Similuk

National Institute of Allergy and Infectious Diseases, National Institutes of Health

Co-authored papers 3

Christopher J Mungall

International Society for Biocuration, Lawrence Berkeley National Laboratory, University of Edinburgh, University of Edinburgh School of Biological Sciences

Co-authored papers 3

Melissa A Haendel

Co-authored papers 3

Nicole Vasilevsky

Critical Path Institute

Co-authored papers 3

Michael Gargano

Co-authored papers 3

Sergi Beltran

Hospital Universitari Vall d'Hebron

Co-authored papers 3

Melissa A Haendel

American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison

Co-authored papers 3

Teresa N Sparks

University of California san francisco

Co-authored papers 2

Leslie Matalonga

The Barcelona Institute of Science and Technology

Co-authored papers 2

Emilia M Swietlik

University of Cambridge, Heart and Lung Research Institute

Co-authored papers 2

Markus S Ladewig

University of Colorado Anschutz Medical Campus