Publications by authors named "Pedro Louro"

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A Comparison Study of Deep Learning Methodologies for Music Emotion Recognition.
Pedro Lima Louro, Hugo Redinho, Ricardo Malheiro, Rui Pedro Paiva, Renato Panda

Sensors (Basel)· March 2024

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A high affinity and specificity anti-HER2 single-domain antibody (VHH) that targets trastuzumab's epitope with versatile biochemical, biological, and medical applications.
Shahryar Khoshtinat Nikkhoi, Hediyeh Heydarzadeh, Venu Gopal Vandavasi, Ge Yang, Pedro Louro

Immunol Res· February 2024

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Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Francesca Peluso, Stefano G Caraffi, Gianluca Contrò, Lara Valeri, Manuela Napoli, Pedro Louro

J Med Genet· November 2023

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ANKRD11 pathogenic variants and 16q24.3 microdeletions share an altered DNA methylation signature in patients with KBG syndrome.
Zain Awamleh, Sanaa Choufani, Cheryl Cytrynbaum, Fowzan S Alkuraya, Stephen Scherer, Pedro Louro

Hum Mol Genet· April 2023

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A Collective Intelligence Platform to Support Older Cancer Survivors: Towards the Definition of LifeChamps System and Big Data Reference Architecture.
Zoe Valero-Ramon, Pedro Louro, Luis Irio, Ilias Dimitriadis, Marinos Poiitis

Stud Health Technol Inform· June 2022

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Challenges and Considerations on Risk-Reducing Surgery in Patients with Advanced Breast Cancer.
Leonor Vasconcelos de Matos, Leonor Fernandes, Pedro Louro, Ana Plácido, Manuel Barros

Curr Oncol· January 2021

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Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental Diseases.
Uirá Souto Melo, Robert Schöpflin, Rocio Acuna-Hidalgo, Martin Atta Mensah, Björn Fischer-Zirnsak, Pedro Louro

Am J Hum Genet· June 2020

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Woodhouse-Sakati Syndrome: First report of a Portuguese case.
Pedro Louro, João Durães, Diana Oliveira, Sandra Paiva, Lina Ramos

Am J Med Genet A· November 2019

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16q22.1 microdeletion and anticipatory guidance.
Sarah Abdullah, Mayada Helal, Lucie Dupuis, D James Stavropoulos, Pedro Louro

Am J Med Genet A· July 2019

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Reciprocal nerve staining (RNS) for the concurrent detection of choline acetyltransferase and myelin basic protein on paraffin-embedded sections.
Antonio Merolli, Pedro Louro, Joachim Kohn

J Neurosci Methods· January 2019

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Development of a Device-Assisted Nerve-Regeneration Procedure in Disruptive Lesions of the Brachial Plexus.
Antonio Merolli, Maria Lucia Manunta, Yong Mao, Gerolamo Masala, Giovanni Mario Careddu, Pedro Louro

J Reconstr Microsurg· July 2018

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Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
Mira Kharbanda, Daniela T Pilz, Susan Tomkins, Kate Chandler, Anand Saggar, Pedro Louro

Eur J Med Genet· February 2017

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Phenotyping GABA transaminase deficiency: a case description and literature review.
Pedro Louro, Lina Ramos, Conceição Robalo, Cândida Cancelinha, Alexandra Dinis

J Inherit Metab Dis· September 2016

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Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations.
Charlotte W Ockeloen, Marjolein H Willemsen, Sonja de Munnik, Bregje W M van Bon, Nicole de Leeuw, Pedro Louro

Eur J Hum Genet· September 2015

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Further delineation of the KBG syndrome caused by ANKRD11 aberrations.
Charlotte W Ockeloen, Marjolein H Willemsen, Sonja de Munnik, Bregje W M van Bon, Nicole de Leeuw, Pedro Louro

Eur J Hum Genet· September 2015

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