Publications by authors named "J Sanchez Estella"

Article Synopsis
  • The study investigates the effectiveness of targeted next generation sequencing (NGS) for identifying chromosomal abnormalities in patients with myeloid neoplasms using plasma cell-free DNA (cfDNA) samples from 2821 patients.
  • Results showed that 54.5% of samples had mutations associated with neoplasms, with distinct rates of abnormalities observed in myeloid (59%) and lymphoid (41%) neoplasms, and a strong concordance between cfDNA NGS results and traditional bone marrow cytogenetic data.
  • The research concludes that liquid biopsy through targeted NGS is a reliable method for detecting chromosomal abnormalities, potentially offering an alternative to invasive bone marrow biopsies for monitoring
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Transcranial direct current stimulation is one of the non-invasive techniques whose main mechanism of action is based on its modulation of cortical excitability. The objective of this study is to analyze the variables (i.e, demographics, clinicals, stimulation parameters) that could influence into the responses during rehabilitation of the upper extremity in patients with stroke.

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Until very recently, we considered Virtual Reality as something that was very close, but it was still science fiction. However, today Virtual Reality is being integrated into many different areas of our lives, from videogames to different industrial use cases and, of course, it is starting to be used in medicine. There are two great general classifications for Virtual Reality.

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Patients with chronic lymphocytic leukemia (CLL) that develop resistance to Bruton tyrosine kinase (BTK) inhibitors are typically positive for mutations in BTK or phospholipase c gamma 2 (PLCγ2). We developed a high sensitivity (HS) assay utilizing wild-type blocking polymerase chain reaction achieved via bridged and locked nucleic acids. We used this high sensitivity assay in combination with Sanger sequencing and next generation sequencing (NGS) and tested cellular DNA and cell-free DNA (cfDNA) from patients with CLL treated with the BTK inhibitor, ibrutinib.

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Introduction: Detection of mutations in the myeloid differentiation primary response gene 88 (MYD88) has clinical implications on diagnosis and therapy, especially in patients with Waldenström's macroglobulinemia (WM) and IgM monoclonal gammopathy of unknown significance (IgM-MGUS). We describe a method that provides greatly increased sensitivity for detecting minority mutations in MYD88.

Methods: We used a locked nucleic acid oligonucleotide to block amplification of wild-type DNA during polymerase chain reaction (PCR).

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