Information theory approaches to improve glioma diagnostic workflows in surgical neuropathology

Autor: Lokman Cevik, Marilyn Vazquez Landrove, Mehmet Tahir Aslan, Vasilii Khammad, Francisco Jose Garagorry Guerra, Yolanda Cabello‐Izquierdo, Wesley Wang, Jing Zhao, Aline Paixao Becker, Catherine Czeisler, Anne Costa Rendeiro, Lucas Luis Sousa Véras, Maicon Fernando Zanon, Rui Manuel Reis, Marcus de Medeiros Matsushita, Koray Ozduman, M. Necmettin Pamir, Ayca Ersen Danyeli, Thomas Pearce, Michelle Felicella, Jennifer Eschbacher, Naomi Arakaki, Horacio Martinetto, Anil Parwani, Diana L. Thomas, José Javier Otero

Publikováno v: Brain pathology (Zurich, Switzerland). 32(5)

Aims Resource-strained healthcare ecosystems often struggle with the adoption of the World Health Organization (WHO) recommendations for the classification of central nervous system (CNS) tumors. The generation of robust clinical diagnostic aids and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::716b0acac826da43b3077320adeda1d8
https://pubmed.ncbi.nlm.nih.gov/35014126

Author response for 'Astrocyte Regional Heterogeneity Revealed Through Machine Learning‐based Glial Neuroanatomical Assays'

Autor: null Jessica Blackburn, null Michele Joana Alves, null Mehmet Tahir Aslan, null Lokman Cevik, null Jing Zhao, null Catherine M. Czeisler, null José Javier Otero

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d5e841f7d1225bf12366f09e65271ad
https://doi.org/10.1002/cne.25105/v3/response1

Neonatal apneic phenotype in a murine congenital central hypoventilation syndrome model is induced through non‐cell autonomous developmental mechanisms

Autor: Sakima A. Smith, Michele Joana Alves, Jillian Liu, Lisa A. Baer, Caroline C. Szujewski, Talita M. Silva, Mikayla Jones, Mehmet Tahir Aslan, Jose Otero, Thiago S. Moreira, Catherine Czeisler, Alfredo J. Garcia, Jessica Blackburn, Amber Kempton, Kristin I. Stanford, Jean-Charles Viemari, Diego Alzate-Correa, Marina Y. Shimada, Jessica Zuniga, Giuliana Zaza, Ana C. Takakura, Abby Silbaugh, Behiye Kaya, Silvio A. Fernandes-Junior, Elizabeth M. Burke

Publikováno v: Brain Pathology
Brain Pathology, Wiley, 2020, ⟨10.1111/bpa.12877⟩
Brain Pathology, 2020, ⟨10.1111/bpa.12877⟩
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

International audience; Congenital central hypoventilation syndrome (CCHS) represents a rare genetic disorder usually caused by mutations in the homeodomain transcription factor PHOX2B. Some CCHS patients suffer mainly from deficiencies in CO 2 and/o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf7041df13148a5fc016e444646f500e
https://hal.archives-ouvertes.fr/hal-03051874

Abstract 5222: Decoding >30 thousand individuals to analyze the most common genetic disorder: Hereditary hemochromatosis (HH)

Autor: Raghu Metpally, Ryan Colonie, Ferit Akova, David J. Carey, Heinric Williams, Aris Baras, Anita Mathew, John D. Overton, Mehmet Tahir Aslan, Nefize Sertac Kip, Marc S. Williams, Adam Cook

Publikováno v: Cancer Research. 76:5222-5222

Background: Hereditary hemochromatosis (HH), one of the most common single gene disorders that alter the body's ability to regulate iron, causes excess iron deposition in liver, heart, pancreas, joints and pituitary gland, with resultant cirrhosis, c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::193e7dd5897bfc1a1af97a0a6fc2a925
https://doi.org/10.1158/1538-7445.am2016-5222