Results 211 to 220 of about 3,788,707 (345)

An Analysis for IDH‐Mutant Grade 4 Astrocytoma Based on WHO CNS 5: Implication of Clinical Practice

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Purpose There is ongoing debate regarding the therapeutic approach and prognosis for IDH‐mutant grade 4 astrocytoma, a newly defined subtype of diffuse glioma in the 2021 WHO classification system for central nervous system tumors (WHO CNS 5). The aim of this study was to explore the clinical outcome and prognosticators for newly diagnosed IDH‐
Xianxin Qiu, Liping Liang, Lingchao Chen, Pengjie Hong, Wanzun Lin, Jiabing Liu, Zhirui Zhou, Wenjia Zhu, Tianqi Wu, Mingyuan Pan, Yihua Zhong, Jing Gao, Zhiyong Qin, Yang Wang   +13 more
wiley   +1 more source

Factors associated with antibiotic use during pregnancy in Sweden: a population-based cohort study. [PDF]

BMC Pregnancy Childbirth
Nakitanda AO, Pazzagli L, Pasternak B, Odsbu I.   +3 more
europepmc   +1 more source

THE QUENCHING OF THE IODINE FLUORESCENCE SPECTRUM [PDF]

, 1958
C. Arnot, C. A. McDowell
openalex   +1 more source

The contribution of de novo coding mutations to autism spectrum disorder

Nature, 2014
I. Iossifov, B. O’Roak, Stephan J Sanders, M. Ronemus, Niklas Krumm, D. Levy, H. Stessman, Kali T. Witherspoon, Laura Vives, Karynne E. Patterson, Joshua D. Smith, B. Paeper, D. Nickerson, Jeanselle Dea, Shan Dong, Luis E. Gonzalez, Jeffrey D. Mandell, S. Mane, M. Murtha, C. Sullivan, Michael F. Walker, Zainulabedin Waqar, Liping Wei, A. Willsey, B. Yamrom, Yoon-ha Lee, E. Grabowska, Ertugrul Dalkic, Zi-Hua Wang, S. Marks, P. Andrews, A. Leotta, J. Kendall, I. Hakker, J. Rosenbaum, Beicong Ma, L. Rodgers, J. Troge, G. Narzisi, Seungtai Yoon, M. Schatz, Kenny Q. Ye, W. McCombie, J. Shendure, E. Eichler, M. State, M. Wigler   +46 more
semanticscholar   +1 more source

Pathway Analyses of Inherited Neuropathies Identify Putative Common Mechanisms of Axon Degeneration

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Inherited neuropathies (IN) are associated with over 100 different genetic mutations presenting with a variety of phenotypes. This complexity suggests multiple pathways may converge onto a limited number of downstream pathways to effect axonal injury.
Christopher R. Cashman, Craig Blackstone, Reza Sadjadi   +2 more
wiley   +1 more source

Resonance-Enhanced Multiphoton Ionization Spectroscopy of Monocyclic and Polycyclic Aromatic Hydrocarbons in the Gas Phase. [PDF]

Rapid Commun Mass Spectrom
Schwarz C, Etscheidt F, Gehm C, Passig J, Ehlert S, Streibel T, Zimmermann R.   +6 more
europepmc   +1 more source

The Spectrum of o Ceti as photographed at Stonyhurst College Observatory [PDF]

, 1898
W. Sidgreaves
openalex   +1 more source

EEG Response to Sedation Interruption Complements Behavioral Assessment After Severe Brain Injury

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Accurate assessment of the level of consciousness and potential to recover in patients with severe brain injury underpins crucial decisions in the intensive care unit but remains a major challenge for the clinical team. The neurological wake‐up test is a widely used assessment tool. However, many patients' behavioral responses during
Charlotte Maschke, Loretta Norton, Catherine Duclos, Miriam Han, Kira Dolhan, Geoffrey Laforge, Allison Frantz, Xiaoyu Wang, Hassan Al‐Hayawi, Tianyu Zhang, Raphaël Lavoie, Adrian M. Owen, Stefanie Blain‐Moraes   +12 more
wiley   +1 more source

Light on Catalytic Reaction Mechanisms: Uncovering the Conformation of Thiourea-Based Organocatalysts and Their Interaction with Nitroolefins Using Mid-infrared Spectroscopy. [PDF]

J Phys Chem Lett
Ferrari P, Lemmens AK, Buma WJ.
europepmc   +1 more source

Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To provide a comprehensive clinical and genetic characterization of individuals with arthrogryposis multiplex congenita (AMC), focusing on the distribution of genetic etiologies across the neuromuscular spectrum and comparing myogenic and neurogenic subtypes. Methods A total of 105 individuals with AMC were clinically and genetically
Florencia Pérez‐Vidarte, Berta Estévez‐Arias, Leslie Matalonga, Delia Yubero, Anna Codina, Carlos Ortez, Julita Medina, Lidia DeSena DeCabo, Laura Carrera‐García, Jesica Expósito‐Escudero, Cristina Jou, Eduardo F. Tizzano, Andres Nascimento, Daniel Natera‐de Benito   +13 more
wiley   +1 more source