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Parkinsonism & Related Disorders|December 19, 2017
Before and after the veterans affairs cooperative program 468 study: Deep brain stimulator target selection for treatment of Parkinson's diseaseDerek G Southwell, Martin J Rutkowski, Marta San Luciano, et al.
Clinical Genetics|May 28, 2026
Novel Postzygotic Variants Associated With Hypomelanosis of Ito Expand the ACTB-Related Neurocutaneous Disease SpectrumEstella Castillon, Paul Rollier, Didier Bessis, et al.
Archives of Neurology|May 11, 2011
Mild cognitive impairment, dementia, and their subtypes in oldest old womenKristine Yaffe, Laura E Middleton, Li-Yung Lui, et al.
Neurobiology of Aging|April 27, 2010
Cognition, glucose metabolism and amyloid burden in Alzheimer's diseaseAnsgar J Furst, Gil D Rabinovici, Ara H Rostomian, et al.
Prenatal Diagnosis|June 26, 2024
Discovery of pathogenic variants in EFEMP2 and RAG1 and undetectable fetal phenotype: A challenge of prenatal exome sequencingMaud Favier, Rodolph Dard, Guillaume Gorincour, et al.
Acta Neuropathologica|October 31, 2009
Sporadic corticobasal syndrome due to FTLD-TDPMaria Carmela Tartaglia, Manu Sidhu, Victor Laluz, et al.
Human Brain Mapping|April 4, 2020
Global resting-state functional connectivity of neural oscillations in tinnitus with and without hearing lossCarly Demopoulos, Xuan Duong, Leighton B Hinkley, et al.
Molecular Genetics & Genomic Medicine|April 16, 2025
First Prenatal Case of Genotypically and Phenotypically Overlapping Double Molecular Diagnosis of Van den Ende-Gupta and 22q11.2 Deletion SyndromesCaroline Racine, Aurore Garde, Olivia Martz, et al.
European Journal of Medical Genetics|March 24, 2025
Lack of behavioural improvement with sirolimus in a patient with MTOR-related macrocephaly with pigmentary mosaicism: A new case reportBertille Bonniaud, Maxime Luu, Coline Cormier, et al.
Prenatal Diagnosis|February 11, 2024
Early prenatal diagnosis of causative homozygous variants in ASCC1 in a fetus with cystic hygroma and additional homozygous variants of unknown significance associated with a neurological phenotype not visible in early gestation: Dual diagnosis or not?Maud Favier, Julian Delanne, Guillaume Gorincour, et al.
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