Results 261 to 270 of about 600,045 (285)

Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG)

Journal of Inherited Metabolic Disease, 2017
V. de Diego, A. Martínez-Monseny, J. Muchart, D. Cuadras, R. Montero, R. Artuch, C. Pérez-Cerdá, B. Perez, B. Pérez-Dueñas, A. Poretti, M. Serrano, S. Aguilera-Albesa, R. C. Candela, M. Marina, F. Carratalá, M. Couce, A. Felipe, Óscar García, M. García-Silva, L. Gutiérrez-Solana, A. Macaya, Maria Concepción Miranda, L. López, E. López-Laso, M. Póo, P. Quijada-Fraile, B. Robles, C. Sierra-Córcoles, Ramón Velázquez Fragua   +28 more
semanticscholar   +1 more source

Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy

Genetics in Medicine, 2022
Takafumi Sakakibara, Jun Tohyama, Yume Suzuki   +2 more
exaly  

Cerebellar Atrophy in Multiple System Atrophy (Cerebellar Type) and Its Implication for Network Connectivity

Cerebellum, 2020
Zhiqun Wang, Shaozhen Ji, Zhigang Chen
exaly  

Cerebellar degeneration with hodgkin's disease

Ca-A Cancer Journal for Clinicians, 1979
Paul P. Carbone
exaly  

Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures

Human Genetics, 2016
B. Tabarki, Nabil A. Almajhad, A. Alhashem, R. Shaheen, F. Alkuraya   +4 more
semanticscholar   +1 more source

Milder progressive cerebellar atrophy caused by biallelic SEPSECS mutations

Journal of Human Genetics, 2016
Kazuhiro Iwama, M. Sasaki, S. Hirabayashi, Chihiro Ohba, E. Iwabuchi, S. Miyatake, M. Nakashima, N. Miyake, S. Ito, H. Saitsu, N. Matsumoto   +10 more
semanticscholar   +1 more source

Cerebellar Atrophy in Adult Survivors of Childhood Cerebellar Tumor

Journal of the International Neuropsychological Society, 2016
Alyssa S. Ailion, Tricia Z. King, Li-Ya Wang, E. Michelle, H. Mao, Robin Morris, B. Crosson   +6 more
semanticscholar   +1 more source

Atrophy of the Cerebellar Vermis: Relevance to the Symptoms of Schizophrenia

International Journal of Neuroscience, 1991
Stanley R Kay, R Sandyk, S R Kay
exaly  

Progressive Cerebellar Atrophy and a Novel Homozygous Pathogenic DNAJC19 Variant as a Cause of Dilated Cardiomyopathy Ataxia Syndrome.

Pediatric Neurology, 2016
Amal M. Al Teneiji, K. Siriwardena, Kristen A. George, S. Mital, S. Mercimek-Mahmutoglu   +4 more
semanticscholar   +1 more source

Diagnostic Approach to Childhood-Onset Cerebellar Atrophy: A 10-Year Retrospective Study of 300 Patients

Journal of Child Neurology, 2012
Grace Yoon, Almundher Al-Maawali
exaly