Results 131 to 140 of about 1,273,570 (277)

SPG4 and Dementia: Expanding the Clinical Spectrum

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza   +19 more
wiley   +1 more source

Other title: Title from HTML header (viewed May 20, 2011): CTCDD-Ct. Council on Developmental Disabilities; Other title: Connecticut Council on Developmental Disabilities

open access: yes, 2015
Updated irregularly; Began in 2002?; Title from home page (publisher's Web site, viewed May 20, 2011).; At head of title: Connecticut.; Harvested from the web on 12/22/15Official website of the Connecticut Developmental Disabilities Council.

core   +1 more source

Developmental assets and hedonic well-being among youths: In the perspective of students’ characteristics

open access: yesBahir Dar Journal of Education
This study examined the effect of gender and school types on developmental assets and hedonic well-being, encompassing positive affect, negative affect, and life satisfaction.
Meseret Ayalew Dejenie   +2 more
doaj   +1 more source

Egyptian and Roma Adolescents' Perspectives on Their Developmental Assets in Albania During the COVID-19 Pandemic. [PDF]

open access: yesJ Res Adolesc, 2021
Miconi D   +5 more
europepmc   +1 more source

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone   +8 more
wiley   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

Other title: Title from HTML header (viewed May 20, 2011): CTCDD-Ct. Council on Developmental Disabilities; Other title: Connecticut Council on Developmental Disabilities

open access: yes, 2017
Updated irregularly; Began in 2002?; Title from home page (publisher's Web site, viewed May 20, 2011).; At head of title: Connecticut.; Harvested from the web on 6/7/17Official website of the Connecticut Developmental Disabilities Council.

core  

Spatial and Volumetric Characteristics of Glioblastoma: Associations With Clinical Presentation and Survival

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective We aim to comprehensively analyze how regional tumor and edema characteristics are associated with clinical presentations and survival outcomes in a large cohort of glioblastoma patients. Methods Patients with IDH‐wildtype glioblastoma who received brain MRI from 2010 to 2023 were included.
Daniel J. Zhou   +16 more
wiley   +1 more source

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