Results 41 to 50 of about 1,519,343 (314)

Developmental Milestones of Infancy and Associations with Later Childhood Neurodevelopmental Outcomes in the Adolescent Brain Cognitive Development (ABCD) Study

open access: yesChildren, 2022
The age at attaining infancy developmental milestones has been associated with later neurodevelopmental outcomes, but evidence from large and diverse samples is lacking.
Haoran Zhuo   +3 more
doaj   +1 more source

Development of Clinical Milestones in Parkinson’s Disease After Bilateral Subthalamic Deep Brain Stimulation [PDF]

open access: yesJournal of Movement Disorders, 2022
Objective Deep brain stimulation of the subthalamic nucleus (STN-DBS) in Parkinson’s disease (PD) patients does not halt disease progression, as these patients will progress and develop disabling non-levodopa responsive symptoms.
Jed Noel A. Ong   +6 more
doaj   +1 more source

Current evidence for treatment with nusinersen for spinal muscular atrophy : a systematic review [PDF]

open access: yes, 2019
Recent discovery of nusinersen, an antisense oligonucleotide drug, has provided encouragement for improving treatment of spinal muscular atrophy. No therapeutic options currently exist for this autosomal recessive motor neuron disorder.
Meylemans, Antoon, De Bleecker, Jan
core   +1 more source

Association Between Age of Achieving Gross Motor Development Milestones During Infancy and Body Fat Percentage at 6 to 7 Years of Age

open access: yesMaternal and Child Health Journal, 2021
Objectives The later achievement of gross motor milestones during infancy is associated with adiposity in early childhood. However, the associations between gross motor development and adiposity after entering primary school are unclear.
T. Aoyama   +7 more
semanticscholar   +1 more source

Early motor trajectories predict motor but not cognitive function in preterm- and term-born adults without pre-existing neurological conditions [PDF]

open access: yes, 2020
Very preterm (VP; 0.05). Motor problems in childhood were homotypically associated with poorer motor competence in adulthood. Similarly, early cognitive problems were homotypically associated with adult cognitive outcomes. Thus, both motor and cognitive
Bartmann, Peter   +3 more
core   +1 more source

Early motor developmental milestones and level of neuroticism in young adulthood:a 23-year follow-up study of the Copenhagen Perinatal Cohort [PDF]

open access: yes, 2012
BackgroundStudies investigating early developmental factors in relation to psychopathology have mainly focused on schizophrenia. The personality dimension of neuroticism seems to be a general risk factor for psychopathology, but evidence on associations ...
Flensborg-Madsen, T   +3 more
core   +1 more source

Treatment algorithm for infants diagnosed with spinal muscular atrophy through newborn screening [PDF]

open access: yes, 2018
Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by the degeneration of alpha motor neurons in the spinal cord, leading to muscular atrophy.
Connolly, Anne   +14 more
core   +2 more sources

Similarities and differences in child development from birth to age 3 years by sex and across four countries: a cross-sectional, observational study

open access: yesThe Lancet Global Health, 2018
Summary: Background: Knowledge about typical development is of fundamental importance for understanding and promoting child health and development. We aimed to ascertain when healthy children in four culturally and linguistically different countries ...
Ilgi Ozturk Ertem, ProfMD   +12 more
doaj   +1 more source

Breastfeeding and developmental delay: Findings from the Millennium Cohort Study [PDF]

open access: yes, 2006
OBJECTIVE: We investigated whether the duration and exclusivity of breastfeeding affects the likelihood of gross and fine motor delay in infants and examined the effect of factors that might explain any observed differences.
Kelly, YJ, Quigley, MA, Sacker, A
core   +1 more source

A closer look at ARSA activity in a patient with metachromatic leukodystrophy. [PDF]

open access: yes, 2019
Metachromatic leukodystrophy (MLD) is an autosomal recessive lysosomal storage disease mainly caused by a deficiency of arylsulfatase A activity. The typical clinical course of patients with the late infantile form includes a regression in motor skills ...
Childers, Anna   +6 more
core   +2 more sources

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