Frequent isolation of extended-spectrum beta-lactamase-producing bacteria from fecal samples of individuals with severe motor and intellectual disabilities
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در صورتی که مقاله لاتین مورد نظر شما تا کنون به زبان فارسی ترجمه نشده باشد، واحد ترجمه پایگاه ISI Articles با همکاری تنی چند از اساتید و مترجمان با سابقه، آمادگی دارد آن را در اسرع وقت و با کیفیت مطلوب برای شما ترجمه نماید.
Altered Brain Cholesterol/Isoprenoid Metabolism in a Rat Model of Autism Spectrum Disorders
Typical vs. atypical: Combining auditory Gestalt perception and acoustic analysis of early vocalisations in Rett syndrome
A clinician friendly data warehouse oriented toward narrative reports: Dr. Warehouse
An update on new and unique uses of botulinum toxin in movement disorders
Functional neurological symptom disorder (conversion disorder): A role for microglial-based plasticity mechanisms?
Carbon dioxide therapy in hypocapnic respiratory failure
Diazepam for outpatient treatment of nonconvulsive status epilepticus in pediatric patients with Angelman syndrome
Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease
Modeling the Interplay Between Neurons and Astrocytes in Autism Using Human Induced Pluripotent Stem Cells
Learning to recognize rat social behavior: Novel dataset and cross-dataset application
Case series: Use of Glyceryl Trinitrate patches to improve peripheral circulation in children with severe neurodisability
Under glass weathering of hemp fibers reinforced polypropylene biocomposites: Impact of Volatile Organic Compounds emissions on indoor air quality
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy
Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders
Insulin-Like Growth Factor Binding Protein-3 Deficiency Leads to Behavior Impairment with Monoaminergic and Synaptic Dysfunction
Diagnostic Yield From 339 Epilepsy Patients Screened on a Clinical Gene Panel
Participation of locus coeruleus in breathing control in female rats
A study of epilepsy according to the age at onset and monitored for 3 years in a regional reference paediatric neurology unit
Charting the territory: Describing the functional abilities of children with progressive neurological conditions
The motor repertoire in 3- to 5-month old infants with Down syndrome
Descriptive study of symptomatic epilepsy by age of onset in patients with a 3-year follow-up at the Neuropaediatric Department of a reference centre
Profile of two hundred children with Autism Spectrum Disorder from a tertiary child and adolescent psychiatry centre
Sacral-Alar-Iliac Fixation in Children with Neuromuscular Scoliosis: Minimum 5-Year Follow-Up
Early Life Epilepsies are a Comorbidity of Developmental Brain Disorders
Is insulin growth factor-1 the future for treating autism spectrum disorder and/or schizophrenia?
Finding patients using similarity measures in a rare diseases-oriented clinical data warehouse: Dr. Warehouse and the needle in the needle stack
Cognitive training modifies frequency EEG bands and neuropsychological measures in Rett syndrome
Comparing social reciprocity in preserved speech variant and typical Rett syndrome during the early years of life
Technological aids to support choice strategies by three girls with Rett syndrome
Neurophysiological responses to music and vibroacoustic stimuli in Rett syndrome
Rett syndrome: A preliminary analysis of stereotypy, stress, and negative affect
Recent insights into genotype–phenotype relationships in patients with Rett syndrome using a fine grain scale
Promoting adaptive behaviors by two girls with Rett syndrome through a microswitch-based program
A retrospective practice based evaluation of music therapy: A single-case study of a four-year-old girl with Rett syndrome—Rebecca's story
Changing the perspective on early development of Rett syndrome
Early socio-communicative forms and functions in typical Rett syndrome
Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndrome
Contributing to the early detection of Rett syndrome: The potential role of auditory Gestalt perception
Peculiarities in the gestural repertoire: An early marker for Rett syndrome?
The relationship between MECP2 mutation type and health status and service use trajectories over time in a Rett syndrome population
Epilepsy in Rett syndrome: Association between phenotype and genotype, and implications for practice
Measuring use and cost of health sector and related care in a population of girls and young women with Rett syndrome
Use of equipment and respite services and caregiver health among Australian families living with Rett syndrome
The role of stereotypies in overselectivity process in Rett syndrome