Pages that link to "Q50484810"
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The following pages link to Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society (Q50484810):
Displaying 50 items.
- Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter (Q21261458) (← links)
- Practice Parameter: Evaluation of the child with microcephaly (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society (Q22337000) (← links)
- Chloral hydrate as a sedating agent for neurodiagnostic procedures in children (Q24186803) (← links)
- Intellectual developmental disorders: towards a new name, definition and framework for "mental retardation/intellectual disability" in ICD-11 (Q24635210) (← links)
- Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies (Q28752220) (← links)
- Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability. (Q30489425) (← links)
- SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay (Q30566015) (← links)
- 19q13.33→qter trisomy in a girl with intellectual impairment and seizures (Q30614022) (← links)
- Sedation medication received and adverse events related to sedation for brain MRI in children with and without developmental disabilities (Q33399911) (← links)
- Delayed diagnosis in duchenne muscular dystrophy: data from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet). (Q33435057) (← links)
- Sensory defects and developmental delay among children with congenital rubella syndrome (Q33559976) (← links)
- Fast 3D (1)H MRSI of the corticospinal tract in pediatric brain (Q33704046) (← links)
- Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine (Q33736038) (← links)
- The analysis of genetic aberrations in children with inherited neurometabolic and neurodevelopmental disorders. (Q33737853) (← links)
- Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability (Q33847214) (← links)
- Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies (Q34009396) (← links)
- Etiological Analysis of Neurodevelopmental Disabilities: Single‐Center Eight‐Year Clinical Experience in South China (Q34170024) (← links)
- Clinical whole-exome sequencing for the diagnosis of mendelian disorders (Q34413680) (← links)
- Individual development of preschool children-prevalences and determinants of delays in Germany: a cross-sectional study in Southern Bavaria (Q34502409) (← links)
- Clinical genetic testing for patients with autism spectrum disorders (Q34588012) (← links)
- Fruit flies and intellectual disability (Q34610614) (← links)
- Vision screening for children 36 to <72 months: recommended practices (Q34759897) (← links)
- The differences in clinical aspect between specific language impairment and global developmental delay (Q34791522) (← links)
- A study of the correlation between BSID-III and KICDT for children with developmental delay (Q35010026) (← links)
- American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation (Q35033863) (← links)
- Molecular findings among patients referred for clinical whole-exome sequencing (Q35078373) (← links)
- Predictors of severity and outcome of global developmental delay without definitive etiologic yield: a prospective observational study (Q35093198) (← links)
- Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature (Q35117171) (← links)
- Magnetic resonance imaging (MRI) evaluation of developmental delay in pediatric patients (Q35139797) (← links)
- Developmental delay: when to suspect and how to investigate for an inborn error of metabolism (Q35281339) (← links)
- Brain magnetic resonance imaging findings in developmentally delayed children (Q35550933) (← links)
- Sensitive Diffusion Tensor Imaging Quantification Method to Identify Language Pathway Abnormalities in Children with Developmental Delay (Q35555971) (← links)
- Neuropsychomotor developmental delay: conceptual map, term definitions, uses and limitations (Q35622326) (← links)
- Caregiver opinions about fragile X population screening (Q35629255) (← links)
- Severe intellectual disability and autistic features associated with microduplication 2q23.1. (Q35837621) (← links)
- Neuropsychiatric syndromes in adults with intellectual disability: issues in assessment and treatment (Q35882098) (← links)
- Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience. (Q35910407) (← links)
- Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness. (Q35938000) (← links)
- Evaluation of the revised Nipissing District Developmental Screening (NDDS) tool for use in general population samples of infants and children. (Q35959985) (← links)
- New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants (Q35987709) (← links)
- Investigation of global developmental delay (Q36153611) (← links)
- X linked mental retardation: a clinical guide (Q36239035) (← links)
- Evaluation children with global developmental delay: a prospective study at sultan qaboos university hospital, oman (Q36299030) (← links)
- Aetiologic spectrum of mental retardation & developmental delay in India (Q36436317) (← links)
- Cerebral palsy: comprehensive review and update. (Q36500376) (← links)
- Identifying patterns of developmental delays can help diagnose neurodevelopmental disorders (Q36559059) (← links)
- Functional performance of school children diagnosed with developmental delay up to two years of age (Q36697425) (← links)
- "Intellectual developmental disorders": reflections on the international consensus document for redefining "mental retardation-intellectual disability" in ICD-11. (Q36771085) (← links)
- De novo truncating variants in the AHDC1 gene encoding the AT-hook DNA-binding motif-containing protein 1 are associated with intellectual disability and developmental delay (Q36851443) (← links)
- Identification of a distinct developmental and behavioral profile in children with Dup15q syndrome (Q36876026) (← links)