Works matching DE "DEVELOPMENTAL delay"
Results: 2263
Value of the Goodenough Drawing Test as a research tool to detect developmental delay in South African preschool children.
- Published in:
- South African Journal of Psychology, 2020, v. 50, n. 1, p. 81, doi. 10.1177/0081246319850683
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- Article
Small Group-Delivered Literacy Based Behavioral Interventions for Young Children.
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- Journal of Applied School Psychology, 2022, v. 38, n. 2, p. 148, doi. 10.1080/15377903.2021.1926033
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- Article
Early onset, severe fetal growth restriction with absent or reversed end-diastolic flow velocity waveform in the umbilical artery: Perinatal and long-term outcomes.
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- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2009, v. 49, n. 1, p. 45, doi. 10.1111/j.1479-828X.2008.00938.x
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- Article
Treatment Modalities for Self-injurious Behaviors Observed in the Special-needs Patient: 2 Case Reports.
- Published in:
- 2010
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- Publication type:
- Case Study
Effects of phenylalanine on the survival and neurite outgrowth of rat cortical neurons in primary cultures: possible involvement of brain-derived neurotrophic factor.
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- Molecular & Cellular Biochemistry, 2010, v. 339, n. 1/2, p. 1, doi. 10.1007/s11010-009-0364-2
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- Article
The Association Between Congenital Heart Disease and Autism Spectrum Disorder: A Systematic Review and Meta-Analysis.
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- Pediatric Cardiology, 2023, v. 44, n. 5, p. 1092, doi. 10.1007/s00246-023-03146-5
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- Article
Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
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- Pediatric Cardiology, 2018, v. 39, n. 5, p. 924, doi. 10.1007/s00246-018-1842-7
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- Article
Left Ventricular Non-compaction: Is It Genetic?
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- Pediatric Cardiology, 2015, v. 36, n. 8, p. 1565, doi. 10.1007/s00246-015-1222-5
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- Article
The syntax and interpretation of embedded null subjects in Chinese, and their acquisition by English-speaking learners.
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- EUROSLA Yearbook, 2011, v. 11, p. 191, doi. 10.1075/eurosla.11.11zha
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- Article
Comparison of 5-year safety and efficacy of laser photocoagulation and intravitreal bevacizumab injection in retinopathy of prematurity.
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- Graefe's Archive of Clinical & Experimental Ophthalmology, 2021, v. 259, n. 9, p. 2849, doi. 10.1007/s00417-021-05137-9
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- Article
Demographic, clinical features, and outcomes of pediatric non-penetrating ocular foreign bodies.
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- Graefe's Archive of Clinical & Experimental Ophthalmology, 2020, v. 258, n. 7, p. 1469, doi. 10.1007/s00417-020-04688-7
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- Publication type:
- Article
Posterior vault encephaloceles: from antenatal management to post-surgical follow-up—a cooperative study.
- Published in:
- Child's Nervous System, 2025, v. 41, n. 1, p. 1, doi. 10.1007/s00381-025-06764-x
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- Publication type:
- Article
Early clinico-radiological outcomes following neuroendoscopic cysto-cisternostomy for middle cranial fossa arachnoid cysts: a prospective cohort study with illustrative cases.
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- Child's Nervous System, 2024, v. 40, n. 12, p. 4033, doi. 10.1007/s00381-024-06596-1
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- Article
Occipital encephalocele: a retrospective analysis and assessment of post-surgical neurodevelopmental outcome.
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- Child's Nervous System, 2024, v. 40, n. 12, p. 3945, doi. 10.1007/s00381-024-06506-5
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- Article
Pineocytoma in a child with Pallister–Killian syndrome: a case report and review of the literature.
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- Child's Nervous System, 2024, v. 40, n. 8, p. 2619, doi. 10.1007/s00381-024-06426-4
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- Article
Long-term sequelae of normocephalic pansynostosis: a rare but insidious entity.
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- Child's Nervous System, 2024, v. 40, n. 7, p. 2125, doi. 10.1007/s00381-024-06379-8
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- Article
Yield of genetic evaluation in non-syndromic pediatric moyamoya patients.
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- Child's Nervous System, 2024, v. 40, n. 3, p. 801, doi. 10.1007/s00381-023-06167-w
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- Article
Deep brain stimulation for status dystonicus in a toddler with SCN2A-related disorder.
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- 2023
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- Publication type:
- Case Study
Intracranial cysts: incidental or neurodevelopmental?
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- Child's Nervous System, 2023, v. 39, n. 3, p. 775, doi. 10.1007/s00381-022-05724-z
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- Publication type:
- Article
A novel technique for frame-based MR-guided laser ablation in an infant.
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- Child's Nervous System, 2023, v. 39, n. 2, p. 497, doi. 10.1007/s00381-022-05616-2
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- Article
Neuroendoscopic fenestration for intracranial unilocular cysts and isolated lateral ventricles: four pediatric cases.
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- 2022
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- Publication type:
- Case Study
Suprasellar arachnoid cyst due to ectopic choroid plexus: case report.
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- 2022
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- Publication type:
- Case Study
Occult tethered cord syndrome: a rare, treatable condition.
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- Child's Nervous System, 2022, v. 38, n. 2, p. 387, doi. 10.1007/s00381-021-05353-y
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- Publication type:
- Article
Morphological and surgical results in sagittal synostosis: early craniectomy versus later cranioplasty.
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- Child's Nervous System, 2021, v. 37, n. 7, p. 2335, doi. 10.1007/s00381-021-05178-9
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- Publication type:
- Article
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay.
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- Acta Neuropathologica, 2020, v. 140, n. 6, p. 881, doi. 10.1007/s00401-020-02228-5
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- Publication type:
- Article
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.
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- Acta Neuropathologica, 2020, v. 139, n. 3, p. 415, doi. 10.1007/s00401-019-02109-6
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- Article
Gene hunt is on for mental disability.
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- Nature, 2012, v. 484, n. 7394, p. 302, doi. 10.1038/484302a
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- Article
Assessment of motor development in children with postural asymmetry and the application of neurodevelopmental-based improvement methods.
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- Rheumatology Forum, 2024, v. 10, n. 4, p. 194, doi. 10.5603/rf.90800
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- Publication type:
- Article
An observational study of exotropia with the application of the Classification of Eye Movement Abnormalities and Strabismus.
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- Pan-American Journal of Ophthalmology, 2022, p. 1, doi. 10.4103/pajo.pajo_17_22
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- Publication type:
- Article
Erratum to: Could Fetuin-A Be a Biomarker for Autism Spectrum Disorder and Cognitive Developmental Delay?
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- 2022
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- Correction Notice
Could Fetuin-A Be a Biomarker for Autism Spectrum Disorder and Cognitive Developmental Delay?
- Published in:
- Biochemistry (00062979), 2022, v. 87, n. 6, p. 559, doi. 10.1134/S0006297922060074
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- Publication type:
- Article
Wiedemann‑Steiner syndrome in a 2‑year‑old patient due to a rare nonsense KMT2A mutation of de novo origin: A case report.
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- International Journal of Epigenetics, 2024, v. 4, n. 1, p. N.PAG, doi. 10.3892/ije.2024.20
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- Publication type:
- Article
Hypocalcemia -- a Diagnostic Challenge.
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- Central European Journal of Paediatrics, 2023, v. 19, n. 1, p. 50, doi. 10.5457/p2005-114.337
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- Article
A de novo microdeletion 2p24.3-25.1 identified in a girl with global development delay.
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- BioDiscovery, 2017, p. 1, doi. 10.7750/BioDiscovery.2015.18.1
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- Article
Collaborative Practice.
- Published in:
- Journal for Specialists in Pediatric Nursing, 2007, v. 12, n. 2, p. 123, doi. 10.1111/j.1744-6155.2007.00102.x
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- Publication type:
- Article
Characteristics of the home environment in children with developmental delays: insights from a cross-sectional study in Türkiye.
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- Turkish Journal of Medical Sciences, 2025, v. 55, n. 1, p. 184, doi. 10.55730/1300-0144.5956
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- Article
Clinical and molecular findings in 37 Turkish patients with isolated methylmalonic acidemia.
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- Turkish Journal of Medical Sciences, 2021, v. 51, n. 3, p. 1220, doi. 10.3906/sag-2001-72
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- Publication type:
- Article
Which Bayley-III cut-off values should be used in different developmental levels?
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- Turkish Journal of Medical Sciences, 2020, v. 50, n. 4, p. 764, doi. 10.3906/sag-1910-69
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- Publication type:
- Article
Smith-Magenis Syndrome associated with Autism Spectrum Disorder with delayed diagnosis due to B12 deficiency: a case report.
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- 2024
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- Publication type:
- Abstract
Inventory construction to track cognitive profiles compatible with intellectual disability, ADHD, and dyslexia in children between 6 to 11 years old.
- Published in:
- European Psychiatry, 2021, v. 64, p. S755, doi. 10.1192/j.eurpsy.2021.2001
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- Publication type:
- Article
The psychiatric phenotype of 15q11.2-q13.3 duplications.
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- European Psychiatry, 2021, v. 64, p. S720, doi. 10.1192/j.eurpsy.2021.1908
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- Publication type:
- Article
Behavior problems associated with brain heterotopia.
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- European Psychiatry, 2021, v. 64, p. S638, doi. 10.1192/j.eurpsy.2021.1696
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- Publication type:
- Article
Child psychiatry expertise in the context of parental separation.
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- European Psychiatry, 2021, v. 64, p. S633, doi. 10.1192/j.eurpsy.2021.1683
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- Publication type:
- Article
Infant exposure to lithium through breast milk.
- Published in:
- European Psychiatry, 2021, v. 64, p. S180, doi. 10.1192/j.eurpsy.2021.477
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- Publication type:
- Article
P-753 - Sotos Syndrome - case Study
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- 2012
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- Publication type:
- Abstract
P-700 - Social cognition and the behavioural phenotype of 17q21.31 microdeletion syndrome
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- 2012
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- Publication type:
- Abstract
P01-199 - Developmental lag in ADHD - cross sectional study with continous performance test
- Published in:
- 2010
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- Publication type:
- Abstract
An expansion of phenotype: novel homozygous variant in the MED17 identified in patients with progressive microcephaly and global developmental delay.
- Published in:
- Journal of Neurogenetics, 2022, v. 36, n. 4, p. 108, doi. 10.1080/01677063.2022.2149748
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- Publication type:
- Article
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype.
- Published in:
- Journal of Neurogenetics, 2021, v. 35, n. 2, p. 67, doi. 10.1080/01677063.2021.1892094
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- Publication type:
- Article
Novel mutation in the <italic>KCNJ10</italic> gene in three siblings with seizures, ataxia and no electrolyte abnormalities.
- Published in:
- Journal of Neurogenetics, 2018, v. 32, n. 1, p. 1, doi. 10.1080/01677063.2017.1404057
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- Publication type:
- Article