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Nascer e Crescer, ISSN 0872-0754, 07/2018, Volume 27, Issue 2, pp. 79 - 81
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 03/2010, Volume 8, Issue 1, pp. 101 - 103
  Through the following months of the regression phase, stereotypies become more frequent, and each girl develops her own personal type of repetitive hand... 
Hands | Mental retardation
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 2016, Volume 53, Issue 3, pp. 190 - 199
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 2015, Volume 13, Issue 4, pp. 208 - 212
  Stereotypies are rhythmic, patterned, repetitive, purposeless, and continuous movements which may be categorized into the following two ways: primary, if... 
autism | movement disorders | stereotypies | Autism | Neuropathology | Behavior
Journal Article
Autism, ISSN 1362-3613, 09/2019, p. 136236131986911
Stereotypies are frequently reported in people with autism spectrum disorder (ASD) but remain one of the less explained phenomena. We aimed to describe,... 
Journal Article
Journal of Pediatric Neurology, ISSN 1304-2580, 01/2010, Volume 8, Issue 1, pp. 101 - 103
Journal Article
Movement Disorders, ISSN 0885-3185, 11/2017, Volume 32, Issue 11, pp. 1620 - 1630
ABSTRACT Background Pantothenate kinase‐associated neurodegeneration is a progressive neurological disorder occurring in both childhood and adulthood. The... 
pantothenate kinase‐associated neurodegeneration | clinical rating scale | neurodegeneration with brain iron accumulation | PKAN | dystonia parkinsonism | pantothenate kinase-associated neurodegeneration | STIMULATION | BRAIN IRON ACCUMULATION | RELIABILITY | CLINICAL NEUROLOGY | HALLERVORDEN-SPATZ-SYNDROME | MULTIPLE-SCLEROSIS | MUTATIONS | DEFERIPRONE | PARKINSONS-DISEASE | CHILDHOOD DYSTONIA | Humans | Middle Aged | Parkinsonian Disorders - diagnosis | Parkinsonian Disorders - etiology | Pantothenate Kinase-Associated Neurodegeneration - diagnosis | Young Adult | Ocular Motility Disorders - diagnosis | Adult | Cognitive Dysfunction - diagnosis | Dystonia - etiology | Mental Disorders - diagnosis | Child | Mental Disorders - etiology | Severity of Illness Index | Ocular Motility Disorders - etiology | Reproducibility of Results | Cross-Sectional Studies | Cognitive Dysfunction - etiology | Pantothenate Kinase-Associated Neurodegeneration - complications | Dystonia - diagnosis | Pilot Projects | Pantothenate Kinase-Associated Neurodegeneration - genetics | Adolescent | Aged | Disabled Persons | Medicine, Experimental | Medical research | Nervous system diseases | Parkinson's disease | Basal ganglia | Neurodegeneration | Cognitive ability | Central nervous system diseases | Skull | Dystonia | Children | Movement disorders | Pantothenate kinase
Journal Article
Journal Article
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 06/2007, Volume 144B, Issue 4, pp. 475 - 483
Mutations in the coding sequence of the methyl‐CpG‐binding protein 2 gene (MECP2), which cause Rett syndrome (RTT), have been found in male and female autistic... 
MECP2 | exon 1 | 3′UTR | autism | Detection of Virtually All Mutations‐SSCP | Autism | Detection of Virtually All Mutations-SSCP | Exon 1 | MUTATION ANALYSIS | METHYLATION | 3 ' UTR | RETT-SYNDROME PATIENTS | X-CHROMOSOME | PSYCHIATRY | SPECTRUM DISORDERS | CPG-BINDING PROTEIN-2 | IDENTIFICATION | INDIVIDUALS | GENE | GENETICS & HEREDITY | EXPRESSION | detection of virtually all mutations-SSCP
Journal Article
Journal Article
Revista de Neurología, ISSN 0210-0010, 2005, Volume 40, Issue S01, p. S167
Journal Article
Movement Disorders, ISSN 0885-3185, 11/2007, Volume 22, Issue 15, pp. 2284 - 2287
Journal Article
Revista de Neurologia, ISSN 0210-0010, 01/2004, Volume 38, Issue 1, pp. 53 - 57
Journal Article