Browse Items (4 total)

Tags: 2010, Aberrant Behavior Checklist, behavioral problems, characteristics, features, fragile-x-syndrome, Gotou M, Inoue Y, Irritability, Japanese manuals of, Journal of Physical Therapy Science, Koeda H, lethargy, Mowat-Wilson syndrome, Nanba Y, Naruse S, Pediatric Physical Therapy, Pena Shokeir syndrome, prader-willi, Problematic behaviors, Rehabilitation, Tokuhisa K, Trajectory, Tuberous Sclerosis, Uesugi M, West syndrome

Tags: 2013, behavioral problems, characteristics, Gotou M, Inoue Y, Journal of Physical Therapy Science, lethargy, Mowat-Wilson syndrome, Nanba Y, Otani Y, Pena Shokeir syndrome, Problematic behavior, Rehabilitation, Ryouiku Techou, stereotyped behaviors, Takemasa S, The Japanese version of the Aberrant Behavior Checklist, Trajectory, Tuberous Sclerosis, Uesugi M, West syndrome

Tags: 2017, angelman-syndrome, behavioral problems, bowel incontinence, characteristics, Children, Constipation, Curfs L, Education & Educational Research, Einfeld S, enuresis, Equit M, features, fecal incontinence, hirschsprungs-disease, Mowat D, Mowat-Wilson syndrome, Niemczyk J, Phenotype, psychopathology, Rehabilitation, Research in Developmental Disabilities, Trajectory, urinary incontinence, urinary-incontinence, von Gontard A, Wagner C

Tags: 0 (Homeodomain Proteins), 0 (Repressor Proteins), 0 (ZEB2 protein human), 2016, Adolescent, Adult, American Journal of Medical Genetics Part A, Australia, Behavior Rating Scale, characteristics, Child, Child Preschool, Einfeld S, Evans E, Facies, Female, Gene Expression, Hirschsprung Disease/co [Complications], Hirschsprung Disease/di [Diagnosis], Hirschsprung Disease/ge [Genetics], Hirschsprung Disease/pp [Physiopathology], Homeodomain Proteins/ge [Genetics], Humans, Intellectual Disability/co [Complications], Intellectual Disability/di [Diagnosis], Intellectual Disability/ge [Genetics], Intellectual Disability/pp [Physiopathology], Male, Microcephaly/co [Complications], Microcephaly/di [Diagnosis], Microcephaly/ge [Genetics], Microcephaly/pp [Physiopathology], Middle Aged, Mowat D, Mowat-Wilson syndrome, Mutation, Repressor Proteins/ge [Genetics], Severity Of Illness Index, sleep disturbance/disorders, Sleep Initiation and Maintenance Disorders/co [Complications], Sleep Initiation and Maintenance Disorders/di [Diagnosis], Sleep Initiation and Maintenance Disorders/ge [Genetics], Sleep Initiation and Maintenance Disorders/pp [Physiopathology], Surveys And Questionnaires, Trajectory, Wilson M