نتایج جستجو برای: motor developmental delay

تعداد نتایج: 398022  

Anooshirvan Kazemnejad, Firoozeh Sajedi, Nadia Azari, Roshanak Vameghi, Soheila Shahshahani,

Objectives: This research was performed to compare the results of two parental-based developmental questionnaires. Methods: In this study the developmental status of 196, 4-60 months old children were screened using Ages and Stages Questionnaires (ASQ) and prescreening developmental Questionnaire (PDQ) in 4 primary health care clinics in Tehran. Convenient sampling was used. Data was analyze...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, iran farzad ahmadabadi 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran narjes jafari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran sayena jabbehdari pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad reza alaee 3. department of pediatric endocrinology, pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad ghofrani 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, ahmadabadi f, jafari n, jabbehdari s, alaee mr, ghofrani m, taghdiri mm, tonekaboni sh. biotinidase deficiency: a reversible neurometabolic disorder (an iranian pediatric case series). iran j child neurol. 2013 autumn; 7(4):47- 52.   objective biotinidase deficiency is one of the rare congenital metabolic disorders with autosomal recessive inheritance. if...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran narjes jafari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran farzad ahmad abadi 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran sayena jabbehdari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad-mahdi taghdiri 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran mohammad-reza alaee department of pediatric endocrinology, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, jafari n, ahmad abadi f, jabbehdari s, taghdiri mm, alaee mr, ghofrani m, tonekaboni sh, nejad biglari h. propionic acidemia: diagnosis and neuroimaging findings of this neurometabolic disorder. iran j child neurol. 2014 winter; 8(1):58-61.   objective propionic acidemia is one of the rare congenital neurometabolic disorders with autosomal recessive inher...

2014
Paulina Krawiec Elżbieta Pac-Kożuchowska Beata Mełges Agnieszka Mroczkowska-Juchkiewicz Stanisław Skomra Agnieszka Pawłowska-Kamieniak Katarzyna Kominek

UNLABELLED ᅟ: Mucopolysaccharidosis type III (MPS III; Sanfilippo syndrome) is a metabolic disorder characterized by the deficiency of a lysosomal enzyme catalyzing the catabolic pathway of heparan sulphate. MPS III presents with progressive mental deterioration, speech delay and behavioural problems with subtle somatic features, which can often lead to misdiagnosis with idiopathic developmenta...

Journal: :International journal of pediatric otorhinolaryngology 2012
Susan Amirsalari Jaleh Yousefi Shokofeh Radfar Amin Saburi Seyed Abbas Tavallaie Mohammad Javad Hosseini Sima Noohi Mahdieh Hassan Alifard Mohammad Ajallouyean

INTRODUCTION Multiple handicapped children and children with syndromes and conditions resulting additional disabilities such as cerebral palsy, global developmental delay and autistic spectrum disorder, are now not routinely precluded from receiving a cochlear implant. The primary focus of this study was to determine the effect of cochlear implants on the speech perception and intelligibility o...

Journal: :Expert Syst. Appl. 2007
Chun-Lang Chang

The implementation of early intervention has close relation to the growth development of developmentally-delayed children. The earlier the intervention is involved the more significant effects and results it will bring to the benefits of these young children. However, providing early intervention exclusively without finding out the relationship between the two would eventually leave the problem...

Journal: :Journal of autism and developmental disorders 2005
Grace T Baranek Cassandra D Danko Martie L Skinner Donald B Bailey Deborah D Hatton Jane E Roberts Penny L Mirrett

This study utilized retrospective video analysis to distinguish sensory-motor patterns in infants with fragile X syndrome (FXS) (n = 11) from other infants [i.e., autism (n = 11), other developmental delay (n = 10), typical (n = 11)] at 9-12 months of age. Measures of development, autistic features, and FMRP were assessed at the time of entry into the study. Home videos collected from families ...

2014
Andréa Januario da Silva Luiz Antônio Tavares Neves Jaqueline da Silva Frônio Luiz Cláudio Ribeiro

1 Programa de Pós-Graduação em Saúde Coletiva, Faculdade de Medicina, Universidade Federal de Juiz de Fora, UFJF; Núcleo Interdisciplinar de Estudos do Desenvolvimento Infantil NIEDI, Faculdade de Fisioterapia, UFJF; 3Núcleo de Assessoria, Treinamento e Estudos em Saúde NATES, UFJF, Juiz de Fora, MG, Brasil. 2 Mestre em Saúde Coletiva (UFJF), Departamento de. Saúde Coletiva Faculdade de Medicin...

Journal: :مجله دانشکده پرستاری و مامایی ارومیه 0
زهرا عبدیزدان z abdeyazdan سهیلا احسان پور s ehsanpour الهه همتی e hemmati

developmental millstones in children with normal, low, and very low birth weights.     abdeyazdan z [1] , ehsanpour s [2] *, hemmati e [3]     received: 22 may , 2013 accepted: 11 sep , 2013   abstract   background & aims : in recent years with the development of nicus, survival rates of vlbw and lbw infants has increased in many countries including iran. there is concern that this increased su...

2016
Tsung-Han Hsieh

Children with dysfunctional visual perception often exhibit limited participation in school activities, poor academic performance, and lack of independence in daily life activities. Negative experiences and poor school performance may then further delay social and emotional development. Thus, effective therapies for enhancing visual perceptual function are essential for facilitating integration...

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