DE eng

Search in the Catalogues and Directories

Page: 1 2 3
Hits 1 – 20 of 56

1
Performance of the German version of the PARCA-R questionnaire as a developmental screening tool in two-year-old very preterm infants
In: ISSN: 1932-6203 ; PLOS ONE, Vol. 15, No 9 (2020) P. e0236289 (2020)
BASE
Show details
2
Prospective cohort study on the predictors of fall risk in 119 patients with bilateral vestibulopathy
In: ISSN: 1932-6203 ; PLOS ONE, Vol. 15, No 3 (2020) P. e0228768 (2020)
BASE
Show details
3
Predictive Factors of Swallowing Disorders and Bronchopneumonia in Acute Ischemic Stroke.
In: Journal of stroke and cerebrovascular diseases, vol. 28, no. 8, pp. 2148-2154 (2019)
BASE
Show details
4
Development of a short form of the compulsive internet use scale in Switzerland.
In: International journal of methods in psychiatric research, vol. 28, no. 1, pp. e1765 (2019)
BASE
Show details
5
Do Parents Model Gestures Differently When Children's Gestures Differ?
In: Journal of autism and developmental disorders, vol. 48, no. 5, pp. 1492-1507 (2018)
BASE
Show details
6
Children with mixed developmental language disorder have more insecure patterns of attachment.
In: BMC psychology, vol. 6, no. 1, pp. 54 (2018)
BASE
Show details
7
Detection Test for Language Impairments in Adults and the Aged-A New Screening Test for Language Impairment Associated With Neurodegenerative Diseases: Validation and Normative Data.
In: American journal of Alzheimer's disease and other dementias, vol. 32, no. 7, pp. 382-392 (2017)
BASE
Show details
8
Patient self-reported concerns in inflammatory bowel diseases: A gender-specific subjective quality-of-life indicator.
In: PloS one, vol. 12, no. 2, pp. e0171864 (2017)
BASE
Show details
9
Primary Progressive Aphasia in the Network of French Alzheimer Plan Memory Centers.
In: Journal of Alzheimer's disease, vol. 54, no. 4, pp. 1459-1471 (2016)
BASE
Show details
10
Symptoms Have Modest Accuracy in Detecting Endoscopic and Histologic Remission in Adults With Eosinophilic Esophagitis.
In: Gastroenterology, vol. 150, no. 3, pp. 581-590.e4 (2016)
BASE
Show details
11
Clinical Reasoning: An 82-year-old woman with dissociated aphasia followed by amnesia.
In: Neurology, vol. 87, no. 9, pp. e91-6 (2016)
BASE
Show details
12
Quality of patient information leaflets for Down syndrome screening: A comparison between the UK and Thailand.
Saiklang, P; Skirton, H. - : Australia, 2015
BASE
Show details
13
The diagnostic role of high-speed vocal fold vibratory imaging.
In: Journal of voice : official journal of the Voice Foundation, vol 27, iss 5 (2013)
BASE
Show details
14
Speechreading development in deaf and hearing children: introducing the test of child speechreading.
In: J Speech Lang Hear Res , 56 (2) 416 - 426. (2013) (2013)
BASE
Show details
15
Logopenic aphasia in Alzheimer's disease: clinical variant or clinical feature?
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2012)
BASE
Show details
16
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
In: Journal of Medical Genetics, vol. 49, no. 10, pp. 660-668 (2012)
BASE
Show details
17
Reliability and validity of the cross-culturally adapted French version of the Core Outcome Measures Index (COMI) in patients with low back pain.
In: European Spine Journal, vol. 21, no. 1, pp. 130-137 (2012)
BASE
Show details
18
Autism, language and communication in children with sex chromosome trisomies.
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2011)
Abstract: PURPOSE: Sex chromosome trisomies (SCTs) are found on amniocentesis in 2.3-3.7 per 1000 same-sex births, yet there is a limited database on which to base a prognosis. Autism has been described in postnatally diagnosed cases of Klinefelter syndrome (XXY karyotype), but the prevalence in non-referred samples, and in other trisomies, is unclear. The authors recruited the largest sample including all three SCTs to be reported to date, including children identified on prenatal screening, to clarify this issue. DESIGN: Parents of children with a SCT were recruited either via prenatal screening or via a parental support group, to give a sample of 58 XXX, 19 XXY and 58 XYY cases. Parents were interviewed using the Vineland Adaptive Behavior Scales and completed questionnaires about the communicative development of children with SCTs and their siblings (42 brothers and 26 sisters). RESULTS: Rates of language and communication problems were high in all three trisomies. Diagnoses of autism spectrum disorder (ASD) were found in 2/19 cases of XXY (11%) and 11/58 XYY (19%). After excluding those with an ASD diagnosis, communicative profiles indicative of mild autistic features were common, although there was wide individual variation. CONCLUSIONS: Autistic features have not previously been remarked upon in studies of non-referred samples with SCTs, yet the rate is substantially above population levels in this sample, even when attention is restricted to early-identified cases. The authors hypothesise that X-linked and Y-linked neuroligins may play a significant role in the aetiology of communication impairments and ASD.
Keyword: Child; Child Development Disorders; Education; Educational Status; Female; Humans; Karyotyping; Language Development Disorders; Language Therapy; Male; Pervasive; Prenatal Diagnosis; Psychometrics; Sex Chromosome Aberrations; Special; Speech Therapy; Trisomy
URL: https://doi.org/10.1136/adc.2009.179747
BASE
Hide details
19
Validation of the French version of the alcohol, smoking and substance involvement screening test (ASSIST)
In: ISSN: 1022-6877 ; European Addiction Research, Vol. 17, No 4 (2011) pp. 190-7 (2011)
BASE
Show details
20
[Language disorders in children with morphologic abnormalities of the hippocampus]
In: ISSN: 0929-693X ; EISSN: 1769-664X ; Archives de Pédiatrie ; https://hal.archives-ouvertes.fr/hal-00617747 ; Archives de Pédiatrie, Elsevier, 2010, 17 (7), pp.1008-16 (2010)
BASE
Show details

Page: 1 2 3

Catalogues
0
0
0
0
0
0
0
Bibliographies
0
0
0
0
0
0
0
0
0
Linked Open Data catalogues
0
Online resources
0
0
0
0
Open access documents
56
0
0
0
0
© 2013 - 2024 Lin|gu|is|tik | Imprint | Privacy Policy | Datenschutzeinstellungen ändern