(Q33942663)

30 July 2017

1 reference

title

Williams (Williams Beuren) syndrome: a distinct neurobehavioral disorder (English)

1 reference

30 July 2017

P Kaplan

1

1 reference

PubMed ID

11305686

30 July 2017

P P Wang

series ordinal

2

1 reference

PubMed ID

11305686

30 July 2017

U Francke

series ordinal

3

1 reference

30 July 2017

1 March 2001

1 reference

Journal of Child Neurology

30 July 2017

1 reference

30 July 2017

16

1 reference

30 July 2017

177-190

1 reference

30 July 2017

3

1 reference

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

30 July 2017

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Natural history of Williams syndrome: physical characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Body composition, energy expenditure, and energy intake in patients with Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Neurobehavioral and neurologic outcome in long-term survivors of posterior fossa brain tumors: role of age and perioperative factors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Neurologic features of Williams and Down syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Anomalous brain morphology on magnetic resonance images in Williams syndrome and Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Proximal interstitial deletion of 7q: a case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

The Williams syndrome. Spectrum and significance of ocular features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Unique profile of visuo-perceptual skills in a genetic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

A specific deficit of dorsal stream function in Williams' syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Segregation of form, color, movement, and depth: anatomy, physiology, and perception

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Evidence from two genetic syndromes for a dissociation between verbal and visual-spatial short-term memory.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Language and Williams syndrome: how intact is "intact"?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Linguistic abilities in children with Williams-Beuren syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Linguistic abilities in Italian children with Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Brief report: response to methylphenidate in two children with Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Treatment of children with Williams syndrome with methylphenidate.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Behavioral and emotional disturbance in individuals with Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Periodic limb movement in sleep in children with Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Periodic limb movement disorder and restless legs syndrome in children with attention-deficit hyperactivity disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Cerebral morphologic distinctions between Williams and Down syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Callosal morphology concurs with neurobehavioral and neuropathological findings in two neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Cognitive and language functions of the human cerebellum

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

The neuropathology of Williams syndrome. Report of a 35-year-old man with presenile beta/A4 amyloid plaques and neurofibrillary tangles

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Brain biochemistry in Williams syndrome: evidence for a role of the cerebellum in cognition?

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Sudden death in Williams syndrome: report of ten cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Cerebrovascular stenoses with cerebral infarction in a child with Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Stroke in Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Carotid ultrasound examination in Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Increased prevalence of urinary symptoms and voiding dysfunction in Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Spectrum of renal anomalies in patients with Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Renal findings in 40 individuals with Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Incidence and spectrum of renal abnormalities in Williams-Beuren syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Renal agenesis in British Columbia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Renal insufficiency in Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Williams syndrome associated with chronic renal failure and various endocrinological abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Increased renal medullary echogenicity in patients with Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Standards for children's height at ages 2-9 years allowing for heights of parents

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Idiopathic infantile hypercalcaemia--a continuing enigma

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Williams syndrome: masseter spasm during anaesthesia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Williams-Beuren syndrome: genes and mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Novel arterial pathology in mice and humans hemizygous for elastin

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

CLIP-115, a novel brain-specific cytoplasmic linker protein, mediates the localization of dendritic lamellar bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

The murine CYLN2 gene: genomic organization, chromosome localization, and comparison to the human gene that is located within the 7q11.23 Williams syndrome critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

A novel human gene, WSTF, is deleted in Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

A novel human gene FKBP6 is deleted in Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Recurrent Williams-Beuren syndrome in a sibship suggestive of maternal germ-line mosaicism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

Memory Abilities in Children with Williams Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380101600305

10.1177/088307380101600305

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

11305686