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1. Full Text Remyelinating drug to the rescue in a Williams syndrome model
by Wood, Heather
Nature reviews. Neurology, ISSN 1759-4758, 07/2019, Volume 15, Issue 7, pp. 368 - 369
Drug therapy | Models | Williams syndrome
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2. Embraceable
: A Film About Williams Syndrome
by Kent, Jon, producer,director and Sproutflix (Organization), production company
2011
You think you know the meaning of kindness, charisma, musical passion and joy until you meet Ben Monkaba and others like him with a rare genetic condition... 
Williams syndrome
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3. Full Text Publisher Correction: Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug
by Barak, Boaz and Zhang, Zicong and Liu, Yuanyuan and Nir, Ariel and Trangle, Sari S and Ennis, Michaela and Levandowski, Kirsten M and Wang, Dongqing and Quast, Kathleen and Boulting, Gabriella L and Li, Yi and Bayarsaihan, Dashzeveg and He, Zhigang and Feng, Guoping
Nature neuroscience, ISSN 1097-6256, 06/2019, Volume 22, Issue 7, pp. 1197 - 1197
The original and corrected figures are shown in the accompanying Publisher Correction. 
Deletion | Clonal deletion | Myelin | Williams syndrome
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4. Full Text Extending the positive bias in Williams syndrome: The influence of biographical information on attention allocation
by Boulton, Kelsie A and Porter, Melanie A
Development and Psychopathology, ISSN 0954-5794, 2019, pp. 1 - 14
There is evidence that individuals with Williams syndrome (WS) show an attention bias toward positive social-perceptual (happy) faces. Research has not yet... 
social phenotype | attention bias | Williams syndrome
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5. Spatial representation
: from gene to mind
by Landau, Barbara, 1949 and Hoffman, James E
2012, Oxford series in developmental cognitive neuroscience, ISBN 9780195385373
Cognition disorders | Williams syndrome
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6. Full Text Orofacial findings and dental management of a child with Williams syndrome
by Pereira, Luciana and Soares, Daniela Novaes and De Lima Pedro, Rafael and Da Silva Fidalgo, Tatiana Kelly and Costa, Marcelo Castro and De Araújo Castro, Gloria Fernanda Barbosa
Revista Odonto Ciencia, ISSN 0102-9460, 2016, Volume 31, Issue 1, pp. 41 - 44
Williams syndrome (WS) is a multisystem, congenital and panethnic disorder characterized by developmental and physical abnormalities. Developmental... 
Agenesis | Children | Williams syndrome
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7. Full Text EP10.29: Prenatal diagnosis of Williams syndrome
by Maeda, K and Kaji, T and Nakaoku, D and Yamasaki, M and Kondo, A and Morine, M and Hinokio, K
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 10/2018, Volume 52, Issue S1, pp. 242 - 242
Pregnant women | Medical diagnosis | Prenatal diagnosis | Williams syndrome
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8. The boy who loved too much
: a true story of pathological friendliness
by Latson, Jennifer, author
2017, First Simon & Schuster hardcover edition., ISBN 9781476774053, x, 290 pages
"Twelve-year-old Eli D'Angelo has a genetic disorder that obliterates social inhibitions, making him irrepressibly friendly, indiscriminately trusting, and... 
Parenting | Friends | Trust | Patients | PSYCHOLOGY | Williams syndrome | FAMILY & RELATIONSHIPS | People with Disabilities | SOCIAL SCIENCE | Friendship in children | Neuropsychology | Social interaction in children | Child | Interpersonal Relations
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9. Neurodevelopmental disorders across the lifespan
: a neuroconstructivist approach
by Farran, Emily K and Karmiloff-Smith, Annette
2012, Oxford series in developmental cognitive neuroscience, ISBN 9780199594818
This text presents evidence on development across the lifespan across multiple levels of description (genetic, brain cognitive, environmental). The authors use... 
Developmental psychology | Cognition | Williams syndrome
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10. Full Text Iskustva majki djece s dijagnozom williamsovog sindroma
by Babić, Marina Milić and Jović, Katarina and Napan, Ksenija
Hrvatska Revija Za Rehabilitacijska Istrazivanja, ISSN 1331-3010, 07/2017, Volume 53, Issue 1, pp. 105 - 117
Rare diseases | Parenthood | Williams syndrome
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11. Full Text Vitamin D supplementation during pregnancy: Double‐blind, randomized clinical trial of safety and effectiveness
by Hollis, Bruce W and Johnson, Donna and Hulsey, Thomas C and Ebeling, Myla and Wagner, Carol L
Journal of Bone and Mineral Research, ISSN 0884-0431, 10/2011, Volume 26, Issue 10, pp. 2341 - 2357
The need, safety, and effectiveness of vitamin D supplementation during pregnancy remain controversial. In this randomized, controlled trial, women with a... 
CHOLECALCIFEROL | VITAMIN D | NEONATE | PREGNANCY | cholecalciferol | neonate | vitamin D | pregnancy | ELEVATED 1,25-DIHYDROXYVITAMIN-D | CALCIUM HOMEOSTASIS | AORTIC-STENOSIS | D DEFICIENCY | SERUM | DIETARY-INTAKE | D REQUIREMENTS | ENDOCRINOLOGY & METABOLISM | GROWTH-FACTOR | CIRCULATING 25-HYDROXYVITAMIN-D | WILLIAMS-SYNDROME | Pregnancy | Vitamin D - adverse effects | Double-Blind Method | Humans | Female | Vitamin D - administration & dosage | Dietary Supplements
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12. Full Text Mild macrocytosis in Williams-Beuren syndrome
by Yu, Eric and Feinn, Richard and Bona, Robert and Brink, Benjamin and Sindhar, Sampat and Kozel, Beth and Pober, Barbara R
European journal of medical genetics, ISSN 1769-7212, 08/2019, p. 103740
To evaluate the occurrence and estimate the frequency of macrocytosis in Williams-Beuren syndrome (WBS). Complete blood count (CBC) data from 179 subjects with... 
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13. Full Text Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
by Sanders, Stephan J and Ercan-Sencicek, A. Gulhan and Hus, Vanessa and Luo, Rui and Murtha, Michael T and Moreno-De-Luca, Daniel and Chu, Su H and Moreau, Michael P and Gupta, Abha R and Thomson, Susanne A and Mason, Christopher E and Bilguvar, Kaya and Celestino-Soper, Patricia B.S and Choi, Murim and Crawford, Emily L and Davis, Lea and Davis Wright, Nicole R and Dhodapkar, Rahul M and DiCola, Michael and DiLullo, Nicholas M and Fernandez, Thomas V and Fielding-Singh, Vikram and Fishman, Daniel O and Frahm, Stephanie and Garagaloyan, Rouben and Goh, Gerald S and Kammela, Sindhuja and Klei, Lambertus and Lowe, Jennifer K and Lund, Sabata C and McGrew, Anna D and Meyer, Kyle A and Moffat, William J and Murdoch, John D and O'Roak, Brian J and Ober, Gordon T and Pottenger, Rebecca S and Raubeson, Melanie J and Song, Youeun and Wang, Qi and Yaspan, Brian L and Yu, Timothy W and Yurkiewicz, Ilana R and Beaudet, Arthur L and Cantor, Rita M and Curland, Martin and Grice, Dorothy E and Günel, Murat and Lifton, Richard P and Mane, Shrikant M and Martin, Christa Lese and Martin, Donna M and Shaw, Chad A and Sheldon, Michael and Tischfield, Jay A and Walsh, Christopher A and Morrow, Eric M and Ledbetter, David H and Fombonne, Eric and Lord, Catherine and Brooks, Andrew I and Sutcliffe, James S and Cook, Edwin H and Geschwind, Daniel and Roeder, Kathryn and Devlin, Bernie and State, Matthew W
Neuron, ISSN 0896-6273, 06/2011, Volume 70, Issue 5, pp. 863 - 885
We have undertaken a genome-wide analysis of rare copy-number variation (CNV) in 1124 autism spectrum disorder (ASD) families, each comprised of a single... 
VARIANTS | MICRODELETIONS | HIDDEN-MARKOV MODEL | GENES | EARLY-ONSET | RISK | 16P11.2 | COPY NUMBER VARIATION | REARRANGEMENTS | DELETIONS | NEUROSCIENCES | Oligonucleotide Array Sequence Analysis | Williams Syndrome - genetics | Humans | Child, Preschool | Family Health | Male | Gene Expression Profiling | Gene Duplication - genetics | Female | Cadherins - genetics | Child | Chromosomes, Human, Pair 16 - genetics | Siblings | Genome-Wide Association Study | Chromosomes, Human, X - genetics | Genotype | DNA Copy Number Variations - genetics | Ubiquitin Thiolesterase - genetics | Nerve Tissue Proteins - genetics | Cell Adhesion Molecules, Neuronal - genetics | Proteins - genetics | Phenotype | Child Development Disorders, Pervasive - genetics | Adolescent | Chromosomes, Human, Pair 7 - genetics | Ubiquitin-Specific Peptidase 7 | Studies | Design | Autism | Genomes | Mutation
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14. Williams-beuren-szindróma (Williams-szindróma)
by Györgyi, Miklós and György, Fekete and Irén, Haltrich and Miklós, Tóth and Péter, Reismann
Orvosi Hetilap, ISSN 0030-6002, 11/2017, Volume 158, Issue 47, pp. 1883 - 1888
Genetic analysis | Mental retardation | Williams syndrome
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15. Full Text Long-term Surgical Prognosis of Primary Supravalvular Aortic Stenosis Repair
by Wu, Fei-Yi and Mondal, Abhijit and del Nido, Pedro J and Gauvreau, Kimberlee and Emani, Sitaram M and Baird, Christopher W and Kaza, Aditya K
The Annals of Thoracic Surgery, ISSN 0003-4975, 10/2019, Volume 108, Issue 4, pp. 1202 - 1209
Supravalvular aortic stenosis (SVAS) represents a heterogeneous group, including Williams syndrome, familial elastin arteriopathy, sporadic cases, and others.... 
SURGERY | CARDIAC & CARDIOVASCULAR SYSTEMS | EXPERIENCE | OUTCOMES | RESPIRATORY SYSTEM | WILLIAMS-SYNDROME
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16. Full Text Editorial: Special edition on Williams Syndrome
by Riby, Deborah M and Porter, Melanie A
Journal of Intellectual Disability Research, ISSN 0964-2633, 10/2016, Volume 60, Issue 10, pp. 901 - 902
Upon deciding that there was a timely need to put together a special edition of JIDR on the topic of Williams Syndrome, we were pleasantly surprised at the... 
HETEROGENEITY | REHABILITATION | EDUCATION, SPECIAL | Williams' syndrome | Articles | Research
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17. Spatial representation
: from gene to mind
by Landau, Barbara
2012, Developmental Cognitive Neuroscience, ISBN 9780195385373, cm.
Our experience of the spatial world is a unitary one; we perceive objects and layouts, we remember them and act on them, and we can even talk about them with... 
Biology, life sciences | Williams syndrome | cognitive psychology | Cognition disorders | Space | Dorsal Stream | Object Recognition | Navigation | Language | Ventral Stream | Genes | Development | Williams Syndrome | Cognition
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18. Full Text Williams Syndrome Associated with Isolated Growth Hormone Deficiency: Is It Just a Coincidence?
by Ogur, Gonul and Kara, Cengiz and Yalcin, Hatice Yelda and Yilmaz, Aysegul and Altundag, Engin and Abur, Ummet and Baysal, Kemal and Aydin, Murat
Journal of Clinical Research in Pediatric Endocrinology, ISSN 1308-5727, 06/2017, Volume 9, Issue 2, p. 18
Case studies | Diagnosis | Children | Williams syndrome | Diseases
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19. Dissociating intuitive physics from intuitive psychology: Evidence from Williams syndrome
by Frederik S Kamps and Joshua B Julian and Peter Battaglia and Barbara Landau and Nancy Kanwisher and Daniel D Dilks
Cognition, ISSN 0010-0277, 11/2017, Volume 168, p. 146
Prior work suggests that our understanding of how things work ("intuitive physics") and how people work ("intuitive psychology") are distinct domains of human... 
Social interactions | Cognition & reasoning | Psychology | Spatial discrimination | Cognition | Knowledge | Physics | Williams syndrome
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20. Full Text Health Care Supervision for Children With Williams Syndrome
by Committee on Genetics and Comm Pediat
Pediatrics, ISSN 0031-4005, 05/2001, Volume 107, Issue 5, pp. 1192 - 1204
This set of guidelines is designed to assist the pediatrician to care for children with Williams syndrome diagnosed by clinical features and with regional... 
ADULTS | PEDIATRICS | Care and treatment | Williams syndrome
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