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Artigos de Referência - Deficiências - Síndromes Diversas

Referências

1 - Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome.
Ursula Bellugi 1, Liz Lichtenberger 1, Debra Mills 2, Albert Galaburda 3, Julie R. Korenberg 4.
1 - The Salk Institute for Biological Studies, La Jolla, USA;
2 - University of California, San Diego, USA;
3 - Beth Israel Deaconess Medical Center, Boston, MA, USA;
4 - Cedars-Sinai Medical Center, Los Angeles, USA.
Trends Neurosci. (1999) 22, 197-207.

2 - Coding space within but not between objects: evidence from Balint's syndrome.
A. C. G. Cooper, G, W. Humphreys.
Cognitive Science Research Centre, School of Psychology, University of Birmingham, Edghaston, Birmingham, UK.
Neuropsychologia 38 (2000) 723-733.

3 - Developmental Gerstmann's Syndrome: A Distinct Clinical Entity of Learning Disabilities.
Poovathinal A. Suresh 1, Swapna Sebastian 2.
1 - Department of Neurology; Sree Chitra Tirunal Institute for Medical Sciences and Techonology; and Institute for Communicative and Cognitive Neuro Sciences; Society for Rehabilitation of Cognitive and Communicative Disorders;
2 - Department of Speech Pathology and Audiology; Institute for Communicative and Cognitive Neuro Sciences; Society for Rehabilitation of Cognitive Neuro Sciences; Society for Rehabilitation of Cognitive and Communicative Disorders; Ulloor, Trivadrum, Derala, India.
Pediatric Neurology vol. 22 nº 4 (2002)

4 - Quantitative MR image analysis in subjects with defects in the PAX6 gene.
Samantha L. Free 1, 2, Tejal N. Mitchell 1, 2, Kathleen A. Williamson 3, Amanda J. Churchill 4, Simon D. Simon D. Shorvon 1, Anthony T. Moore 5, Veronica van heyningen 3, and Sanjay M. Sisodiya 1, 2.
1 - Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College london, Queen Square, London, UK;
2 - National Society for Epilepsy, Chalfont-St-Peter, Buchinghamshire, UK;
3 - MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK;
4 - Bristol Eye Hospital, Lower Maudlin Street, Bristol, UK;
5 - Moorfields Eye Hospital,City Road, London, UK.
NeuroImage 0 (2003) 000-000.

5 - Procedural learning deficit in children with Williams syndrome.
Stefano Vicari 1, 2, Samantha Bellucci 1, Giovanni Augusto Carlesimo 2.
1 - IRCCS, Ospedale Pediatrico BAmbino Gesù, Sevizio di Neuro e Riabilitazione, Lungomare Guglielmo Marcomi 36, Rome, Italy;
2 - IRCCS, Clinica Santa Lucia, Rome, Italy.
Neuropsychologia 39 (2001) 665-677.

6 - Neuroradiologic Aspects of West Syndrome.
Nur Aydinli 1, Mine Çaliskan 2, Meral Özmen 1, Erdem Tonguç, 3.
1 - Department of Pediatrics; Division of Pediatric Neurology; Istanbul University; Medical Faculty of Istanbul.
2 - Department of Pediatrics; Division of Pediatric Neurology; Istanbul University; Institute of Child Health.
3 - Institute of Pediatrics; Iltanbul University; Medical Faculty of Istanbul; Istanbul, Turkey.

7 - West Syndrome With Periventricular Leukomalacia: A Morphometric MRI Study.
Hiroshi Ozawa 1, 2, Toshiaki Hashimoto 2, Takashi Endo 3, Junichi Furuscho 3, Yasuyuki Suzuki 4, Eiko Takada 5, yonosuke Ogawa 5, Sachio Takashima 1.
1 - Departments of Mental Retardation and Birth Defect Research; National Institute of Neuroscience;
2 - Department of Child Neurology; National Center Hospital for Mental, Nervous and Muscular Disorders; National Center of Neurology and Psychiatry;
3 - Department of Pediatrics; Showa General Hospital;
4 - Department of Pediatrics; Tokyo Children's Rehabilitation Hospital; Tokyo;
5 - Department of Pediatrics; Saitama Medical Center; Saitama Medical School; Saitama, Japan.
Pediatric Neurology vol.19 nº 5 (1998)

8 - The Williams Syndrome Cognitive Profile.
Carolyn B. Mervis 1, Byron F. Robinson 1, Jacquelyn Bertrand 2, Colleen A. Morris 3, Bonita P. Klein-Tasman 4, Sharon C. Armstrong 5.
1 - University of Louisville;
2 - Centers for Disease Control;
3 - University of Nevada School of Medicine;
4 - Emory University;
5 - Ohio State University.
Brain and Cognition 44, 604-628 (2000)

9 - The Aicardi-Goutières Syndrome: Variable Clinical Expression in Two Siblings.
Aad Verrips 1, Johan A. P. Hiel 1, Fons J. M. Gabreëls 1, Pieter Wesseling 2, Jan J. Rotteveel 1.
1 - Department of Pediatric Neurology and;
2 - Pathology University Hospital Nijmegen: Nijmegen, The Netherlands.
Pediatric Neurology vol. 16 nº 4 (1997)

10 - Cerebral Perfusion in Children With Alice in Wonderland Syndrome.
Yung-Ting Kuo 1, 2, Nan-Chang Chiu 2, Ein-Yiao Shen 2, Che-Sheng Ho 2, Ming-Che Wu 3.
1 - Department of Pediatrics; Taipei Municipal Wan-Fang Hospital and;
2 - Department of Pediatrics;
3 - Nuclear Medicine; Machay Memorial Hospital; Taipei, Taiwan.

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