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Co-authors
(17)
Enrico Bertini
1
Ingrid E. Scheffer
1
Sabrina Giglio
1
Elena Parrini
1
Chantal Missirian
1
Journals
(1)
Neurology
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Authors
E. Pallesi
E. Pallesi,Neuroscience
Edit
E. Pallesi
Publications:
1
|
Citations:
13
Fields:
Neuroscience
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Collaborated with
17 co-authors
in 2009
|
Cited by
118 authors
Cumulative
Annual
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Publications
(1)
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Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion
(
Citations: 13
)
C. Cardoso
,
A. Boys
,
E. Parrini
,
C. Mignon-Ravix
,
J. M. McMahon
,
S. Khantane
,
E. Bertini
,
E. Pallesi
,
C. Missirian
,
O. Zuffardi
,
F. Novara
,
L. Villard
http://academic.research.microsoft.com/io.ashx?type=5&id=37725007&selfId1=28524385&selfId2=0&maxNumber=12&query=
Journal:
Neurology
, vol. 72, no. 9, pp. 784-792, 2009
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Citations
(13 times by 13 publications)
Neuronal migration disorders
(
Citations: 13
)
Renzo Guerrini
,
Elena Parrini
Journal:
Neurobiology of Disease - NEUROBIOL DISEASE
, vol. 38, no. 2, pp. 154-166, 2010
5q14.3 Deletion Manifesting as Mitochondrial Disease and Autism: Case Report
(
Citations: 7
)
Herbert Ezugha
,
Michael Goldenthal
,
Ignacio Valencia
,
Carol E. Anderson
,
Agustin Legido
,
Harold Marks
Journal:
Journal of Child Neurology - JCN
, vol. 25, no. 10, pp. 1232-1235, 2010
Severe mental retardation, seizures, and hypotonia due to deletions of MEF2C
(
Citations: 5
)
Beata A. Nowakowska
,
Ewa Obersztyn
,
Krystyna Szymańska
,
Monika Bekiesińska-Figatowska
,
Zhilian Xia
,
Christian B. Ricks
,
Ewa Bocian
,
David W. Stockton
,
Krzysztof Szczałuba
,
Magdalena Nawara
,
Ankita Patel
,
Daryl A. Scott
http://academic.research.microsoft.com/io.ashx?type=5&id=34289455&selfId1=28524385&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Medical Genetics Part B-neuropsychiatric Genetics - AM J MED GENET PART B
, vol. 9999B, 2010
Neurodevelopmental disorders in children with severe to profound sensorineural hearing loss: a clinical study: Neurodevelopmental Disorders in Children with SNHL
(
Citations: 1
)
ANNA M CHILOSI
,
ALESSANDRO COMPARINI
,
MARIA F SCUSA
,
STEFANO BERRETTINI
,
FRANCESCA FORLI
,
ROBERTA BATTINI
,
PAOLA CIPRIANI
,
GIOVANNI CIONI
Journal:
Developmental Medicine and Child Neurology - DEVELOP MED CHILD NEUROL
, vol. 52, no. 9, pp. 856-862, 2010
Array Comparative Genomic Hybridization as a Diagnostic Tool for Syndromic Heart Defects
(
Citations: 2
)
Jeroen Breckpot
,
Bernard Thienpont
,
Hilde Peeters
,
Thomy de Ravel
,
Amihood Singer
,
Maissa Rayyan
,
Karel Allegaert
,
Christine Vanhole
,
Benedicte Eyskens
,
Joris Robert Vermeesch
,
Marc Gewillig
,
Koenraad Devriendt
Journal:
Journal of Pediatrics - J PEDIAT
, vol. 156, no. 5, pp. 810-817.e4, 2010
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