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Co-authors
(166)
Montserrat Baiget
41
Maria Jesus Barcelo (María Jesús Barceló)
13
Laura Alias
12
Manel Baena
10
Adoracion Vencesla (Adoración Venceslá)
8
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Authors
Eduardo F. Tizzano
Eduardo F. Tizzano,Hospital de la Santa Creu i Sant Pau,Genetics & Genealogy,Neuroscience,Pathology
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Eduardo F. Tizzano
Hospital de la Santa Creu i Sant Pau
Publications:
54
|
Citations:
304
Fields:
Genetics & Genealogy
,
Neuroscience
,
Pathology
View FAQ about top research areas and Fields of study
Collaborated with
166 co-authors
from 1991 to 2011
|
Cited by
1082 authors
Cumulative
Annual
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Publications
(54)
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Ultrasound evaluation of fetal movements in pregnancies at risk for severe spinal muscular atrophy
(
Citations: 1
)
Juan Parra
,
Rebeca Martínez-Hernández
,
Eva Also-Rallo
,
Laura Alias
,
María Jesús Barceló
,
María Amenedo
,
Carmen Medina
,
Raquel Senosiain
,
Joaquim Calaf
,
Montserrat Baiget
,
Sara Bernal
,
Eduardo F. Tizzano
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, no. 2, pp. 97-101, 2011
Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability
Eva Also-Rallo
,
Laura Alías
,
Rebeca Martínez-Hernández
,
Lidia Caselles
,
María J Barceló
,
Montserrat Baiget
,
Sara Bernal
,
Eduardo F Tizzano
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 10, pp. 1059-1065, 2011
Plastin 3 expression in discordant spinal muscular atrophy (SMA) siblings
Sara Bernal
,
Eva Also-Rallo
,
Rebeca Martínez-Hernández
,
Laura Alías
,
Francisco Javier Rodríguez-Alvarez
,
José M. Millán
,
Concepción Hernández-Chico
,
Montserrat Baiget
,
Eduardo F. Tizzano
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, no. 6, pp. 413-419, 2011
The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor
(
Citations: 2
)
S. Bernal
,
L. Alias
,
M. J. Barcelo
,
E. Also-Rallo
,
R. Martinez-Hernandez
,
J. Gamez
,
E. Guillen-Navarro
,
J. Rosell
,
I. Hernando
,
F. J. Rodriguez-Alvarez
,
S. Borrego
,
J. M. Millan
E. F. Tizzano
http://academic.research.microsoft.com/io.ashx?type=5&id=30640742&selfId1=23762198&selfId2=0&maxNumber=12&query=
Journal:
Journal of Medical Genetics - J MED GENET
, vol. 47, no. 9, pp. 640-642, 2010
Measurement of muscle strength with a handheld dynamometer in patients with chronic spinal muscular atrophy
(
Citations: 1
)
A Febrer
,
N Rodriguez
,
L Alias
,
E Tizzano
Journal:
Journal of Rehabilitation Medicine - J REHABIL MED
, vol. 42, no. 3, pp. 228-231, 2010
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Citations
(304 times by 267 publications)
Nuclear Receptor Rev-erb Alpha (Nr1d1) Functions in Concert with Nr2e3 to Regulate Transcriptional Networks in the Retina
Nissa J. Mollema
,
Yang Yuan
,
Austin S. Jelcick
,
Andrew J. Sachs
,
Désirée von Alpen
,
Daniel Schorderet
,
Pascal Escher
,
Neena B. Haider
,
Ellen Nollen
Journal:
PLOS One
, vol. 6, no. 3, 2011
A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites
Jessica X Chong
,
A Afşin Oktay
,
Zunyan Dai
,
Kathryn J Swoboda
,
Thomas W Prior
,
Carole Ober
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 10, pp. 1045-1051, 2011
Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III
Galina Yu Zheleznyakova
,
Anton V Kiselev
,
Viktor G Vakharlovsky
,
Mathias Rask-Andersen
,
Rohit Chavan
,
Anna A Egorova
,
Helgi B Schiöth
,
Vladislav S Baranov
Journal:
BMC Medical Genetics - BMC MED GENET
, vol. 12, no. 1, pp. 1-9, 2011
Detection of Spinal Muscular Atrophy Carriers in a Sample of the Brazilian Population
K. C. Bueno
,
S. P. Gouvea
,
A. B. Genari
,
C. A. Funayama
,
D. L. Zanette
,
W. A. Silva Jr
,
A. B. Oliveira
,
R. H. Scola
,
L. C. Werneck
,
W. Marques Jr
Journal:
Neuroepidemiology
, vol. 36, pp. 105-108, 2011
Treatment of spinal muscular atrophy cells with drugs that upregulate SMN expression reveals inter- and intra-patient variability
Eva Also-Rallo
,
Laura Alías
,
Rebeca Martínez-Hernández
,
Lidia Caselles
,
María J Barceló
,
Montserrat Baiget
,
Sara Bernal
,
Eduardo F Tizzano
Journal:
European Journal of Human Genetics - EUR J HUMAN GENET
, vol. 19, no. 10, pp. 1059-1065, 2011
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