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Co-authors
(59)
Michael G. Hanna
15
Dimitri M. Kullmann
7
Stephanie Schorge
7
S. Veronica Tan
5
Emma Matthews
4
Journals
(11)
NEUROMUSCULAR DISORD
5
Neurology
2
Case Reports
2
DIS MODEL MECH
1
J PHYSIOL-LONDON
1
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Authors
Sanjeev Rajakulendran
Sanjeev Rajakulendran,Imperial College London,Neuroscience,Pathology,Genetics & Genealogy
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Sanjeev Rajakulendran
Imperial College London
Publications:
17
|
Citations:
25
Fields:
Neuroscience
,
Pathology
,
Genetics & Genealogy
View FAQ about top research areas and Fields of study
Collaborated with
59 co-authors
from 2007 to 2011
|
Cited by
109 authors
Cumulative
Annual
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Publications
(17)
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Candidate Screening of the TRPC3 Gene in Cerebellar Ataxia
Esther B. E. Becker
,
Brent L. Fogel
,
Sanjeev Rajakulendran
,
Anna Dulneva
,
Michael G. Hanna
,
Susan L. Perlman
,
Daniel H. Geschwind
,
Kay E. Davies
Journal:
Cerebellum
, vol. 10, no. 2, pp. 296-299, 2011
Subacute combined degeneration of the spinal cord due to vitamin B12 deficiency
Jon Fenton
,
Sanjeev Rajakulendran
,
Roger Chinn
,
John C Janssen
Journal:
Case Reports
, vol. 2011, 2011
P27 Genotype-phenotype correlation and longitudinal three year natural history study in the non-dystrophic myotonias in the UK
D. L. Raja Rayan
,
E. Matthews
,
S. Rajakulendran
,
G. Barreto
,
S. V. Tan
,
L. Dewar
,
J. Burge
,
R. C. Griggs
,
R. Barohn
,
M. G. Hanna
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, pp. S14-S14, 2011
P29 Genotype-phenotype correlation and longitudinal study of Andersen-Tawil Syndrome in the UK
D. L. Raja Rayan
,
S. Rajakulendran
,
G. Barreto
,
S. V. Tan
,
L. Dewar
,
R. C. Griggs
,
M. G. Hanna
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, pp. S14-S14, 2011
Familial cerebral cavernomas due to a KRIT1 mutation presenting with epilepsy
Sanjeev Rajakulendran
,
Sreeman Andole
,
Angus Kennedy
Journal:
Case Reports
, vol. 2011, 2011
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Citations
(25 times by 22 publications)
Fístula colecistocólica: un hallazgo casual en colangiopancreatografía retrógrada endoscópica programada por coledocolitiasis
Josefina Morales Ruiz
,
Sonia González Castillo
,
Julio Pleguezuelo Díaz
Journal:
Gastroenterology
, vol. 34, no. 8, pp. 585-586, 2011
Human ataxias: a genetic dissection of inositol triphosphate receptor ( ITPR1)-dependent signaling
(
Citations: 7
)
Stephanie Schorge
,
Joyce van de Leemput
,
Andrew Singleton
,
Henry Houlden
,
John Hardy
Journal:
Trends in Neurosciences - TRENDS NEUROSCI
, vol. 33, no. 5, pp. 211-219, 2010
Ca V 2.1 channelopathies
(
Citations: 2
)
Daniela Pietrobon
Journal:
Pflugers Archiv-european Journal of Physiology - PFLUGERS ARCH-EUR J PHYSIOL
, vol. 460, no. 2, pp. 375-393, 2010
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2
(
Citations: 1
)
Elide Mantuano
,
Silvia Romano
,
Liana Veneziano
,
Cinzia Gellera
,
Barbara Castellotti
,
Sara Caimi
,
Daniela Testa
,
Margherita Estienne
,
Giovanna Zorzi
,
Marianna Bugiani
,
Yusuf A. Rajabally
,
Maria J Garcìa Barcina
http://academic.research.microsoft.com/io.ashx?type=5&id=35349926&selfId1=25370204&selfId2=0&maxNumber=12&query=
Journal:
Journal of The Neurological Sciences - J NEUROL SCI
, vol. 291, no. 1, pp. 30-36, 2010
Episodic cerebellar dysfunction in a bichon frise: a canine case of episodic ataxia?
A. L. Hopkins
,
J. Clarke
Journal:
Journal of Small Animal Practice - J SMALL ANIM PRACT
, vol. 51, no. 8, pp. 444-446, 2010
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