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Co-authors
(700)
Katherine M. D Bushby
127
Hanns Lochmuller (Hanns Lochmüller)
62
Francesco Muntoni
42
Steven H. Laval
38
Rita Barresi
34
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(42)
NEUROMUSCULAR DISORD
106
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Academic
Authors
Volker Straub
Volker Straub,Newcastle University,Neuroscience,Pathology,Genetics & Genealogy
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Volker Straub
Newcastle University
Publications:
196
|
Citations:
2912
Fields:
Neuroscience
,
Pathology
,
Genetics & Genealogy
View FAQ about top research areas and Fields of study
Collaborated with
700 co-authors
from 1992 to 2011
|
Cited by
6583 authors
Cumulative
Annual
Sort by:
Publications
(196)
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Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect
(
Citations: 4
)
Jan Senderek
,
Juliane S. Müller
,
Marina Dusl
,
Tim M. Strom
,
Velina Guergueltcheva
,
Irmgard Diepolder
,
Steven H. Laval
,
Susan Maxwell
,
Judy Cossins
,
Sabine Krause
,
Nuria Muelas
,
Juan J. Vilchez
Volker Straub
http://academic.research.microsoft.com/io.ashx?type=5&id=49005382&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 88, no. 2, pp. 162-172, 2011
P63 A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy
(
Citations: 4
)
P. Hicks
,
A. Sarkozy
,
N. Muelas
,
K. Koehler
,
A. Huebner
,
G. Hudson
,
P. F. Chinnery
,
R. Barresi
,
M. Eagle
,
T. Polvikoski
,
G. Bailey
,
J. Miller
V. Straub
http://academic.research.microsoft.com/io.ashx?type=5&id=49477727&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, pp. S24-S25, 2011
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study
(
Citations: 2
)
Sebahattin Cirak
,
Virginia Arechavala-Gomeza
,
Michela Guglieri
,
Lucy Feng
,
Silvia Torelli
,
Karen Anthony
,
Stephen Abbs
,
Maria Elena Garralda
,
John Bourke
,
Dominic J Wells
,
George Dickson
,
Matthew JA Wood
Volker Straub
http://academic.research.microsoft.com/io.ashx?type=5&id=49175286&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
Lancet
, vol. 378, no. 9791, pp. 595-605, 2011
3FC2.2 Muscle MRI in congenital myopathies due to Ryanodine receptor type 1 (RYR1) gene mutations
(
Citations: 1
)
A. Klein
,
H. Jungbluth
,
E. Clement
,
S. Lillis
,
S. Abbs
,
P. Munot
,
M. Pane
,
E. Wraige
,
U. Schara
,
V. Straub
,
E. M. Mercuri
,
F. Muntoni
Journal:
European Journal of Paediatric Neurology - EUR J PAEDIATR NEUROL
, vol. 15, pp. S28-S28, 2011
P3.41. Clinical and genetic findings in a large cohort of patients with congenital myopathies due to mutations in the skeletal muscle ryanodine receptor (RYR1) gene
S. Lillis
,
I. Oprea
,
M. Scoto
,
S. Robb
,
A. Manzur
,
V. Straub
,
H. Roper
,
P. Y. Jeannet
,
U. B. Jensen
,
E. Wraige
,
N. Trump
,
W. Rakowicz
http://academic.research.microsoft.com/io.ashx?type=5&id=49477963&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, no. 9, pp. 694-694, 2011
Sort by:
Citations
(2912 times by 1809 publications)
Consensus Statement on Standard of Care for Congenital Myopathies
Ching H. Wang
,
James J. Dowling
,
Kathryn North
,
Mary K. Schroth
,
Thomas Sejersen
,
Frederic Shapiro
,
Jonathan Bellini
,
Hali Weiss
,
Marc Guillet
,
Kimberly Amburgey
,
Susan Apkon
,
Enrico Bertini
http://academic.research.microsoft.com/io.ashx?type=5&id=57196580&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
Journal of Child Neurology - JCN
, vol. 27, no. 3, pp. 363-382, 2012
Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer
Satoshi Inoue
,
Rameshwar Patil
,
Jose Portilla-Arias
,
Hui Ding
,
Bindu Konda
,
Andres Espinoza
,
Dmitriy Mongayt
,
Janet L. Markman
,
Adam Elramsisy
,
H. Westley Phillips
,
Keith L. Black
,
Eggehard Holler
http://academic.research.microsoft.com/io.ashx?type=5&id=57402676&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
PLOS One
, vol. 7, no. 2, 2012
Co-Regulation of Cell Polarization and Migration by Caveolar Proteins PTRF/Cavin-1 and Caveolin-1
Michelle M. Hill
,
Noor Huda Daud
,
Cho Sanda Aung
,
Dorothy Loo
,
Sally Martin
,
Samantha Murphy
,
Debra M. Black
,
Rachael Barry
,
Fiona Simpson
,
Libin Liu
,
Paul F. Pilch
,
John F. Hancock
http://academic.research.microsoft.com/io.ashx?type=5&id=57407325&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
PLOS One
, vol. 7, no. 8, 2012
Long-term Restoration of Cardiac Dystrophin Expression in Golden Retriever Muscular Dystrophy Following rAAV6-mediated Exon Skipping
Lawrence T Bish
,
Meg M Sleeper
,
Sean C Forbes
,
Bingjing Wang
,
Caryn Reynolds
,
Gretchen E Singletary
,
Dennis Trafny
,
Kevin J Morine
,
Julio Sanmiguel
,
Sylvain Cecchini
,
Tamas Virag
,
Adeline Vulin
http://academic.research.microsoft.com/io.ashx?type=5&id=56566500&selfId1=2265969&selfId2=0&maxNumber=12&query=
Journal:
Molecular Therapy - MOL THER
, vol. 20, no. 3, pp. 580-589, 2012
TRIM32 Regulates Skeletal Muscle Stem Cell Differentiation and Is Necessary for Normal Adult Muscle Regeneration
Sarah Nicklas
,
Anthony Otto
,
Xiaoli Wu
,
Pamela Miller
,
Sandra Stelzer
,
Yefei Wen
,
Shihuan Kuang
,
Klaus Wrogemann
,
Ketan Patel
,
Hao Ding
,
Jens C. Schwamborn
Journal:
PLOS One
, vol. 7, no. 1, 2012
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