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Co-authors
(135)
Akbar Soltanzadeh
4
Hajir Sikaroodi
4
Askar Ghorbani
4
P. Lederlin
3
Antoine E. Tarazi
3
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(11)
CLIN NEUROPHYSIOL
5
REV MED INTERNE
3
AMER J HUM GENET
2
NEUROMUSCULAR DISORD
2
ANTI-CANCER DRUG
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Authors
Shahriar Nafissi
Shahriar Nafissi,Tehran University of Medical Sciences,Neuroscience,Physiology,Genetics & Genealogy
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Shahriar Nafissi
Tehran University of Medical Sciences
Publications:
24
|
Citations:
27
Fields:
Neuroscience
,
Physiology
,
Genetics & Genealogy
View FAQ about top research areas and Fields of study
Collaborated with
135 co-authors
from 1991 to 2011
|
Cited by
106 authors
Cumulative
Annual
Sort by:
Publications
(24)
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RefWorks
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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
Shahriar Nafissi
http://academic.research.microsoft.com/io.ashx?type=5&id=49005382&selfId1=24406449&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 88, no. 2, pp. 162-172, 2011
KIF1A, an Axonal Transporter of Synaptic Vesicles, Is Mutated in Hereditary Sensory and Autonomic Neuropathy Type 2
Jean-Baptiste Rivière
,
Siriram Ramalingam
,
Valérie Lavastre
,
Masoud Shekarabi
,
Sébastien Holbert
,
Julie Lafontaine
,
Myriam Srour
,
Nancy Merner
,
Daniel Rochefort
,
Pascale Hince
,
Rébecca Gaudet
,
Anne-Marie Mes-Masson
Shahriar Nafissi
http://academic.research.microsoft.com/io.ashx?type=5&id=49005496&selfId1=24406449&selfId2=0&maxNumber=12&query=
Journal:
American Journal of Human Genetics - AMER J HUM GENET
, vol. 89, no. 2, pp. 219-230, 2011
P5.17 Congenital Myasthenic Syndromes with COLQ mutations: Long term follow-up
P. Richard
,
T. Kuntzer
,
S. Nafissi
,
K. Gaudon
,
D. Sternberg
,
E. Fournier
,
A. Gevin
,
B. Eymard
,
T. Stojkovic
Journal:
Neuromuscular Disorders - NEUROMUSCULAR DISORD
, vol. 21, no. 9, pp. 728-729, 2011
Silibinin inhibits invasive properties of human glioblastoma U87MG cells through suppression of cathepsin B and nuclear factor kappa B-mediated induction of matrix metalloproteinase 9
(
Citations: 1
)
Majid Momeny
,
Mohsen Malehmir
,
Majid Zakidizaji
,
Reza Ghasemi
,
Habibeh Ghadimi
,
Mohammad A. Shokrgozar
,
Amir H. Emami
,
Shahriar Nafissi
,
Ardeshir Ghavamzadeh
,
Seyed H. Ghaffari
Journal:
Anti-cancer Drugs - ANTI-CANCER DRUG
, vol. 21, no. 3, pp. 252-260, 2010
P12-3 Electrophysiologic findings in Guillain Barré syndrome
S. Nafissi
,
S. Yadegari
,
N. Kazemi
,
H. Sikaroodi
,
A. Ghorbani
,
A. Soltanzadeh
Journal:
Clinical Neurophysiology - CLIN NEUROPHYSIOL
, vol. 121, pp. S172-S172, 2010
Sort by:
Citations
(27 times by 27 publications)
CAG Repeat Variants in the POLG1 Gene Encoding mtDNA Polymerase-Gamma and Risk of Breast Cancer in African-American Women
Sami Azrak
,
Vanniarajan Ayyasamy
,
Gary Zirpoli
,
Christine Ambrosone
,
Elisa V. Bandera
,
Dana H. Bovbjerg
,
Lina Jandorf
,
Gregory Ciupak
,
Warren Davis
,
Karen S. Pawlish
,
Ping Liang
,
Keshav Singh
Journal:
PLOS One
, vol. 7, no. 1, 2012
Neuromuskuläre Signalübertragung im Erwachsenenalter
S. Kröger
,
B. Schoser
Journal:
Nervenarzt
, vol. 82, no. 6, pp. 707-711, 2011
Radiation-inducible promoter mediated puma gene for the treatment of tongue squamous cell carcinoma
D. Yu
,
W. Zhao
,
X. Wu
Journal:
International Journal of Oral and Maxillofacial Surgery - INT J ORAL MAXILLOFAC SURG
, vol. 40, no. 10, pp. 1069-1070, 2011
Neurologic Wilson's disease
(
Citations: 5
)
Matthew T. Lorincz
Journal:
Annals of The New York Academy of Sciences - ANN N Y ACAD SCI
, vol. 1184, no. 1, pp. 173-187, 2010
Antimetastatic efficacy of silibinin: molecular mechanisms and therapeutic potential against cancer
(
Citations: 4
)
Gagan Deep
,
Rajesh Agarwal
Journal:
Cancer and Metastasis Reviews - CANCER METAST REV
, vol. 29, no. 3, pp. 447-463, 2010
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