Search research articles
Contact Us
Filters
Showing results (41-50 of 49) with videos related to
Page
of 5
Sort By:
You have reached the last page of results.
This site can display upto 49 results.
Proceedings of the National Academy of Sciences of the United States of America
|
August 16, 2000
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
K Jurkat-Rott, N Mitrovic, C Hang, et al.
Annals of Neurology
|
September 11, 1999
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
H Lerche, C Biervert, A K Alekov, et al.
Neurology
|
March 12, 2010
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2
Y G Weber, R Roebling, J Kassubek, et al.
Neurology
|
July 8, 2011
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias
M Strupp, R Kalla, J Claassen, et al.
Anesthesia and Analgesia
|
January 7, 2000
A multicenter study of 4-chloro-m-cresol for diagnosing malignant hyperthermia susceptibility
C P Baur, L Bellon, P Felleiter, et al.
European Journal of Neurology
|
June 26, 2001
EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. First of two parts
T Gasser, M Dichgans, J Finsterer, et al.
European Journal of Neurology
|
September 14, 2001
EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts
T Gasser, M Dichgans, J Finsterer, et al.
European Journal of Human Genetics : EJHG
|
April 18, 2003
Recent advances in the diagnosis of malignant hyperthermia susceptibility: how confident can we be of genetic testing?
R L Robinson, M J Anetseder, V Brancadoro, et al.
Neurology
|
October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation
N P Davies, P Imbrici, D Fialho, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Proceedings of the National Academy of Sciences of the United States of America
|
August 16, 2000
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
K Jurkat-Rott, N Mitrovic, C Hang, et al.
Annals of Neurology
|
September 11, 1999
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
H Lerche, C Biervert, A K Alekov, et al.
Neurology
|
March 12, 2010
Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2
Y G Weber, R Roebling, J Kassubek, et al.
Neurology
|
July 8, 2011
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxias
M Strupp, R Kalla, J Claassen, et al.
Anesthesia and Analgesia
|
January 7, 2000
A multicenter study of 4-chloro-m-cresol for diagnosing malignant hyperthermia susceptibility
C P Baur, L Bellon, P Felleiter, et al.
European Journal of Neurology
|
June 26, 2001
EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. First of two parts
T Gasser, M Dichgans, J Finsterer, et al.
European Journal of Neurology
|
September 14, 2001
EFNS Task Force on Molecular Diagnosis of Neurologic Disorders: guidelines for the molecular diagnosis of inherited neurologic diseases. Second of two parts
T Gasser, M Dichgans, J Finsterer, et al.
European Journal of Human Genetics : EJHG
|
April 18, 2003
Recent advances in the diagnosis of malignant hyperthermia susceptibility: how confident can we be of genetic testing?
R L Robinson, M J Anetseder, V Brancadoro, et al.
Neurology
|
October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation
N P Davies, P Imbrici, D Fialho, et al.
Page
of 5