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Human & Experimental Toxicology
|
September 1, 1992
A case of porphyria due to carbaryl intoxication
H Sargin, S Cirak, S Gürçay
Der Nervenarzt
|
July 6, 2018
[Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable]
G Wunderlich, A Abicht, A Brunn, et al.
Child: Care, Health and Development
|
June 9, 2012
Emotional impact of genetic trials in progressive paediatric disorders: a dose-ranging exon-skipping trial in Duchenne muscular dystrophy
M E Garralda, H McConachie, A Le Couteur, et al.
Revue Neurologique
|
July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies
C Paketci, M Karakaya, P Edem, et al.
Neuropediatrics
|
June 15, 2006
Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum
A Olmez, G Uyanik, R K Ozgül, et al.
Neurology
|
January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathies
M Lommel, S Cirak, T Willer, et al.
Neuromuscular Disorders : NMD
|
February 12, 2013
Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom
L Maggi, M Scoto, S Cirak, et al.
Neuromuscular Disorders : NMD
|
July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement
T Cullup, P J Lamont, S Cirak, et al.
Neurology
|
January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures
R Straussberg, L Basel-Vanagaite, S Kivity, et al.
Neurology
|
June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patients
M Scoto, S Cirak, R Mein, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Human & Experimental Toxicology
|
September 1, 1992
A case of porphyria due to carbaryl intoxication
H Sargin, S Cirak, S Gürçay
Der Nervenarzt
|
July 6, 2018
[Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable]
G Wunderlich, A Abicht, A Brunn, et al.
Child: Care, Health and Development
|
June 9, 2012
Emotional impact of genetic trials in progressive paediatric disorders: a dose-ranging exon-skipping trial in Duchenne muscular dystrophy
M E Garralda, H McConachie, A Le Couteur, et al.
Revue Neurologique
|
July 26, 2020
Clinical, electrophysiological and genetic characteristics of childhood hereditary polyneuropathies
C Paketci, M Karakaya, P Edem, et al.
Neuropediatrics
|
June 15, 2006
Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum
A Olmez, G Uyanik, R K Ozgül, et al.
Neurology
|
January 13, 2010
Correlation of enzyme activity and clinical phenotype in POMT1-associated dystroglycanopathies
M Lommel, S Cirak, T Willer, et al.
Neuromuscular Disorders : NMD
|
February 12, 2013
Congenital myopathies--clinical features and frequency of individual subtypes diagnosed over a 5-year period in the United Kingdom
L Maggi, M Scoto, S Cirak, et al.
Neuromuscular Disorders : NMD
|
July 13, 2012
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement
T Cullup, P J Lamont, S Cirak, et al.
Neurology
|
January 12, 2005
An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures
R Straussberg, L Basel-Vanagaite, S Kivity, et al.
Neurology
|
June 15, 2011
SEPN1-related myopathies: clinical course in a large cohort of patients
M Scoto, S Cirak, R Mein, et al.
Page
of 2