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Pathologie-Biologie
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October 31, 2009
[High prevalence of community- and hospital-acquired infections of methicillin-resistant Staphylococcus aureus containing Panton-Valentine leukocidin gene in Algiers]
K Antri, N Rouzic, I Boubekri, et al.
Journal of the Neurological Sciences
|
January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients
M Tazir, L Ali-Pacha, A M'Zahem, et al.
Journal of Hepatology
|
June 1, 1987
Vitamin E deficiency and its clinical significance in adults with primary biliary cirrhosis and other forms of chronic liver disease
G P Jeffrey, D P Muller, A K Burroughs, et al.
Nature Genetics
|
November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
P Bomont, L Cavalier, F Blondeau, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene
M Chaouch, Y Allal, A De Sandre-Giovannoli, et al.
Annals of Human Genetics
|
June 14, 2008
Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western Africa
T Hamadouche, Y Poitelon, E Genin, et al.
Neuromolecular Medicine
|
June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease
O Dubourg, H Azzedine, C Verny, et al.
New Microbes and New Infections
|
June 25, 2015
Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria from 2005 to 2012
N Ramdani-Bouguessa, H Ziane, S Bekhoucha, et al.
Neurology
|
August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
H Azzedine, N Ravisé, C Verny, et al.
Neurology
|
December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P Richard, K Gaudon, H Haddad, et al.
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Search research articles
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Showing results (21-30 of 32) with videos related to
Sort By:
Page
of 4
Pathologie-Biologie
|
October 31, 2009
[High prevalence of community- and hospital-acquired infections of methicillin-resistant Staphylococcus aureus containing Panton-Valentine leukocidin gene in Algiers]
K Antri, N Rouzic, I Boubekri, et al.
Journal of the Neurological Sciences
|
January 15, 2009
Ataxia with oculomotor apraxia type 2: a clinical and genetic study of 19 patients
M Tazir, L Ali-Pacha, A M'Zahem, et al.
Journal of Hepatology
|
June 1, 1987
Vitamin E deficiency and its clinical significance in adults with primary biliary cirrhosis and other forms of chronic liver disease
G P Jeffrey, D P Muller, A K Burroughs, et al.
Nature Genetics
|
November 4, 2000
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
P Bomont, L Cavalier, F Blondeau, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene
M Chaouch, Y Allal, A De Sandre-Giovannoli, et al.
Annals of Human Genetics
|
June 14, 2008
Founder effect and estimation of the age of the c.892C>T (p.Arg298Cys) mutation in LMNA associated to Charcot-Marie-Tooth subtype CMT2B1 in families from North Western Africa
T Hamadouche, Y Poitelon, E Genin, et al.
Neuromolecular Medicine
|
June 16, 2006
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease
O Dubourg, H Azzedine, C Verny, et al.
New Microbes and New Infections
|
June 25, 2015
Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria from 2005 to 2012
N Ramdani-Bouguessa, H Ziane, S Bekhoucha, et al.
Neurology
|
August 23, 2006
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
H Azzedine, N Ravisé, C Verny, et al.
Neurology
|
December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
P Richard, K Gaudon, H Haddad, et al.
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of 4