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Neurology. Genetics
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October 8, 2024
A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family: The Exception That Proves the Rule
Kristl G Claeys, Marco Savarese, Per Harald Jonson, et al.
Journal of Clinical Microbiology
|
May 1, 1996
Endocarditis of native aortic and mitral valves due to Corynebacterium accolens: report of a case and application of phenotypic and genotypic techniques for identification
G Claeys, H Vanhouteghem, P Riegel, et al.
Journal of Mother and Child
|
March 8, 2021
A Patient with neonatal cholestasis
Kristl G Claeys, Luc Breysem, Eric Legius, et al.
Neurology
|
November 24, 2012
Myopathy with lobulated fibers, cores, and rods caused by a mutation in collagen VI
Kristl G Claeys, Simone Schrading, Ahmet Bozkurt, et al.
Neuromuscular Disorders : NMD
|
January 17, 2021
Respiratory decline in adult patients with Becker muscular dystrophy: A longitudinal study
Bram De Wel, Sofie Willaert, Aleksandra Nadaj-Pakleza, et al.
Journal of Clinical Microbiology
|
November 29, 2001
Case of catheter sepsis with Ralstonia gilardii in a child with acute lymphoblastic leukemia
G Wauters, G Claeys, G Verschraegen, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
December 30, 1998
Cardioverter-lead electrode infection due to Corynebacterium amycolatum
M Vaneechoutte, D De Bleser, G Claeys, et al.
Acta Neurologica Belgica
|
April 22, 2024
Recommendations for the management of myasthenia gravis in Belgium
Jan L De Bleecker, Gauthier Remiche, Alicia Alonso-Jiménez, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 22, 2017
Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis
Maxim De Schaepdryver, Andreas Jeromin, Benjamin Gille, et al.
Neurology
|
February 21, 2012
Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrum
A Béhin, C Jardel, K G Claeys, et al.
Page
of 28
Search research articles
Search
Showing results (121-130 of 275) with videos related to
Sort By:
Page
of 28
Neurology. Genetics
|
October 8, 2024
A Titin Truncating Variant Causing a Dominant Myopathy With Cardiac Involvement in a Large Family: The Exception That Proves the Rule
Kristl G Claeys, Marco Savarese, Per Harald Jonson, et al.
Journal of Clinical Microbiology
|
May 1, 1996
Endocarditis of native aortic and mitral valves due to Corynebacterium accolens: report of a case and application of phenotypic and genotypic techniques for identification
G Claeys, H Vanhouteghem, P Riegel, et al.
Journal of Mother and Child
|
March 8, 2021
A Patient with neonatal cholestasis
Kristl G Claeys, Luc Breysem, Eric Legius, et al.
Neurology
|
November 24, 2012
Myopathy with lobulated fibers, cores, and rods caused by a mutation in collagen VI
Kristl G Claeys, Simone Schrading, Ahmet Bozkurt, et al.
Neuromuscular Disorders : NMD
|
January 17, 2021
Respiratory decline in adult patients with Becker muscular dystrophy: A longitudinal study
Bram De Wel, Sofie Willaert, Aleksandra Nadaj-Pakleza, et al.
Journal of Clinical Microbiology
|
November 29, 2001
Case of catheter sepsis with Ralstonia gilardii in a child with acute lymphoblastic leukemia
G Wauters, G Claeys, G Verschraegen, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
December 30, 1998
Cardioverter-lead electrode infection due to Corynebacterium amycolatum
M Vaneechoutte, D De Bleser, G Claeys, et al.
Acta Neurologica Belgica
|
April 22, 2024
Recommendations for the management of myasthenia gravis in Belgium
Jan L De Bleecker, Gauthier Remiche, Alicia Alonso-Jiménez, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 22, 2017
Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis
Maxim De Schaepdryver, Andreas Jeromin, Benjamin Gille, et al.
Neurology
|
February 21, 2012
Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrum
A Béhin, C Jardel, K G Claeys, et al.
Page
of 28