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The Journal of Rheumatology
|
November 1, 1993
31P magnetic resonance muscle spectroscopy in fibromyalgia
E Joos, K De Meirleir, K Vandenborne, et al.
Child and Adolescent Psychiatry and Mental Health
|
July 30, 2014
Psychosis in an adolescent girl: a common manifestation in Niemann-Pick Type C disease
Sara Wouters, Linda De Meirleir, Edward Campforts, et al.
British Medical Journal (Clinical Research Ed.)
|
March 9, 1985
The role of endogenous opiates in thermal regulation of the body during exercise
K De Meirleir, T Arentz, W Hollmann, et al.
Pediatric Neurology
|
July 3, 1998
Dancing eye syndrome and hyperphosphatasemia
D E Hasaerts, F K Gorus, L J De Meirleir
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunit
L J de Meirleir, W Lissens, E Vamos, et al.
Acta Clinica Belgica
|
January 1, 1980
Hypothyroidism with normal thyroid hormone levels as a consequence of autoimmune thyroiditis and peripheral resistance to thyroid hormone
K De Meirleir, J Golstein, M H Jonckheer, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1988
Multimodal evoked potential studies in leukodystrophies of children
L J De Meirleir, M J Taylor, W J Logan
Medical Hypotheses
|
February 28, 2003
Type I interferons induce proteins susceptible to act as thyroid receptor (TR) corepressors and to signal the TR for destruction by the proteasome: possible etiology for unexplained chronic fatigue
P Englebienne, M Verhas, C V Herst, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
May 1, 2002
Antiviral pathway activation in chronic fatigue syndrome and acute infection
Kenny De Meirleir, Robert J Suhadolnik, Bernard Lebleu, et al.
Pediatric Research
|
December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency
A K Cardozo, L De Meirleir, I Liebaers, et al.
Page
of 25
Search research articles
Search
Showing results (41-50 of 250) with videos related to
Sort By:
Page
of 25
The Journal of Rheumatology
|
November 1, 1993
31P magnetic resonance muscle spectroscopy in fibromyalgia
E Joos, K De Meirleir, K Vandenborne, et al.
Child and Adolescent Psychiatry and Mental Health
|
July 30, 2014
Psychosis in an adolescent girl: a common manifestation in Niemann-Pick Type C disease
Sara Wouters, Linda De Meirleir, Edward Campforts, et al.
British Medical Journal (Clinical Research Ed.)
|
March 9, 1985
The role of endogenous opiates in thermal regulation of the body during exercise
K De Meirleir, T Arentz, W Hollmann, et al.
Pediatric Neurology
|
July 3, 1998
Dancing eye syndrome and hyperphosphatasemia
D E Hasaerts, F K Gorus, L J De Meirleir
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pyruvate dehydrogenase deficiency due to a mutation of the E1 alpha subunit
L J de Meirleir, W Lissens, E Vamos, et al.
Acta Clinica Belgica
|
January 1, 1980
Hypothyroidism with normal thyroid hormone levels as a consequence of autoimmune thyroiditis and peripheral resistance to thyroid hormone
K De Meirleir, J Golstein, M H Jonckheer, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
February 1, 1988
Multimodal evoked potential studies in leukodystrophies of children
L J De Meirleir, M J Taylor, W J Logan
Medical Hypotheses
|
February 28, 2003
Type I interferons induce proteins susceptible to act as thyroid receptor (TR) corepressors and to signal the TR for destruction by the proteasome: possible etiology for unexplained chronic fatigue
P Englebienne, M Verhas, C V Herst, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
May 1, 2002
Antiviral pathway activation in chronic fatigue syndrome and acute infection
Kenny De Meirleir, Robert J Suhadolnik, Bernard Lebleu, et al.
Pediatric Research
|
December 5, 2000
Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency
A K Cardozo, L De Meirleir, I Liebaers, et al.
Page
of 25