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G Matthijs

Showing results (101-110 of 157) with videos related to

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Journal of Manipulative and Physiological Therapeutics|November 8, 2025
Effect of Cervical Lateral Flexion Prepositioning on Segmental Cervical Axial Rotation of C1 and C2: A Computed Tomography Cadaveric InvestigationAnja Matthijs, Omer C G Matthijs, Gunther Ch Windisch, et al.
Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.
PM & R : the Journal of Injury, Function, and Rehabilitation|September 18, 2013
Co-contractive activation of the superficial multifidus during volitional preemptive abdominal contractionOmer C G Matthijs, Gregory S Dedrick, C Roger James, et al.
Journal of Inherited Metabolic Disease|October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylationJ Jaeken, W Vleugels, L Régal, et al.
Human Mutation|September 12, 2000
Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extensionB Gérard, N Ginet, G Matthijs, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A case with rare type of congenital disorder of glycosylation: PGM1-CDGA Küçükçongar, L Tümer, F Süheyl Ezgü, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 21, 2009
TDP-43 M311V mutation in familial amyotrophic lateral sclerosisR Lemmens, V Race, N Hersmus, et al.
Archives of Disease in Childhood|September 25, 2001
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannoseC J Hendriksz, P McClean, M J Henderson, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
ALG11-CDG: Three novel mutations and further characterization of the phenotypeL Regal, P M van Hasselt, F Foulquier, et al.
The European Journal of Neuroscience|August 24, 2005
Tissue distribution of the murine phosphomannomutases Pmm1 and Pmm2 during brain developmentK Cromphout, L Keldermans, A Snellinx, et al.
Pageof 16

Showing results (101-110 of 157) with videos related to

Sort By:
Pageof 16
Journal of Manipulative and Physiological Therapeutics|November 8, 2025
Effect of Cervical Lateral Flexion Prepositioning on Segmental Cervical Axial Rotation of C1 and C2: A Computed Tomography Cadaveric InvestigationAnja Matthijs, Omer C G Matthijs, Gunther Ch Windisch, et al.
Journal of Medical Genetics|May 1, 1997
Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndromeK Devriendt, P Petit, G Matthijs, et al.
PM & R : the Journal of Injury, Function, and Rehabilitation|September 18, 2013
Co-contractive activation of the superficial multifidus during volitional preemptive abdominal contractionOmer C G Matthijs, Gregory S Dedrick, C Roger James, et al.
Journal of Inherited Metabolic Disease|October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylationJ Jaeken, W Vleugels, L Régal, et al.
Human Mutation|September 12, 2000
Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extensionB Gérard, N Ginet, G Matthijs, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A case with rare type of congenital disorder of glycosylation: PGM1-CDGA Küçükçongar, L Tümer, F Süheyl Ezgü, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 21, 2009
TDP-43 M311V mutation in familial amyotrophic lateral sclerosisR Lemmens, V Race, N Hersmus, et al.
Archives of Disease in Childhood|September 25, 2001
Successful treatment of carbohydrate deficient glycoprotein syndrome type 1b with oral mannoseC J Hendriksz, P McClean, M J Henderson, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
ALG11-CDG: Three novel mutations and further characterization of the phenotypeL Regal, P M van Hasselt, F Foulquier, et al.
The European Journal of Neuroscience|August 24, 2005
Tissue distribution of the murine phosphomannomutases Pmm1 and Pmm2 during brain developmentK Cromphout, L Keldermans, A Snellinx, et al.
Pageof 16