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Aad Verrips

Showing results (41-50 of 62) with videos related to

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Rheumatology (Oxford, England)|April 2, 2016
The value of routine creatine kinase and thyroid stimulating hormone testing in patients with suspected fibromyalgia: a cross-sectional studyNienke Lesuis, Judith van Vliet, Nadine Boers, et al.
The Journal of Pain|March 31, 2018
Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2Judith van Vliet, Alide A Tieleman, Aad Verrips, et al.
Journal of Inherited Metabolic Disease|September 13, 2017
Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosisBianca M L Stelten, Olivier Bonnot, Hidde H Huidekoper, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|November 22, 2017
Extremely Painful Multifocal Acquired Predominant Axonal Sensorimotor Neuropathy of the Upper LimbDoris Lieba-Samal, Jeroen J J van Eijk, Marieke H J van Rosmalen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 30, 2024
Chenodeoxycholic acid (CDCA) treatment during pregnancy in women with cerebrotendinous xanthomatosis (CTX): Lessons learned from 19 pregnanciesTzipora C Falik Zaccai, Sharon Hassin-Baer, Nehama Cohen Kfir, et al.
Human Mutation|April 1, 2006
The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardationJeroen van Reeuwijk, Svetlana Maugenre, Christa van den Elzen, et al.
Neuromuscular Disorders : NMD|August 21, 2018
A recurrent de novo DYNC1H1 tail domain mutation causes spinal muscular atrophy with lower extremity predominance, learning difficulties and mild brain abnormalitySophelia Hoi Shan Chan, Nens van Alfen, Inger Johanne Thuestad, et al.
Journal of Neurology|March 5, 2013
Pure adult-onset spastic paraplegia caused by a novel mutation in the KIAA0196 (SPG8) geneSusanne T de Bot, Sascha Vermeer, Wendy Buijsman, et al.
Acta Neuropathologica|March 4, 2010
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literatureCasper Jansen, Willem Voet, Mark W Head, et al.
Neurology|December 12, 2018
Long-term treatment effect in cerebrotendinous xanthomatosis depends on age at treatment startBianca M L Stelten, Hidde H Huidekoper, Bart P C van de Warrenburg, et al.
Pageof 7

Showing results (41-50 of 62) with videos related to

Sort By:
Pageof 7
Rheumatology (Oxford, England)|April 2, 2016
The value of routine creatine kinase and thyroid stimulating hormone testing in patients with suspected fibromyalgia: a cross-sectional studyNienke Lesuis, Judith van Vliet, Nadine Boers, et al.
The Journal of Pain|March 31, 2018
Qualitative and Quantitative Aspects of Pain in Patients With Myotonic Dystrophy Type 2Judith van Vliet, Alide A Tieleman, Aad Verrips, et al.
Journal of Inherited Metabolic Disease|September 13, 2017
Autism spectrum disorder: an early and frequent feature in cerebrotendinous xanthomatosisBianca M L Stelten, Olivier Bonnot, Hidde H Huidekoper, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|November 22, 2017
Extremely Painful Multifocal Acquired Predominant Axonal Sensorimotor Neuropathy of the Upper LimbDoris Lieba-Samal, Jeroen J J van Eijk, Marieke H J van Rosmalen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 30, 2024
Chenodeoxycholic acid (CDCA) treatment during pregnancy in women with cerebrotendinous xanthomatosis (CTX): Lessons learned from 19 pregnanciesTzipora C Falik Zaccai, Sharon Hassin-Baer, Nehama Cohen Kfir, et al.
Human Mutation|April 1, 2006
The expanding phenotype of POMT1 mutations: from Walker-Warburg syndrome to congenital muscular dystrophy, microcephaly, and mental retardationJeroen van Reeuwijk, Svetlana Maugenre, Christa van den Elzen, et al.
Neuromuscular Disorders : NMD|August 21, 2018
A recurrent de novo DYNC1H1 tail domain mutation causes spinal muscular atrophy with lower extremity predominance, learning difficulties and mild brain abnormalitySophelia Hoi Shan Chan, Nens van Alfen, Inger Johanne Thuestad, et al.
Journal of Neurology|March 5, 2013
Pure adult-onset spastic paraplegia caused by a novel mutation in the KIAA0196 (SPG8) geneSusanne T de Bot, Sascha Vermeer, Wendy Buijsman, et al.
Acta Neuropathologica|March 4, 2010
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literatureCasper Jansen, Willem Voet, Mark W Head, et al.
Neurology|December 12, 2018
Long-term treatment effect in cerebrotendinous xanthomatosis depends on age at treatment startBianca M L Stelten, Hidde H Huidekoper, Bart P C van de Warrenburg, et al.
Pageof 7