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Showing results (141-150 of 340) with videos related to

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Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1987
Hereditary mitochondrial hypertrophic cardiomyopathy with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosisG J van Ekeren, A M Stadhouders, G J Egberink, et al.
Journal of the Mechanical Behavior of Biomedical Materials|October 20, 2023
Depth profiling via nanoindentation for characterisation of the elastic modulus and hydraulic properties of thin hydrogel layersDichu Xu, Maria Luisa Hernandez Miranda, Nicholas D Evans, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 2001
Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trialC Noordam, I Van der Burgt, R C Sengers, et al.
Archives of Neurology|December 1, 1981
Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liverM J Prick, F J Gabreëls, W O Renier, et al.
Neuropediatrics|March 8, 2000
Preterm birth in Sjögren-Larsson syndromeM A Willemsen, J J Rotteveel, P H van Domburg, et al.
Journal of Tissue Engineering and Regenerative Medicine|June 8, 2012
Tantalum trabecular metal - addition of human skeletal cells to enhance bone implant interface strength and clinical applicationJ O Smith, B G Sengers, A Aarvold, et al.
Clinical Neurology and Neurosurgery|June 24, 1998
Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical studyH J ter Laak, Q H Leyten, F J Gabreëls, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 2, 2010
[Haematological abnormalities in premature babies due to placental mesenchymal dysplasia]Florien B Sengers, Gesina van Lijnschoten, Jacqueline P van der Sluijs-Bens, et al.
Acta Neuropathologica|January 1, 1993
Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsiesQ H Leyten, H J ter Laak, F J Gabreëls, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Pageof 34

Showing results (141-150 of 340) with videos related to

Sort By:
Pageof 34
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1987
Hereditary mitochondrial hypertrophic cardiomyopathy with mitochondrial myopathy of skeletal muscle, congenital cataract and lactic acidosisG J van Ekeren, A M Stadhouders, G J Egberink, et al.
Journal of the Mechanical Behavior of Biomedical Materials|October 20, 2023
Depth profiling via nanoindentation for characterisation of the elastic modulus and hydraulic properties of thin hydrogel layersDichu Xu, Maria Luisa Hernandez Miranda, Nicholas D Evans, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 1, 2001
Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trialC Noordam, I Van der Burgt, R C Sengers, et al.
Archives of Neurology|December 1, 1981
Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liverM J Prick, F J Gabreëls, W O Renier, et al.
Neuropediatrics|March 8, 2000
Preterm birth in Sjögren-Larsson syndromeM A Willemsen, J J Rotteveel, P H van Domburg, et al.
Journal of Tissue Engineering and Regenerative Medicine|June 8, 2012
Tantalum trabecular metal - addition of human skeletal cells to enhance bone implant interface strength and clinical applicationJ O Smith, B G Sengers, A Aarvold, et al.
Clinical Neurology and Neurosurgery|June 24, 1998
Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical studyH J ter Laak, Q H Leyten, F J Gabreëls, et al.
Nederlands Tijdschrift Voor Geneeskunde|April 2, 2010
[Haematological abnormalities in premature babies due to placental mesenchymal dysplasia]Florien B Sengers, Gesina van Lijnschoten, Jacqueline P van der Sluijs-Bens, et al.
Acta Neuropathologica|January 1, 1993
Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsiesQ H Leyten, H J ter Laak, F J Gabreëls, et al.
Annals of Clinical Biochemistry|May 1, 1992
Maturation of mitochondrial and other isoenzymes of creatine kinase in skeletal muscle of preterm born infantsJ Smeitink, W Ruitenbeek, T van Lith, et al.
Pageof 34