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E Morava

Showing results (51-60 of 96) with videos related to

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Die Nahrung|January 1, 1984
Effect of soya consumption on hepatic monooxygenase enzyme system and some lipid parameters in ratsM Antal, K Nagy, M Bedö, et al.
Biorxiv : the Preprint Server for Biology|July 17, 2025
Predicting disease-overarching therapeutic approaches for Congenital Disorders of Glycosylation using multi-OMICSI J J Muffels, R Budhraja, R Shah, et al.
American Journal of Medical Genetics|November 24, 1999
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian populationP Gyürüs, J Molnár, B Melegh, et al.
Orvosi Hetilap|October 17, 2001
[Kennedy disease in a patient with progressive speech disorder]J Kárteszi, E Morava, M Czakó, et al.
Molecular Genetics and Metabolism|July 31, 2025
Predicting disease-overarching therapeutic approaches for congenital disorders of glycosylation using multi-OMICSI J J Muffels, R Budhraja, R Shah, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Partial craniosynostosis in a patient with deletion 22q11J Karteszi, W Kress, M Szasz, et al.
International Journal of Pediatric Otorhinolaryngology|June 4, 2013
Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutationH G X M Thomeer, E Morava, B M Verbist, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 6, 2008
Decreased bone density and treatment in patients with autosomal recessive cutis laxaC Noordam, S Funke, N V Knoers, et al.
Molecular Therapy. Methods & Clinical Development|August 14, 2025
Are viral vector-mediated therapies compatible with aberrant glycosylation?I J J Muffels, R Budhraja, S Radenkovic, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 5, 2007
Early cardiac involvement in children carrying the A3243G mtDNA mutationS B Wortmann, R J Rodenburg, A P Backx, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
Die Nahrung|January 1, 1984
Effect of soya consumption on hepatic monooxygenase enzyme system and some lipid parameters in ratsM Antal, K Nagy, M Bedö, et al.
Biorxiv : the Preprint Server for Biology|July 17, 2025
Predicting disease-overarching therapeutic approaches for Congenital Disorders of Glycosylation using multi-OMICSI J J Muffels, R Budhraja, R Shah, et al.
American Journal of Medical Genetics|November 24, 1999
Trinucleotide repeat polymorphism at five disease loci in mixed Hungarian populationP Gyürüs, J Molnár, B Melegh, et al.
Orvosi Hetilap|October 17, 2001
[Kennedy disease in a patient with progressive speech disorder]J Kárteszi, E Morava, M Czakó, et al.
Molecular Genetics and Metabolism|July 31, 2025
Predicting disease-overarching therapeutic approaches for congenital disorders of glycosylation using multi-OMICSI J J Muffels, R Budhraja, R Shah, et al.
Genetic Counseling (Geneva, Switzerland)|January 22, 2005
Partial craniosynostosis in a patient with deletion 22q11J Karteszi, W Kress, M Szasz, et al.
International Journal of Pediatric Otorhinolaryngology|June 4, 2013
Otological aspects and surgical outcome in a consanguineous family with a novel ANKH gene mutationH G X M Thomeer, E Morava, B M Verbist, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 6, 2008
Decreased bone density and treatment in patients with autosomal recessive cutis laxaC Noordam, S Funke, N V Knoers, et al.
Molecular Therapy. Methods & Clinical Development|August 14, 2025
Are viral vector-mediated therapies compatible with aberrant glycosylation?I J J Muffels, R Budhraja, S Radenkovic, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 5, 2007
Early cardiac involvement in children carrying the A3243G mtDNA mutationS B Wortmann, R J Rodenburg, A P Backx, et al.
Pageof 10