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E Fransen

Showing results (121-130 of 130) with videos related to

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European Urology Focus|December 19, 2018
Urothelial Carcinoma in Bladder Diverticula: A Multicenter Analysis of Characteristics and Clinical OutcomesCharlotte S Voskuilen, Roland Seiler, Michael Rink, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
Urologic Oncology|June 9, 2018
Metric substage according to micro and extensive lamina propria invasion improves prognostics in T1 bladder cancerElisabeth E Fransen van de Putte, Wolfgang Otto, Arndt Hartmann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 19, 2018
Divergent Biological Response to Neoadjuvant Chemotherapy in Muscle-invasive Bladder CancerRoland Seiler, Ewan A Gibb, Natalie Q Wang, et al.
European Journal of Medical Genetics|March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
European Urology|April 10, 2017
Impact of Molecular Subtypes in Muscle-invasive Bladder Cancer on Predicting Response and Survival after Neoadjuvant ChemotherapyRoland Seiler, Hussam Al Deen Ashab, Nicholas Erho, et al.
American Journal of Human Genetics|April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics|October 6, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
European Urology Focus|December 19, 2018
Urothelial Carcinoma in Bladder Diverticula: A Multicenter Analysis of Characteristics and Clinical OutcomesCharlotte S Voskuilen, Roland Seiler, Michael Rink, et al.
Human Molecular Genetics|October 1, 1996
Positional cloning of a gene involved in hereditary multiple exostosesW Wuyts, W Van Hul, J Wauters, et al.
Urologic Oncology|June 9, 2018
Metric substage according to micro and extensive lamina propria invasion improves prognostics in T1 bladder cancerElisabeth E Fransen van de Putte, Wolfgang Otto, Arndt Hartmann, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 19, 2018
Divergent Biological Response to Neoadjuvant Chemotherapy in Muscle-invasive Bladder CancerRoland Seiler, Ewan A Gibb, Natalie Q Wang, et al.
European Journal of Medical Genetics|March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individualsE K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.
Journal of Medical Genetics|May 22, 2007
Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairmentE Van Eyken, G Van Camp, E Fransen, et al.
B-ENT|January 30, 2008
Familial aggregation of tinnitus: a European multicentre studyJ J Hendrickx, J R Huyghe, K Demeester, et al.
European Urology|April 10, 2017
Impact of Molecular Subtypes in Muscle-invasive Bladder Cancer on Predicting Response and Survival after Neoadjuvant ChemotherapyRoland Seiler, Hussam Al Deen Ashab, Nicholas Erho, et al.
American Journal of Human Genetics|April 17, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
American Journal of Human Genetics|October 6, 2018
A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar DysgenesisHeather E Olson, Nolwenn Jean-Marçais, Edward Yang, et al.
Pageof 13