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Bogdanovic

Showing results (541-550 of 824) with videos related to

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Behavioural Brain Research|October 28, 2008
Influence of environmental manipulation on exploratory behaviour in male BDNF knockout miceShun-Wei Zhu, Alina Codita, Nenad Bogdanovic, et al.
Molecular Psychiatry|June 26, 2020
Amyloid, tau, and astrocyte pathology in autosomal-dominant Alzheimer's disease variants: AβPParc and PSEN1DE9Laetitia Lemoine, Per-Göran Gillberg, Nenad Bogdanovic, et al.
International Journal of Clinical and Experimental Pathology|September 9, 2014
Prognostic significance of mucin expression in urothelial bladder cancerSlavica Stojnev, Ana Ristic-Petrovic, Ljubinka Jankovic Velickovic, et al.
Haematologica|March 15, 2006
The incidence of hemorrhagic cystitis and BK-viruria in allogeneic hematopoietic stem cell recipients according to intensity of the conditioning regimenGéraldine Giraud, Gordana Bogdanovic, Peter Priftakis, et al.
Abdominal Radiology (New York)|April 4, 2016
Subtypes and clinical significance of common bile duct varices in portal vein thrombosis: diagnosis and follow-up by Doppler US and EUSIvica Grgurevic, Milan Kujundzic, Marko Banic, et al.
Brain : a Journal of Neurology|July 26, 2016
Reward sensitivity deficits modulated by dopamine are associated with apathy in Parkinson's diseaseKinan Muhammed, Sanjay Manohar, Michael Ben Yehuda, et al.
European Journal of Radiology|June 21, 2017
In-depth analysis of interreader agreement and accuracy in categorical assessment of brown adipose tissue in (18)FDG-PET/CTAnton S Becker, Caroline Zellweger, Khoschy Schawkat, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 11, 2007
Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformationsBethan E Hoskins, Carl H Cramer, Velibor Tasic, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's diseaseJ A Prince, L Feuk, S L Sawyer, et al.
Neuroreport|May 31, 1996
Abundance of the longer A beta 42 in neocortical and cerebrovascular amyloid beta deposits in Swedish familial Alzheimer's disease and Down's syndromeR N Kalaria, D L Cohen, B D Greenberg, et al.
Pageof 83

Showing results (541-550 of 824) with videos related to

Sort By:
Pageof 83
Behavioural Brain Research|October 28, 2008
Influence of environmental manipulation on exploratory behaviour in male BDNF knockout miceShun-Wei Zhu, Alina Codita, Nenad Bogdanovic, et al.
Molecular Psychiatry|June 26, 2020
Amyloid, tau, and astrocyte pathology in autosomal-dominant Alzheimer's disease variants: AβPParc and PSEN1DE9Laetitia Lemoine, Per-Göran Gillberg, Nenad Bogdanovic, et al.
International Journal of Clinical and Experimental Pathology|September 9, 2014
Prognostic significance of mucin expression in urothelial bladder cancerSlavica Stojnev, Ana Ristic-Petrovic, Ljubinka Jankovic Velickovic, et al.
Haematologica|March 15, 2006
The incidence of hemorrhagic cystitis and BK-viruria in allogeneic hematopoietic stem cell recipients according to intensity of the conditioning regimenGéraldine Giraud, Gordana Bogdanovic, Peter Priftakis, et al.
Abdominal Radiology (New York)|April 4, 2016
Subtypes and clinical significance of common bile duct varices in portal vein thrombosis: diagnosis and follow-up by Doppler US and EUSIvica Grgurevic, Milan Kujundzic, Marko Banic, et al.
Brain : a Journal of Neurology|July 26, 2016
Reward sensitivity deficits modulated by dopamine are associated with apathy in Parkinson's diseaseKinan Muhammed, Sanjay Manohar, Michael Ben Yehuda, et al.
European Journal of Radiology|June 21, 2017
In-depth analysis of interreader agreement and accuracy in categorical assessment of brown adipose tissue in (18)FDG-PET/CTAnton S Becker, Caroline Zellweger, Khoschy Schawkat, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 11, 2007
Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformationsBethan E Hoskins, Carl H Cramer, Velibor Tasic, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Lack of replication of association findings in complex disease: an analysis of 15 polymorphisms in prior candidate genes for sporadic Alzheimer's diseaseJ A Prince, L Feuk, S L Sawyer, et al.
Neuroreport|May 31, 1996
Abundance of the longer A beta 42 in neocortical and cerebrovascular amyloid beta deposits in Swedish familial Alzheimer's disease and Down's syndromeR N Kalaria, D L Cohen, B D Greenberg, et al.
Pageof 83