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A Maat

Showing results (31-40 of 52) with videos related to

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Circulation|June 1, 1995
Prediction of improvement of regional left ventricular function after surgical revascularization. A comparison of low-dose dobutamine echocardiography with 201Tl single-photon emission computed tomographyM Arnese, J H Cornel, A Salustri, et al.
Heart (British Cardiac Society)|August 15, 2006
Outcome after redo coronary artery bypass grafting in patients with ischaemic cardiomyopathy and viable myocardiumV Rizzello, D Poldermans, A F L Schinkel, et al.
Archives of Neurology|June 15, 2007
A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystoniaLiesbeth Spruijt, Hubert J Smeets, Alexandra Hendrickx, et al.
International Journal of Radiation Oncology, Biology, Physics|February 1, 2015
Stereotactic body radiation therapy for oligometastases to the lung: a phase 2 studyJoost J Nuyttens, Noëlle C M G van der Voort van Zyp, Cornelis Verhoef, et al.
Heart (British Cardiac Society)|April 9, 2005
Long term prognostic value of myocardial viability and ischaemia during dobutamine stress echocardiography in patients with ischaemic cardiomyopathy undergoing coronary revascularisationV Rizzello, D Poldermans, A F L Schinkel, et al.
Genomics|October 1, 1990
Genetic heterogeneity in tuberous sclerosisL A Janssen, L A Sandkuyl, E C Merkens, et al.
Genetic Testing|October 18, 2005
Large deletion at the TSC1 locus in a family with tuberous sclerosis complexM Nellist, O Sancak, M A Goedbloed, et al.
European Journal of Human Genetics : EJHG|September 30, 2010
Characterisation of TSC1 promoter deletions in tuberous sclerosis complex patientsAns M W van den Ouweland, Peter Elfferich, Bernard A Zonnenberg, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardationS M van der Maarel, I H Scholten, J A Maat-Kievit, et al.
Cell Reports|November 23, 2022
Calreticulin mutations affect its chaperone function and perturb the glycoproteomePatrick M Schürch, Liliana Malinovska, Mohammad Hleihil, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Circulation|June 1, 1995
Prediction of improvement of regional left ventricular function after surgical revascularization. A comparison of low-dose dobutamine echocardiography with 201Tl single-photon emission computed tomographyM Arnese, J H Cornel, A Salustri, et al.
Heart (British Cardiac Society)|August 15, 2006
Outcome after redo coronary artery bypass grafting in patients with ischaemic cardiomyopathy and viable myocardiumV Rizzello, D Poldermans, A F L Schinkel, et al.
Archives of Neurology|June 15, 2007
A MELAS-associated ND1 mutation causing leber hereditary optic neuropathy and spastic dystoniaLiesbeth Spruijt, Hubert J Smeets, Alexandra Hendrickx, et al.
International Journal of Radiation Oncology, Biology, Physics|February 1, 2015
Stereotactic body radiation therapy for oligometastases to the lung: a phase 2 studyJoost J Nuyttens, Noëlle C M G van der Voort van Zyp, Cornelis Verhoef, et al.
Heart (British Cardiac Society)|April 9, 2005
Long term prognostic value of myocardial viability and ischaemia during dobutamine stress echocardiography in patients with ischaemic cardiomyopathy undergoing coronary revascularisationV Rizzello, D Poldermans, A F L Schinkel, et al.
Genomics|October 1, 1990
Genetic heterogeneity in tuberous sclerosisL A Janssen, L A Sandkuyl, E C Merkens, et al.
Genetic Testing|October 18, 2005
Large deletion at the TSC1 locus in a family with tuberous sclerosis complexM Nellist, O Sancak, M A Goedbloed, et al.
European Journal of Human Genetics : EJHG|September 30, 2010
Characterisation of TSC1 promoter deletions in tuberous sclerosis complex patientsAns M W van den Ouweland, Peter Elfferich, Bernard A Zonnenberg, et al.
European Journal of Human Genetics : EJHG|January 1, 1995
Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardationS M van der Maarel, I H Scholten, J A Maat-Kievit, et al.
Cell Reports|November 23, 2022
Calreticulin mutations affect its chaperone function and perturb the glycoproteomePatrick M Schürch, Liliana Malinovska, Mohammad Hleihil, et al.
Pageof 6