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Rachel E Harrison

Showing results (1-10 of 15) with videos related to

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Journal of Alternative and Complementary Medicine (New York, N.Y.)|January 11, 2011
Multipractitioner Upledger CranioSacral Therapy: descriptive outcome study 2007-2008Rachel E Harrison, John S Page
Circulation|February 3, 2005
Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhoodRachel E Harrison, Rolf Berger, Sheila G Haworth, et al.
Circulation|February 9, 2005
Investigation of second genetic hits at the BMPR2 locus as a modulator of disease progression in familial pulmonary arterial hypertensionRajiv D Machado, Victoria James, Mark Southwood, et al.
European Journal of Medical Genetics|August 14, 2022
Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UKSchaida Schirwani, Fleur S van Dijk, Matthew Cauldwell, et al.
American Journal of Medical Genetics. Part A|April 30, 2015
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillanceBianca Russell, Jennifer J Johnston, Leslie G Biesecker, et al.
Trials|February 2, 2024
Cancer Precision-Prevention trial of Metformin in adults with Li Fraumeni syndrome (MILI) undergoing yearly MRI surveillance: a randomised controlled trial protocolMiriam Dixon-Zegeye, Rachel Shaw, Linda Collins, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disordersAlistair T Pagnamenta, Yoshiko Murakami, John M Taylor, et al.
Circulation|March 25, 2009
Stress Doppler echocardiography in relatives of patients with idiopathic and familial pulmonary arterial hypertension: results of a multicenter European analysis of pulmonary artery pressure response to exercise and hypoxiaEkkehard Grünig, Sylvia Weissmann, Nicola Ehlken, et al.
Muscle & Nerve|July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathyJohnnie Turner, Christine C Bruels, Audrey L Daugherty, et al.
Human Mutation|January 24, 2006
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertensionRajiv D Machado, Micheala A Aldred, Victoria James, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Alternative and Complementary Medicine (New York, N.Y.)|January 11, 2011
Multipractitioner Upledger CranioSacral Therapy: descriptive outcome study 2007-2008Rachel E Harrison, John S Page
Circulation|February 3, 2005
Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhoodRachel E Harrison, Rolf Berger, Sheila G Haworth, et al.
Circulation|February 9, 2005
Investigation of second genetic hits at the BMPR2 locus as a modulator of disease progression in familial pulmonary arterial hypertensionRajiv D Machado, Victoria James, Mark Southwood, et al.
European Journal of Medical Genetics|August 14, 2022
Amniotic band sequence in vascular Ehlers-Danlos Syndrome (EDS): Experience of the EDS National Diagnostic Services in the UKSchaida Schirwani, Fleur S van Dijk, Matthew Cauldwell, et al.
American Journal of Medical Genetics. Part A|April 30, 2015
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillanceBianca Russell, Jennifer J Johnston, Leslie G Biesecker, et al.
Trials|February 2, 2024
Cancer Precision-Prevention trial of Metformin in adults with Li Fraumeni syndrome (MILI) undergoing yearly MRI surveillance: a randomised controlled trial protocolMiriam Dixon-Zegeye, Rachel Shaw, Linda Collins, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disordersAlistair T Pagnamenta, Yoshiko Murakami, John M Taylor, et al.
Circulation|March 25, 2009
Stress Doppler echocardiography in relatives of patients with idiopathic and familial pulmonary arterial hypertension: results of a multicenter European analysis of pulmonary artery pressure response to exercise and hypoxiaEkkehard Grünig, Sylvia Weissmann, Nicola Ehlken, et al.
Muscle & Nerve|July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathyJohnnie Turner, Christine C Bruels, Audrey L Daugherty, et al.
Human Mutation|January 24, 2006
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertensionRajiv D Machado, Micheala A Aldred, Victoria James, et al.
Pageof 2