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Journal of Alternative and Complementary Medicine (New York, N.Y.)
|
January 11, 2011
Multipractitioner Upledger CranioSacral Therapy: descriptive outcome study 2007-2008
Rachel E Harrison, John S Page
Circulation
|
February 3, 2005
Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood
Rachel 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 hypertension
Rajiv 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 UK
Schaida 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 surveillance
Bianca 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 protocol
Miriam 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 disorders
Alistair 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 hypoxia
Ekkehard Grünig, Sylvia Weissmann, Nicola Ehlken, et al.
Muscle & Nerve
|
July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy
Johnnie 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 hypertension
Rajiv D Machado, Micheala A Aldred, Victoria James, et al.
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Search research articles
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Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Journal of Alternative and Complementary Medicine (New York, N.Y.)
|
January 11, 2011
Multipractitioner Upledger CranioSacral Therapy: descriptive outcome study 2007-2008
Rachel E Harrison, John S Page
Circulation
|
February 3, 2005
Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood
Rachel 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 hypertension
Rajiv 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 UK
Schaida 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 surveillance
Bianca 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 protocol
Miriam 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 disorders
Alistair 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 hypoxia
Ekkehard Grünig, Sylvia Weissmann, Nicola Ehlken, et al.
Muscle & Nerve
|
July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy
Johnnie 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 hypertension
Rajiv D Machado, Micheala A Aldred, Victoria James, et al.
Page
of 2