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F Cox

Showing results (761-770 of 782) with videos related to

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Blood Cells, Molecules & Diseases|April 23, 2018
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Molecular Genetics and Metabolism|July 30, 2018
Nitisinone arrests ochronosis and decreases rate of progression of Alkaptonuria: Evaluation of the effect of nitisinone in the United Kingdom National Alkaptonuria CentreL R Ranganath, M Khedr, A M Milan, et al.
British Journal of Cancer|March 9, 2018
Expression of dihydropyrimidine dehydrogenase (DPD) and hENT1 predicts survival in pancreatic cancerN O Elander, K Aughton, P Ghaneh, et al.
Data in Brief|September 29, 2018
Data on items of AKUSSI in Alkaptonuria collected over three years from the United Kingdom National Alkaptonuria Centre and the impact of nitisinoneR Griffin, E E Psarelli, T F Cox, et al.
Journal of Magnetic Resonance Imaging : JMRI|November 3, 2020
Consensus-Based Technical Recommendations for Clinical Translation of Renal Phase Contrast MRIAnneloes de Boer, Giulia Villa, Octavia Bane, et al.
Magma (New York, N.Y.)|December 14, 2019
Consensus-based technical recommendations for clinical translation of renal ASL MRIFabio Nery, Charlotte E Buchanan, Anita A Harteveld, et al.
Journal of Medical Genetics|September 23, 2008
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disordersD T Miller, Y Shen, L A Weiss, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
Redefining the MED13L syndromeAbidemi Adegbola, Luciana Musante, Bert Callewaert, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Human Mutation|March 26, 2014
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathyPhillipa J Lamont, William Wallefeld, David Hilton-Jones, et al.
Pageof 79

Showing results (761-770 of 782) with videos related to

Sort By:
Pageof 79
Blood Cells, Molecules & Diseases|April 23, 2018
Safety, efficacy, and authorization of eliglustat as a first-line therapy in Gaucher disease type 1Pramod K Mistry, Manisha Balwani, Hagit N Baris, et al.
Molecular Genetics and Metabolism|July 30, 2018
Nitisinone arrests ochronosis and decreases rate of progression of Alkaptonuria: Evaluation of the effect of nitisinone in the United Kingdom National Alkaptonuria CentreL R Ranganath, M Khedr, A M Milan, et al.
British Journal of Cancer|March 9, 2018
Expression of dihydropyrimidine dehydrogenase (DPD) and hENT1 predicts survival in pancreatic cancerN O Elander, K Aughton, P Ghaneh, et al.
Data in Brief|September 29, 2018
Data on items of AKUSSI in Alkaptonuria collected over three years from the United Kingdom National Alkaptonuria Centre and the impact of nitisinoneR Griffin, E E Psarelli, T F Cox, et al.
Journal of Magnetic Resonance Imaging : JMRI|November 3, 2020
Consensus-Based Technical Recommendations for Clinical Translation of Renal Phase Contrast MRIAnneloes de Boer, Giulia Villa, Octavia Bane, et al.
Magma (New York, N.Y.)|December 14, 2019
Consensus-based technical recommendations for clinical translation of renal ASL MRIFabio Nery, Charlotte E Buchanan, Anita A Harteveld, et al.
Journal of Medical Genetics|September 23, 2008
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disordersD T Miller, Y Shen, L A Weiss, et al.
European Journal of Human Genetics : EJHG|March 12, 2015
Redefining the MED13L syndromeAbidemi Adegbola, Luciana Musante, Bert Callewaert, et al.
Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.
Human Mutation|March 26, 2014
Novel mutations widen the phenotypic spectrum of slow skeletal/β-cardiac myosin (MYH7) distal myopathyPhillipa J Lamont, William Wallefeld, David Hilton-Jones, et al.
Pageof 79