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Molecular Genetics and Metabolism
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March 31, 2007
Molecular and clinical characterization of a Moroccan Cog7 deficient patient
Bobby G Ng, Christian Kranz, E E O Hagebeuk, et al.
The European Respiratory Journal
|
January 24, 2009
Leukotriene B4 release by human lung macrophages via receptor- not voltage-operated Ca2+ channels
T K Finney-Hayward, P Bahra, S Li, et al.
Neurology
|
February 12, 2004
Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survival
P G Barth, C B L M Majoie, J Gootjes, et al.
Human Genetics
|
August 13, 2015
'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes
Nuria C Bramswig, C W Ockeloen, J C Czeschik, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1987
Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders
R J Wanders, C W van Roermund, M J van Wijland, et al.
Parkinsonism & Related Disorders
|
October 26, 2017
Non-motor symptoms and quality of life in dopa-responsive dystonia patients
E R Timmers, A Kuiper, M Smit, et al.
European Journal of Human Genetics : EJHG
|
April 21, 2001
Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome
S M Houten, J Koster, G J Romeijn, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 22, 2009
Expression of transient receptor potential C6 channels in human lung macrophages
Tricia K Finney-Hayward, Mariana Oana Popa, Parmjit Bahra, et al.
Journal of Medical Genetics
|
July 7, 2009
The unfolding clinical spectrum of POLG mutations
M J Blok, B J van den Bosch, E Jongen, et al.
American Journal of Medical Genetics
|
January 20, 1997
Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation: clinical, biochemical and DNA analyses in a four-generation family
M G Ausems, E Bakker, R Berger, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 136) with videos related to
Sort By:
Page
of 14
Molecular Genetics and Metabolism
|
March 31, 2007
Molecular and clinical characterization of a Moroccan Cog7 deficient patient
Bobby G Ng, Christian Kranz, E E O Hagebeuk, et al.
The European Respiratory Journal
|
January 24, 2009
Leukotriene B4 release by human lung macrophages via receptor- not voltage-operated Ca2+ channels
T K Finney-Hayward, P Bahra, S Li, et al.
Neurology
|
February 12, 2004
Neuroimaging of peroxisome biogenesis disorders (Zellweger spectrum) with prolonged survival
P G Barth, C B L M Majoie, J Gootjes, et al.
Human Genetics
|
August 13, 2015
'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes
Nuria C Bramswig, C W Ockeloen, J C Czeschik, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 15, 1987
Peroxisomal very long-chain fatty acid beta-oxidation in human skin fibroblasts: activity in Zellweger syndrome and other peroxisomal disorders
R J Wanders, C W van Roermund, M J van Wijland, et al.
Parkinsonism & Related Disorders
|
October 26, 2017
Non-motor symptoms and quality of life in dopa-responsive dystonia patients
E R Timmers, A Kuiper, M Smit, et al.
European Journal of Human Genetics : EJHG
|
April 21, 2001
Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome
S M Houten, J Koster, G J Romeijn, et al.
American Journal of Respiratory Cell and Molecular Biology
|
October 22, 2009
Expression of transient receptor potential C6 channels in human lung macrophages
Tricia K Finney-Hayward, Mariana Oana Popa, Parmjit Bahra, et al.
Journal of Medical Genetics
|
July 7, 2009
The unfolding clinical spectrum of POLG mutations
M J Blok, B J van den Bosch, E Jongen, et al.
American Journal of Medical Genetics
|
January 20, 1997
Asymptomatic and late-onset ornithine transcarbamylase deficiency caused by a A208T mutation: clinical, biochemical and DNA analyses in a four-generation family
M G Ausems, E Bakker, R Berger, et al.
Page
of 14