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T M Cox

Showing results (71-80 of 146) with videos related to

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Gastroenterology|April 21, 2001
Intestinal iron uptake determined by divalent metal transporter is enhanced in HFE-deficient mice with hemochromatosisW J Griffiths, W S Sly, T M Cox
QJM : Monthly Journal of the Association of Physicians|September 5, 2015
Orphan drugs: expensive yet necessaryH I Hyry, J C Roos, T M Cox
The Quarterly Journal of Medicine|July 1, 1987
Molecular forms of porphobilinogen deaminase in acute intermittent porphyria. A study by Western immunoblottingA V Nunn, L C Gardner, T M Cox
The Quarterly Journal of Medicine|September 1, 1986
Acute myopericarditis in influenza A infectionC M Proby, D Hackett, S Gupta, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
Pathological bone fractures preceded by sustained hypercalcaemia in type 1 Gaucher diseaseC D Byrne, L Bermann, C Constant, et al.
QJM : Monthly Journal of the Association of Physicians|December 1, 2014
Orphan drugs: expensive yet necessaryH I Hyry, J C P Roos, T M Cox
Analytical Biochemistry|October 1, 1988
Zinc chelatase in human lymphocytes: detection of the enzymatic defect in erythropoietic protoporphyriaA V Nunn, P Norris, J L Hawk, et al.
QJM : Monthly Journal of the Association of Physicians|March 19, 2004
Twin pairs showing discordance of phenotype in adult Gaucher's diseaseR H Lachmann, I R Grant, D Halsall, et al.
The Biochemical Journal|May 7, 1999
Alteration of substrate specificity by a naturally-occurring aldolase B mutation (Ala337-->Val) in fructose intoleranceP Rellos, M Ali, M Vidailhet, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|May 25, 2001
Tartrate-resistant acid phosphatase (Acp 5): identification in diverse human tissues and dendritic cellsA R Hayman, P Macary, P J Lehner, et al.
Pageof 15

Showing results (71-80 of 146) with videos related to

Sort By:
Pageof 15
Gastroenterology|April 21, 2001
Intestinal iron uptake determined by divalent metal transporter is enhanced in HFE-deficient mice with hemochromatosisW J Griffiths, W S Sly, T M Cox
QJM : Monthly Journal of the Association of Physicians|September 5, 2015
Orphan drugs: expensive yet necessaryH I Hyry, J C Roos, T M Cox
The Quarterly Journal of Medicine|July 1, 1987
Molecular forms of porphobilinogen deaminase in acute intermittent porphyria. A study by Western immunoblottingA V Nunn, L C Gardner, T M Cox
The Quarterly Journal of Medicine|September 1, 1986
Acute myopericarditis in influenza A infectionC M Proby, D Hackett, S Gupta, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
Pathological bone fractures preceded by sustained hypercalcaemia in type 1 Gaucher diseaseC D Byrne, L Bermann, C Constant, et al.
QJM : Monthly Journal of the Association of Physicians|December 1, 2014
Orphan drugs: expensive yet necessaryH I Hyry, J C P Roos, T M Cox
Analytical Biochemistry|October 1, 1988
Zinc chelatase in human lymphocytes: detection of the enzymatic defect in erythropoietic protoporphyriaA V Nunn, P Norris, J L Hawk, et al.
QJM : Monthly Journal of the Association of Physicians|March 19, 2004
Twin pairs showing discordance of phenotype in adult Gaucher's diseaseR H Lachmann, I R Grant, D Halsall, et al.
The Biochemical Journal|May 7, 1999
Alteration of substrate specificity by a naturally-occurring aldolase B mutation (Ala337-->Val) in fructose intoleranceP Rellos, M Ali, M Vidailhet, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|May 25, 2001
Tartrate-resistant acid phosphatase (Acp 5): identification in diverse human tissues and dendritic cellsA R Hayman, P Macary, P J Lehner, et al.
Pageof 15