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T M Cox

Showing results (91-100 of 146) with videos related to

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The Journal of Investigative Dermatology|September 1, 1990
Genetic heterogeneity in erythropoietic protoporphyria: a study of the enzymatic defect in nine affected familiesP G Norris, A V Nunn, J L Hawk, et al.
Human Mutation|October 26, 1999
Metachromatic leucodystrophy: a newly identified mutation in arylsulphatase A, D281Y, found as a compound heterozygote with I179L in an adult onset caseD J Halsall, E P Halligan, T S Elsey, et al.
The British Journal of Radiology|October 20, 2011
Quantifying the Erlenmeyer flask deformityA Carter, P S Rajan, P Deegan, et al.
The American Journal of Tropical Medicine and Hygiene|April 1, 1993
Biology and pathology of Schistosoma mansoni and Schistosoma japonicum infections in several strains of nude miceA W Cheever, I A Eltoum, Z A Andrade, et al.
Journal of Medical Genetics|October 1, 1996
Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British populationC L James, P Rellos, M Ali, et al.
The Quarterly Journal of Medicine|April 1, 1988
Cyclophosphamide-induced liver necrosis: a possible interaction with azathioprineS Shaunak, J M Munro, K Weinbren, et al.
QJM : Monthly Journal of the Association of Physicians|January 24, 2014
Limits on use of health economic assessments for rare diseasesH I Hyry, A D Stern, T M Cox, et al.
The Quarterly Journal of Medicine|July 1, 1992
Successful treatment of bone marrow failure in Gaucher's disease with low-dose modified glucocerebrosidaseP K Mistry, S Davies, A Corfield, et al.
QJM : Monthly Journal of the Association of Physicians|February 20, 1999
Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage diseaseA L Kelly, D A Rhodes, J M Roland, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|January 20, 2000
Osteoclastic tartrate-resistant acid phosphatase (Acp 5): its localization to dendritic cells and diverse murine tissuesA R Hayman, A J Bune, J R Bradley, et al.
Pageof 15

Showing results (91-100 of 146) with videos related to

Sort By:
Pageof 15
The Journal of Investigative Dermatology|September 1, 1990
Genetic heterogeneity in erythropoietic protoporphyria: a study of the enzymatic defect in nine affected familiesP G Norris, A V Nunn, J L Hawk, et al.
Human Mutation|October 26, 1999
Metachromatic leucodystrophy: a newly identified mutation in arylsulphatase A, D281Y, found as a compound heterozygote with I179L in an adult onset caseD J Halsall, E P Halligan, T S Elsey, et al.
The British Journal of Radiology|October 20, 2011
Quantifying the Erlenmeyer flask deformityA Carter, P S Rajan, P Deegan, et al.
The American Journal of Tropical Medicine and Hygiene|April 1, 1993
Biology and pathology of Schistosoma mansoni and Schistosoma japonicum infections in several strains of nude miceA W Cheever, I A Eltoum, Z A Andrade, et al.
Journal of Medical Genetics|October 1, 1996
Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British populationC L James, P Rellos, M Ali, et al.
The Quarterly Journal of Medicine|April 1, 1988
Cyclophosphamide-induced liver necrosis: a possible interaction with azathioprineS Shaunak, J M Munro, K Weinbren, et al.
QJM : Monthly Journal of the Association of Physicians|January 24, 2014
Limits on use of health economic assessments for rare diseasesH I Hyry, A D Stern, T M Cox, et al.
The Quarterly Journal of Medicine|July 1, 1992
Successful treatment of bone marrow failure in Gaucher's disease with low-dose modified glucocerebrosidaseP K Mistry, S Davies, A Corfield, et al.
QJM : Monthly Journal of the Association of Physicians|February 20, 1999
Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage diseaseA L Kelly, D A Rhodes, J M Roland, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|January 20, 2000
Osteoclastic tartrate-resistant acid phosphatase (Acp 5): its localization to dendritic cells and diverse murine tissuesA R Hayman, A J Bune, J R Bradley, et al.
Pageof 15