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T M Cox

Showing results (101-110 of 146) with videos related to

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QJM : Monthly Journal of the Association of Physicians|January 1, 1997
Pro-inflammatory cytokines and the pathogenesis of Gaucher's disease: increased release of interleukin-6 and interleukin-10M J Allen, B J Myer, A M Khokher, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|January 1, 1997
Skeletal muscle weakness and dysphagia caused by acid maltase deficiency: nutritional consequences of coincident celiac sprueT S King, J R Anderson, E P Wraight, et al.
Medizinische Klinik (Munich, Germany : 1983)|September 15, 1993
[Acute hepatorenal failure in hereditary fructose intolerance]U Rosien, T M Cox, M Ali, et al.
Journal of Neurochemistry|January 1, 1997
The tau protein in human cerebrospinal fluid in Alzheimer's disease consists of proteolytically derived fragmentsG V Johnson, P Seubert, T M Cox, et al.
BMJ (Clinical Research Ed.)|September 30, 1989
Imaging amyloidosis in Still's diseaseP Hawkins, S R Bloom, J Cassar, et al.
Human Genetics|October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresisD K Lord, I Dunham, R D Campbell, et al.
Genetic Counseling (Geneva, Switzerland)|March 23, 2007
Aldolase B mutations in Turkish families from central AnatoliaH G Karabulut, D Halsall, B D Sayin, et al.
Gut|July 1, 1979
Rôle of calcitonin in diarrhoea associated with medullary carcinoma of the thyroidT M Cox, E A Fagan, C J Hillyard, et al.
Infection and Immunity|April 1, 1993
Schistosoma japonicum-infected mice show reduced hepatic fibrosis and eosinophilia and selective inhibition of interleukin-5 secretion by CD4+ cells after treatment with anti-interleukin-2 antibodiesA W Cheever, Y Xu, A Sher, et al.
Journal of Medical Genetics|June 1, 1994
Null alleles of the aldolase B gene in patients with hereditary fructose intoleranceM Ali, G Tunçman, N C Cross, et al.
Pageof 15

Showing results (101-110 of 146) with videos related to

Sort By:
Pageof 15
QJM : Monthly Journal of the Association of Physicians|January 1, 1997
Pro-inflammatory cytokines and the pathogenesis of Gaucher's disease: increased release of interleukin-6 and interleukin-10M J Allen, B J Myer, A M Khokher, et al.
JPEN. Journal of Parenteral and Enteral Nutrition|January 1, 1997
Skeletal muscle weakness and dysphagia caused by acid maltase deficiency: nutritional consequences of coincident celiac sprueT S King, J R Anderson, E P Wraight, et al.
Medizinische Klinik (Munich, Germany : 1983)|September 15, 1993
[Acute hepatorenal failure in hereditary fructose intolerance]U Rosien, T M Cox, M Ali, et al.
Journal of Neurochemistry|January 1, 1997
The tau protein in human cerebrospinal fluid in Alzheimer's disease consists of proteolytically derived fragmentsG V Johnson, P Seubert, T M Cox, et al.
BMJ (Clinical Research Ed.)|September 30, 1989
Imaging amyloidosis in Still's diseaseP Hawkins, S R Bloom, J Cassar, et al.
Human Genetics|October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresisD K Lord, I Dunham, R D Campbell, et al.
Genetic Counseling (Geneva, Switzerland)|March 23, 2007
Aldolase B mutations in Turkish families from central AnatoliaH G Karabulut, D Halsall, B D Sayin, et al.
Gut|July 1, 1979
Rôle of calcitonin in diarrhoea associated with medullary carcinoma of the thyroidT M Cox, E A Fagan, C J Hillyard, et al.
Infection and Immunity|April 1, 1993
Schistosoma japonicum-infected mice show reduced hepatic fibrosis and eosinophilia and selective inhibition of interleukin-5 secretion by CD4+ cells after treatment with anti-interleukin-2 antibodiesA W Cheever, Y Xu, A Sher, et al.
Journal of Medical Genetics|June 1, 1994
Null alleles of the aldolase B gene in patients with hereditary fructose intoleranceM Ali, G Tunçman, N C Cross, et al.
Pageof 15