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Lancet (London, England)
|
September 22, 1990
Precocious familial gout
J S Cameron, C S Ogg, F Moro, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
NAD synthesis in human erythrocytes: study of adenylyl transferase activities in patients bearing purine enzyme disorders
S Sestini, M Pescaglini, C Magagnoli, et al.
Bioscience Reports
|
May 1, 1982
Formation and degradation of deoxyadenosine nucleotides in inherited adenosine deaminase deficiency
H A Simmonds, D R Webster, D Perrett, et al.
The American Journal of Physiology
|
August 1, 1980
Micropuncture study of tubular transport of urate and PAH in the pig kidney
F Roch-Ramel, F White, L Vowles, et al.
Biochemical Pharmacology
|
March 15, 1982
GTP depletion and other erythrocyte abnormalities in inherited PNP deficiency
H A Simmonds, A R Watson, D R Webster, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
Evidence of a new syndrome involving hereditary uric acid over-production, neurological complications and deafness
H A Simmonds, D R Webster, J Wilson, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1989
Deoxy GTP accumulates in thymocytes, but not in T or B lymphocytes in simulated PNP deficiency
A Taddeo, L D Fairbanks, H A Simmonds, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
Congenital chloride losing enteropathy associated with tophaceous gouty arthritis
G Nuki, M L Watson, B C Williams, et al.
Archives of Disease in Childhood
|
October 1, 1983
Hypoxanthine guanine phosphoribosyl transferase deficiency presenting with gout and renal failure in infancy
P C Holland, M J Dillon, J Pincott, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
New perspectives in the diagnosis and treatment of adenosine deaminase (ADA) deficiency
R J Levinsky, E G Davies, H A Simmonds, et al.
Page
of 25
Search research articles
Search
Showing results (131-140 of 250) with videos related to
Sort By:
Page
of 25
Lancet (London, England)
|
September 22, 1990
Precocious familial gout
J S Cameron, C S Ogg, F Moro, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
NAD synthesis in human erythrocytes: study of adenylyl transferase activities in patients bearing purine enzyme disorders
S Sestini, M Pescaglini, C Magagnoli, et al.
Bioscience Reports
|
May 1, 1982
Formation and degradation of deoxyadenosine nucleotides in inherited adenosine deaminase deficiency
H A Simmonds, D R Webster, D Perrett, et al.
The American Journal of Physiology
|
August 1, 1980
Micropuncture study of tubular transport of urate and PAH in the pig kidney
F Roch-Ramel, F White, L Vowles, et al.
Biochemical Pharmacology
|
March 15, 1982
GTP depletion and other erythrocyte abnormalities in inherited PNP deficiency
H A Simmonds, A R Watson, D R Webster, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
Evidence of a new syndrome involving hereditary uric acid over-production, neurological complications and deafness
H A Simmonds, D R Webster, J Wilson, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1989
Deoxy GTP accumulates in thymocytes, but not in T or B lymphocytes in simulated PNP deficiency
A Taddeo, L D Fairbanks, H A Simmonds, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1991
Congenital chloride losing enteropathy associated with tophaceous gouty arthritis
G Nuki, M L Watson, B C Williams, et al.
Archives of Disease in Childhood
|
October 1, 1983
Hypoxanthine guanine phosphoribosyl transferase deficiency presenting with gout and renal failure in infancy
P C Holland, M J Dillon, J Pincott, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1984
New perspectives in the diagnosis and treatment of adenosine deaminase (ADA) deficiency
R J Levinsky, E G Davies, H A Simmonds, et al.
Page
of 25