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Archives of Disease in Childhood
|
October 1, 1990
Kawasaki disease: echocardiographic features in 91 cases presenting in the United Kingdom
A Suzuki, E J Tizard, V Gooch, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 1, 1989
Autosomal recessive polycystic kidney disease
B S Kaplan, J Fay, V Shah, et al.
Archives of Disease in Childhood
|
March 1, 1989
Antineutrophil cytoplasm antibodies in Kawasaki disease
C O Savage, J Tizard, D Jayne, et al.
Clinical and Experimental Immunology
|
December 12, 2007
T cell activation profiles in Kawasaki syndrome
P A Brogan, V Shah, L A Clarke, et al.
European Journal of Pediatrics
|
January 7, 1999
Validation of new blood pressure monitors for children: defects by default
C D Goonasekera, A M Wade, M Slattery, et al.
Blood Pressure
|
December 19, 1998
Performance of a new blood pressure monitor in children and young adults: the difficulties in clinical validation
C D Goonasekera, A M Wade, M Slattery, et al.
The British Journal of Dermatology
|
January 4, 2007
Nephro-urological complications of epidermolysis bullosa in paediatric patients
S M H Chan, M J Dillon, P G Duffy, et al.
European Journal of Pediatrics
|
March 1, 1985
Isolated glucocorticoid deficiency: metabolic and endocrine studies in a 5-year-old boy
G Soltesz, M J Dillon, P A Jenkins, 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.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1980
Hypertension in a four-year-old child: gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids
C H Shackleton, J W Honour, M J Dillon, et al.
Page
of 21
Search research articles
Search
Showing results (121-130 of 206) with videos related to
Sort By:
Page
of 21
Archives of Disease in Childhood
|
October 1, 1990
Kawasaki disease: echocardiographic features in 91 cases presenting in the United Kingdom
A Suzuki, E J Tizard, V Gooch, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 1, 1989
Autosomal recessive polycystic kidney disease
B S Kaplan, J Fay, V Shah, et al.
Archives of Disease in Childhood
|
March 1, 1989
Antineutrophil cytoplasm antibodies in Kawasaki disease
C O Savage, J Tizard, D Jayne, et al.
Clinical and Experimental Immunology
|
December 12, 2007
T cell activation profiles in Kawasaki syndrome
P A Brogan, V Shah, L A Clarke, et al.
European Journal of Pediatrics
|
January 7, 1999
Validation of new blood pressure monitors for children: defects by default
C D Goonasekera, A M Wade, M Slattery, et al.
Blood Pressure
|
December 19, 1998
Performance of a new blood pressure monitor in children and young adults: the difficulties in clinical validation
C D Goonasekera, A M Wade, M Slattery, et al.
The British Journal of Dermatology
|
January 4, 2007
Nephro-urological complications of epidermolysis bullosa in paediatric patients
S M H Chan, M J Dillon, P G Duffy, et al.
European Journal of Pediatrics
|
March 1, 1985
Isolated glucocorticoid deficiency: metabolic and endocrine studies in a 5-year-old boy
G Soltesz, M J Dillon, P A Jenkins, 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.
The Journal of Clinical Endocrinology and Metabolism
|
April 1, 1980
Hypertension in a four-year-old child: gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids
C H Shackleton, J W Honour, M J Dillon, et al.
Page
of 21