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Pediatric Nephrology (Berlin, Germany)
|
March 1, 1992
Cadaveric renal transplantation in children under 5 years of age
M M Fitzpatrick, P G Duffy, O N Fernando, et al.
Clinical Endocrinology
|
December 1, 1993
Tissue resistance to 1,25-dihydroxyvitamin D without a mutation of the vitamin D receptor gene
M Hewison, A R Rut, K Kristjansson, et al.
Archives of Disease in Childhood
|
June 1, 1980
Pseudohypoaldosteronism
M J Dillon, J V Leonard, J M Buckler, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 16, 1999
A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation in Jansen's metaphyseal chondrodysplasia
E Schipani, C Langman, J Hunzelman, et al.
Lancet (London, England)
|
March 15, 1986
Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy
D B Dunger, K E Davies, M Pembrey, et al.
Journal of the Royal Society of Medicine
|
April 1, 1994
Chronic rash associated with congenital rubella
L S Ostlere, D Harris, H P Stevens, et al.
Archives of Disease in Childhood
|
August 24, 2002
Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside
M K H Chan, A T Tucker, S Madden, et al.
Kidney International
|
January 1, 1988
Intravascular platelet activation in the hemolytic uremic syndrome
M D Walters, M Levin, C Smith, et al.
Lancet (London, England)
|
November 9, 1991
Isolation of measles virus from child with Kawasaki disease
D Whitby, J G Hoad, E J Tizard, et al.
The Journal of Pediatrics
|
November 1, 1990
Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome)
L Jadresic, J Leake, I Gordon, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 206) with videos related to
Sort By:
Page
of 21
Pediatric Nephrology (Berlin, Germany)
|
March 1, 1992
Cadaveric renal transplantation in children under 5 years of age
M M Fitzpatrick, P G Duffy, O N Fernando, et al.
Clinical Endocrinology
|
December 1, 1993
Tissue resistance to 1,25-dihydroxyvitamin D without a mutation of the vitamin D receptor gene
M Hewison, A R Rut, K Kristjansson, et al.
Archives of Disease in Childhood
|
June 1, 1980
Pseudohypoaldosteronism
M J Dillon, J V Leonard, J M Buckler, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 16, 1999
A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation in Jansen's metaphyseal chondrodysplasia
E Schipani, C Langman, J Hunzelman, et al.
Lancet (London, England)
|
March 15, 1986
Deletion on the X chromosome detected by direct DNA analysis in one of two unrelated boys with glycerol kinase deficiency, adrenal hypoplasia, and Duchenne muscular dystrophy
D B Dunger, K E Davies, M Pembrey, et al.
Journal of the Royal Society of Medicine
|
April 1, 1994
Chronic rash associated with congenital rubella
L S Ostlere, D Harris, H P Stevens, et al.
Archives of Disease in Childhood
|
August 24, 2002
Erythromelalgia: an endothelial disorder responsive to sodium nitroprusside
M K H Chan, A T Tucker, S Madden, et al.
Kidney International
|
January 1, 1988
Intravascular platelet activation in the hemolytic uremic syndrome
M D Walters, M Levin, C Smith, et al.
Lancet (London, England)
|
November 9, 1991
Isolation of measles virus from child with Kawasaki disease
D Whitby, J G Hoad, E J Tizard, et al.
The Journal of Pediatrics
|
November 1, 1990
Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome)
L Jadresic, J Leake, I Gordon, et al.
Page
of 21