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Journal D'Urologie
|
January 1, 1982
[Comparative experimental study of the renal consequences of vesico-ureteric reflux and of ureteric obstruction in the sheep foetus (author's transl)]
G Vallancien, D Beurton, R Szemat, et al.
Human Molecular Genetics
|
November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
A Fuchshuber, G Jean, O Gribouval, et al.
Kidney International
|
December 1, 1986
H deficiency in two brothers with atypical dense intramembranous deposit disease
M Levy, L Halbwachs-Mecarelli, M C Gubler, et al.
Kidney International
|
November 1, 1987
Ontogenesis of angiotensin-I converting enzyme in human kidney
F Mounier, N Hinglais, M Sich, et al.
Kidney International
|
July 1, 1997
Development of human fetal kidney in obstructive uropathy: correlations with ultrasonography and urine biochemistry
F Daïkha-Dahmane, M Dommergues, F Muller, et al.
Fetal Diagnosis and Therapy
|
June 16, 2001
Pathogenesis of twin-twin transfusion syndrome: the renin-angiotensin system hypothesis
D Mahieu-Caputo, F Muller, D Joly, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
August 1, 1997
Clinical and pathophysiological aspects of immune complex glomerulonephritis associated with Entamoeba histolytica abscess of the liver
M Lecuit, F Martinez, G Deray, et al.
Kidney International. Supplement
|
July 1, 1993
A specific glomerular lesion of the graft: allograft glomerulopathy
R Habib, A Zurowska, N Hinglais, et al.
Kidney International
|
April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution
M C Gubler, B Knebelmann, A Beziau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 12, 2000
[Prenatal diagnosis of autosomal recessive polycystic kidney disease]
M F Gagnadoux, T Attié, J Amiel, et al.
Page
of 20
Search research articles
Search
Showing results (141-150 of 195) with videos related to
Sort By:
Page
of 20
Journal D'Urologie
|
January 1, 1982
[Comparative experimental study of the renal consequences of vesico-ureteric reflux and of ureteric obstruction in the sheep foetus (author's transl)]
G Vallancien, D Beurton, R Szemat, et al.
Human Molecular Genetics
|
November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis
A Fuchshuber, G Jean, O Gribouval, et al.
Kidney International
|
December 1, 1986
H deficiency in two brothers with atypical dense intramembranous deposit disease
M Levy, L Halbwachs-Mecarelli, M C Gubler, et al.
Kidney International
|
November 1, 1987
Ontogenesis of angiotensin-I converting enzyme in human kidney
F Mounier, N Hinglais, M Sich, et al.
Kidney International
|
July 1, 1997
Development of human fetal kidney in obstructive uropathy: correlations with ultrasonography and urine biochemistry
F Daïkha-Dahmane, M Dommergues, F Muller, et al.
Fetal Diagnosis and Therapy
|
June 16, 2001
Pathogenesis of twin-twin transfusion syndrome: the renin-angiotensin system hypothesis
D Mahieu-Caputo, F Muller, D Joly, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
August 1, 1997
Clinical and pathophysiological aspects of immune complex glomerulonephritis associated with Entamoeba histolytica abscess of the liver
M Lecuit, F Martinez, G Deray, et al.
Kidney International. Supplement
|
July 1, 1993
A specific glomerular lesion of the graft: allograft glomerulopathy
R Habib, A Zurowska, N Hinglais, et al.
Kidney International
|
April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distribution
M C Gubler, B Knebelmann, A Beziau, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
October 12, 2000
[Prenatal diagnosis of autosomal recessive polycystic kidney disease]
M F Gagnadoux, T Attié, J Amiel, et al.
Page
of 20