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Gastroenterology
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February 24, 2001
Diffuse esophageal leiomyomatosis with perirectal involvement mimicking Hirschsprung disease
P Guillem, F Delcambre, L Cohen-Solal, et al.
American Journal of Medical Genetics
|
May 30, 1998
Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1
C Stavrou, A Pierides, I Zouvani, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]
D Graber, C Antignac, G Deschenes, et al.
Human Molecular Genetics
|
November 11, 1999
Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin
M Attard, G Jean, L Forestier, et al.
Clinical Genetics
|
July 14, 2011
Maternal uniparental disomy of chromosome 16 in a patient with adenine phosphoribosyltransferase deficiency
I Ceballos-Picot, G Guest, V Moriniere, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 31, 2001
Benign familial hematuria associated with a novel COL4A4 mutation
S Ozen, D Ertoy, L Heidet, et al.
The International Journal of Pediatric Nephrology
|
January 1, 1985
Diffuse arterial calcified elastopathy--a new cause of renovascular hypertension in children
M C Gubler, C Antignac, M Broyer, et al.
American Journal of Diseases of Children (1960)
|
July 1, 1993
Pathological case of the month. Alport syndrome and diffuse leiomyomatosis
P Cochat, C Guyot, C Antignac, et al.
Genomics
|
July 1, 1990
Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor
C Jeanpierre, C Antignac, C Beroud, 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.
Page
of 11
Search research articles
Search
Showing results (41-50 of 103) with videos related to
Sort By:
Page
of 11
Gastroenterology
|
February 24, 2001
Diffuse esophageal leiomyomatosis with perirectal involvement mimicking Hirschsprung disease
P Guillem, F Delcambre, L Cohen-Solal, et al.
American Journal of Medical Genetics
|
May 30, 1998
Medullary cystic kidney disease with hyperuricemia and gout in a large Cypriot family: no allelism with nephronophthisis type 1
C Stavrou, A Pierides, I Zouvani, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
March 10, 2001
[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]
D Graber, C Antignac, G Deschenes, et al.
Human Molecular Genetics
|
November 11, 1999
Severity of phenotype in cystinosis varies with mutations in the CTNS gene: predicted effect on the model of cystinosin
M Attard, G Jean, L Forestier, et al.
Clinical Genetics
|
July 14, 2011
Maternal uniparental disomy of chromosome 16 in a patient with adenine phosphoribosyltransferase deficiency
I Ceballos-Picot, G Guest, V Moriniere, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 31, 2001
Benign familial hematuria associated with a novel COL4A4 mutation
S Ozen, D Ertoy, L Heidet, et al.
The International Journal of Pediatric Nephrology
|
January 1, 1985
Diffuse arterial calcified elastopathy--a new cause of renovascular hypertension in children
M C Gubler, C Antignac, M Broyer, et al.
American Journal of Diseases of Children (1960)
|
July 1, 1993
Pathological case of the month. Alport syndrome and diffuse leiomyomatosis
P Cochat, C Guyot, C Antignac, et al.
Genomics
|
July 1, 1990
Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor
C Jeanpierre, C Antignac, C Beroud, 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.
Page
of 11