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European Journal of Clinical Investigation
|
August 3, 2002
Sodium bicarbonate treatment and ubiquitin gene expression in acidotic human subjects with chronic renal failure
R G Roberts, C P F Redfern, K A Graham, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 3, 2002
Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor
Rosemary L Donne, Ian Abbs, Peter Barany, et al.
Journal of Medical Genetics
|
October 1, 1993
Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134)
R Wadey, S Daw, A Wickremasinghe, et al.
Molecular Immunology
|
August 3, 2005
Does complement factor B have a role in the pathogenesis of atypical HUS?
David Kavanagh, Elizabeth J Kemp, Anna Richards, et al.
Nature Genetics
|
May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus
M Satoda, F Zhao, G A Diaz, et al.
Human Molecular Genetics
|
June 1, 1995
Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
R Wadey, S Daw, C Taylor, et al.
Blood
|
October 5, 2007
Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome
Celia J Fang, Veronique Fremeaux-Bacchi, M Kathryn Liszewski, et al.
Human Genetics
|
March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion
S V Hodgson, M E Robertson, C N Fear, et al.
American Journal of Human Genetics
|
November 1, 1992
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome
A H Carey, D Kelly, S Halford, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 22, 2008
Efficacy of plasma therapy in atypical hemolytic uremic syndrome with complement factor H mutations
Anne-Laure Lapeyraque, Eric Wagner, Véronique Phan, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 137) with videos related to
Sort By:
Page
of 14
European Journal of Clinical Investigation
|
August 3, 2002
Sodium bicarbonate treatment and ubiquitin gene expression in acidotic human subjects with chronic renal failure
R G Roberts, C P F Redfern, K A Graham, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
December 3, 2002
Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor
Rosemary L Donne, Ian Abbs, Peter Barany, et al.
Journal of Medical Genetics
|
October 1, 1993
Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134)
R Wadey, S Daw, A Wickremasinghe, et al.
Molecular Immunology
|
August 3, 2005
Does complement factor B have a role in the pathogenesis of atypical HUS?
David Kavanagh, Elizabeth J Kemp, Anna Richards, et al.
Nature Genetics
|
May 10, 2000
Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus
M Satoda, F Zhao, G A Diaz, et al.
Human Molecular Genetics
|
June 1, 1995
Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome
R Wadey, S Daw, C Taylor, et al.
Blood
|
October 5, 2007
Membrane cofactor protein mutations in atypical hemolytic uremic syndrome (aHUS), fatal Stx-HUS, C3 glomerulonephritis, and the HELLP syndrome
Celia J Fang, Veronique Fremeaux-Bacchi, M Kathryn Liszewski, et al.
Human Genetics
|
March 1, 1987
Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion
S V Hodgson, M E Robertson, C N Fear, et al.
American Journal of Human Genetics
|
November 1, 1992
Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome
A H Carey, D Kelly, S Halford, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 22, 2008
Efficacy of plasma therapy in atypical hemolytic uremic syndrome with complement factor H mutations
Anne-Laure Lapeyraque, Eric Wagner, Véronique Phan, et al.
Page
of 14