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Molecular Immunology
|
July 2, 2013
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
Edwin K S Wong, Tim H J Goodship, David Kavanagh
Journal of Medical Genetics
|
January 1, 1988
Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy
J Goodship, S Malcolm, M E Robertson, et al.
Clinical Dysmorphology
|
July 1, 1992
New dysmorphic syndrome with choanal atresia in siblings
J Burn, C McKeown, J Wagget, et al.
Prenatal Diagnosis
|
August 26, 1998
Prenatal diagnosis of mosaic trisomy 8 with investigations of the extent and origin of trisomic cells
A L Webb, J Wolstenholme, J Evans, et al.
European Journal of Clinical Investigation
|
September 27, 2003
Effect of insulin upon protein degradation in cultured human myocytes
R G Roberts, C P F Redfern, T H J Goodship
Journal of Medical Genetics
|
November 1, 1991
Transmission of Proteus syndrome from father to son?
J Goodship, A Redfearn, D Milligan, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 1, 2011
Plasma therapy for atypical haemolytic uraemic syndrome associated with heterozygous factor H mutations
Jon Jin Kim, Tim H J Goodship, Jane Tizard, et al.
Clinical Kidney Journal
|
September 29, 2015
Use of eculizumab in crescentic IgA nephropathy: proof of principle and conundrum?
Troels Ring, Birgitte Bang Pedersen, Giedrius Salkus, et al.
QJM : Monthly Journal of the Association of Physicians
|
April 23, 2015
A national specialized service in England for atypical haemolytic uraemic syndrome-the first year's experience
N S Sheerin, D Kavanagh, T H J Goodship, et al.
American Journal of Human Genetics
|
July 13, 2000
Autozygosity mapping of a seckel syndrome locus to chromosome 3q22. 1-q24
J Goodship, H Gill, J Carter, et al.
Page
of 14
Search research articles
Search
Showing results (21-30 of 137) with videos related to
Sort By:
Page
of 14
Molecular Immunology
|
July 2, 2013
Complement therapy in atypical haemolytic uraemic syndrome (aHUS)
Edwin K S Wong, Tim H J Goodship, David Kavanagh
Journal of Medical Genetics
|
January 1, 1988
Service experience using DNA analysis for genetic prediction in Duchenne muscular dystrophy
J Goodship, S Malcolm, M E Robertson, et al.
Clinical Dysmorphology
|
July 1, 1992
New dysmorphic syndrome with choanal atresia in siblings
J Burn, C McKeown, J Wagget, et al.
Prenatal Diagnosis
|
August 26, 1998
Prenatal diagnosis of mosaic trisomy 8 with investigations of the extent and origin of trisomic cells
A L Webb, J Wolstenholme, J Evans, et al.
European Journal of Clinical Investigation
|
September 27, 2003
Effect of insulin upon protein degradation in cultured human myocytes
R G Roberts, C P F Redfern, T H J Goodship
Journal of Medical Genetics
|
November 1, 1991
Transmission of Proteus syndrome from father to son?
J Goodship, A Redfearn, D Milligan, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 1, 2011
Plasma therapy for atypical haemolytic uraemic syndrome associated with heterozygous factor H mutations
Jon Jin Kim, Tim H J Goodship, Jane Tizard, et al.
Clinical Kidney Journal
|
September 29, 2015
Use of eculizumab in crescentic IgA nephropathy: proof of principle and conundrum?
Troels Ring, Birgitte Bang Pedersen, Giedrius Salkus, et al.
QJM : Monthly Journal of the Association of Physicians
|
April 23, 2015
A national specialized service in England for atypical haemolytic uraemic syndrome-the first year's experience
N S Sheerin, D Kavanagh, T H J Goodship, et al.
American Journal of Human Genetics
|
July 13, 2000
Autozygosity mapping of a seckel syndrome locus to chromosome 3q22. 1-q24
J Goodship, H Gill, J Carter, et al.
Page
of 14