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E R Maher

Showing results (21-30 of 171) with videos related to

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Postgraduate Medical Journal|June 1, 1984
Acute renal failure due to glomerulonephritis associated with staphylococcal infectionE R Maher, D V Hamilton, S Thiru, et al.
Cancer|April 15, 1992
Phenotypic variation in hereditary nonpolyposis colon cancer syndrome. Association with infiltrative fibromatosis (desmoid tumor)E R Maher, B Morson, R Beach, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|February 15, 2007
The genetics of paragangliomas: a reviewT P C Martin, R M Irving, E R Maher
Human Molecular Genetics|May 1, 1996
Expression of the von Hippel-Lindau disease tumour suppressor gene during human embryogenesisF M Richards, P N Schofield, S Fleming, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 4, 1998
Independent segregation of von Hippel-Lindau disease and cerebral cavernomasA R Webster, R B Fisher, L Ginsberg, et al.
Familial Cancer|February 3, 2009
SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosisAlex Henderson, F Douglas, P Perros, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1992
Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC)A T Moore, E R Maher, D J Koch, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1988
Cyclosporin in the treatment of steroid-responsive and steroid-resistant nephrotic syndrome in adultsE R Maher, P Sweny, M Chappel, et al.
Clinical Genetics|August 1, 1994
Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new casesM Elliott, R Bayly, T Cole, et al.
Journal of Medical Genetics|October 10, 1997
Uptake of genetic testing for cancer predispositionD G Evans, E R Maher, R Macleod, et al.
Pageof 18

Showing results (21-30 of 171) with videos related to

Sort By:
Pageof 18
Postgraduate Medical Journal|June 1, 1984
Acute renal failure due to glomerulonephritis associated with staphylococcal infectionE R Maher, D V Hamilton, S Thiru, et al.
Cancer|April 15, 1992
Phenotypic variation in hereditary nonpolyposis colon cancer syndrome. Association with infiltrative fibromatosis (desmoid tumor)E R Maher, B Morson, R Beach, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|February 15, 2007
The genetics of paragangliomas: a reviewT P C Martin, R M Irving, E R Maher
Human Molecular Genetics|May 1, 1996
Expression of the von Hippel-Lindau disease tumour suppressor gene during human embryogenesisF M Richards, P N Schofield, S Fleming, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 4, 1998
Independent segregation of von Hippel-Lindau disease and cerebral cavernomasA R Webster, R B Fisher, L Ginsberg, et al.
Familial Cancer|February 3, 2009
SDHB-associated renal oncocytoma suggests a broadening of the renal phenotype in hereditary paragangliomatosisAlex Henderson, F Douglas, P Perros, et al.
Ophthalmic Paediatrics and Genetics|June 1, 1992
Incidence and significance of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in familial adenomatous polyposis coli (FAPC)A T Moore, E R Maher, D J Koch, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1988
Cyclosporin in the treatment of steroid-responsive and steroid-resistant nephrotic syndrome in adultsE R Maher, P Sweny, M Chappel, et al.
Clinical Genetics|August 1, 1994
Clinical features and natural history of Beckwith-Wiedemann syndrome: presentation of 74 new casesM Elliott, R Bayly, T Cole, et al.
Journal of Medical Genetics|October 10, 1997
Uptake of genetic testing for cancer predispositionD G Evans, E R Maher, R Macleod, et al.
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