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C Hogan

Showing results (361-370 of 484) with videos related to

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Lancet (London, England)|April 13, 2010
Maternal mortality for 181 countries, 1980-2008: a systematic analysis of progress towards Millennium Development Goal 5Margaret C Hogan, Kyle J Foreman, Mohsen Naghavi, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1990
Genetic linkage map of 46 DNA markers on human chromosome 16T P Keith, P Green, S T Reeders, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 10, 2013
Evaluating health-related quality of life in patients with polycystic liver disease and determining the impact of symptoms and liver volumeTitus F M Wijnands, Myrte K Neijenhuis, Wietske Kievit, et al.
Nephrology (Carlton, Vic.)|July 16, 2013
Risk factors for hospitalization among older, incident haemodialysis patientsKimberly L Schoonover, Latonya J Hickson, Suzanne M Norby, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|April 1, 2011
Successful ABO-incompatible kidney transplantation with antibody removal and standard immunosuppressionS M Flint, R G Walker, C Hogan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 16, 2008
Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletionJoaquim Calado, Yves Sznajer, Daniel Metzger, et al.
Kidney International Reports|September 13, 2021
Mitochondriopathy Manifesting as Inherited Tubulointerstitial Nephropathy Without Symptomatic Other Organ InvolvementAlessia Buglioni, Linda Hasadsri, Samih H Nasr, et al.
Journal of the American College of Surgeons|March 28, 2016
Outcomes and Durability of Hepatic Reduction after Combined Partial Hepatectomy and Cyst Fenestration for Massive Polycystic Liver DiseaseFouad T Chebib, Amber Harmon, Maria V Irazabal Mira, et al.
BMC Nephrology|May 27, 2017
The effect of disease severity markers on quality of life in autosomal dominant polycystic kidney disease: a systematic review, meta-analysis and meta-regressionMyrte K Neijenhuis, Wietske Kievit, Ronald D Perrone, et al.
Pediatrics|August 1, 1994
Screening for lead poisoning in an urban pediatric clinic using samples obtained by fingerstickD J Schonfeld, M R Cullen, P M Rainey, et al.
Pageof 49

Showing results (361-370 of 484) with videos related to

Sort By:
Pageof 49
Lancet (London, England)|April 13, 2010
Maternal mortality for 181 countries, 1980-2008: a systematic analysis of progress towards Millennium Development Goal 5Margaret C Hogan, Kyle J Foreman, Mohsen Naghavi, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1990
Genetic linkage map of 46 DNA markers on human chromosome 16T P Keith, P Green, S T Reeders, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|December 10, 2013
Evaluating health-related quality of life in patients with polycystic liver disease and determining the impact of symptoms and liver volumeTitus F M Wijnands, Myrte K Neijenhuis, Wietske Kievit, et al.
Nephrology (Carlton, Vic.)|July 16, 2013
Risk factors for hospitalization among older, incident haemodialysis patientsKimberly L Schoonover, Latonya J Hickson, Suzanne M Norby, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|April 1, 2011
Successful ABO-incompatible kidney transplantation with antibody removal and standard immunosuppressionS M Flint, R G Walker, C Hogan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 16, 2008
Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletionJoaquim Calado, Yves Sznajer, Daniel Metzger, et al.
Kidney International Reports|September 13, 2021
Mitochondriopathy Manifesting as Inherited Tubulointerstitial Nephropathy Without Symptomatic Other Organ InvolvementAlessia Buglioni, Linda Hasadsri, Samih H Nasr, et al.
Journal of the American College of Surgeons|March 28, 2016
Outcomes and Durability of Hepatic Reduction after Combined Partial Hepatectomy and Cyst Fenestration for Massive Polycystic Liver DiseaseFouad T Chebib, Amber Harmon, Maria V Irazabal Mira, et al.
BMC Nephrology|May 27, 2017
The effect of disease severity markers on quality of life in autosomal dominant polycystic kidney disease: a systematic review, meta-analysis and meta-regressionMyrte K Neijenhuis, Wietske Kievit, Ronald D Perrone, et al.
Pediatrics|August 1, 1994
Screening for lead poisoning in an urban pediatric clinic using samples obtained by fingerstickD J Schonfeld, M R Cullen, P M Rainey, et al.
Pageof 49