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International Journal of Nephrology
|
July 16, 2011
Peritoneal dialysis tailored to pediatric needs
C P Schmitt, A Zaloszyc, B Schaefer, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 27, 2014
Fetal intervention for severe lower urinary tract obstruction: a multicenter case-control study comparing fetal cystoscopy with vesicoamniotic shunting
R Ruano, N Sananes, H Sangi-Haghpeykar, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 13, 2014
Urological fistulas after fetal cystoscopic laser ablation of posterior urethral valves: surgical technical aspects
N Sananes, R Favre, C J Koh, et al.
Molecular Syndromology
|
December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly
E Schaefer, A Zaloszyc, J Lauer, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
International Journal of Nephrology
|
July 16, 2011
Peritoneal dialysis tailored to pediatric needs
C P Schmitt, A Zaloszyc, B Schaefer, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
August 27, 2014
Fetal intervention for severe lower urinary tract obstruction: a multicenter case-control study comparing fetal cystoscopy with vesicoamniotic shunting
R Ruano, N Sananes, H Sangi-Haghpeykar, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology
|
May 13, 2014
Urological fistulas after fetal cystoscopic laser ablation of posterior urethral valves: surgical technical aspects
N Sananes, R Favre, C J Koh, et al.
Molecular Syndromology
|
December 23, 2011
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly
E Schaefer, A Zaloszyc, J Lauer, et al.
Page
of 1