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The Journal of Small Animal Practice|April 4, 2017
Congenital duodenocolic fistula in a dogA Lecoindre, D Saade, P Barthez, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|March 9, 2005
United Arab Emirates National Newborn Screening Programme: an evaluation 1998-2000H al-Hosani, M Salah, D Saade, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|November 26, 2004
Prevalence of iodine deficiency disorders in the United Arab Emirates measured by raised TSH levelsH Al-Hosani, H Osman, L Abdel Wareth, et al.
Urology Case Reports|August 24, 2019
Advanced small-cell bladder cancer into a ureterocele: A case report and literature reviewCamila R T Burity, Fábio T Ferreira, André F Veiga, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|May 17, 2006
The National Congenital Anomalies Register in the United Arab EmiratesH Al Hosani, M Salah, H Abu-Zeid, et al.
Urology Annals|September 20, 2013
Challenges on percutaneous nephrolithotomy in pregnancy: Supine position approach through ultrasound guidanceAdriano Fregonesi, Fernando G F Dias, Ricardo D Saade, et al.
The Journal of Urology|November 17, 2007
Quantitative (stereological) and qualitative study of rat epididymis after vasectomy and percutaneous epididymal sperm aspirationRicardo D Saade, Paulo A Neves, Sidney Glina, et al.
Eastern Mediterranean Health Journal = La Revue De Sante De La Mediterranee Orientale = Al-Majallah Al-Sihhiyah Li-Sharq Al-Mutawassit|June 17, 2014
Expanding the comprehensive national neonatal screening programme in the United Arab Emirates from 1995 to 2011H Al Hosani, M Salah, H M Osman, et al.
Urology Case Reports|May 26, 2021
Localized primary melanoma of male urethra with a 4-year follow upC R T Burity, S B Linica, R D Saade, et al.
Acta Neuropathologica|August 30, 2019
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvementS Donkervoort, R Sabouny, P Yun, et al.
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