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Amin J Barakat

Showing results (1-10 of 7) with videos related to

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Pediatric Annals|March 6, 2013
Presentation of renal disease in childrenAmin J Barakat
International Journal of Pediatrics|June 13, 2012
Presentation of the child with renal disease and guidelines for referral to the pediatric nephrologistAmin J Barakat
Clinical Genetics|September 18, 2024
Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A reviewAmin J Barakat, Merlin G Butler
American Journal of Medical Genetics. Part A|April 18, 2018
Barakat syndrome revisitedAmin J Barakat, Margarita Raygada, Owen M Rennert
Pediatric Investigation|August 28, 2020
Rapid strep testing in children with recently treated streptococcal pharyngitisAmin J Barakat, Coni Evans, Monica Gill, et al.
Clinical Dysmorphology|June 15, 2004
22q13 deletion syndrome with central diabetes insipidus: a previously unreported associationAmin J Barakat, Phillip L Pearl, Maria T Acosta, et al.
The World Allergy Organization Journal|January 4, 2013
Hereditary angioedema caused by c1-esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategiesRichard G Gower, Paula J Busse, Emel Aygören-Pürsün, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Pediatric Annals|March 6, 2013
Presentation of renal disease in childrenAmin J Barakat
International Journal of Pediatrics|June 13, 2012
Presentation of the child with renal disease and guidelines for referral to the pediatric nephrologistAmin J Barakat
Clinical Genetics|September 18, 2024
Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A reviewAmin J Barakat, Merlin G Butler
American Journal of Medical Genetics. Part A|April 18, 2018
Barakat syndrome revisitedAmin J Barakat, Margarita Raygada, Owen M Rennert
Pediatric Investigation|August 28, 2020
Rapid strep testing in children with recently treated streptococcal pharyngitisAmin J Barakat, Coni Evans, Monica Gill, et al.
Clinical Dysmorphology|June 15, 2004
22q13 deletion syndrome with central diabetes insipidus: a previously unreported associationAmin J Barakat, Phillip L Pearl, Maria T Acosta, et al.
The World Allergy Organization Journal|January 4, 2013
Hereditary angioedema caused by c1-esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategiesRichard G Gower, Paula J Busse, Emel Aygören-Pürsün, et al.
Pageof 1