Showing results (631-640 of 825) with videos related to

Sort By:
Pageof 83
Circulation|November 22, 2000
Severely impaired baroreflex-buffering in patients with monogenic hypertension and neurovascular contactJ Jordan, H R Toka, K Heusser, et al.
International Journal of Molecular Sciences|April 3, 2021
microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic DystrophySarah U Morton, Christopher R Sefton, Huanqing Zhang, et al.
Indian Journal of Gastroenterology : Official Journal of the Indian Society of Gastroenterology|May 17, 2000
Laparoscopic management of hydatid cyst of liverA N Dalvi, A A Deshpande, R Prabhu, et al.
The Thoracic and Cardiovascular Surgeon|October 1, 1995
Surgical considerations in the management of significant acute mitral regurgitation following mitral valvotomyM Khaja, V Naithani, M E Mukadam, et al.
Postgraduate Medical Journal|July 8, 2009
Congenital and acquired conditions of the aortic root: multidetector computed tomography featuresH A Vargas, E T D Hoey, D Gopalan, et al.
NPJ Genomic Medicine|September 6, 2022
Integrating rapid exome sequencing into NICU clinical care after a pilot research studyAlissa M D'Gama, Maya C Del Rosario, Mairead A Bresnahan, et al.
Journal of Biotechnology|September 20, 2005
Purification and characterization of a new bioscouring pectate lyase from Bacillus pumilus BK2Barbara G Klug-Santner, Wolfgang Schnitzhofer, Maria Vrsanská, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2024
"It's hard to wait": Provider perspectives on current genomic care in safety-net NICUsAlissa M D'Gama, Monica H Wojcik, Sonia Hills, et al.
Kidney International|December 15, 2000
Relationship between nonphenacetin combined analgesics and nephropathy: a review. Ad Hoc Committee of the International Study Group on Analgesics and NephropathyA R Feinstein, L A Heinemann, G C Curhan, et al.
American Journal of Medical Genetics. Part A|January 20, 2018
Three-generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndromeBianca Quiñones-Pérez, Grace E VanNoy, Meghan C Towne, et al.
Pageof 83