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E HARMS

Showing results (221-230 of 308) with videos related to

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The Journal of Pediatrics|January 1, 1995
Intact survival with transfusion-associated graft-versus-host disease proved by human leukocyte antigen typing of lymphocytes in skin biopsy specimensR Hentschel, E B Broecker, G Kolde, et al.
The American Surgeon|August 19, 2008
Breast MR for the evaluation of occult nipple dischargeVincent E Mortellaro, Julia Marshall, Steven E Harms, et al.
Applications in Plant Sciences|April 13, 2023
DNA assays for genetic discrimination of three <i>Phragmites australis</i> subspecies in the United StatesDenise L Lindsay, Xin Guan, Nathan E Harms, et al.
AJR. American Journal of Roentgenology|March 1, 1992
Arterial injury from penetrating trauma: evaluation with single-acquisition fat-suppressed MR imagingJ J Yaquinto, S E Harms, P T Siemers, et al.
Radiology|December 1, 1991
Three-dimensional gadolinium-enhanced MR imaging of the breast: pulse sequence with fat suppression and magnetization transfer contrast. Work in progressW B Pierce, S E Harms, D P Flamig, et al.
Annals of Neurology|October 17, 2001
Individual blood-brain barrier phenylalanine transport determines clinical outcome in phenylketonuriaJ Weglage, D Wiedermann, J Denecke, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1994
Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samplesR Rossi, S Danzebrink, K Linnenbürger, et al.
The Journal of Infectious Diseases|April 16, 1998
Persistent infection with small colony variant strains of Staphylococcus aureus in patients with cystic fibrosisB Kahl, M Herrmann, A S Everding, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiencyK P Zimmer, T Matsuura, J P Colombo, et al.
Pediatric Nephrology (Berlin, Germany)|June 29, 2000
Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiencyE Kuwertz-Bröking, H G Koch, T Marquardt, et al.
Pageof 31

Showing results (221-230 of 308) with videos related to

Sort By:
Pageof 31
The Journal of Pediatrics|January 1, 1995
Intact survival with transfusion-associated graft-versus-host disease proved by human leukocyte antigen typing of lymphocytes in skin biopsy specimensR Hentschel, E B Broecker, G Kolde, et al.
The American Surgeon|August 19, 2008
Breast MR for the evaluation of occult nipple dischargeVincent E Mortellaro, Julia Marshall, Steven E Harms, et al.
Applications in Plant Sciences|April 13, 2023
DNA assays for genetic discrimination of three <i>Phragmites australis</i> subspecies in the United StatesDenise L Lindsay, Xin Guan, Nathan E Harms, et al.
AJR. American Journal of Roentgenology|March 1, 1992
Arterial injury from penetrating trauma: evaluation with single-acquisition fat-suppressed MR imagingJ J Yaquinto, S E Harms, P T Siemers, et al.
Radiology|December 1, 1991
Three-dimensional gadolinium-enhanced MR imaging of the breast: pulse sequence with fat suppression and magnetization transfer contrast. Work in progressW B Pierce, S E Harms, D P Flamig, et al.
Annals of Neurology|October 17, 2001
Individual blood-brain barrier phenylalanine transport determines clinical outcome in phenylketonuriaJ Weglage, D Wiedermann, J Denecke, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1994
Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samplesR Rossi, S Danzebrink, K Linnenbürger, et al.
The Journal of Infectious Diseases|April 16, 1998
Persistent infection with small colony variant strains of Staphylococcus aureus in patients with cystic fibrosisB Kahl, M Herrmann, A S Everding, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
A novel point mutation at codon 269 of the ornithine transcarbamylase (OTC) gene causing neonatal onset of OTC deficiencyK P Zimmer, T Matsuura, J P Colombo, et al.
Pediatric Nephrology (Berlin, Germany)|June 29, 2000
Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiencyE Kuwertz-Bröking, H G Koch, T Marquardt, et al.
Pageof 31