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The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
August 12, 2003
Long-term follow-up of arrhythmias in pediatric orthotopic heart transplant recipients: incidence and correlation with rejection
N J Kertesz, J A Towbin, S Clunie, et al.
American Journal of Medical Genetics
|
May 26, 1999
Maternally inherited nonsyndromic hearing loss
R A Friedman, Y Bykhovskaya, C M Sue, et al.
The Journal of Biological Chemistry
|
July 21, 1998
Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2
P J Kozel, R A Friedman, L C Erway, et al.
The American Journal of Otology
|
May 23, 2000
Prognostic factors for hearing preservation in vestibular schwannoma surgery
D E Brackmann, R M Owens, R A Friedman, et al.
The Journal of Clinical Psychiatry
|
January 28, 1999
Predictors of response to acute treatment of chronic and double depression with sertraline or imipramine
R M Hirschfeld, J M Russell, P L Delgado, et al.
Pacing and Clinical Electrophysiology : PACE
|
May 4, 2000
Recommendations for extraction of chronically implanted transvenous pacing and defibrillator leads: indications, facilities, training. North American Society of Pacing and Electrophysiology Lead Extraction Conference Faculty
C J Love, B L Wilkoff, C L Byrd, et al.
Journal of the American College of Cardiology
|
January 12, 2001
Congenital heart block: development of late-onset cardiomyopathy, a previously underappreciated sequela
J P Moak, K S Barron, T J Hougen, et al.
Journal of Affective Disorders
|
June 28, 2001
Sertraline versus imipramine to prevent relapse in chronic depression
L M Koran, A J Gelenberg, S G Kornstein, et al.
Human Molecular Genetics
|
September 1, 1996
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4
Y J de Kok, E R Vossenaar, C W Cremers, et al.
Gene
|
October 3, 1998
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19
D A Scott, J H Greinwald, J R Marietta, et al.
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Search research articles
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Showing results (91-100 of 100) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 100 results.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation
|
August 12, 2003
Long-term follow-up of arrhythmias in pediatric orthotopic heart transplant recipients: incidence and correlation with rejection
N J Kertesz, J A Towbin, S Clunie, et al.
American Journal of Medical Genetics
|
May 26, 1999
Maternally inherited nonsyndromic hearing loss
R A Friedman, Y Bykhovskaya, C M Sue, et al.
The Journal of Biological Chemistry
|
July 21, 1998
Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2
P J Kozel, R A Friedman, L C Erway, et al.
The American Journal of Otology
|
May 23, 2000
Prognostic factors for hearing preservation in vestibular schwannoma surgery
D E Brackmann, R M Owens, R A Friedman, et al.
The Journal of Clinical Psychiatry
|
January 28, 1999
Predictors of response to acute treatment of chronic and double depression with sertraline or imipramine
R M Hirschfeld, J M Russell, P L Delgado, et al.
Pacing and Clinical Electrophysiology : PACE
|
May 4, 2000
Recommendations for extraction of chronically implanted transvenous pacing and defibrillator leads: indications, facilities, training. North American Society of Pacing and Electrophysiology Lead Extraction Conference Faculty
C J Love, B L Wilkoff, C L Byrd, et al.
Journal of the American College of Cardiology
|
January 12, 2001
Congenital heart block: development of late-onset cardiomyopathy, a previously underappreciated sequela
J P Moak, K S Barron, T J Hougen, et al.
Journal of Affective Disorders
|
June 28, 2001
Sertraline versus imipramine to prevent relapse in chronic depression
L M Koran, A J Gelenberg, S G Kornstein, et al.
Human Molecular Genetics
|
September 1, 1996
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4
Y J de Kok, E R Vossenaar, C W Cremers, et al.
Gene
|
October 3, 1998
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19
D A Scott, J H Greinwald, J R Marietta, et al.
Page
of 10