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Seidman

Showing results (651-660 of 3,640) with videos related to

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American Journal of Preventive Medicine|January 11, 2024
First Responders During COVID-19: Career Calling, PTSD, and Work Self-EfficacyAndrew J Seidman, Wendi Born, Erin Corriveau
Elife|June 14, 2017
Effects of myosin variants on interacting-heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypesLorenzo Alamo, James S Ware, Antonio Pinto, et al.
Cell|September 7, 1990
A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutationA A Geisterfer-Lowrance, S Kass, G Tanigawa, et al.
Human Genetics|December 23, 2003
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontiaDolrudee Jumlongras, Jenn-Yih Lin, Anas Chapra, et al.
Cell|June 3, 1994
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereL Thierfelder, H Watkins, C MacRae, et al.
The Israel Medical Association Journal : IMAJ|January 7, 2015
Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinicMichael Arad, Lorenzo Monserrat, Shiraz Haron-Khun, et al.
Kidney International|February 14, 1998
A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13B J Mathis, S H Kim, K Calabrese, et al.
Annals of Neurology|April 1, 1997
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1Z Argov, E Tiram, I Eisenberg, et al.
Circulation|January 30, 2002
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderlyHideshi Niimura, Kristen K Patton, William J McKenna, et al.
The American Journal of Cardiology|April 6, 2000
Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutationE J Gruver, D Fatkin, G A Dodds, et al.
Pageof 364

Showing results (651-660 of 3,640) with videos related to

Sort By:
Pageof 364
American Journal of Preventive Medicine|January 11, 2024
First Responders During COVID-19: Career Calling, PTSD, and Work Self-EfficacyAndrew J Seidman, Wendi Born, Erin Corriveau
Elife|June 14, 2017
Effects of myosin variants on interacting-heads motif explain distinct hypertrophic and dilated cardiomyopathy phenotypesLorenzo Alamo, James S Ware, Antonio Pinto, et al.
Cell|September 7, 1990
A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutationA A Geisterfer-Lowrance, S Kass, G Tanigawa, et al.
Human Genetics|December 23, 2003
A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontiaDolrudee Jumlongras, Jenn-Yih Lin, Anas Chapra, et al.
Cell|June 3, 1994
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomereL Thierfelder, H Watkins, C MacRae, et al.
The Israel Medical Association Journal : IMAJ|January 7, 2015
Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinicMichael Arad, Lorenzo Monserrat, Shiraz Haron-Khun, et al.
Kidney International|February 14, 1998
A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13B J Mathis, S H Kim, K Calabrese, et al.
Annals of Neurology|April 1, 1997
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1Z Argov, E Tiram, I Eisenberg, et al.
Circulation|January 30, 2002
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderlyHideshi Niimura, Kristen K Patton, William J McKenna, et al.
The American Journal of Cardiology|April 6, 2000
Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutationE J Gruver, D Fatkin, G A Dodds, et al.
Pageof 364