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The Israel Medical Association Journal : IMAJ
|
January 7, 2015
Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic
Michael Arad, Lorenzo Monserrat, Shiraz Haron-Khun, et al.
Kidney International
|
February 14, 1998
A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13
B 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-q1
Z Argov, E Tiram, I Eisenberg, et al.
Circulation
|
January 30, 2002
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly
Hideshi 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 mutation
E J Gruver, D Fatkin, G A Dodds, et al.
Nature Genetics
|
April 1, 1993
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
H Watkins, C MacRae, L Thierfelder, et al.
Muscle & Nerve
|
June 18, 2003
Adult Hallervorden-Spatz syndrome simulating amyotrophic lateral sclerosis
O M Vasconcelos, D H Harter, C Duffy, et al.
Pediatrics
|
December 1, 1987
Primary sclerosing cholangitis in children: study of five cases and review of the literature
A Sisto, P Feldman, L Garel, et al.
Current Protocols
|
October 26, 2022
Multiplexed Single-Nucleus RNA Sequencing Using Lipid-Oligo Barcodes
Qi Zhang, Seong Won Kim, Joshua M Gorham, et al.
The Pediatric Infectious Disease Journal
|
August 5, 2000
Leukocytosis in children with Escherichia coli O157:H7 enteritis developing the hemolytic-uremic syndrome
C Buteau, F Proulx, M Chaibou, et al.
Page
of 54
Search research articles
Search
Showing results (151-160 of 533) with videos related to
Sort By:
Page
of 54
The Israel Medical Association Journal : IMAJ
|
January 7, 2015
Merits and pitfalls of genetic testing in a hypertrophic cardiomyopathy clinic
Michael Arad, Lorenzo Monserrat, Shiraz Haron-Khun, et al.
Kidney International
|
February 14, 1998
A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13
B 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-q1
Z Argov, E Tiram, I Eisenberg, et al.
Circulation
|
January 30, 2002
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly
Hideshi 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 mutation
E J Gruver, D Fatkin, G A Dodds, et al.
Nature Genetics
|
April 1, 1993
A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3
H Watkins, C MacRae, L Thierfelder, et al.
Muscle & Nerve
|
June 18, 2003
Adult Hallervorden-Spatz syndrome simulating amyotrophic lateral sclerosis
O M Vasconcelos, D H Harter, C Duffy, et al.
Pediatrics
|
December 1, 1987
Primary sclerosing cholangitis in children: study of five cases and review of the literature
A Sisto, P Feldman, L Garel, et al.
Current Protocols
|
October 26, 2022
Multiplexed Single-Nucleus RNA Sequencing Using Lipid-Oligo Barcodes
Qi Zhang, Seong Won Kim, Joshua M Gorham, et al.
The Pediatric Infectious Disease Journal
|
August 5, 2000
Leukocytosis in children with Escherichia coli O157:H7 enteritis developing the hemolytic-uremic syndrome
C Buteau, F Proulx, M Chaibou, et al.
Page
of 54