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Journal of the American College of Cardiology
|
July 6, 2024
Exercise Testing to Unmask Latent LVOT Obstruction in a Highly Symptomatic Patient With Hypertrophic Cardiomyopathy
Mustafa Husaini, Richard G Bach, Sharon Cresci
Das Deutsche Gesundheitswesen
|
April 16, 1970
[Fibrinolysis incidence in arteriosclerosis-induced illnesses as well as in arteriosclerosis positive and negative syntropic diseases]
F H Schulz, G Bach, A Künzel
American Journal of Human Genetics
|
September 1, 1980
Metachromatic leukodystrophy in the habbanite Jews: high frequency in a genetic isolate and screening for heterozygotes
J Zlotogora, G Bach, Y Barak, et al.
Clinical Genetics
|
April 1, 1987
Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate
G Bach, A Dagan, B Herz, et al.
Das Deutsche Gesundheitswesen
|
June 15, 1972
[Vitamin B 6 deficiency in hematologic diseases]
D Nelius, G Bach, J Schulz, et al.
Acta Biologica Et Medica Germanica
|
January 1, 1971
[Standardization of the latex fixation test for the demonstration of the rheumatoid factor. 3. Nature of the rheumatoid factor in normal serum, in serum of patients with rheumatoid arthritis, and in serum of the aged]
H Grieble, G Bach, T Anderson, et al.
Clinical Genetics
|
January 1, 1982
Pseudodeficiency of alpha-galactosidase A
G Bach, E Rosenmann, A Karni, et al.
Pediatric Research
|
August 1, 1980
Letter to the editor: about the inheritance of the aryl sulfatase A
J Zlotogora, T Cohen, E Elian, et al.
Israel Journal of Medical Sciences
|
January 1, 1983
Tay-Sachs disease among Moroccan Jews
J Vecht, M Zeigler, M Segal, et al.
Human Genetics
|
March 1, 1991
Hunter syndrome in Jews in Israel: further evidence for prenatal selection favoring the Hunter allele
J Zlotogora, T Schaap, M Zeigler, et al.
Page
of 37
Search research articles
Search
Showing results (101-110 of 363) with videos related to
Sort By:
Page
of 37
Journal of the American College of Cardiology
|
July 6, 2024
Exercise Testing to Unmask Latent LVOT Obstruction in a Highly Symptomatic Patient With Hypertrophic Cardiomyopathy
Mustafa Husaini, Richard G Bach, Sharon Cresci
Das Deutsche Gesundheitswesen
|
April 16, 1970
[Fibrinolysis incidence in arteriosclerosis-induced illnesses as well as in arteriosclerosis positive and negative syntropic diseases]
F H Schulz, G Bach, A Künzel
American Journal of Human Genetics
|
September 1, 1980
Metachromatic leukodystrophy in the habbanite Jews: high frequency in a genetic isolate and screening for heterozygotes
J Zlotogora, G Bach, Y Barak, et al.
Clinical Genetics
|
April 1, 1987
Diagnosis of arylsulfatase A deficiency in intact cultured cells using a fluorescent derivative of cerebroside sulfate
G Bach, A Dagan, B Herz, et al.
Das Deutsche Gesundheitswesen
|
June 15, 1972
[Vitamin B 6 deficiency in hematologic diseases]
D Nelius, G Bach, J Schulz, et al.
Acta Biologica Et Medica Germanica
|
January 1, 1971
[Standardization of the latex fixation test for the demonstration of the rheumatoid factor. 3. Nature of the rheumatoid factor in normal serum, in serum of patients with rheumatoid arthritis, and in serum of the aged]
H Grieble, G Bach, T Anderson, et al.
Clinical Genetics
|
January 1, 1982
Pseudodeficiency of alpha-galactosidase A
G Bach, E Rosenmann, A Karni, et al.
Pediatric Research
|
August 1, 1980
Letter to the editor: about the inheritance of the aryl sulfatase A
J Zlotogora, T Cohen, E Elian, et al.
Israel Journal of Medical Sciences
|
January 1, 1983
Tay-Sachs disease among Moroccan Jews
J Vecht, M Zeigler, M Segal, et al.
Human Genetics
|
March 1, 1991
Hunter syndrome in Jews in Israel: further evidence for prenatal selection favoring the Hunter allele
J Zlotogora, T Schaap, M Zeigler, et al.
Page
of 37