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Schweizerische Medizinische Wochenschrift
|
January 20, 1973
[Wilson's disease in Switzerland. Clinical, genetic and biochemical studies]
A Tschumi, J P Colombo, H Moser
Schweizerische Medizinische Wochenschrift
|
February 26, 1977
[Morbidity and mortality in cystic fibrosis. Results of 20 years of experience]
R Kraemer, E Stoll, H Moser, et al.
BMJ (Clinical Research Ed.)
|
November 10, 1990
Screening for carriers of cystic fibrosis among partners of people heterozygous for the disease
F H Sennhauser, S Liechti-Gallati, H Moser
Molecular and Chemical Neuropathology
|
June 1, 1990
Cognitive impairment in adult-onset adrenoleukodystrophy
D Edwin, L Speedie, S Naidu, et al.
Schweizerische Medizinische Wochenschrift
|
May 25, 1996
[Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]
R Spiegel, A Hagmann, E Boltshauser, et al.
European Journal of Applied Physiology and Occupational Physiology
|
May 18, 1979
Intra- and extravascular volume changes in the human forearm after static hand grip exercise
W Schnizer, H Hinneberg, H Moser, et al.
Haemostasis
|
January 1, 1992
Interferon-gamma-induced expression of tissue factor activity during human monocyte to macrophage maturation
C Scheibenbogen, H Moser, S Krause, et al.
Human Molecular Genetics
|
November 1, 1992
A polymorphic synonymous mutation (K54K) in the human 70 kD peroxisomal membrane protein gene (PMP1)
J Gärtner, C Obie, H Moser, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie
|
November 1, 1985
[Prenatal diagnosis of osteogenesis imperfecta, type II, following AID]
U Gigon, R Meudt, A Zimmermann, et al.
Developments in Biological Standardization
|
January 1, 1982
Herpes simplex virus subunit vaccine: characterization of the virus strain used and testing of the vaccine
J Hilfenhaus, H Moser, A Herrmann, et al.
Page
of 43
Search research articles
Search
Showing results (171-180 of 423) with videos related to
Sort By:
Page
of 43
Schweizerische Medizinische Wochenschrift
|
January 20, 1973
[Wilson's disease in Switzerland. Clinical, genetic and biochemical studies]
A Tschumi, J P Colombo, H Moser
Schweizerische Medizinische Wochenschrift
|
February 26, 1977
[Morbidity and mortality in cystic fibrosis. Results of 20 years of experience]
R Kraemer, E Stoll, H Moser, et al.
BMJ (Clinical Research Ed.)
|
November 10, 1990
Screening for carriers of cystic fibrosis among partners of people heterozygous for the disease
F H Sennhauser, S Liechti-Gallati, H Moser
Molecular and Chemical Neuropathology
|
June 1, 1990
Cognitive impairment in adult-onset adrenoleukodystrophy
D Edwin, L Speedie, S Naidu, et al.
Schweizerische Medizinische Wochenschrift
|
May 25, 1996
[Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]
R Spiegel, A Hagmann, E Boltshauser, et al.
European Journal of Applied Physiology and Occupational Physiology
|
May 18, 1979
Intra- and extravascular volume changes in the human forearm after static hand grip exercise
W Schnizer, H Hinneberg, H Moser, et al.
Haemostasis
|
January 1, 1992
Interferon-gamma-induced expression of tissue factor activity during human monocyte to macrophage maturation
C Scheibenbogen, H Moser, S Krause, et al.
Human Molecular Genetics
|
November 1, 1992
A polymorphic synonymous mutation (K54K) in the human 70 kD peroxisomal membrane protein gene (PMP1)
J Gärtner, C Obie, H Moser, et al.
Zeitschrift Fur Geburtshilfe Und Perinatologie
|
November 1, 1985
[Prenatal diagnosis of osteogenesis imperfecta, type II, following AID]
U Gigon, R Meudt, A Zimmermann, et al.
Developments in Biological Standardization
|
January 1, 1982
Herpes simplex virus subunit vaccine: characterization of the virus strain used and testing of the vaccine
J Hilfenhaus, H Moser, A Herrmann, et al.
Page
of 43