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Archives of Dermatology
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September 18, 2001
Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband
K Nomura, K Umeki, I Hatayama, et al.
Dermatology (Basel, Switzerland)
|
June 1, 2001
Sézary syndrome with acute progressive pulmonary infiltration after improvement of skin eruption
D Sawamura, K Harada, T Aizu, et al.
Clinical and Experimental Immunology
|
April 1, 1990
Experimental murine thyroiditis induced by porcine thyroid peroxidase and its transfer by the antigen-specific T cell line
T Kotani, K Umeki, K Hirai, et al.
Acta Dermato-Venereologica
|
July 1, 1997
Dominant dystrophic epidermolysis bullosa albopapuloidea Pasini -- ultrastructural observations of albopapuloid lesions and a type VII collagen DNA polymorphism study of a family
K Nomura, K Umeki, D Sawamura, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1981
[Experimental and clinical studies on determination of urinary low molecular weight proteins by laser nephelometer (author's transl)]
S Matsunaga, K Umeki, H Nakagawa, et al.
Immunology Letters
|
January 1, 1985
Epitopic difference among rat thyroglobulins
T Kotani, M Maeda, K Umeki, et al.
Journal of Biochemistry
|
November 1, 1972
Crystallization of an -amylase and evidence for the presence of a glucose-forming enzyme in human urine
N Minamiura, K Umeki, K Tsujino, et al.
Journal of Medicine
|
January 1, 1995
Hepatocyte growth factor and acute phase proteins in patients with chronic liver diseases
G Shiota, K Umeki, J Okano, et al.
Journal of Dermatological Science
|
January 1, 1996
A keratin K14 gene mutation in a Japanese patient with the Dowling-Meara type of epidermolysis bullosa simplex
K Umeki, K Nomura, K Harada, et al.
Journal of Biochemistry
|
December 1, 1974
A glucose-forming amylase in human liver
K Tsujino, M Yoshimura, K Umeki, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 62) with videos related to
Sort By:
Page
of 7
Archives of Dermatology
|
September 18, 2001
Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband
K Nomura, K Umeki, I Hatayama, et al.
Dermatology (Basel, Switzerland)
|
June 1, 2001
Sézary syndrome with acute progressive pulmonary infiltration after improvement of skin eruption
D Sawamura, K Harada, T Aizu, et al.
Clinical and Experimental Immunology
|
April 1, 1990
Experimental murine thyroiditis induced by porcine thyroid peroxidase and its transfer by the antigen-specific T cell line
T Kotani, K Umeki, K Hirai, et al.
Acta Dermato-Venereologica
|
July 1, 1997
Dominant dystrophic epidermolysis bullosa albopapuloidea Pasini -- ultrastructural observations of albopapuloid lesions and a type VII collagen DNA polymorphism study of a family
K Nomura, K Umeki, D Sawamura, et al.
Rinsho Byori. the Japanese Journal of Clinical Pathology
|
May 1, 1981
[Experimental and clinical studies on determination of urinary low molecular weight proteins by laser nephelometer (author's transl)]
S Matsunaga, K Umeki, H Nakagawa, et al.
Immunology Letters
|
January 1, 1985
Epitopic difference among rat thyroglobulins
T Kotani, M Maeda, K Umeki, et al.
Journal of Biochemistry
|
November 1, 1972
Crystallization of an -amylase and evidence for the presence of a glucose-forming enzyme in human urine
N Minamiura, K Umeki, K Tsujino, et al.
Journal of Medicine
|
January 1, 1995
Hepatocyte growth factor and acute phase proteins in patients with chronic liver diseases
G Shiota, K Umeki, J Okano, et al.
Journal of Dermatological Science
|
January 1, 1996
A keratin K14 gene mutation in a Japanese patient with the Dowling-Meara type of epidermolysis bullosa simplex
K Umeki, K Nomura, K Harada, et al.
Journal of Biochemistry
|
December 1, 1974
A glucose-forming amylase in human liver
K Tsujino, M Yoshimura, K Umeki, et al.
Page
of 7