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Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
June 1, 1990
[A case of penicillin-resistant pneumococcal meningitis and antibiotic susceptibility of Streptococcus pneumoniae isolated from children]
K Himi, S Miyamoto, H Ohshimi, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
May 1, 1996
Clinical significance and time course of antibodies to glutamic acid decarboxylase in Japanese children with type I (insulin-dependent) diabetes mellitus
S Sugihara, S Konda, K Wataki, et al.
British Journal of Haematology
|
November 1, 1996
A novel human leukaemic cell line, CTS, has a t(6;11) chromosomal translocation and characteristics of pluripotent stem cells
H Kakuda, T Sato, Y Hayashi, et al.
The New England Journal of Medicine
|
March 5, 1998
Inactivating mutations in the 25-hydroxyvitamin D3 1alpha-hydroxylase gene in patients with pseudovitamin D-deficiency rickets
S Kitanaka, K Takeyama, A Murayama, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1985
Low serum concentrations of 1,25-dihydroxyvitamin D in human magnesium deficiency
R K Rude, J S Adams, E Ryzen, et al.
Frontiers in Immunology
|
September 21, 2023
Predictive values of immune indicators on respiratory failure in the early phase of COVID-19 due to Delta and precedent variants
K Nagaoka, H Kawasuji, Y Takegoshi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1996
Induction of Graves-like disease in mice by immunization with fibroblasts transfected with the thyrotropin receptor and a class II molecule
N Shimojo, Y Kohno, K Yamaguchi, et al.
Human Genetics
|
July 1, 1996
Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiency
S Yamamoto, H Abe, T Kohgo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 24, 1999
No enzyme activity of 25-hydroxyvitamin D3 1alpha-hydroxylase gene product in pseudovitamin D deficiency rickets, including that with mild clinical manifestation
S Kitanaka, A Murayama, T Sakaki, et al.
International Journal of Molecular Medicine
|
December 16, 1998
Establishment of a new human megakaryoblastic cell line, CMY, with chromosome 17p abnormalities
N Miura, T Sato, A Fuse, et al.
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of 26
Search research articles
Search
Showing results (241-250 of 254) with videos related to
Sort By:
Page
of 26
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
June 1, 1990
[A case of penicillin-resistant pneumococcal meningitis and antibiotic susceptibility of Streptococcus pneumoniae isolated from children]
K Himi, S Miyamoto, H Ohshimi, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
May 1, 1996
Clinical significance and time course of antibodies to glutamic acid decarboxylase in Japanese children with type I (insulin-dependent) diabetes mellitus
S Sugihara, S Konda, K Wataki, et al.
British Journal of Haematology
|
November 1, 1996
A novel human leukaemic cell line, CTS, has a t(6;11) chromosomal translocation and characteristics of pluripotent stem cells
H Kakuda, T Sato, Y Hayashi, et al.
The New England Journal of Medicine
|
March 5, 1998
Inactivating mutations in the 25-hydroxyvitamin D3 1alpha-hydroxylase gene in patients with pseudovitamin D-deficiency rickets
S Kitanaka, K Takeyama, A Murayama, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 1, 1985
Low serum concentrations of 1,25-dihydroxyvitamin D in human magnesium deficiency
R K Rude, J S Adams, E Ryzen, et al.
Frontiers in Immunology
|
September 21, 2023
Predictive values of immune indicators on respiratory failure in the early phase of COVID-19 due to Delta and precedent variants
K Nagaoka, H Kawasuji, Y Takegoshi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 1, 1996
Induction of Graves-like disease in mice by immunization with fibroblasts transfected with the thyrotropin receptor and a class II molecule
N Shimojo, Y Kohno, K Yamaguchi, et al.
Human Genetics
|
July 1, 1996
Two novel gene mutations (Glu174-->Lys, Phe383-->Tyr) causing the "hepatic" form of carnitine palmitoyltransferase II deficiency
S Yamamoto, H Abe, T Kohgo, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 24, 1999
No enzyme activity of 25-hydroxyvitamin D3 1alpha-hydroxylase gene product in pseudovitamin D deficiency rickets, including that with mild clinical manifestation
S Kitanaka, A Murayama, T Sakaki, et al.
International Journal of Molecular Medicine
|
December 16, 1998
Establishment of a new human megakaryoblastic cell line, CMY, with chromosome 17p abnormalities
N Miura, T Sato, A Fuse, et al.
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of 26