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Brain & Development
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July 1, 1996
Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency
H Wada, M Woo, H Nishio, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
April 1, 1996
[A case of empyema caused by Salmonella enteritidis in a patient with sequela of pulmonary tuberculosis]
H Suzuki, T Okamura, A Imamura, et al.
No to Hattatsu = Brain and Development
|
September 1, 1996
[Benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency]
H Wada, H Nishio, S Nagaki, et al.
Journal of Medical Genetics
|
October 21, 1999
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders
N Shimozawa, A Imamura, Z Zhang, et al.
Pancreas
|
March 27, 2003
Clinicopathologic evaluation after resection for ductal adenocarcinoma of the pancreas: a retrospective, single-institution experience
S Takai, S Satoi, H Toyokawa, et al.
Psychiatric Genetics
|
January 25, 2002
Lack of association between the hKCa3 gene and Japanese schizophrenia patients
A Imamura, T Tsujita, T Kayashima, et al.
International Urology and Nephrology
|
April 9, 1999
Influence of luteinizing hormone-releasing hormone analogues on serum levels of prostatic acid phosphatase and prostatic specific antigen in patients with metastatic carcinoma of the prostate
I Sasagawa, Y Kubota, T Nakada, et al.
Leukemia
|
February 13, 2002
Expression of endothelial cell-associated molecules in AML cells
M Watarai, H Miwa, M Shikami, et al.
Biochemical and Biophysical Research Communications
|
August 27, 1999
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients
N Shimozawa, Z Zhang, Y Suzuki, et al.
Clinical and Laboratory Haematology
|
August 11, 2006
Gene expression changes in a patient presenting nonleukaemic nasal granulocytic sarcoma to acute myelogenous leukaemia using 40 K cDNA microarray
H Teramoto, H Miwa, V Patel, et al.
Page
of 19
Search research articles
Search
Showing results (171-180 of 189) with videos related to
Sort By:
Page
of 19
Brain & Development
|
July 1, 1996
Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency
H Wada, M Woo, H Nishio, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
April 1, 1996
[A case of empyema caused by Salmonella enteritidis in a patient with sequela of pulmonary tuberculosis]
H Suzuki, T Okamura, A Imamura, et al.
No to Hattatsu = Brain and Development
|
September 1, 1996
[Benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency]
H Wada, H Nishio, S Nagaki, et al.
Journal of Medical Genetics
|
October 21, 1999
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders
N Shimozawa, A Imamura, Z Zhang, et al.
Pancreas
|
March 27, 2003
Clinicopathologic evaluation after resection for ductal adenocarcinoma of the pancreas: a retrospective, single-institution experience
S Takai, S Satoi, H Toyokawa, et al.
Psychiatric Genetics
|
January 25, 2002
Lack of association between the hKCa3 gene and Japanese schizophrenia patients
A Imamura, T Tsujita, T Kayashima, et al.
International Urology and Nephrology
|
April 9, 1999
Influence of luteinizing hormone-releasing hormone analogues on serum levels of prostatic acid phosphatase and prostatic specific antigen in patients with metastatic carcinoma of the prostate
I Sasagawa, Y Kubota, T Nakada, et al.
Leukemia
|
February 13, 2002
Expression of endothelial cell-associated molecules in AML cells
M Watarai, H Miwa, M Shikami, et al.
Biochemical and Biophysical Research Communications
|
August 27, 1999
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients
N Shimozawa, Z Zhang, Y Suzuki, et al.
Clinical and Laboratory Haematology
|
August 11, 2006
Gene expression changes in a patient presenting nonleukaemic nasal granulocytic sarcoma to acute myelogenous leukaemia using 40 K cDNA microarray
H Teramoto, H Miwa, V Patel, et al.
Page
of 19