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Journal of the Neurological Sciences
|
February 10, 1998
Tomaculous neuropathy in Charcot-Marie-Tooth disease with myelin protein zero gene mutation
N Tachi, N Kozuka, K Ohya, et al.
International Journal of Hematology
|
December 24, 1997
Rapid progression of chronic myelomonocytic leukemia following diaminodiphenyl sulphone treatment for dermatitis herpetiformis
Y Kanda, S Chiba, N Hirano, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 16, 1999
Immunosuppressive effect of deoxyspergualin in proliferative glomerulonephritis
O Hotta, T Furuta, S Chiba, et al.
Nihon Kokyuki Gakkai Zasshi = the Journal of the Japanese Respiratory Society
|
October 30, 2001
[A case of pulmonary lymphangioleiomyomatosis originally treated as bronchial asthma]
K Nakagome, Y Ohbu, N Yamamoto, et al.
Journal of the Neurological Sciences
|
December 1, 1990
High serum adenosine deaminase activity and its correlation with lymphocyte subsets in myasthenia gravis
S Chiba, H Matsumoto, Y Motoi, et al.
Journal of Biochemistry
|
May 1, 1990
Allosteric properties, substrate specificity, and subsite affinities of honeybee alpha-glucosidase I
A Kimura, S Takewaki, H Matsui, et al.
Fundamental and Applied Toxicology : Official Journal of the Society of Toxicology
|
October 1, 1990
Biochemical changes in rat erythrocytes caused by ethylene oxide exposure
K Mori, N Inoue, K Fujishiro, et al.
Pediatric Neurology
|
July 1, 1990
Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophy
N Tachi, M Tachi, K Sasaki, et al.
Acta Paediatrica Japonica : Overseas Edition
|
January 20, 1999
An infant with Costello syndrome complicated with fatal hypertrophic obstructive cardiomyopathy
H Tomita, S Fuse, K Ikeda, et al.
Histology and Histopathology
|
October 1, 1996
Immunocytochemical localization of myotonin protein kinase on muscle from patients with congenital myotonic dystrophy
N Tachi, N Kozuka, K Ohya, et al.
Page
of 105
Search research articles
Search
Showing results (541-550 of 1,046) with videos related to
Sort By:
Page
of 105
Journal of the Neurological Sciences
|
February 10, 1998
Tomaculous neuropathy in Charcot-Marie-Tooth disease with myelin protein zero gene mutation
N Tachi, N Kozuka, K Ohya, et al.
International Journal of Hematology
|
December 24, 1997
Rapid progression of chronic myelomonocytic leukemia following diaminodiphenyl sulphone treatment for dermatitis herpetiformis
Y Kanda, S Chiba, N Hirano, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 16, 1999
Immunosuppressive effect of deoxyspergualin in proliferative glomerulonephritis
O Hotta, T Furuta, S Chiba, et al.
Nihon Kokyuki Gakkai Zasshi = the Journal of the Japanese Respiratory Society
|
October 30, 2001
[A case of pulmonary lymphangioleiomyomatosis originally treated as bronchial asthma]
K Nakagome, Y Ohbu, N Yamamoto, et al.
Journal of the Neurological Sciences
|
December 1, 1990
High serum adenosine deaminase activity and its correlation with lymphocyte subsets in myasthenia gravis
S Chiba, H Matsumoto, Y Motoi, et al.
Journal of Biochemistry
|
May 1, 1990
Allosteric properties, substrate specificity, and subsite affinities of honeybee alpha-glucosidase I
A Kimura, S Takewaki, H Matsui, et al.
Fundamental and Applied Toxicology : Official Journal of the Society of Toxicology
|
October 1, 1990
Biochemical changes in rat erythrocytes caused by ethylene oxide exposure
K Mori, N Inoue, K Fujishiro, et al.
Pediatric Neurology
|
July 1, 1990
Dystrophin analysis in the differential diagnosis of autosomal recessive muscular dystrophy of childhood and Duchenne muscular dystrophy
N Tachi, M Tachi, K Sasaki, et al.
Acta Paediatrica Japonica : Overseas Edition
|
January 20, 1999
An infant with Costello syndrome complicated with fatal hypertrophic obstructive cardiomyopathy
H Tomita, S Fuse, K Ikeda, et al.
Histology and Histopathology
|
October 1, 1996
Immunocytochemical localization of myotonin protein kinase on muscle from patients with congenital myotonic dystrophy
N Tachi, N Kozuka, K Ohya, et al.
Page
of 105