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The British Journal of Dermatology
|
April 12, 2001
An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem
Y Ichiki, T Akiyama, N Shimozawa, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 29, 1988
Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder
Y Suzuki, N Shimozawa, T Orii, et al.
Electroencephalography and Clinical Neurophysiology
|
March 1, 1988
Origin and clinical significance of subcortical components in short-latency somatosensory evoked potentials in children
Y Tomita, T Tanaka, N Kamimura, et al.
Clinical Chemistry
|
November 20, 1997
Very long chain fatty acid analysis of dried blood spots on filter paper to screen for adrenoleukodystrophy
K Inoue, Y Suzuki, S Yajima, et al.
American Journal of Human Genetics
|
December 5, 1998
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D
M Honsho, S Tamura, N Shimozawa, et al.
Biochemical Pharmacology
|
February 1, 1991
Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases
Y Suzuki, N Shimozawa, S Yajima, et al.
Clinical Genetics
|
February 9, 2000
Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells
Z Zhang, Y Suzuki, N Shimozawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
January 5, 2000
Glucose metabolism evaluated by positron emission tomography in Lafora disease
Z Kato, K Yasuda, K Ishii, et al.
Brain & Development
|
July 1, 1994
Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy
A Imamura, Y Komori, O Fukutomi, et al.
American Journal of Human Genetics
|
April 1, 1993
Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect
N Shimozawa, Y Suzuki, T Orii, et al.
Page
of 17
Search research articles
Search
Showing results (41-50 of 167) with videos related to
Sort By:
Page
of 17
The British Journal of Dermatology
|
April 12, 2001
An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem
Y Ichiki, T Akiyama, N Shimozawa, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 29, 1988
Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder
Y Suzuki, N Shimozawa, T Orii, et al.
Electroencephalography and Clinical Neurophysiology
|
March 1, 1988
Origin and clinical significance of subcortical components in short-latency somatosensory evoked potentials in children
Y Tomita, T Tanaka, N Kamimura, et al.
Clinical Chemistry
|
November 20, 1997
Very long chain fatty acid analysis of dried blood spots on filter paper to screen for adrenoleukodystrophy
K Inoue, Y Suzuki, S Yajima, et al.
American Journal of Human Genetics
|
December 5, 1998
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D
M Honsho, S Tamura, N Shimozawa, et al.
Biochemical Pharmacology
|
February 1, 1991
Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases
Y Suzuki, N Shimozawa, S Yajima, et al.
Clinical Genetics
|
February 9, 2000
Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells
Z Zhang, Y Suzuki, N Shimozawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
January 5, 2000
Glucose metabolism evaluated by positron emission tomography in Lafora disease
Z Kato, K Yasuda, K Ishii, et al.
Brain & Development
|
July 1, 1994
Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy
A Imamura, Y Komori, O Fukutomi, et al.
American Journal of Human Genetics
|
April 1, 1993
Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect
N Shimozawa, Y Suzuki, T Orii, et al.
Page
of 17