Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Orii

Showing results (151-160 of 276) with videos related to

Pageof 28
Sort By:
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|March 22, 2001
Experience with artificial liver support in 16 living related liver transplant recipientsN Kawagishi, N Ohkohchi, K Fujimori, et al.
Biotherapy (Dordrecht, Netherlands)|January 1, 1992
Lymphocyte responses to food antigens in food sensitive patients with allergic tension-fatigue syndromeN Kondo, S Shinoda, H Agata, 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 infancyA Imamura, Y Komori, O Fukutomi, et al.
Acta Paediatrica Japonica : Overseas Edition|October 1, 1996
Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defectY Suzuki, N Shimozawa, A Imamura, et al.
Human Genetics|October 19, 1978
Lysosomal acid hydrolases in established lymphoblastoid cell lines, transformed by Epstein-Barr virus, from patients with genetic lysosomal storage diseasesR Minami, Y Watanabe, T Kudoh, et al.
The Tohoku Journal of Experimental Medicine|April 1, 1992
Severe infantile sialidosis--the characteristics of oligosaccharides isolated from the urine and the abdominal ascitesY Nakamura, Y Takahashi, S Yamaguchi, et al.
Clinical Genetics|November 1, 1996
Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidationK Inoue, Y Suzuki, S Yajima, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disordersY Suzuki, N Shimozawa, A Imamura, et al.
Journal of Investigational Allergology & Clinical Immunology|March 1, 1995
Evaluation of lymphocyte proliferative responses to casein hydrolysate formula in cow's milk-sensitive children: response of peripheral blood mononuclear cells to hydrolysate formulaT Nishida, N Kondo, H Agata, et al.
Brain & Development|September 1, 1993
Adrenoleukomyeloneuropathy presenting as cerebellar ataxia in a young child: a probable variant of adrenoleukodystrophyM Kurihara, K Kumagai, S Yagishita, et al.
Pageof 28

Showing results (151-160 of 276) with videos related to

Sort By:
Pageof 28
Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|March 22, 2001
Experience with artificial liver support in 16 living related liver transplant recipientsN Kawagishi, N Ohkohchi, K Fujimori, et al.
Biotherapy (Dordrecht, Netherlands)|January 1, 1992
Lymphocyte responses to food antigens in food sensitive patients with allergic tension-fatigue syndromeN Kondo, S Shinoda, H Agata, 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 infancyA Imamura, Y Komori, O Fukutomi, et al.
Acta Paediatrica Japonica : Overseas Edition|October 1, 1996
Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defectY Suzuki, N Shimozawa, A Imamura, et al.
Human Genetics|October 19, 1978
Lysosomal acid hydrolases in established lymphoblastoid cell lines, transformed by Epstein-Barr virus, from patients with genetic lysosomal storage diseasesR Minami, Y Watanabe, T Kudoh, et al.
The Tohoku Journal of Experimental Medicine|April 1, 1992
Severe infantile sialidosis--the characteristics of oligosaccharides isolated from the urine and the abdominal ascitesY Nakamura, Y Takahashi, S Yamaguchi, et al.
Clinical Genetics|November 1, 1996
Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidationK Inoue, Y Suzuki, S Yajima, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disordersY Suzuki, N Shimozawa, A Imamura, et al.
Journal of Investigational Allergology & Clinical Immunology|March 1, 1995
Evaluation of lymphocyte proliferative responses to casein hydrolysate formula in cow's milk-sensitive children: response of peripheral blood mononuclear cells to hydrolysate formulaT Nishida, N Kondo, H Agata, et al.
Brain & Development|September 1, 1993
Adrenoleukomyeloneuropathy presenting as cerebellar ataxia in a young child: a probable variant of adrenoleukodystrophyM Kurihara, K Kumagai, S Yagishita, et al.
Pageof 28