Long-Term Follow-up Posthematopoietic Stem Cell Transplantation in a Japanese Patient with Type-VII Mucopolysaccharidosis

por Orii, Kenji, Suzuki, Yasuyuki, Tomatsu, Shunji, Orii, Tadao, Fukao, Toshiyuki
Publicado no Diagnostics (Basel) (2020)

Assessment of Activity of Daily Life in Mucopolysaccharidosis Type II Patients with Hematopoietic Stem Cell Transplantation

por Suzuki, Yasuyuki, Taylor, Madeleine, Orii, Kenji, Fukao, Toshiyuki, Orii, Tadao, Tomatsu, Shunji
Publicado no Diagnostics (Basel) (2020)

Physiological role of oxygenated cytochrome o: observations on whole-cell suspensions of Vitreoscilla.

por Webster, D A, Orii, Y
Publicado em 1978

Wiki-Pi: A Web-Server of Annotated Human Protein-Protein Interactions to Aid in Discovery of Protein Function

por Orii, Naoki, Ganapathiraju, Madhavi K.
Publicado em 2012

Research prioritization through prediction of future impact on biomedical science: a position paper on inference-analytics

por Ganapathiraju, Madhavi K, Orii, Naoki
Publicado em 2013

Лісовідновний процес свіжого дубово-соснового субору у ДП «Колківське лісове господарство»

por Mykhailo Shevchuk, Vitalii Myroniuk, Orii Kurchyk
Publicado em 2021-09-01

Sequence organization and gene expression of pGD1, a plasmid found in a wild isolate of Dictyostelium.

por Orii, H, Tanaka, Y, Yanagisawa, K
Publicado em 1989

Defect in biosynthesis of mitochondrial acetoacetyl-coenzyme A thiolase in cultured fibroblasts from a boy with 3-ketothiolase deficiency.

por Yamaguchi, S, Orii, T, Sakura, N, Miyazawa, S, Hashimoto, T
Publicado em 1988

Assessment of Cardiac Sarcoidosis with Advanced Imaging Modalities

por Orii, Makoto, Imanishi, Toshio, Akasaka, Takashi
Publicado em 2014

Anesthesia management of arthroscopic ankle arthrodesis for a hemophilia patient after living-donor liver transplantation

por Shibata, Reiko, Orii, Ryo, Ako, Rie
Publicado no Intractable Rare Dis Res (2019)

Growth charts for patients with Hunter syndrome()

por Patel, Pravin, Suzuki, Yasuyuki, Maeda, Miho, Yasuda, Eriko, Shimada, Tsutomu, Orii, Kenji E., Orii, Tadao, Tomatsu, Shunji
Publicado em 2014

Presentation and Treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome)

por Stapleton, Molly, Kubaski, Francyne, Mason, Robert W., Yabe, Hiromasa, Suzuki, Yasuyuki, Orii, Kenji E., Orii, Tadao, Tomatsu, Shunji
Publicado no Expert Opin Orphan Drugs (2017)

Mutation analysis of very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: identification and characterization of mutant VLCAD cDNAs from four patients.

por Souri, M., Aoyama, T., Orii, K., Yamaguchi, S., Hashimoto, T.
Publicado em 1996

Mucopolysaccharidosis IVA: identification of mutations and methylation study in GALNS gene

por Tomatsu, S, Nishioka, T, Montano, A, Gutierrez, M, Pena, O, Orii, K, Sly, W, Yamaguchi, S, Orii, T, Paschke, E, Kircher, S, Noguchi, A
Publicado em 2004

Activities of Daily Living in patients with Hunter syndrome: Impact of enzyme replacement therapy and hematopoietic stem cell transplantation

por Tanjuakio, Julian, Suzuki, Yasuyuki, Patel, Pravin, Yasuda, Eriko, Kubaski, Francyne, Tanaka, Akemi, Yabe, Hiromasa, Mason, Robert W., Montaño, Adriana M., Orii, Kenji E., Orii, Koji O., Fukao, Toshiyuki, Orii, Tadao, Tomatsu, Shunji
Publicado no Mol Genet Metab (2014)

Effect of Erythropoietin Administration on Myocardial Viability and Coronary Microvascular Dysfunction in Anterior Acute Myocardial Infarction: Randomized Controlled Trial in the J...

por Makoto Orii, Kumiko Hirata, Kazushi Takemoto, Takashi Akasaka
Publicado em 2018-10-01

Identification of a novel exonic mutation at -13 from 5' splice site causing exon skipping in a girl with mitochondrial acetoacetyl-coenzyme A thiolase deficiency.

por Fukao, T, Yamaguchi, S, Wakazono, A, Orii, T, Hoganson, G, Hashimoto, T
Publicado em 1994

A new type of plasmid from a wild isolate of Dictyostelium species: the existence of closely situated long inverted repeats.

por Orii, H, Suzuki, K, Tanaka, Y, Yanagisawa, K
Publicado em 1987

Identification of three mutant alleles of the gene for mitochondrial acetoacetyl-coenzyme A thiolase. A complete analysis of two generations of a family with 3-ketothiolase deficie...

por Fukao, T, Yamaguchi, S, Orii, T, Schutgens, R B, Osumi, T, Hashimoto, T
Publicado em 1992

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

por Shimozawa, N, Tsukamoto, T, Suzuki, Y, Orii, T, Fujiki, Y
Publicado em 1992