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Intracerebral cell transplantation therapy for murine GM1 gangliosidosis

Brain & development (Tokyo. 1979), 2009-11, Vol.31 (10), p.717-724

2009

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Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double-blind, parallel-group, phase 3 trial

Lancet neurology, 2021-12, Vol.20 (12), p.1027-1037

2021

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Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan

Genetics in medicine, 2024-08, Vol.26 (8), p.101165, Article 101165

2024

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Long-term efficacy of hematopoietic stem cell transplantation on brain involvement in patients with mucopolysaccharidosis type II: A nationwide survey in Japan

Molecular genetics and metabolism, 2012-11, Vol.107 (3), p.513-520

2012

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Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III)

Human molecular genetics, 2015-04, Vol.24 (7), p.1856-1868

2015

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Acid Ceramidase Deficiency in Mice Results in a Broad Range of Central Nervous System Abnormalities

The American journal of pathology, 2017-04, Vol.187 (4), p.864-883

2017

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104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)

Journal of neurology, 2024-05, Vol.271 (5), p.2810-2823

2024

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Genotype-phenotype correlation and the antibody formation against idursulfase in the course of enzyme replacement therapy in mucopolysaccharidosis type II

Molecular genetics and metabolism, 2014-02, Vol.111 (2), p.S52-S52

2014

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Effects of cytoskeletal inhibitors on ooplasmic segregation and microtubule organization during fertilization and early development in the ascidian Molgula occidentalis

Developmental biology, 1989-04, Vol.132 (2), p.331-342

1989

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Farber disease: characterization of behavior and brain pathology in a new murine model

Molecular genetics and metabolism, 2014-02, Vol.111 (2), p.S93

2014

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Genotype of mucopolysaccharidosis type II severe form and the efficacy of enzyme replacement therapy or hematopoietic stem cell transplantation on cognitive function

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.S111-S112

2015

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Spatial distribution of brain ceramides in an acid ceramidase deficient murine model: Subsequent histological manifestations and functional deficits

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.S38-S39

2015

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Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations

Journal of human genetics, 2010-01, Vol.55 (1), p.18-22

2010

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Microtubules in ascidian eggs during meiosis, fertilization, and mitosis

Cell motility and the cytoskeleton, 1988, Vol.9 (3), p.219-230

1988

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Cortical contraction and ooplasmic movement in centrifuged or artificially constricted eggs ofCiona intestinalis

Wilhelm Roux's Archives of Developmental Biology, 1984-05, Vol.193 (3), p.127-132

1984

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The cortical contraction related to the ooplasmic segregation inCiona intestinalis eggs

Wilhelm Roux's Archives of Developmental Biology, 1981-07, Vol.190 (4), p.208-214

1981

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Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population

Gastroenterology (New York, N.Y. 1943), 2016-05, Vol.150 (5), p.1171-1182

2016

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Hepatocellular carcinoma diagnosis using a novel electrochemiluminescence immunoassay targeting serum IgM-free AIM

Clinical journal of gastroenterology, 2022-02, Vol.15 (1), p.41-51

2022

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Novel Electrocardiographic Criteria for the Diagnosis of Left Ventricular Hypertrophy in the Japanese General Population

International Heart Journal, 2019/05/30, Vol.60(3), pp.679-687

2019

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Sexual dimorphism of body size in an African fossil ape, Nacholapithecus kerioi

Journal of human evolution, 2018-10, Vol.123, p.129-140

2018

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Correction to: Hepatocellular carcinoma diagnosis using a novel electrochemiluminescence immunoassay targeting serum IgM‑free AIM

Clinical journal of gastroenterology, 2022-02, Vol.15 (1), p.52-52

2022

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Successful entecavir plus prednisolone treatment for hepatitis B virus-associated membranoproliferative glomerulonephritis: A case report

Medicine (Baltimore), 2019-01, Vol.98 (2), p.e14014-e14014

2019

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Sex determination using mastoid process measurements: standards for Japanese human skeletons of the medieval and early modern periods

Anthropological Science, 2008, Vol.116(2), pp.105-113

2008

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Novel Electrocardiographic Criteria for the Diagnosis of Left Ventricular Hypertrophy in the Japanese General Population

International Heart Journal, 2019, pp.18-511

2019

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Intracerebral cell transplantation therapy for murine GM1 gangliosidosis

Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double-blind, parallel-group, phase 3 trial

Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan

Long-term efficacy of hematopoietic stem cell transplantation on brain involvement in patients with mucopolysaccharidosis type II: A nationwide survey in Japan

Ataxia is the major neuropathological finding in arylsulfatase G-deficient mice: similarities and dissimilarities to Sanfilippo disease (mucopolysaccharidosis type III)

Acid Ceramidase Deficiency in Mice Results in a Broad Range of Central Nervous System Abnormalities

104-week efficacy and safety of cipaglucosidase alfa plus miglustat in adults with late-onset Pompe disease: a phase III open-label extension study (ATB200-07)

Genotype-phenotype correlation and the antibody formation against idursulfase in the course of enzyme replacement therapy in mucopolysaccharidosis type II

Effects of cytoskeletal inhibitors on ooplasmic segregation and microtubule organization during fertilization and early development in the ascidian Molgula occidentalis

Farber disease: characterization of behavior and brain pathology in a new murine model

Genotype of mucopolysaccharidosis type II severe form and the efficacy of enzyme replacement therapy or hematopoietic stem cell transplantation on cognitive function

Spatial distribution of brain ceramides in an acid ceramidase deficient murine model: Subsequent histological manifestations and functional deficits

Mutant alleles associated with late-onset ornithine transcarbamylase deficiency in male patients have recurrently arisen and have been retained in some populations

Microtubules in ascidian eggs during meiosis, fertilization, and mitosis

Cortical contraction and ooplasmic movement in centrifuged or artificially constricted eggs ofCiona intestinalis

The cortical contraction related to the ooplasmic segregation inCiona intestinalis eggs

Genomic Landscape of Esophageal Squamous Cell Carcinoma in a Japanese Population

Hepatocellular carcinoma diagnosis using a novel electrochemiluminescence immunoassay targeting serum IgM-free AIM

Novel Electrocardiographic Criteria for the Diagnosis of Left Ventricular Hypertrophy in the Japanese General Population

Sexual dimorphism of body size in an African fossil ape, Nacholapithecus kerioi

Correction to: Hepatocellular carcinoma diagnosis using a novel electrochemiluminescence immunoassay targeting serum IgM‑free AIM

Epidemiology conduction of paediatric rheumatic diseases based on the registry database of the Pediatric Rheumatology Association of Japan

Successful entecavir plus prednisolone treatment for hepatitis B virus-associated membranoproliferative glomerulonephritis: A case report

Sex determination using mastoid process measurements: standards for Japanese human skeletons of the medieval and early modern periods

Novel Electrocardiographic Criteria for the Diagnosis of Left Ventricular Hypertrophy in the Japanese General Population

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