A. Hattori

发表

Current state of Wilson disease patients in central Japan.

K. Hayashi, S. Kaneko, H. Goto, 2010, Internal medicine.

Ursodeoxycholic acid induces glutathione synthesis through activation of PI3K/Akt pathway in HepG2 cells.

K. Hayashi, H. Goto, K. Takagi, 2009, Biochemical pharmacology.

Tonsillectomy plus steroid pulse therapy is the most effective treatment in adult patients with C-Grade I IgA nephropathy, and the weight of the extracted palatine tonsils and Yamamoto scale have no significant correlation with the effects of this treatment.

T. Moriyama, N. Kondo, A. Hattori, 2019, Auris, nasus, larynx.

Increase in P-glycoprotein accompanied by activation of protein kinase Calpha and NF-kappaB p65 in the livers of rats with streptozotocin-induced diabetes.

K. Takagi, J. Ueyama, S. Kagota, 2008, Biochimica et biophysica acta.

Hemojuvelin hemochromatosis receiving iron chelation therapy with deferasirox: improvement of liver disease activity, cardiac and hematological function

S. Tomoyasu, T. Nakamaki, Kenshi Suzuki, 2011, European journal of haematology.

Various copper and iron overload patterns in the livers of patients with Wilson disease and idiopathic copper toxicosis

K. Hayashi, H. Goto, J. Ueyama, 2013, Medical Molecular Morphology.

Patients with chronic hepatitis C may be more sensitive to iron hepatotoxicity than patients with HFE-hemochromatosis.

K. Hayashi, H. Goto, A. Piperno, 2010, Internal medicine.

Platelet cyclo-oxygenase deficiency in a Japanese.

H. Kaido, T. Hato, A. Hattori, 2009, Scandinavian journal of haematology.

Iron chelation therapy for a case of transfusion-independent MDS-RARS with significant iron overload

T. Naoe, Yasuhiro Suzuki, H. Nagai, 2012, International Journal of Hematology.

AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis.

Ai Harashima, M. Kawanaka, A. Hattori, 2003, Hepatology research : the official journal of the Japan Society of Hepatology.

ATP7B analysis of a Wilson disease family

H. Goto, J. Ueyama, K. Hayashi, 2013 .

Hereditary hemochromatosis in a male patient with TFR2 (1861_1872del12) gene mutation: the second biopsy 19 years after diagnosis

G. Yamada, M. Kawanaka, A. Hattori, 2011 .

Special stain and X‐ray probe microanalysis of livers with Wilson disease

K. Hayashi, H. Goto, Y. Katano, 2009, Hepatology research : the official journal of the Japan Society of Hepatology.

Compound load of copper and iron in the livers of pretreatment patients with Wilson's disease

K. Yoshioka, Ai Harashima, M. Yano, 2004 .

A male patient with ferroportin disease B and a female patient with iron overload similar to ferroportin disease B

T. Sohda, T. Yamashita, Y. Tatsumi, 2014, Clinical Journal of Gastroenterology.

BIOCHEMICAL STAGING OF THE CHRONIC HEPATIC LESIONS OF WILSON DISEASE

K. Hayashi, H. Goto, H. Toyoda, 2014, Nagoya journal of medical science.

PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus

S. Miyano, Y. Shiraishi, K. Chiba, 2016, International Journal of Hematology.

Clinicopathological study of Japanese patients with genetic iron overload syndromes

H. Miyajima, N. Tomosugi, Y. Tatsumi, 2012, Pathology international.

Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.

K. Hayashi, H. Goto, T. Ishikawa, 2012, Blood cells, molecules & diseases.

Iron overload patients with unknown etiology from national survey in Japan

A. Gotoh, N. Komatsu, Y. Kohgo, 2017, International Journal of Hematology.

A Single Amino Acid Mutation Converts (R)-5-Diphosphomevalonate Decarboxylase into a Kinase*

H. Kawaide, H. Hemmi, T. Yoshimura, 2016, The Journal of Biological Chemistry.

(R)-Mevalonate 3-Phosphate Is an Intermediate of the Mevalonate Pathway in Thermoplasma acidophilum*♦

H. Kawaide, H. Hemmi, T. Yoshimura, 2014, The Journal of Biological Chemistry.

Liver structures of a patient with idiopathic copper toxicosis

K. Goto, Y. Murakami, T. Shinohara, 2012, Medical Molecular Morphology.

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders

M. Yamagishi, K. Yoshioka, H. Miyajima, 2010, Journal of Gastroenterology.

In Vivo Formation of the Protein Disulfide Bond That Enhances the Thermostability of Diphosphomevalonate Decarboxylase, an Intracellular Enzyme from the Hyperthermophilic Archaeon Sulfolobus solfataricus

H. Hemmi, T. Yoshimura, S. Goda, 2015, Journal of bacteriology.

diphosphomevalonate decarboxylase, an intracellular enzyme from the hyperthermophilic

H. Hemmi, T. Yoshimura, S. Goda, 2015 .

Assessment of the capillary zone electrophoretic behavior of proteins in the presence of electroosmotic modifiers: Protein‐polyamine interaction studied using a polyacrylamide‐coated capillary

A. Hattori, K. Kubo, 2001, Electrophoresis.

Potential of the international scoring system for the diagnosis of Wilson disease to differentiate Japanese patients who need anti‐copper treatment

K. Hayashi, H. Goto, Y. Katano, 2011, Hepatology research : the official journal of the Japan Society of Hepatology.

Title Measurement of serum hepcidin-25 levels as a potential test for diagnosinghemochromatosis and related disorders

M. Yamagishi, K. Yoshioka, H. Miyajima, 2017 .

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders

M. Yamagishi, K. Yoshioka, H. Miyajima, 2010, Journal of Gastroenterology.