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Longitudinal Associations of Toothbrushing With Obesity and Hyperglycemia

Journal of epidemiology, 2020-12, Vol.30 (12), p.556-565

2020

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Periodontal Status and Metabolic Syndrome in Middle‐Aged Japanese

Journal of periodontology (1970), 2012-11, Vol.83 (11), p.1363-1371

2012

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Association between periodontitis and fibrotic progression of non‐alcoholic fatty liver among Japanese adults

Journal of clinical periodontology, 2021-03, Vol.48 (3), p.368-377

2021

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Tooth loss and metabolic syndrome in middle-aged Japanese adults

Journal of clinical periodontology, 2016-06, Vol.43 (6), p.482-491

2016

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Relationship of toothbrushing to metabolic syndrome in middle‐aged adults

Journal of clinical periodontology, 2018-05, Vol.45 (5), p.538-547

2018

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Association of periodontal status with liver abnormalities and metabolic syndrome

Journal of Oral Science, 2015, Vol.57(4), pp.335-343

2015

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Relationship between Receiving a Workplace Oral Health Examination Including Oral Health Instruction and Oral Health Status in the Japanese Adult Population

Journal of Occupational Health, 2011-05, Vol.53 (3), p.222-229

2011

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Actual Seagoing Operation in Polar Region Ice-covered Waters - from Author’s Experience of Voyage in the Antarctic Ocean by JS SHIRASE

Marine Engineering, 2018/09/01, Vol.53(5), pp.682-687

Shinagawa, Takashi

2018

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Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan

Endocrine Journal, 2007, Vol.54(6), pp.1021-1025

2007

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A case report of undifferentiated carcinoma with osteoclast-like giant cells of the pancreas and literature review

Clinical journal of gastroenterology, 2010-08, Vol.3 (4), p.195-203

2010

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極水域における氷海航行の実際 -「しらせ」での南極海航海の体験から

マリンエンジニアリング, 2018/09/01, Vol.53(5), pp.682-687

品川, 隆

2018

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Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency

Metabolism, clinical and experimental, 2010-11, Vol.59 (11), p.1628-1632

2010

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IVS9-9C>A, not IVS9-9A>C, mutation in CYP21A2 causes classic salt-wasting steroid 21-hydroxylase deficiency

Metabolism, clinical and experimental, 2010, Vol.59 (10), p.e12-e12

2010

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Japanese Familial Patients with Male-Limited Precocious Puberty

Endocrine Journal, 2000, Vol.47(6), pp.777-782

2000

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Japanese Familial Patients with Male-Limited Precocious Puberty

ENDOCRINE JOURNAL, 2000, Vol.47 (6), p.777-782

2000

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Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia

Endocrine Journal, 1997, Vol.44(3), pp.441-446

1997

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Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP27A2 Detected by the Neonatal Mass-Screening Program in Japan

ENDOCRINE JOURNAL, 2007, Vol.54 (6), p.1021-1025

2007

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Detection of the Missense Mutation A218V in the Steroidogenic Acute Regulatory Protein Gene of a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia

Clinical Pediatric Endocrinology, 1997, Vol.6(1), pp.33-37

1997

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Detection of the Missense Mutation A218V in the Steroidogenic Acute Regulatory Protein Gene of a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia

Clinical Pediatric Endocrinology, 1997, Vol.6 (1), p.33-37

1997

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Natural history of minute hepatocellular carcinoma smaller than three centimeters complicating cirrhosis: a study in 22 patients

Gastroenterology (New York, N.Y. 1943), 1986-02, Vol.90 (2), p.289-298

1986

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Diagnosis of small hepatocellular carcinoma by computed tomography: Correlation of CT findings and histopathology

Journal of gastroenterology and hepatology, 1989-10, Vol.4 (5), p.395-404

1989

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An autopsy case of hepatocellular carcinoma producing human chorionic gonadotropin (hCG)

Nippon Shokakibyo Gakkai Zasshi, 1994, Vol.91(12), pp.2269-2273

1994

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Incidence of portal vein thrombosis in liver cirrhosis. An angiographic study in 708 patients

Gastroenterology (New York, N.Y. 1943), 1985-08, Vol.89 (2), p.279-286

1985

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Natural history of minute hepatocellular carcinoma smaller than three centimeters complicating cirrhosis

Gastroenterology (New York, N.Y. 1943), 1986-02, Vol.90 (2), p.289-298

1986

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Diagnosis and clinical features of small hepatocellular carcinoma with emphasis on the utility of real-time ultrasonography: a study in 51 patients

Gastroenterology (New York, N.Y. 1943), 1984-03, Vol.86 (3), p.495-502

1984

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Longitudinal Associations of Toothbrushing With Obesity and Hyperglycemia

Periodontal Status and Metabolic Syndrome in Middle‐Aged Japanese

Association between periodontitis and fibrotic progression of non‐alcoholic fatty liver among Japanese adults

Tooth loss and metabolic syndrome in middle-aged Japanese adults

Relationship of toothbrushing to metabolic syndrome in middle‐aged adults

Association of periodontal status with liver abnormalities and metabolic syndrome

Relationship between Receiving a Workplace Oral Health Examination Including Oral Health Instruction and Oral Health Status in the Japanese Adult Population

Actual Seagoing Operation in Polar Region Ice-covered Waters - from Author’s Experience of Voyage in the Antarctic Ocean by JS SHIRASE

Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP21A2 Detected by the Neonatal Mass-Screening Program in Japan

A case report of undifferentiated carcinoma with osteoclast-like giant cells of the pancreas and literature review

極水域における氷海航行の実際 -「しらせ」での南極海航海の体験から

Novel intronic CYP21A2 mutation in a Japanese patient with classic salt-wasting steroid 21-hydroxylase deficiency

IVS9-9C>A, not IVS9-9A>C, mutation in CYP21A2 causes classic salt-wasting steroid 21-hydroxylase deficiency

Japanese Familial Patients with Male-Limited Precocious Puberty

Japanese Familial Patients with Male-Limited Precocious Puberty

Homozygous Q258X Mutation in the Steroidogenic Acute Regulatory Gene in a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia

Nonclassic Steroid 21-Hydroxylase Deficiency due to a Homozygous V281L Mutation in CYP27A2 Detected by the Neonatal Mass-Screening Program in Japan

Detection of the Missense Mutation A218V in the Steroidogenic Acute Regulatory Protein Gene of a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia

Detection of the Missense Mutation A218V in the Steroidogenic Acute Regulatory Protein Gene of a Japanese Patient with Congenital Lipoid Adrenal Hyperplasia

Natural history of minute hepatocellular carcinoma smaller than three centimeters complicating cirrhosis: a study in 22 patients

Diagnosis of small hepatocellular carcinoma by computed tomography: Correlation of CT findings and histopathology

An autopsy case of hepatocellular carcinoma producing human chorionic gonadotropin (hCG)

Incidence of portal vein thrombosis in liver cirrhosis. An angiographic study in 708 patients

Natural history of minute hepatocellular carcinoma smaller than three centimeters complicating cirrhosis

Diagnosis and clinical features of small hepatocellular carcinoma with emphasis on the utility of real-time ultrasonography: a study in 51 patients

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