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No Enzyme Activity of 25-Hydroxyvitamin D3 1α-Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

The journal of clinical endocrinology and metabolism, 1999-11, Vol.84 (11), p.4111-4117

1999

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Congenital hypothyroidism caused by a unique thyroid peroxidase allele containing two mutations, C1708T and C2737T

Journal of pediatric endocrinology & metabolism : JPEM, 2004, Vol.17 (2), p.231

2004

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A 15-year-old girl with pubertal masculinization due to bilateral gonadoblastoma and 45,X/46,X,+mar karyotype

Kurume medical journal, 1994, Vol.41 (3), p.155

1994

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Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: Molecular analysis in four patients

Genes chromosomes & cancer, 1999-05, Vol.25 (1), p.40-45

1999

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No Enzyme Activity of 25-Hydroxyvitamin D sub(3) 1 alpha -Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

The journal of clinical endocrinology and metabolism, 1999-11, Vol.84 (11), p.4111-4117

1999

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A point mutation in exon 3 (His 107→Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement

Human genetics, 1996-04, Vol.97 (4), p.435-437

1996

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P1148A in fibrillin-1 is not a mutation leading to Shprintzen-Goldberg syndrome

Human mutation, 1997, Vol.10 (4), p.326-327

1997

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Carbonic anhydrase II deficiency in a Japanese patient produced by a nonsense mutation (TAT →TAG) at Tyr-40 in exon 2, (Y40X)

Human mutation, 1995, Vol.5 (4), p.348-350

1995

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Turner Syndrome and Occlusion of the Internal Carotid Artery

Journal of child neurology, 1993-10, Vol.8 (4), p.412-415

1993

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Abnormal Low Ratio of Cholic Acid to Chenodeoxycholic Acid in a Cholestatic Infant with Severe Hypoglycemia

Journal of pediatric gastroenterology and nutrition, 1991-04, Vol.12 (3), p.383-387

1991

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Abnormal Low Ratio of Cholic Acid to Chenodeoxycholic Acid in a Cholestatic Infant with Severe Hypoglycemia

Journal of pediatric gastroenterology and nutrition, 1991-04, Vol.12 (3), p.383-387

1991

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Hereditary Nephrogenic Diabetes Insipidus Type‐2

Pediatrics international, 1988-12, Vol.30 (6), p.714-716

1988

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A molecular deletion study with Southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11-12 and on an atypical PWS patient with apparently normal karyotype

Jinrui idengaku zasshi. Japanese journal of human genetics, 1988-12, Vol.33 (4), p.477-486

1988

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Hereditary Nephrogenic Diabetes Insipidus Type-2

Pediatrics International, 1988, Vol.30 (6), p.714-716

1988

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ASPLENIA AND POLYSPLENIA SYNDROME

Acta pathologica japonica, 1982-05, Vol.32 (3), p.505-511

1982

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FUNDAMENTAL AND CLINICAL EVALUATION OF CEFMENOXIME IN CHILDREN

The Japanese Journal of Antibiotics, 1982/11/25, Vol.35(11), pp.2599-2614

1982

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FUNDAMENTAL AND CLINICAL STUDIES OF T-1982 (CEFBUPERAZONE) IN THE PEDIATRIC FIELD

The Japanese Journal of Antibiotics, 1983/04/25, Vol.36(4), pp.888-909

1983

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CLINICAL EFFECT OF MIDECAMYCIN ACETATE ON WHOOPING COUGH

The Japanese Journal of Antibiotics, 1982/08/25, Vol.35(8), pp.2022-2033

1982

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EFFECT OF MIDECAMYCIN ACETATE ON INTESTINAL BACTERIAL FLORA OF CHILDREN, AND RESULTS OF CLINICAL STUDY ON MIDECAMYCIN ACETATE IN TREATMENT OF MYCOPLASMAL PNEUMONIA

The Japanese Journal of Antibiotics, 1982/11/25, Vol.35(11), pp.2491-2529

1982

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FUNDAMENTAL AND CLINICAL STUDIES OF CEFTAZIDIME IN THE PEDIATRIC FIELD

The Japanese Journal of Antibiotics, 1984/03/25, Vol.37(3), pp.537-553

1984

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小児科領域におけるCeftazidimeの基礎的・臨床的検討

The Japanese Journal of Antibiotics, 1984/03/25, Vol.37(3), pp.537-553

1984

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Ampicillin坐剤 (KS-R 1) の小児における基礎的, 臨床的検討

The Japanese Journal of Antibiotics, 1983/07/25, Vol.36(7), pp.1900-1951

1983

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小児科領域におけるT-1982 (Cefbuperazone) の基礎的・臨床的検討

The Japanese Journal of Antibiotics, 1983/04/25, Vol.36(4), pp.888-909

1983

Volltextzugriff (PDF)

小児におけるCefmenoximeの基礎的, 臨床的検討

The Japanese Journal of Antibiotics, 1982/11/25, Vol.35(11), pp.2599-2614

1982

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No Enzyme Activity of 25-Hydroxyvitamin D3 1α-Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

Congenital hypothyroidism caused by a unique thyroid peroxidase allele containing two mutations, C1708T and C2737T

A 15-year-old girl with pubertal masculinization due to bilateral gonadoblastoma and 45,X/46,X,+mar karyotype

Gonadoblastoma, mixed germ cell tumor, and Y chromosomal genotype: Molecular analysis in four patients

No Enzyme Activity of 25-Hydroxyvitamin D sub(3) 1 alpha -Hydroxylase Gene Product in Pseudovitamin D Deficiency Rickets, Including That with Mild Clinical Manifestation

A point mutation in exon 3 (His 107→Tyr) in two unrelated Japanese patients with carbonic anhydrase II deficiency with central nervous system involvement

P1148A in fibrillin-1 is not a mutation leading to Shprintzen-Goldberg syndrome

Carbonic anhydrase II deficiency in a Japanese patient produced by a nonsense mutation (TAT →TAG) at Tyr-40 in exon 2, (Y40X)

Turner Syndrome and Occlusion of the Internal Carotid Artery

Abnormal Low Ratio of Cholic Acid to Chenodeoxycholic Acid in a Cholestatic Infant with Severe Hypoglycemia

Abnormal Low Ratio of Cholic Acid to Chenodeoxycholic Acid in a Cholestatic Infant with Severe Hypoglycemia

Hereditary Nephrogenic Diabetes Insipidus Type‐2

A molecular deletion study with Southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11-12 and on an atypical PWS patient with apparently normal karyotype

Hereditary Nephrogenic Diabetes Insipidus Type-2

ASPLENIA AND POLYSPLENIA SYNDROME

FUNDAMENTAL AND CLINICAL EVALUATION OF CEFMENOXIME IN CHILDREN

FUNDAMENTAL AND CLINICAL STUDIES OF T-1982 (CEFBUPERAZONE) IN THE PEDIATRIC FIELD

FUNDAMENTAL AND CLINICAL STUDIES ON AMPICILLIN SUPPOSITORY (KS-R1) IN CHILDREN

CLINICAL EFFECT OF MIDECAMYCIN ACETATE ON WHOOPING COUGH

EFFECT OF MIDECAMYCIN ACETATE ON INTESTINAL BACTERIAL FLORA OF CHILDREN, AND RESULTS OF CLINICAL STUDY ON MIDECAMYCIN ACETATE IN TREATMENT OF MYCOPLASMAL PNEUMONIA

FUNDAMENTAL AND CLINICAL STUDIES OF CEFTAZIDIME IN THE PEDIATRIC FIELD

小児科領域におけるCeftazidimeの基礎的・臨床的検討

Ampicillin坐剤 (KS-R 1) の小児における基礎的, 臨床的検討

小児科領域におけるT-1982 (Cefbuperazone) の基礎的・臨床的検討

小児におけるCefmenoximeの基礎的, 臨床的検討

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