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Standards for Growth and Growth Velocity in Turner's Syndrome

Pediatrics international, 1992-04, Vol.34 (2), p.206-221

Suwa, Seizo

1992

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Longitudinal Standards for Height and Height Velocity for Japanese Children from Birth to Maturity

Clinical Pediatric Endocrinology, 1992, Vol.1(1), pp.5-13

1992

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Standard Growth Charts for Height and Weight of Japanese Children from Birth to 17 Years Based on a Cross-sectional Survey of National Data

Clinical Pediatric Endocrinology, 1993, Vol.2(2), pp.87-97

1993

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A Novel Missense Mutation of Mineralocorticoid Receptor Gene in One Japanese Family with a Renal Form of Pseudohypoaldosteronism Type 1

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4690-4694

2000

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A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17.ALPHA.-Hydroxylase/ 17, 20-Lyase Deficiency, but without Obvious CYP 17 Gene Mutations

Endocrine journal, 1999, Vol.46 (2), p.285-292

1999

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Nationwide survey of neonatal mass-screening for congenital adrenal hyperplasia in Japan

Screening (Amsterdam), 1994-12, Vol.3 (3), p.141-151

Suwa, Seizo

1994

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“Growth without Growth Hormone”in a Young Female with Remitted Langerhans Cell Histiocytosis：A Case Report

Clinical Pediatric Endocrinology, 1999, Vol.8 (1), p.17-22

1999

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“Growth without Growth Hormone” in a Young Female with Remitted Langerhans Cell Histiocytosis: A Case Report

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1999, Vol.8 (1), p.17-22

1999

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The prevalence of islet cell antibodies in Japanese insulin-dependent and non-insulin-dependent diabetic patients studied by indirect immunofluorescence and by a new method

Diabetes (New York, N.Y.), 1986-03, Vol.35 (3), p.335-340

1986

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A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1

The journal of clinical endocrinology and metabolism, 2000-12, Vol.85 (12), p.4690-4694

2000

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Guideline for the Treatment of Patients with 21-OHase Deficiency Detected by Neonatal Screening (Revised in 1999)

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1999, Vol.8 (1), p.61-65

1999

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Guideline for Neonatal Mass-screening for Congenital Hypothyroidism

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1999, Vol.8 (1), p.51-55

1999

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Cerebral Infarction in Three Infant Cases of Congenital Adrenal Hyperplasia

Clinical Pediatric Endocrinology, 1997, Vol.6(1), pp.11-14

1997

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Quantitation of urinary gonadotropins in normal children

Pediatric research, 1990-10, Vol.28 (4), p.401-404

1990

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Massive Enlargement of an Ovarian Follicle after Administration of Nasal GnRH Analogue in Two Girls with Central Precocious Puberty

Clinical Pediatric Endocrinology, 1999, Vol.8 (1), p.11-16

1999

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Massive Enlargement of an Ovarian Follicle after Administration of Nasal GnRH Analogue in Two Girls with Central Precocious Puberty

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1999, Vol.8 (1), p.11-16

1999

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Guideline for the Treatment of Patients with 21-OHase Deficiency Detected by Neonatal Screening (Revised in 1999)

Clinical Pediatric Endocrinology, 1999, Vol.8 (1), p.61-65

1999

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Guidelines for Diagnosing Steroid 21-Hydroxylase Deficiency

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1999, Vol.8 (1), p.57-60

1999

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A boy with psychosocial short stature followed up from infancy to adulthood

Pediatrics international, 1995-04, Vol.37 (2), p.283-287

SUWA, SEIZO

1995

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Paradoxical Growth Hormone (GH) Response to Insulin Hypoglycemia in a Case of Diencephalic Syndrome

Clinical Pediatric Endocrinology, 1994, Vol.3(Supple5), pp.234-235

1994

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Adrenarche in Childhood: I. Development of a New Enzyme-linked Immunosorbent Assay (ELISA) for Dehydroepiandrosterone Sulfate (DHEAS) and Determination of Serum DHEAS Levels in Normal Children

Clinical Pediatric Endocrinology, 1994, Vol.3(2), pp.97-104

1994

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A Girl with Infant-onset Autoimmune Thyroiditis

Clinical Pediatric Endocrinology, 1995, Vol.4(Supple6), pp.119-120

1995

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Four-year Experience of Growth Hormone Treatment in Children with Non-endocrine Short Stature

Clinical Pediatric Endocrinology, 1996, Vol.5(Supple7), pp.1-9

1996

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Resumption of Puberty in Girls and Boys with Central Precocious Puberty After Withdrawal of Long-Term Therapy with LHRH-Analogue D-Ser-6-LHRH

Clinical Pediatric Endocrinology, 1994, Vol.3 (1), p.45-54

1994

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Standards for Growth and Growth Velocity in Turner's Syndrome

Longitudinal Standards for Height and Height Velocity for Japanese Children from Birth to Maturity

Standard Growth Charts for Height and Weight of Japanese Children from Birth to 17 Years Based on a Cross-sectional Survey of National Data

A Novel Missense Mutation of Mineralocorticoid Receptor Gene in One Japanese Family with a Renal Form of Pseudohypoaldosteronism Type 1

A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17.ALPHA.-Hydroxylase/ 17, 20-Lyase Deficiency, but without Obvious CYP 17 Gene Mutations

Nationwide survey of neonatal mass-screening for congenital adrenal hyperplasia in Japan

“Growth without Growth Hormone”in a Young Female with Remitted Langerhans Cell Histiocytosis：A Case Report

“Growth without Growth Hormone” in a Young Female with Remitted Langerhans Cell Histiocytosis: A Case Report

The prevalence of islet cell antibodies in Japanese insulin-dependent and non-insulin-dependent diabetic patients studied by indirect immunofluorescence and by a new method

A novel missense mutation of mineralocorticoid receptor gene in one Japanese family with a renal form of pseudohypoaldosteronism type 1

Guideline for the Treatment of Patients with 21-OHase Deficiency Detected by Neonatal Screening (Revised in 1999)

Guideline for Neonatal Mass-screening for Congenital Hypothyroidism

Cerebral Infarction in Three Infant Cases of Congenital Adrenal Hyperplasia

Quantitation of urinary gonadotropins in normal children

Massive Enlargement of an Ovarian Follicle after Administration of Nasal GnRH Analogue in Two Girls with Central Precocious Puberty

Massive Enlargement of an Ovarian Follicle after Administration of Nasal GnRH Analogue in Two Girls with Central Precocious Puberty

Guideline for the Treatment of Patients with 21-OHase Deficiency Detected by Neonatal Screening (Revised in 1999)

Guidelines for Diagnosing Steroid 21-Hydroxylase Deficiency

A boy with psychosocial short stature followed up from infancy to adulthood

Paradoxical Growth Hormone (GH) Response to Insulin Hypoglycemia in a Case of Diencephalic Syndrome

Adrenarche in Childhood: I. Development of a New Enzyme-linked Immunosorbent Assay (ELISA) for Dehydroepiandrosterone Sulfate (DHEAS) and Determination of Serum DHEAS Levels in Normal Children

A Girl with Infant-onset Autoimmune Thyroiditis

Human Corticotropin-Releasing Hormone (hCRH) Test: Sex and Age Differences in Plasma ACTH and Cortisol Responses and their Reproducibility in Healthy Adults

Four-year Experience of Growth Hormone Treatment in Children with Non-endocrine Short Stature

Resumption of Puberty in Girls and Boys with Central Precocious Puberty After Withdrawal of Long-Term Therapy with LHRH-Analogue D-Ser-6-LHRH

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