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The current status of 492 adult women with Turner syndrome: a questionnaire survey by the Foundation for Growth Science

Endocrine Journal, 2021, Vol.68(9), pp.1081-1089

2021

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The current status of 492 adult women with Turner syndrome : a questionnaire survey by the Foundation for Growth Science

ENDOCRINE JOURNAL, 2021, Vol.68 (9), p.1081-1089

2021

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Prevalence of diverse complications and its association with karyotypes in Japanese adult women with Turner syndrome—a questionnaire survey by the Foundation for Growth Science

Endocrine Journal, 2018, Vol.65(5), pp.509-519

2018

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Women with Turner syndrome are at high risk of lifestyle-related disease —From questionnaire surveys by the Foundation for Growth Science in Japan

Endocrine Journal, 2016, Vol.63(5), pp.449-456

2016

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Prevalence of diverse complications and its association with karyotypes in Japanese adult women with Turner syndrome - a questionnaire survey by the Foundation for Growth Science

ENDOCRINE JOURNAL, 2018, Vol.65 (5), p.509-519

2018

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Women with Turner syndrome are at high risk of lifestyle-related disease - From questionnaire surveys by the Foundation for Growth Science in Japan

ENDOCRINE JOURNAL, 2016-05, Vol.63 (5), p.449-456

2016

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Development and validation of a new questionnaire assessing quality of life in adults with hypopituitarism: Adult Hypopituitarism Questionnaire (AHQ)

PloS one, 2012-09, Vol.7 (9), p.e44304-e44304

2012

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Effects of financial support on treatment of adolescents with growth hormone deficiency: a retrospective study in Japan

BMC health services research, 2016-10, Vol.16 (1), p.602-602, Article 602

2016

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Recent Status in the Occurrence of Leukemia in Growth Hormone-Treated Patients in Japan

The journal of clinical endocrinology and metabolism, 1999-06, Vol.84 (6), p.1961-1965

1999

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Adult Height in Patients with Turner Syndrome and Association with Lifestyle-related Diseases after Human Growth Hormone Treatment in Japan

Pediatric endocrinology reviews : PER, 2017-03, Vol.14 Suppl 1 (Suppl 1), p.252

2017

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The current status of 492 adult women with Turner syndrome: a questionnaire survey by the Foundation for Growth Science

Endocrine Journal, 2021, pp.EJ20-0617

2021

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Adult Heights of 258 Girls with Turner Syndrome on Low Dose of Growth Hormone Therapy in Japan

Clinical Pediatric Endocrinology, 2010, Vol.19(3), pp.63-68

2010

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The Mechanism of Arginine- and Insulin-Induced GH Release in Humans

Endocrine Journal, 2000, Vol.47(SupplMarch), pp.S23-S27

HANEW, KUNIHIKO

2000

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Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations

Cytogenetic and genome research, 2016-01, Vol.150 (2), p.86-92

2016

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Studies of Very Severe Short Stature with Severe GH Deficiency: From the Data Registered with the Foundation for Growth Science

Endocrine Journal, 2005, Vol.52(1), pp.37-43

2005

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Adult Heights of 258 Girls with Turner Syndrome on Low Dose of Growth Hormone Therapy in Japan

Clinical Pediatric Endocrinology, 2010, Vol.19 (3), p.63-68

2010

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Clinical Characteristics, Etiologies and Pathophysiology of Patients with Severe Short Stature with Severe GH Deficiency：Questionnaire Study on the Data Registered with the Foundation for Growth Science, Japan

ENDOCRINE JOURNAL, 2006, Vol.53 (2), p.259-265

2006

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Effects of financial support on treatment of adolesJapancents with growth hormone deficiency: a retrospective study in Japan

BMC health services research, 2016-10, Vol.16 (1)

2016

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Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome

The journal of clinical endocrinology and metabolism, 2004-07, Vol.89 (7), p.3359-3364

2004

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Studies of Very Severe Short Stature with Severe GH Deficiency: From the Data Registered with the Foundation for Growth Science

ENDOCRINE JOURNAL, 2005, Vol.52 (1), p.37-43

2005

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No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment

Clinical Pediatric Endocrinology, 2006, Vol.15(1), pp.15-21

2006

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The effects of human leptin fragment(126-140) on pituitary functions in man

European journal of endocrinology, 2003-11, Vol.149 (5), p.407

Hanew, Kunihiko

2003

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Plasma Chromogranin A in Pheochromocytoma, Primary Hyperparathyroidism and Pituitary Adenoma in Comparison with Catecholamine, Parathyroid Hormone and Pituitary Hormones

Endocrine Journal, 1997, Vol.44(2), pp.319-327

1997

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Final Height of Growth Hormone (GH)-Treated Short Children Registered at the Foundation for Growth Science in Japan: Comparison between the Pituitary Human GH Era and the Recombinant Human GH Era

Clinical Pediatric Endocrinology, 2001, Vol.10(1), pp.53-62

2001

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The current status of 492 adult women with Turner syndrome: a questionnaire survey by the Foundation for Growth Science

The current status of 492 adult women with Turner syndrome : a questionnaire survey by the Foundation for Growth Science

Prevalence of diverse complications and its association with karyotypes in Japanese adult women with Turner syndrome—a questionnaire survey by the Foundation for Growth Science

Women with Turner syndrome are at high risk of lifestyle-related disease —From questionnaire surveys by the Foundation for Growth Science in Japan

Prevalence of diverse complications and its association with karyotypes in Japanese adult women with Turner syndrome - a questionnaire survey by the Foundation for Growth Science

Women with Turner syndrome are at high risk of lifestyle-related disease - From questionnaire surveys by the Foundation for Growth Science in Japan

Development and validation of a new questionnaire assessing quality of life in adults with hypopituitarism: Adult Hypopituitarism Questionnaire (AHQ)

Effects of financial support on treatment of adolescents with growth hormone deficiency: a retrospective study in Japan

Recent Status in the Occurrence of Leukemia in Growth Hormone-Treated Patients in Japan

Adult Height in Patients with Turner Syndrome and Association with Lifestyle-related Diseases after Human Growth Hormone Treatment in Japan

The current status of 492 adult women with Turner syndrome: a questionnaire survey by the Foundation for Growth Science

Adult Heights of 258 Girls with Turner Syndrome on Low Dose of Growth Hormone Therapy in Japan

The Mechanism of Arginine- and Insulin-Induced GH Release in Humans

Complex X-Chromosomal Rearrangements in Two Women with Ovarian Dysfunction: Implications of Chromothripsis/Chromoanasynthesis-Dependent and -Independent Origins of Complex Genomic Alterations

Clinical Characteristics, Etiologies and Pathophysiology of Patients with Severe Short Stature with Severe GH Deficiency: Questionnaire Study on the Data Registered with the Foundation for Growth Science, Japan

Studies of Very Severe Short Stature with Severe GH Deficiency: From the Data Registered with the Foundation for Growth Science

Adult Heights of 258 Girls with Turner Syndrome on Low Dose of Growth Hormone Therapy in Japan

Clinical Characteristics, Etiologies and Pathophysiology of Patients with Severe Short Stature with Severe GH Deficiency：Questionnaire Study on the Data Registered with the Foundation for Growth Science, Japan

Effects of financial support on treatment of adolesJapancents with growth hormone deficiency: a retrospective study in Japan

Protein-Tyrosine Phosphatase, Nonreceptor Type 11 Mutation Analysis and Clinical Assessment in 45 Patients with Noonan Syndrome

Studies of Very Severe Short Stature with Severe GH Deficiency: From the Data Registered with the Foundation for Growth Science

No Improvement of Adult Height in Non-growth Hormone (GH) Deficient Short Children with GH Treatment

The effects of human leptin fragment(126-140) on pituitary functions in man

Plasma Chromogranin A in Pheochromocytoma, Primary Hyperparathyroidism and Pituitary Adenoma in Comparison with Catecholamine, Parathyroid Hormone and Pituitary Hormones

Final Height of Growth Hormone (GH)-Treated Short Children Registered at the Foundation for Growth Science in Japan: Comparison between the Pituitary Human GH Era and the Recombinant Human GH Era

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