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The prevalence of heterozygous CYP21A2 deficiency in patients with idiopathic acne, hirsutism, or both

Endocrine, 2020-03, Vol.67 (3), p.665-672

2020

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Mixed hypogonadism: a neglected combined form of hypogonadism

Endocrine, 2024-02, Vol.83 (2), p.488-493

2024

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Pulsatile gonadotropin releasing hormone therapy for spermatogenesis in congenital hypogonadotropic hypogonadism patients who had poor response to combined gonadotropin therapy

Archives of Endocrinology and Metabolism, 2024-05, Vol.68, p.e230101

2024

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Desmopressin Suppresses Gonadotropin-Induced Spermatogenesis in Patients With Pituitary Stalk Interruption Syndrome: A Retrospective, Single-Center Cohort Study

Endocrine practice, 2021-02, Vol.27 (2), p.124-130

2021

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One-pot preparation of boronic acid and PEG bi-functionalized silica particles for separation and purification of catecholamine from rat serum

New journal of chemistry, 2015-01, Vol.39 (11), p.8848-8854

2015

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Clinical Characteristics and Spermatogenesis in Patients with Congenital Hypogonadotropic Hypogonadism Caused by FGFR1 Mutations

International journal of endocrinology, 2020-11, Vol.2020, p.8873532-11

2020

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Air water intake device based on heat slow-release system

Journal of physics. Conference series, 2021-06, Vol.1952 (3), p.32065

2021

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The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2020-07, Vol.105 (7), p.1-2299

2020

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Novel rare variants in FGFR1 and clinical characteristics analysis in a series of congenital hypogonadotropic hypogonadism patients

Clinical endocrinology (Oxford), 2021-07, Vol.95 (1), p.153-162

2021

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Spontaneous Perforation in Crohn’s Disease: A Report of Two Cases

Inflammatory bowel diseases, 2022-03, Vol.28 (3), p.e40-e42

2022

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Hydrophilic surface molecularly imprinted naringin prepared via reverse atom transfer radical polymerization with excellent recognition ability in a pure aqueous phase

RSC advances, 2017, Vol.7 (45), p.28082-28091

2017

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Relationship between growth hormone deficiency and nonalcoholic fatty liver disease in patients with pituitary stalk interruption syndrome

Clinical endocrinology (Oxford), 2022-11, Vol.97 (5), p.612-621

2022

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Mutation of c.244GT in NR5A1 gene causing 46, XY DSD by affecting RNA splicing

Orphanet journal of rare diseases, 2021-08, Vol.16 (1)

2021

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Bone Mineral Density in Pituitary Stalk Interruption Syndrome: The Role of Insulin-Like Growth Factor-1 and Testosterone at Different Skeletal Sites

Endocrine practice, 2022-11, Vol.28 (11), p.1118-1124

2022

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High prevalence of hypertension and target organ damage in patients with 11β‐hydroxylase deficiency

Clinical endocrinology (Oxford), 2022-05, Vol.96 (5), p.657-665

2022

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Increased Bone Mineral Density in Male Patients With Idiopathic Hypogonadotropic Hypogonadism Who Undergo Sex Hormone Therapy: Findings From Cross-Sectional and Longitudinal Studies

Endocrine practice, 2021-09, Vol.27 (9), p.934-940

2021

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Efficacy of Pulsatile Gonadotropin-Releasing Hormone Therapy in Male Patients: Comparison between Pituitary Stalk Interruption Syndrome and Congenital Hypogonadotropic Hypogonadism

Endocrine practice, 2022-05, Vol.28 (5), p.521-527

2022

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Aromatase Inhibitor Increases the Height of Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Endocrine practice, 2020-09, Vol.26 (9), p.997-1002

2020

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Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations

European journal of endocrinology, 2017-10, Vol.177 (4), p.389

2017

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Novel NR5A1 mutations found in Chinese patients with 46, XY disorders of sex development

Clinical endocrinology (Oxford), 2018-11, Vol.89 (5), p.613-620

2018

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Gonadotropin Therapy Once a Week for Spermatogenesis in Hypogonadotropic Hypogonadism

Endocrine practice, 2021-11, Vol.27 (11), p.1119-1127

2021

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Personalization of Saliency Estimation

Yu, Bingqing

2018

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Novel NR 5A1 mutations found in Chinese patients with 46, XY disorders of sex development

Clinical endocrinology (Oxford), 2018-11, Vol.89 (5), p.613-620

2018

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Efficacy and safety of letrozole in treatment of male children with disorders of sex development

Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban, 2020-05, Vol.49 (3), p.297

2020

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Generation of Spatial-Temporal Panoramas with a Single Moving Camera

2016 13th Conference on Computer and Robot Vision (CRV), 2016, p.289-295

2016

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The prevalence of heterozygous CYP21A2 deficiency in patients with idiopathic acne, hirsutism, or both

Mixed hypogonadism: a neglected combined form of hypogonadism

Pulsatile gonadotropin releasing hormone therapy for spermatogenesis in congenital hypogonadotropic hypogonadism patients who had poor response to combined gonadotropin therapy

Desmopressin Suppresses Gonadotropin-Induced Spermatogenesis in Patients With Pituitary Stalk Interruption Syndrome: A Retrospective, Single-Center Cohort Study

One-pot preparation of boronic acid and PEG bi-functionalized silica particles for separation and purification of catecholamine from rat serum

Clinical Characteristics and Spermatogenesis in Patients with Congenital Hypogonadotropic Hypogonadism Caused by FGFR1 Mutations

Air water intake device based on heat slow-release system

The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency

Novel rare variants in FGFR1 and clinical characteristics analysis in a series of congenital hypogonadotropic hypogonadism patients

Spontaneous Perforation in Crohn’s Disease: A Report of Two Cases

Hydrophilic surface molecularly imprinted naringin prepared via reverse atom transfer radical polymerization with excellent recognition ability in a pure aqueous phase

Relationship between growth hormone deficiency and nonalcoholic fatty liver disease in patients with pituitary stalk interruption syndrome

Mutation of c.244GT in NR5A1 gene causing 46, XY DSD by affecting RNA splicing

Bone Mineral Density in Pituitary Stalk Interruption Syndrome: The Role of Insulin-Like Growth Factor-1 and Testosterone at Different Skeletal Sites

High prevalence of hypertension and target organ damage in patients with 11β‐hydroxylase deficiency

Increased Bone Mineral Density in Male Patients With Idiopathic Hypogonadotropic Hypogonadism Who Undergo Sex Hormone Therapy: Findings From Cross-Sectional and Longitudinal Studies

Efficacy of Pulsatile Gonadotropin-Releasing Hormone Therapy in Male Patients: Comparison between Pituitary Stalk Interruption Syndrome and Congenital Hypogonadotropic Hypogonadism

Aromatase Inhibitor Increases the Height of Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations

Novel NR5A1 mutations found in Chinese patients with 46, XY disorders of sex development

Gonadotropin Therapy Once a Week for Spermatogenesis in Hypogonadotropic Hypogonadism

Personalization of Saliency Estimation

Novel NR 5A1 mutations found in Chinese patients with 46, XY disorders of sex development

Efficacy and safety of letrozole in treatment of male children with disorders of sex development

Generation of Spatial-Temporal Panoramas with a Single Moving Camera

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