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T2DM Self-Management via Smartphone Applications: A Systematic Review and Meta-Analysis

PloS one, 2016-11, Vol.11 (11), p.e0166718-e0166718

2016

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Percent body fat was negatively correlated with Testosterone levels in male

PloS one, 2024-01, Vol.19 (1), p.e0294567-e0294567

2024

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Thymoma in multiple endocrine neoplasia type 1: a case report and systematic review

Endocrine, 2023-11, Vol.82 (2), p.442-449

2023

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High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiency

Endocrine, 2022-04, Vol.76 (1), p.151-161

2022

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Triglyceride glucose-waist circumference: the optimum index to screen nonalcoholic fatty liver disease in non-obese adults

BMC gastroenterology, 2023-11, Vol.23 (1), p.1-376, Article 376

2023

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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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Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia

Frontiers in nutrition (Lausanne), 2023-03, Vol.10, p.1109824-1109824

2023

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Combined therapy with GnRH analogue and growth hormone increases adult height in children with short stature and normal pubertal onset

Endocrine, 2020-09, Vol.69 (3), p.615-624

2020

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

Orphanet journal of rare diseases, 2021-08, Vol.16 (1), p.370-370, Article 370

2021

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Classification of CHD7 Rare Variants in Chinese Congenital Hypogonadotropic Hypogonadism Patients and Analysis of Their Clinical Characteristics

Frontiers in genetics, 2022-01, Vol.12, p.770680-770680

2022

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Metabolic Effects of Recombinant Human Growth Hormone Replacement Therapy on Juvenile Patients after Craniopharyngioma Resection

International journal of endocrinology, 2022-07, Vol.2022, p.1-9

2022

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Novel Microdeletion in the X Chromosome Leads to Kallmann Syndrome, Ichthyosis, Obesity, and Strabismus

Frontiers in genetics, 2020-06, Vol.11, p.596-596

2020

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Case Report: Novel Compound Heterozygotic Variants in PPP2R3C Gene Causing Syndromic 46, XY Gonadal Dysgenesis and Literature Review

Frontiers in genetics, 2022-06, Vol.13

2022

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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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Growth Hormone Is Beneficial for Induction of Spermatogenesis in Adult Patients With Congenital Combined Pituitary Hormone Deficiency

Frontiers in endocrinology (Lausanne), 2022-04, Vol.13, p.868047-868047

2022

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Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy

Therapeutic advances in endocrinology and metabolism, 2020, Vol.11, p.2042018820924556-2042018820924556

2020

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Assisted reproductive techniques with congenital hypogonadotropic hypogonadism patients: a systematic review and meta-analysis

BMC endocrine disorders, 2018-11, Vol.18 (1), p.85-85, Article 85

2018

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The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant

Frontiers in endocrinology (Lausanne), 2023-02, Vol.13, p.1015773-1015773

2023

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The diagnostic value of the olfactory evaluation for congenital hypogonadotropic hypogonadism

Frontiers in endocrinology (Lausanne), 2022-09, Vol.13, p.909623-909623

2022

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Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism

Heliyon, 2023-04, Vol.9 (4), p.e14779-e14779, Article e14779

2023

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Corrigendum to “Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism” [Heliyon 9(4) (March 2023) e14779]

Heliyon, 2023-05, Vol.9 (5), p.e15657-e15657, Article e15657

2023

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Dietary or Enteral Medium-Chain Triglyceride Usage in a Chinese General Hospital

Asia Pacific Journal of Clinical Nutrition, 2015-09, Vol.24 (3), p.387-393

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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Gonadotropin-Induced Spermatogenesis in CHH Patients with Cryptorchidism

International journal of endocrinology, 2019, Vol.2019, p.6743489-6

2019

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T2DM Self-Management via Smartphone Applications: A Systematic Review and Meta-Analysis

Percent body fat was negatively correlated with Testosterone levels in male

Thymoma in multiple endocrine neoplasia type 1: a case report and systematic review

High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiency

Triglyceride glucose-waist circumference: the optimum index to screen nonalcoholic fatty liver disease in non-obese adults

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

Mixed hypogonadism: a neglected combined form of hypogonadism

Prediabetes is associated with loss of appendicular skeletal muscle mass and sarcopenia

Combined therapy with GnRH analogue and growth hormone increases adult height in children with short stature and normal pubertal onset

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

Classification of CHD7 Rare Variants in Chinese Congenital Hypogonadotropic Hypogonadism Patients and Analysis of Their Clinical Characteristics

Metabolic Effects of Recombinant Human Growth Hormone Replacement Therapy on Juvenile Patients after Craniopharyngioma Resection

Novel Microdeletion in the X Chromosome Leads to Kallmann Syndrome, Ichthyosis, Obesity, and Strabismus

Case Report: Novel Compound Heterozygotic Variants in PPP2R3C Gene Causing Syndromic 46, XY Gonadal Dysgenesis and Literature Review

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

Growth Hormone Is Beneficial for Induction of Spermatogenesis in Adult Patients With Congenital Combined Pituitary Hormone Deficiency

Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy

Assisted reproductive techniques with congenital hypogonadotropic hypogonadism patients: a systematic review and meta-analysis

The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant

The diagnostic value of the olfactory evaluation for congenital hypogonadotropic hypogonadism

Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism

Corrigendum to “Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism” [Heliyon 9(4) (March 2023) e14779]

Dietary or Enteral Medium-Chain Triglyceride Usage in a Chinese General Hospital

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

Gonadotropin-Induced Spermatogenesis in CHH Patients with Cryptorchidism

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