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Nonremission and Recurrent Tumor‐Induced Osteomalacia: A Retrospective Study

Journal of bone and mineral research, 2020-03, Vol.35 (3), p.469-477

2020

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EFFICACY AND SAFETY OF BISPHOSPHONATE THERAPY IN MCCUNE-ALBRIGHT SYNDROME-RELATED POLYOSTOTIC FIBROUS DYSPLASIA: A SINGLE-CENTER EXPERIENCE

Endocrine practice, 2019-01, Vol.25 (1), p.23-30

2019

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Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: Effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism

Molecular and cellular endocrinology, 2015-01, Vol.399, p.32-42

2015

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Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas

PloS one, 2012-09, Vol.7 (9), p.e45567-e45567

2012

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Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese

PloS one, 2016-11, Vol.11 (11), p.e0166634-e0166634

2016

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Bone Volumetric Density, Microarchitecture, and Estimated Bone Strength in Tumor-Induced Rickets/Osteomalacia Versus X-linked Hypophosphatemia in Chinese Adolescents

Frontiers in endocrinology (Lausanne), 2022-06, Vol.13, p.883981-883981

2022

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Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism

European journal of endocrinology, 2013-11, Vol.169 (5), p.629

2013

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Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese

Clinical endocrinology (Oxford), 2014-08, Vol.81 (2), p.222-230

2014

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Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia

PloS one, 2012-06, Vol.7 (6), p.e38643

2012

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A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient

Bone (New York, N.Y.), 2014-02, Vol.59, p.114-121

2014

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FGF23 analysis of a Chinese family with autosomal dominant hypophosphatemic rickets

Journal of bone and mineral metabolism, 2012-01, Vol.30 (1), p.78-84

2012

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Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients

Bone (New York, N.Y.), 2012-09, Vol.51 (3), p.563-569

2012

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A Recurrent Mutation c.617G>A in the ACVR1 Gene Causes Fibrodysplasia Ossificans Progressiva in Two Chinese Patients

Calcified tissue international, 2009-05, Vol.84 (5), p.361-365

2009

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Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia

Bone (New York, N.Y.), 2019-04, Vol.121, p.212-220

2019

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Germinal mosaicism of GATA3 in a family with HDR syndrome

American journal of medical genetics. Part A, 2009-04, Vol.149A (4), p.776-778

2009

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Primary hyperparathyroidism in Chinese children and adolescents: A single‐centre experience at Peking Union Medical College Hospital

Clinical endocrinology (Oxford), 2017-12, Vol.87 (6), p.865-873

2017

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Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati–Engelmann Disease: Assessed by HR‐pQCT

Journal of bone and mineral research, 2022-01, Vol.37 (1), p.78-86

2022

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PRIMARY HYPERPARATHYROIDISM DURING PREGNANCY: A CASE SERIES OF 8 PATIENTS

Endocrine practice, 2019-11, Vol.25 (11), p.1127-1136

2019

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Early Discrimination Between Tumor‐Induced Rickets/Osteomalacia and X‐Linked Hypophosphatemia in Chinese Children and Adolescents: A Retrospective Case–Control Study

Journal of bone and mineral research, 2021-09, Vol.36 (9), p.1739-1748

2021

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Surgical Treatments of Tumor-Induced Osteomalacia Lesions in Long Bones: Seventeen Cases with More Than One Year of Follow-up

Journal of bone and joint surgery. American volume, 2015-07, Vol.97 (13), p.1084

2015

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Primary hyperparathyroidism in women: a tale of two cities--New York and Beijing

International journal of fertility & women's medicine, 2000-03, Vol.45 (2), p.158

2000

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Familial isolated primary hyperparathyroidism/hyperparathyroidism‐jaw tumour syndrome caused by germline gross deletion or point mutations of CDC 73 gene in Chinese

Clinical endocrinology (Oxford), 2014-08, Vol.81 (2), p.222-230

2014

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MEN1 c.825-1GA mutation in a family with multiple endocrine neoplasia type 1: a case report

Molecular medicine reports, 2015-10, p.6152

2015

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MEN1 c.825-1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report

Molecular medicine reports, 2015-10, Vol.12 (4), p.6152-6156

2015

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Report of a case with Alstrom syndrome

Zhonghua er ke za zhi, 2004-06, Vol.42 (6), p.471

2004

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Nonremission and Recurrent Tumor‐Induced Osteomalacia: A Retrospective Study

EFFICACY AND SAFETY OF BISPHOSPHONATE THERAPY IN MCCUNE-ALBRIGHT SYNDROME-RELATED POLYOSTOTIC FIBROUS DYSPLASIA: A SINGLE-CENTER EXPERIENCE

Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: Effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism

Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas

Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese

Bone Volumetric Density, Microarchitecture, and Estimated Bone Strength in Tumor-Induced Rickets/Osteomalacia Versus X-linked Hypophosphatemia in Chinese Adolescents

Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism

Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese

Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia

A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient

FGF23 analysis of a Chinese family with autosomal dominant hypophosphatemic rickets

Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients

A Recurrent Mutation c.617G>A in the ACVR1 Gene Causes Fibrodysplasia Ossificans Progressiva in Two Chinese Patients

Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia

Germinal mosaicism of GATA3 in a family with HDR syndrome

Primary hyperparathyroidism in Chinese children and adolescents: A single‐centre experience at Peking Union Medical College Hospital

Alteration of Bone Density, Microarchitecture, and Strength in Patients with Camurati–Engelmann Disease: Assessed by HR‐pQCT

PRIMARY HYPERPARATHYROIDISM DURING PREGNANCY: A CASE SERIES OF 8 PATIENTS

Early Discrimination Between Tumor‐Induced Rickets/Osteomalacia and X‐Linked Hypophosphatemia in Chinese Children and Adolescents: A Retrospective Case–Control Study

Surgical Treatments of Tumor-Induced Osteomalacia Lesions in Long Bones: Seventeen Cases with More Than One Year of Follow-up

Primary hyperparathyroidism in women: a tale of two cities--New York and Beijing

Familial isolated primary hyperparathyroidism/hyperparathyroidism‐jaw tumour syndrome caused by germline gross deletion or point mutations of CDC 73 gene in Chinese

MEN1 c.825-1GA mutation in a family with multiple endocrine neoplasia type 1: a case report

MEN1 c.825-1G>A mutation in a family with multiple endocrine neoplasia type 1: A case report

Report of a case with Alstrom syndrome

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