Effects of romosozumab on bone ultrastructure and density in a patient with primary osteoporosis caused by a novel heterozygous WNT1 mutation

被引：0

作者：

Montero-Lopez, Rodrigo ^{[1
]}

Blaschitz, Alexandra ^{[1
]}

Tischlinger, Katharina ^{[1
]}

Wimleitner, Marlene ^{[1
]}

Hoertenhuber, Thomas ^{[1
]}

Klinger, Markus ^{[2
]}

Cejka, Daniel ^{[3
]}

Hoegler, Wolfgang ^{[1
]}

机构：

[1] Johannes Kepler Univ Linz, Dept Paediat & Adolescent Med, Linz, Austria

[2] Kepler Univ Hosp, Inst Nucl Med, Linz, Austria

[3] Ordensklinikum Linz Elisabethinen, Dept Internal Med 3, Nephrol, Transplantat Med,Rheumatol, Linz, Austria

来源：

HORMONE RESEARCH IN PAEDIATRICS | 2023年 / 96卷

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

P1-28

引用

页码：162 / 163

页数：2

共 13 条

[1] Heterozygous Mutation in WNT1 gene in Brothers with Early- Onset Osteoporosis
Al Mukaddam, Mona
Kallish, Staci
Raper, Anna
Asher, Stephanie
Khan, Amna N.
JOURNAL OF BONE AND MINERAL RESEARCH, 2019, 34 : 192 - 192
[2] EARLY-ONSET OSTEOPOROSIS IN A PATIENT DUE TO NOVEL MUTATION OF THE WNT1 GENE
Karaseva, E.
Eremkina, A.
Salimkhanov, R.
Myakota, A.
Sevostyanenko, E.
Mokrysheva, N.
AGING CLINICAL AND EXPERIMENTAL RESEARCH, 2024, 36 : S237 - S237
[3] Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 gene
Campopiano, Maria Cristina
Fogli, Antonella
Michelucci, Angela
Mazoni, Laura
Longo, Antonella
Borsari, Simona
Pardi, Elena
Benelli, Elena
Sardella, Chiara
Pierotti, Laura
Dinoi, Elisa
Marcocci, Claudio
Cetani, Filomena
FRONTIERS IN ENDOCRINOLOGY, 2022, 13
[4] Low bone mass in mice with conditional Wnt1 deletion and a Wnt1 mutation causing early-onset osteoporosis
Vollersen, Nele
Yorgan, Timur
Rolvien, Tim
Amling, Michael
Schinke, Thorsten
JOURNAL OF BONE AND MINERAL RESEARCH, 2018, 33 : 5 - 5
[5] Complex heterozygous WNT1 mutation in severe recessive osteogenesis imperfecta of a Chinese patient
Lu, Yanqin
Dai, Yunzhang
Wang, Yanzhou
Zhai, Naixiang
Zhang, Jian
Liu, Junlong
Yin, Xiaoli
Li, Tianyou
Ren, Xiuzhi
Han, Jinxiang
INTRACTABLE & RARE DISEASES RESEARCH, 2018, 7 (01) : 19 - 24
[6] Hereditary Spherocytosis Caused by a Novel Compound Heterozygous Mutation of SPTA1 and Autoimmune Hepatitis in a Pediatric Patient
Qin, Yu-Mei
Chen, Yan-Yun
Liao, Lin
Chen, Min
Lin, Fa-Quan
IRANIAN JOURNAL OF PEDIATRICS, 2023, 33 (01)
[7] Acromicric Dysplasia Caused by a Novel Heterozygous Mutation of FBN1 and Effects of Growth Hormone Treatment
Jin, Hyung Suk
Song, Ho Young
Cho, Sung Yoon
Ki, Chang-Seok
Yang, Song Hyun
Kim, Ok-Hwa
Kim, Su Jin
ANNALS OF LABORATORY MEDICINE, 2017, 37 (01) : 92 - 94
[8] A novel compound heterozygous mutation of MYSM1 gene in a patient with bone marrow failure syndrome 4
Zhan, X.
Zhao, A.
Wu, B.
Yang, Y.
Wan, L.
Tan, P.
Huang, J.
Lu, Y.
BRITISH JOURNAL OF BIOMEDICAL SCIENCE, 2021, 78 (04) : 239 - 243
[9] A novel mutation in TPRS1 gene caused tricho-rhino-phalangeal syndrome in a Chinese patient with severe osteoporosis
SHAO CongTIAN JunSHI DonghongYU ChunxiaoXU ChaoWANG Laicheng GAO Ling and ZHAO Jiajun Department of Endocrinology and MetabolismProvincial Hospital Affiliated to Shandong UniversityInstitute of Endocrinology Shandong Academy of Clinical MedicineJinanShandong China Shandong Medical Imaging Research InstituteJinanShandong China Chromosome Biology LaboratoryDepartment of Gynaecology and Obstetrics Department of Scientific Center Provincial Hospital Affiliated to Shandong UniversityJinanShandong China Department of Endocrinology and MetabolismWeihai Hospital Medical College of Qingdao UniversityWeihaiShandong China
中华医学杂志（英文版）, 2011, (10) : 1583 - 1585
[10] A novel mutation in TPRS1 gene caused tricho-rhino-phalangeal syndrome in a Chinese patient with severe osteoporosis
Shao Cong
Tian Jun
Shi Dong-hong
Yu Chun-xiao
Xu Chao
Wang Lai-cheng
Gao Ling
Zhao Jia-jun
CHINESE MEDICAL JOURNAL, 2011, 124 (10) : 1583 - 1585

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