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Items: 1 to 20 of 1711

1.
New scenarios in secondary hyperparathyroidism: etelcalcetide. Position paper of working group on CKD-MBD of the Italian Society of Nephrology
Antonio Bellasi, Mario Cozzolino, Fabio Malberti, Giovanni Cancarini, Ciro Esposito, Carlo Maria Guastoni, Patrizia Ondei, Giuseppe Pontoriero, Ugo Teatini, Giuseppe Vezzoli, Marzia Pasquali, Piergiorgio Messa, Francesco Locatelli
J Nephrol. 2020; 33(2): 211–221. Published online 2019 Dec 18. doi: 10.1007/s40620-019-00677-0
PMCID:
PMC7118036
ArticlePDF–673K
2.
The dietary management of calcium and phosphate in children with CKD stages 2-5 and on dialysis—clinical practice recommendation from the Pediatric Renal Nutrition Taskforce
Louise McAlister, Pearl Pugh, Laurence Greenbaum, Dieter Haffner, Lesley Rees, Caroline Anderson, An Desloovere, Christina Nelms, Michiel Oosterveld, Fabio Paglialonga, Nonnie Polderman, Leila Qizalbash, José Renken-Terhaerdt, Jetta Tuokkola, Bradley Warady, Johan Vande Walle, Vanessa Shaw, Rukshana Shroff
Pediatr Nephrol. 2020; 35(3): 501–518. Published online 2019 Oct 30. doi: 10.1007/s00467-019-04370-z
PMCID:
PMC6969014
ArticlePDF–505K
3.
Prevention and treatment of renal osteodystrophy in children on chronic renal failure: European guidelines
G. Klaus, A. Watson, A. Edefonti, M. Fischbach, K. Rönnholm, F. Schaefer, E. Simkova, C. J. Stefanidis, V. Strazdins, J. Vande Walle, C. Schröder, A. Zurowska, M. Ekim
Pediatr Nephrol. 2006 Feb; 21(2): 151–159. Published online 2005 Oct 25. doi: 10.1007/s00467-005-2082-7
PMCID:
PMC1766475
ArticlePDF–186K
4.
Experience of X-linked hypophosphatemic rickets in the Gulf Cooperation Council countries: case series
Fahad Al-Juraibah, Adnan Al Shaikh, Afaf Al-Sagheir, Amir Babiker, Asma Al Nuaimi, Ayed Al Enezi, George S Mikhail, Hassan A Mundi, Hubert K Penninckx, Huda Mustafa, Majid Al Ameri, Mohamed Al-Dubayee, Nadia S Ali, Nagla Fawzy, Sameer Al Shammari, Tarek Fiad
Endocrinol Diabetes Metab Case Rep. 2024 Apr 1; 2024(2): 23-0098. Published online 2024 Apr 11. doi: 10.1530/EDM-23-0098
PMCID:
PMC11046327
ArticlePDF–782K
5.
Vitamin D-Dependent Rickets Type 1A in Two Siblings with a Hypomorphic CYP27B1 Variant Frequent in the African Population
Joana de Brito Chagas, Carolina Cordinhã, Carmen do Carmo, Cristina Alves, Karen E. Heath, Sérgio B. Sousa, Clara Gomes
J Pediatr Genet. 2024 Mar; 13(1): 43–49. Published online 2021 Oct 25. doi: 10.1055/s-0041-1736559
PMCID:
PMC10984714
ArticlePDF–915K
6.
Intact FGF23 concentration in healthy infants, children, and adolescents, and diagnostic usefulness in patients with X-linked hypophosphatemic rickets
G. I. Baroncelli, M. R. Sessa, C. Pelosini, S. Bertelloni, A. Michelucci, B. Toschi, P. Piaggi, D. Peroni, P. Comberiati
J Endocrinol Invest. 2024; 47(4): 873–882. Published online 2023 Nov 22. doi: 10.1007/s40618-023-02202-4
PMCID:
PMC10965647
ArticlePDF–666K
7.
Serum 25-hydroxyvitamin D threshold and risk of rickets in young children: a systematic review and individual participant data meta-analysis to inform the development of dietary requirements for vitamin D
Magali Rios-Leyvraz, Tom D. Thacher, Aashima Dabas, Heba Hassan Elsedfy, Giampiero I. Baroncelli, Kevin D. Cashman
Eur J Nutr. 2024; 63(3): 673–695. Published online 2024 Jan 27. doi: 10.1007/s00394-023-03299-2
PMCID:
PMC10948504
ArticlePDF–1.0M
8.
一个PHEX基因新发变异导致的X-连锁低磷性佝偻病家系
张 玉海, 张 娴, 方 团育, 全 会标, 陈 开宁, 盛 志峰
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2021 Jun 28; 46(6): 658–665. Chinese. doi: 10.11817/j.issn.1672-7347.2021.200072
PMCID:
PMC10930202
ArticlePDF–1.3M
9.
Novel Mutation in CYP2R1 Causing Vitamin D-Dependent Rickets Type 1b
Jayakrishnan C Menon, Archana Kumari, Shruti M Sajjan, Preeti Dabadghao
JCEM Case Rep. 2024 Mar; 2(3): luae024. Published online 2024 Mar 4. doi: 10.1210/jcemcr/luae024
PMCID:
PMC10911226
ArticlePDF–498K
10.
Multi-segment osteotomy with interlocking intramedullary nail fixation in the treatment of lower limb deformity in older children with hypophosphatemic rickets
Ming Lu, Haifeng You, Yukun Wang
Front Pediatr. 2024; 12: 1332531. Published online 2024 Feb 19. doi: 10.3389/fped.2024.1332531
PMCID:
PMC10909947
ArticlePDF–8.0M
11.
Family analysis and literature study of hereditary hypophosphatemic rickets with hypercalciuria
Lufeng Wang, Gulimire Kulaixi, Jiazireya Zaiyinati, Guzhalikezi Aibai, Danyang Du, Yanying Guo
BMC Pediatr. 2024; 24: 121. Published online 2024 Feb 14. doi: 10.1186/s12887-024-04589-2
PMCID:
PMC10865686
ArticlePDF–1.1M
12.
Rickets Types and Treatment with Vitamin D and Analogues
Giacomo Biasucci, Valentina Donini, Giuseppe Cannalire
Nutrients. 2024 Feb; 16(3): 416. Published online 2024 Jan 31. doi: 10.3390/nu16030416
PMCID:
PMC10857029
ArticlePDF–771K
13.
A PAI‐1 antagonist ameliorates hypophosphatemia in the Hyp vitamin D‐resistant rickets model mouse
Cheng Qian, Nobuaki Ito, Kunikazu Tsuji, Shingo Sato, Katsushi Kikuchi, Toshitaka Yoshii, Toshio Miyata, Yoshinori Asou
FEBS Open Bio. 2024 Feb; 14(2): 290–299. Published online 2023 Dec 25. doi: 10.1002/2211-5463.13745
PMCID:
PMC10839342
ArticlePDF–914K
14.
Rickets – A case report
Deepjyoti Mudgade, Himanshu M. Srivastava, Sameera M. R. Qureshi, Amit Handa
J Oral Maxillofac Pathol. 2023 Oct-Dec; 27(4): 781. Published online 2023 Dec 20. doi: 10.4103/jomfp.jomfp_233_23
PMCID:
PMC10829471
ArticlePDF–1.1M
15.
FGF23‐related hypophosphatemic rickets preceding the onset of systemic lupus erythematosus: A juvenile case
Yoko tabei, Yoshiaki Ohtsu, Masaharu Shimada, Aya Wada, Emi Hamajima, Yoshimitsu Osawa, Takumi Takizawa
Clin Case Rep. 2024 Jan; 12(1): e8420. Published online 2024 Jan 12. doi: 10.1002/ccr3.8420
PMCID:
PMC10784849
ArticlePDF–718K
16.
Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
Nouf F Bin Rubaian, Bashayer S Al-Awam, Samah M Aljohani, Serene R Almuhaidib
Clin Cosmet Investig Dermatol. 2024; 17: 13–16. Published online 2024 Jan 3. doi: 10.2147/CCID.S438505
PMCID:
PMC10771772
ArticlePDF–476K
17.
CYP3A4 Mutation Causes Vitamin D-Dependent Rickets Type 3: A Case Report in Saudi Arabia
Abdullah Al-Ashwal, Asma Al Zahrani, Nada Dammas, Lujain Aletani, Raghad Alhuthil
Cureus. 2023 Dec; 15(12): e49976. Published online 2023 Dec 5. doi: 10.7759/cureus.49976
PMCID:
PMC10765270
ArticlePDF–437K
18.
X-linked hypophosphatemic rickets: from diagnosis to management
Eujin Park, Hee Gyung Kang
Clin Exp Pediatr. 2024 Jan; 67(1): 17–25. Published online 2023 Jun 14. doi: 10.3345/cep.2022.01459
PMCID:
PMC10764665
ArticlePDF–2.3M
19.
A De Novo Mosaic PHEX Variant Causing Sporadic X-Linked Hypophosphatemic Rickets in a 2-Year-Old Girl
Kok-Siong Poon, Karen Mei-Ling Tan, Margaret Zacharin, Cindy Wei-Li Ho
J Pediatr Genet. 2023 Dec; 12(4): 308–311. Published online 2021 Jun 1. doi: 10.1055/s-0041-1728746
PMCID:
PMC10756725
ArticlePDF–1.5M
20.
The contribution of a novel PHEX gene mutation to X-linked hypophosphatemic rickets: a case report and an analysis of the gene mutation dosage effect in a rat model
Xiaoming Chen, Cijing Cai, Shaocong Lun, Qiuli Ye, Weiyuan Pan, Yushi Chen, Yuexuan Wu, Taoshan Feng, Faming Su, Choudi Ma, Jiaxin Luo, Meilian Liu, Guoda Ma
Front Endocrinol (Lausanne) 2023; 14: 1251718. Published online 2023 Dec 5. doi: 10.3389/fendo.2023.1251718
PMCID:
PMC10728720
ArticlePDF–6.3M

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