Results 251 to 260 of about 511,382 (289)

Unprecedented coexistence of Dent’s disease type 1 and Wilson’s disease in a two-year-old Chinese boy: implications for precision medicine

BMC Nephrology
Qingxian Mao, Wai W. Cheung, Ruochen Che, Fei Zhao, Xueqin Cheng, Guixia Ding   +5 more
openaire   +1 more source

Keras Slim ResNet-Based Prediction of Furcation Management Recommendations Among Dentists. [PDF]

Int J Dent
Yadalam PK, Arumuganainar D, Mosaddad SA, Heboyan A, Duraisami NK.   +4 more
europepmc   +1 more source

Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report. [PDF]

Contemp Clin Dent
Rani N, Yadav S, Kaur A, Kaur CK, Kumar U.   +4 more
europepmc   +1 more source

Metagenomics as an Effective Diagnostic Approach for Exploring Oral Microbial Diversity and Dental Diseases: A Narrative Review. [PDF]

Int J Clin Pediatr Dent
Walia T, Srivastava N, Shetty RM, Rana V.   +3 more
europepmc   +1 more source

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Drosophila Clc-c as a model of human CLC-5 and Dent Disease type 1

Physiology, 2023
Introduction: Dent Disease type 1 (DD1) results from X-linked, mutations in CLC-5 (2Cl-/H+ exchanger) and results in progressive renal failure by 20-40. DD1 is characterized by kidney Ca2+ mishandling, and subsequent hypercalcuria, calcium oxalate (CaOx) kidney stones, and kidney calcification as well as proteinuria.
Carmen Reynolds, Christopher Gillen, Julian Dow, Michael Romero   +3 more
openaire   +1 more source

Inherited hypercalciuric syndromes: dent’s disease (CLC-5) and familial hypomagnesemia with hypercalciuria (paracellin-1)

Seminars in Nephrology, 2004
Dent's disease and familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) are inherited diseases in which hypercalciuria, nephrocalcinosis, and renal failure are prominent features. Dent's disease resembles a Fanconi syndrome, with impaired reabsorption in the proximal tubule; FHHNC, with urinary loss of magnesium and calcium, is ...
Stephen J, Knohl, Steven J, Scheinman
openaire   +2 more sources

Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene

Pediatric and Developmental Pathology, 2022
The study aims to explore the clinicopathological features and whether the nonsense mutations of CLCN5 gene have effect on the renal expression of CLC-5 protein and megalin/cubilin complex in children with Dent-1 disease. The clinicopathological features and genetic examination of three patients with Dent-1 disease were investigated. The expression of
Panpan, Zhai, Weigang, Lv, Xiaoqing, Yang, Yanjie, Huang, Wensheng, Zhai, Xianqing, Ren, Xia, Zhang, Meng, Yang, Jian, Zhang, Ting, Guo, Minghui, Bai, Yueli, Yang, Ying, Ding, Yanshi, Huang   +13 more
openaire   +2 more sources