Maria Isabel Luis-Yanes
Overview
Explore the profile of Maria Isabel Luis-Yanes including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
45
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Garcia-Nieto V, Claverie-Martin F, Moraleda-Mesa T, Perdomo-Ramirez A, Fraga-Rodriguez G, Luis-Yanes M, et al.
Nefrologia (Engl Ed)
. 2024 Feb;
44(1):23-31.
PMID: 38350738
Renal diseases associated with hypomagnesemia are a complex and diverse group of tubulopathies caused by mutations in genes encoding proteins that are expressed in the thick ascending limb of the...
2.
Perdomo-Ramirez A, Cordoba-Lanus E, Trujillo-Frias C, Gonzalez-Navasa C, Ramos-Trujillo E, Luis-Yanes M, et al.
Int J Mol Sci
. 2023 May;
24(9).
PMID: 37176161
Renal hypouricemia (RHUC) is a rare inherited disorder characterized by impaired urate reabsorption in the proximal tubule resulting in low urate serum levels and increased urate excretion. Some patients may...
3.
Garcia-Nieto V, Gonzalez-Rodriguez J, Cabrera-Sevilla J, Martin-Fernandez de Basoa M, Luis-Yanes M
Pediatr Nephrol
. 2023 Apr;
38(11):3845-3848.
PMID: 37052691
Background: Fractional tubular reabsorption of phosphate (TRP) has been used for over 60 years to establish the existence of renal phosphate loss. It is a parameter of corrected volume per...
4.
Garcia-Nieto V, Monge-Zamorano M, Luis-Yanes M, Moraleda-Mesa T
Indian J Pediatr
. 2021 May;
88(7):738.
PMID: 33983540
No abstract available.
5.
Rodriguez-Rubio E, Gil-Pena H, Chocron S, Madariaga L, de la Cerda-Ojeda F, Fernandez-Fernandez M, et al.
Orphanet J Rare Dis
. 2021 Apr;
16(1):154.
PMID: 33794951
No abstract available.
6.
Rodriguez-Rubio E, Gil-Pena H, Chocron S, Madariaga L, de la Cerda-Ojeda F, Fernandez-Fernandez M, et al.
Orphanet J Rare Dis
. 2021 Feb;
16(1):104.
PMID: 33639975
Background: X-linked hypophosphatemia (XLH) is a hereditary rare disease caused by loss-of-function mutations in PHEX gene leading tohypophosphatemia and high renal loss of phosphate. Rickets and growth retardation are the...
7.
Luis-Yanes M, Martinez Gomez G, Tapia-Romero C, Tejera-Carreno P, Garcia-Nieto V
Nefrologia (Engl Ed)
. 2020 Jun;
40(6):672-673.
PMID: 32571524
No abstract available.
8.
Garcia-Nieto V, Garcia-Rodriguez V, Luis-Yanes M, Monge M, Arango-Sancho P, Garin E
Eur J Pediatr
. 2019 Feb;
178(4):525-531.
PMID: 30706159
Severe (grades IV and V) vesicoureteral reflux (VUR) is a risk factor for acute pyelonephritis, renal scars, and renal failure. This study evaluates albumin and N-acetylglucosaminidase (NAG) urinary excretion, and...
9.
Garcia-Nieto V, Luis-Yanes M, Arango-Sancho P
Pediatr Nephrol
. 2017 Jun;
32(9):1639-1640.
PMID: 28624981
No abstract available.
10.
Gonzalez-Rodriguez J, Luis-Yanes M, Ingles-Torres E, Arango-Sancho P, Cabrera-Sevilla J, Duque-Fernandez M, et al.
Intractable Rare Dis Res
. 2016 Dec;
5(4):284-289.
PMID: 27904825
Sclerosing bone dysplasias are a series of clinically and genetically heterogeneous diseases characterized by functional failure of the osteoclasts in bone resorption, leading to an excessive amount of bone mineral...