Page last updated: 2024-10-17

citric acid, anhydrous and Genetic Predisposition

citric acid, anhydrous has been researched along with Genetic Predisposition in 8 studies

Citric Acid: A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.
citric acid : A tricarboxylic acid that is propane-1,2,3-tricarboxylic acid bearing a hydroxy substituent at position 2. It is an important metabolite in the pathway of all aerobic organisms.

Research Excerpts

ExcerptRelevanceReference
"Urolithiasis is one of the commonest problems in pediatric nephrology."1.36Clinical manifestations and etiology of renal stones in children less than 14 years age. ( Heidari, A; Sepahi, MA; Shajari, A, 2010)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's8 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Pop, A1
Williams, M1
Struys, EA1
Monné, M1
Jansen, EEW1
De Grassi, A1
Kanhai, WA1
Scarcia, P1
Ojeda, MRF1
Porcelli, V1
van Dooren, SJM1
Lennertz, P1
Nota, B1
Abdenur, JE1
Coman, D1
Das, AM1
El-Gharbawy, A1
Nuoffer, JM1
Polic, B1
Santer, R1
Weinhold, N1
Zuccarelli, B1
Palmieri, F1
Palmieri, L1
Salomons, GS1
Li, K1
Luo, Y1
Mo, Y1
Shen, J1
Liu, X1
Li, H1
Schwaderer, AL1
Kusumi, K1
Ayoob, RM1
Hardies, K1
de Kovel, CG1
Weckhuysen, S1
Asselbergh, B1
Geuens, T1
Deconinck, T1
Azmi, A1
May, P1
Brilstra, E1
Becker, F1
Barisic, N1
Craiu, D1
Braun, KP1
Lal, D1
Thiele, H1
Schubert, J1
Weber, Y1
van 't Slot, R1
Nürnberg, P1
Balling, R1
Timmerman, V1
Lerche, H1
Maudsley, S1
Helbig, I1
Suls, A1
Koeleman, BP1
De Jonghe, P1
Sepahi, MA1
Heidari, A1
Shajari, A1
Zhu, C1
Ye, Z1
Chen, Z1
Xia, D1
Hu, J1
García Nieto, V1
Dublán García, K1
Luis Yanes, MI1
Sáez-Torres, C1
Grases, F1
Rodrigo, D1
García-Raja, AM1
Gómez, C1
Frontera, G1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
SLC13A5 Deficiency: A Prospective Natural History Study - United States Only[NCT06144957]17 participants (Anticipated)Observational2021-12-01Recruiting
SLC13A5 Deficiency: A Prospective Natural History Study - Remote Only (International)[NCT04681781]20 participants (Anticipated)Observational2021-03-01Enrolling by invitation
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

1 review available for citric acid, anhydrous and Genetic Predisposition

ArticleYear
Pediatric nephrolithiasis and the link to bone metabolism.
    Current opinion in pediatrics, 2014, Volume: 26, Issue:2

    Topics: Absorptiometry, Photon; Bone and Bones; Bone Density; Bone Density Conservation Agents; Child; Child

2014

Other Studies

7 other studies available for citric acid, anhydrous and Genetic Predisposition

ArticleYear
An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants.
    Journal of inherited metabolic disease, 2018, Volume: 41, Issue:2

    Topics: Anion Transport Proteins; Biological Assay; Brain Diseases, Metabolic, Inborn; Cells, Cultured; Chil

2018
Association between vitamin D receptor gene polymorphisms and idiopathic hypocitraturia in a Chinese Bai population.
    Urolithiasis, 2019, Volume: 47, Issue:3

    Topics: Adult; Asian People; Case-Control Studies; China; Citric Acid; Female; Genetic Association Studies;

2019
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
    Brain : a journal of neurology, 2015, Volume: 138, Issue:Pt 11

    Topics: Adolescent; Anodontia; Brain Diseases; Child; Citric Acid; Developmental Disabilities; Epilepsy; Fem

2015
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
    Brain : a journal of neurology, 2015, Volume: 138, Issue:Pt 11

    Topics: Adolescent; Anodontia; Brain Diseases; Child; Citric Acid; Developmental Disabilities; Epilepsy; Fem

2015
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
    Brain : a journal of neurology, 2015, Volume: 138, Issue:Pt 11

    Topics: Adolescent; Anodontia; Brain Diseases; Child; Citric Acid; Developmental Disabilities; Epilepsy; Fem

2015
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia.
    Brain : a journal of neurology, 2015, Volume: 138, Issue:Pt 11

    Topics: Adolescent; Anodontia; Brain Diseases; Child; Citric Acid; Developmental Disabilities; Epilepsy; Fem

2015
Clinical manifestations and etiology of renal stones in children less than 14 years age.
    Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia, 2010, Volume: 21, Issue:1

    Topics: Adolescent; Child; Child, Preschool; Citric Acid; Cystinuria; Dysuria; Female; Fever; Genetic Predis

2010
Association between vitamin D receptor gene polymorphisms and idiopathic hypocitraturia in the Chinese population.
    Urologia internationalis, 2010, Volume: 85, Issue:1

    Topics: Asian People; Biomarkers; Case-Control Studies; China; Citric Acid; Gene Frequency; Genetic Predispo

2010
[Are simple renal cysts another manifestation of prelithiasis in infancy?].
    Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 2010, Volume: 30, Issue:3

    Topics: Adolescent; Child; Child, Preschool; Citric Acid; Comorbidity; Disease Susceptibility; Female; Follo

2010
Risk factors for urinary stones in healthy schoolchildren with and without a family history of nephrolithiasis.
    Pediatric nephrology (Berlin, Germany), 2013, Volume: 28, Issue:4

    Topics: Biomarkers; Calcium; Chi-Square Distribution; Child; Child, Preschool; Citric Acid; Female; Genetic

2013