‘Cystinuria Support’ – a new dedicated forum for patients with the rare disease cystinuria

‘Cystinuria Support’ – a new dedicated forum for patients with the rare disease cystinuria

Bibliographic Details
Main Authors:	M. Bultitude, K Thomas
Format:	Article
Language:	English
Published:	Elsevier 2020-07-01
Series:	European Urology Open Science
Online Access:	http://www.sciencedirect.com/science/article/pii/S2666168320330585

Similar Items

Defining the inheritance of cystinuria: Is it always autosomal recessive?
by: G. Zhou, et al.
Published: (2020-07-01)

Metabolic consequences of cystinuria
by: Lauren E. Woodard, et al.
Published: (2019-06-01)

Cystinuria in association with cataract
by: Prabhakar Singh, et al.
Published: (2020-01-01)

Recurrent nephrolithiasis: Cystinuria
by: Lalić Tijana, et al.
Published: (2016-01-01)

Cystinuria: an inborn cause of urolithiasis
by: Eggermann Thomas, et al.
Published: (2012-04-01)

CASE REPORT OF A PATIENT WITH CYSTINURIA
by: Matej Kemperle, et al.
Published: (2020-04-01)

Pediatric Cystinuria Patient With Novel Mutation in
by: Yoshitaka Watanabe MD, PhD, et al.
Published: (2019-07-01)

The diagnosis, genetics and management of patients with cystinuria
by: Wong, Kathie
Published: (2018)

Molecular genetic studies on cystinuria
by: Harnevik, Lotta
Published: (2007)

Digenic Inheritance in Cystinuria Mouse Model.
by: Meritxell Espino, et al.
Published: (2015-01-01)

Cystinuria : an investigation of suggested psychological complications
by: Dobrinski, Morris J
Published: (1973)

Genetic analysis and in vitro models of cystinuria
by: Rhodes, Hannah Lucinda
Published: (2015)

CYSTINURIA - A TEN-YEAR FOLLOW-UP OF THE PATIENTS
by: Anđelka Slavković, et al.
Published: (2001-09-01)

The impact of surgical intervention on renal function in cystinuria
by: Serra Sürmeli Döven, et al.
Published: (2018-06-01)

The effect of selenium supplementation on cystine crystal volume in patients with cystinuria
by: Mohammadi Mehrdad, et al.
Published: (2018-12-01)

Oxidative folding and early traffic of the human cystinuria transporter
by: Rius Radrigales, Mònica
Published: (2014)

Persistent Leukocyturia Was a Clue to Diagnosis of Cystinuria in a Female Patient
by: Yoshifusa Abe MD, PhD, et al.
Published: (2014-10-01)

A Novel Variant in Iranian Patient with Cystinuria: A Case Report
by: Ali Mardi, et al.
Published: (2021-09-01)

PATIENT SATISFACTION AND DIETARY OUTCOMES FROM ATTENDING A MULTIDISCIPLINARY CYSTINURIA CLINIC
by: Angela Doherty, et al.
Published: (2012-06-01)

Associating mutations causing cystinuria with disease severity with the aim of providing precision medicine
by: Henry J. Martell, et al.
Published: (2017-08-01)

Clinical profile of a Polish cohort of children and young adults with cystinuria
by: Marcin Tkaczyk, et al.
Published: (2021-01-01)

Ultrasonic lithotripter to eliminate cystinuria related protein-rich renal stone
by: Chin-Wei Kuo, et al.
Published: (2016-06-01)

Diversity of Phenotype and Genetic Etiology of 23 Cystinuria Saudi Patients: A Retrospective Study
by: Malak Alghamdi, et al.
Published: (2020-11-01)

Cystinuria Associated with Different SLC7A9 Gene Variants in the Cat.
by: Keijiro Mizukami, et al.
Published: (2016-01-01)

A Case of Hypotonia-Cystinuria Syndrome With Genito-Urinary Malformations and Extrarenal Involvement
by: Francesca Taroni, et al.
Published: (2019-04-01)

A translational approach to investigate the role of membrane transport proteins in the renal stone disease, cystinuria
by: Rice, Sarah Jayne
Published: (2016)

Successful pre-emptive kidney transplantation in a cystinuria patient with nephrolithiasis-related end-stage renal disease
by: Masatoshi Matsunami, et al.
Published: (2019-07-01)

Cystinuria in Dogs and Cats: What Do We Know after Almost 200 Years?
by: Simona Kovaříková, et al.
Published: (2021-08-01)

Five Novel Mutations in Cystinuria Genes SLC3A1 and SLC7A9
by: Popovska-Jankovic K, et al.
Published: (2009-01-01)

Characterization of the SLC3A1 (D2H) gene and mutation analysis of cystinuria patients in Québec
by: Saadi, Irfan.
Published: (1997)

Tiopronin and/or NSAID? A Case of Nephrotic Syndrome and Acute Interstitial Nephritis in a Young Woman with Cystinuria.
by: Luka Vidović, et al.
Published: (2021-01-01)

An animal model of type A cystinuria due to spontaneous mutation in 129S2/SvPasCrl mice.
by: Marine Livrozet, et al.
Published: (2014-01-01)

Report of SLC3A1/rBAT gene mutations in Iranian cystinuria patients: A direct sequencing study
by: Samaneh Markazi, et al.
Published: (2017-01-01)

No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria
by: Kathrin Olschok, et al.
Published: (2018-10-01)

S-Methyl-L-Ergothioneine to L-Ergothioneine Ratio in Urine Is a Marker of Cystine Lithiasis in a Cystinuria Mouse Model
by: Miguel López de Heredia, et al.
Published: (2021-09-01)

Efficacy of transurethral cystolithotripsy assisted by percutaneous evacuation and the benefit of genetic analysis in a pediatric cystinuria patient with a large bladder stone
by: Tomoki Okada, et al.
Published: (2021-01-01)

Cystinuria in a 13-month-old girl with absence of mutations in the SLC3A1 and SLC7A9 Genes
by: S Krishnamurthy, et al.
Published: (2018-01-01)

Cystinuria in a 13-Month-Old girl with absence of mutations in the SLC3A1 and SLC7A9 genes
by: M D Al-Mendalawi
Published: (2018-01-01)

Detection of Mutation in Exons 3 and 8 of SLC3A1 and Exons 4 and 10 of SLC7A9 Genes in Patients with Cystinuria in Iran
by: Leila Koulivand, et al.
Published: (2014-09-01)

Forum, Dedicated to Inclusive Education
by: Vachkov I.V.
Published: (2015-06-01)