Results 91 to 100 of about 1,864 (192)

Hypouricemia [PDF]

Arthritis & Rheumatism, 1975
openaire   +2 more sources

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2

, 2011
Background: Elevated serum uric acid (UA) is associated with gout, hypertension, cardiovascular and renal disease. Hereditary renal hypouricemia type 1 (RHUC1) is caused by mutations in the renal tubular UA transporter URAT1 and can be complicated by ...
Sawyer, Lindsay, Wright, Alan F, S. Campbell, L. Sawyer, E. J. Holtzman, Shu, Xinhua, A. F. Wright, H. Shalev, D. Landau, X. Shu, A. J. S. Knox, D. Dinour, Campbell, Susan, B.-A. Sela, Sela, Ben-Ami, Landau, Daniel, Shalev, Hanna, Gray, Nicola K, N. K. Gray, Valsamidou, Evgenia, Holtzman, Eliezer J, Gannon, Liat, Knox, Andrew J. S., E. Valsamidou, L. Ganon, Dinour, Dganit   +25 more
core   +1 more source

Hypouricemia and nephroprotection of Coix lacryma-jobi L. seed extract [PDF]

Songklanakarin Journal of Science and Technology (SJST), 2015
The Coix lacryma-jobi L. or Adlay seed has been used as a healthy food and herb in many Asian countries. A previous in vitro study found that it has an inhibitory effect on xanthine oxidase (XOD) activity but its use as a traditional medicine in the ...
Ormjai Taejarernwiriyakul, Naohiko Anzai, Promsuk Jutabha, Wantika Kruanamkam, Suparat Chanluang   +4 more
doaj  

URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews

, 2010
Background. Hereditary renal hypouricemia may be complicated by nephrolithiasis or exercise-induced acute renal failure. Most patients described so far are of Japanese origin and carry the truncating mutation W258X in the uric acid transporter URAT1 ...
G. Burckhardt, Sela, Ben-Ami, Burckhardt, Gerhard, Ganon, Liat, Ron, Rotem, E. J. Holtzman, R. Ron, R. Rachamimov, Knecht, Aaron, A. Bahn, Bahn, Andrew, D. Dinour, A. Knecht, O. Geifman-Holtzman, B.-A. Sela, Holtzman, Eliezer J., U. Gafter, Rachamimov, Ruth, L. Ganon, Gafter, Uzi, Geifman-Holtzman, Ossie, Dinour, Dganit   +21 more
core   +1 more source

Hypouricemia in a patient with metabolic syndrome

Nefrología (English Edition), 2023
Ana Noelia Hernández González, María Teresa Valda de Miguel, Pedro Pablo Ortuño López, José Luis Albero Dolón, Víctor Martínez Jiménez, Juan Bernardo Cabezuelo Romero   +5 more
openaire   +4 more sources

Purine disorders with hypouricemia.

Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki), 2016
Hypouricemia is defined as a serum urate levels less than 2 mg/dL (119 µmol/L). Primary hypouricemia is caused by disorders of purine metabolism and transport. This laboratory finding is sometimes overlooked and, following two genetic defects, should be considered in differential diagnosis of unexplained hypouricemia.
Ivan, Sebesta, Blanka, Stiburkova
openaire   +1 more source

Evaluation of the proximal tubular function in individuals with primary renal hypouricemia: an NMR-based metabonomic study

, 2009
Primary renal hypouricemia (PRH) refers to a rare condition of increased renal urate clearance, caused by an isolated inborn error of membrane transport of urate in the renal proximal tubule.
Elisaf, M. S., Psychogios, N. G., Kostara, C. E., Bairaktari, E. T., Tzovaras, V. T.   +4 more
core  

Urinary amino acids patterns enlighten new predictive models for extensive renal proximal tubular injuries and kidney function. [PDF]

J Transl Int Med
Shi X, Dong Y, Luo W, Hou Z, Xia P, Ye W, Qiu L, Chen L.   +7 more
europepmc   +1 more source

Genetic Insights into Persistent Hypouricemia in Adults: Novel Findings from an Adult Nephrogenetic Clinic. [PDF]

Kidney Dis (Basel)
Dirim AB, Suer I, Kalaycı T, Tahillioglu Y, Safak S, Ucar AR, Mirioglu S, Artan AS, Oto OA, Altınkaynak M, Ozturk S, Senturk L, Turkmen A, Yildiz A, Cefle K, Yazici H, Ozturk S.   +16 more
europepmc   +1 more source

Addison's Disease Mimicking Cerebral Salt Wasting Syndrome: A Case of Severe Hyponatremia. [PDF]

Cureus
Anandan S, Rajendran S, Joy J, Suresh A, Pushpaletha CS.   +4 more
europepmc   +1 more source