Results 131 to 140 of about 10,151 (205)

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN16/CLDN19 mutations in four Chinese families. [PDF]

Sci Rep
Wang C, Ding J, Yang H, Huang L, Wang X.
europepmc   +1 more source

A newborn with type 1 Bartter syndrome: challenges in the treatment and development during 30 months follow-up-a case report. [PDF]

Front Pediatr
Czubilińska-Łada J, Szymańska A, Sienko A, Badeński A, Behrendt J, Szczepanska M.   +5 more
europepmc   +1 more source

Distal Renal Tubular Acidosis as a Renal Manifestation of Sjögren's Syndrome: A Case Report. [PDF]

Cureus
Sharma S, Khalid A, Herrera GA, Al Jaber E.   +3 more
europepmc   +1 more source

Hypercalciuria in Sanjad-Sakati Syndrome: A Retrospective Evaluation of Kidney Involvement Indicators. [PDF]

Cureus
Tresa V, Zeb Shaikh S, Mehmood S, Al-Omairi A, Fatima K, Al Nabhani DA, Al Yaarubi S.   +6 more
europepmc   +1 more source

Prioritising genetic testing for kidney stone disease in adults using a clinical scoring system. [PDF]

Clin Kidney J
Maffei Faccioli F, Cozzolino MG, Moochhala SH.   +2 more
europepmc   +1 more source

Long-term survival and phenotypic expansion in siblings with generalized arterial calcification of infancy. [PDF]

JCEM Case Rep
Resnick O, Ashraf A.
europepmc   +1 more source

Nephrocalcinosis

, 2008
Laughlin Dawes, Kieran Kusel, Daniel Bell   +2 more
openaire   +1 more source

Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis in a 7-Year-Old Girl: A Case Report. [PDF]

Clin Case Rep
Tonny RT, Mumu FA, Sharmim S, Huque SS.
europepmc   +1 more source

Nephrocalcinosis

, 2016
  +5 more sources

Hyperoxaluria by the AGXT gene: a case report. [PDF]

J Med Case Rep
Naghettini AV, Mesquita AL, Santos AN, Moreira JVP, de Oliveira MCM, Fortes PM.   +5 more
europepmc   +1 more source