Results 111 to 120 of about 1,035 (181)

Hereditary kidney disease with auditory abnormalities: analysis of mutations and clinical phenotypes. [PDF]

BMC Med Genomics
Bi J, Guo W, Ji P, Xie Y.
europepmc   +1 more source

Licorice-Induced Pseudohyperaldosteronism Highlights an Underestimated Etiology of Hypertension. [PDF]

Kidney Int Rep
Bendjilali-Sabiani JJ, Cardinale A, Lamy A, Pouget AM, Boyer JC, Taillard V, Reboul P.   +6 more
europepmc   +1 more source

Refractory hypokalaemia and hypertension in pregnancy in a woman with renal artery stenosis. [PDF]

Obstet Med
Phillips J, Iftikhar I, Sunanda G, Jeffs L.   +3 more
europepmc   +1 more source

The Diagnostic Challenge of Potassium-Wasting and Hypertension in Pregnancy: Lessons from a Geller Syndrome Workup. [PDF]

Case Rep Nephrol Dial
Tse JD, Lin R, Wang J.
europepmc   +1 more source

Familial <i>WT1</i>-associated nephropathy - 46, XY Frasier syndrome and 46, XX steroid-resistant nephrotic syndrome in female siblings: A case report and review of literature. [PDF]

World J Nephrol
Khandelwal MH, Piparva KG, Parchwani D.
europepmc   +1 more source

Ticking Down Sodium Levels-An Atypical Link Between Chronic Hyponatremia and Borreliosis. [PDF]

Biology (Basel)
Vlad RM, Vasile C, Mirică A.
europepmc   +1 more source

Two mutations in the thiazide-sensitive NaCl co-transporter gene in a Romanian Gitelman syndrome patient: case report [PDF]

Adelina Mihaescu, Cristina Gug, Ioana Mozos   +2 more
core   +2 more sources

Tetanie und Hypoparathyreodismus, Pseudohypoparathyreodismus [PDF]

, 1979
Scriba, Peter Christian
core  

Clinical characteristics and genetic mutations of 10 Chinese children with cystic fibrosis or cystic frbrosis transmembrane conductance regulator-related disorders. [PDF]

Chin Med J (Engl)
Tan S, Cao L.
europepmc   +1 more source

Glosarium Kedokteran [PDF]

, 2005
Hardaniwati, Menuk, Latief, A., Wonodirekso, Sugito   +2 more
core