Results 221 to 230 of about 2,061,243 (253)
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Acquired autoimmune Bartter syndrome in a patient with primary hypothyroidism

Rheumatology International, 2021
N. Nasir   +5 more
semanticscholar   +1 more source

Prenatal diagnosis of MAGED2 gene mutation causing transient antenatal Bartter syndrome.

European Journal of Medical Genetics, 2021
Satoshi Takemori   +12 more
semanticscholar   +1 more source

BARTTER'S SYNDROME

Klinische Wochenschrift, 1983
GERALD C. TIMMIS   +7 more
  +6 more sources

Bartter’s Syndrome

1982
Bartter’s syndrome was described in 1962 as a condition characterized by hypokalemia and metabolic alkalosis, hyper-reninemia with secondary hyperaldosteronism and normal blood pressure with pressor resistance to angiotensin II and norepinephrine. The histopathology of the kidney included hyperplasia of the juxtaglomerular complex and a number of other
F. C. Bartter, J. A. Rodriguez
openaire   +1 more source

BARTTER SYNDROME IN PREGNANCY

Obstetrics & Gynecology, 2000
J R, Johnson, R S, Miller, P, Samuels
openaire   +2 more sources

Bartter's syndrome

The American Journal of Medicine, 1976
David J. Tomko   +2 more
openaire   +3 more sources

[Bartter syndrome].

La Revue de medecine interne, 1993
Bartter's syndrome, sometimes a familial autosomal recessive condition, is characterized by hypokalaemia with normal kaliuresis, hyperreninaemia with secondary hyperaldosteronism, vascular resistance to angiotensin and overproduction of prostaglandins by the kidneys.
A, de la Blanchardière, F, Duron
openaire   +1 more source

Bartter's syndrome.

Advances in nephrology from the Necker Hospital, 1978
F C, Bartter, J R, Gill, J C, Frolich
  +6 more sources

Bartter Syndrome and Gitelman Syndrome.

The Pediatric clinics of North America, 2019
Rosanna Fulchiero, Patricia W. Seo-Mayer
semanticscholar   +1 more source

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