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Acquired autoimmune Bartter syndrome in a patient with primary hypothyroidism
Rheumatology International, 2021N. Nasir +5 more
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Prenatal diagnosis of MAGED2 gene mutation causing transient antenatal Bartter syndrome.
European Journal of Medical Genetics, 2021Satoshi Takemori +12 more
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Cystic Fibrosis Presenting as Pseudo-Bartter Syndrome: An Important Diagnosis that is Missed!
Indian Journal of Pediatrics, 2020M. Mantoo, M. Kabra, S. K. Kabra
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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
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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
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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
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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
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Advances in nephrology from the Necker Hospital, 1978
F C, Bartter, J R, Gill, J C, Frolich
+6 more sources
F C, Bartter, J R, Gill, J C, Frolich
+6 more sources
Bartter Syndrome and Gitelman Syndrome.
The Pediatric clinics of North America, 2019Rosanna Fulchiero, Patricia W. Seo-Mayer
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