Recent Publications on Bartter Syndrome: |  |
Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.
Type I Bartter syndrome (BS) is caused by mutations of the Na-K-2Cl...
Direct Link | 3rd October, 2008
| Department of Medicine, Nagaoka Red Cross Hospital, Nagaoka, Japan.
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A cytoplasmic domain mutation in ClC-Kb affects long-distance communication across the membrane.
BACKGROUND: ClC-Kb and ClC-Ka are homologous chloride channels that...
Direct Link | 25th September, 2008
| Department of Molecular and Cellular Physiology and Program in Biophysics,
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Bartter syndrome presenting as poor weight gain and abdominal mass in an infant.
Bartter syndrome, a group of disorders that encompasses multiple genetic...
Direct Link | 19th September, 2008
| Department of Pediatrics, University of South Florida, Tampa General
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Disease-Causing Dysfunctions of Barttin in Bartter Syndrome Type IV.
Bartter syndrome type IV is an inherited human condition characterized by...
Direct Link | 9th September, 2008
| *Institut fur Neurophysiologie, Medizinische Hochschule Hannover, and
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Neonatal pseudo-Bartter syndrome due to maternal eating disorder.
A total of 4 of 153 low birth weight infants at our hospital were found to...
Direct Link | 30th August, 2008
| Department of Perinatal Medicine, Perinatal Medical Center for Mother and
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An improved terminology and classification of Bartter-like syndromes.
This Review outlines a terminology and classification of Bartter-like...
Direct Link | 13th August, 2008
| Center for Pediatric and Adolescent Medicine, Philipps University,
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Comment on: Bartter syndrome and cholelithiasis in an infant: is this a mere coincidence? (Eur J Pediatr 2008;167(1):109-110).
This Review outlines a terminology and classification of Bartter-like...
Direct Link | 2nd August, 2008
| The Institute of Kidney Disease, Department of Pediatrics, Severance
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Gitelman syndrome.
Gitelman syndrome (GS), also referred to as familial...
Direct Link | 1st August, 2008
| Department of Human Genetics, Radboud University Nijmegen Medical Centre,
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Reply to correspondence letter by Jae Il Shin and Jae Seung Lee: Bartter syndrome and cholelithiasis in an infant: is this a mere coincidence?
Gitelman syndrome (GS), also referred to as familial...
Direct Link | 29th July, 2008
| Department of Pediatrics, Nephrology Division, Hopital Ste-Justine, 3175
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Functional and structural characterization of PKA-mediated pH(i) gating of ROMK1 channels.
Hyperprostaglandin E syndrome/antenatal Bartter syndrome (HPS/aBS) is a...
Direct Link | 16th July, 2008
| Department of Pharmacology, College of Medicine, National Taiwan
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Female ROMK null mice manifest more severe Bartter II phenotype on renal function and higher PGE2 production.
ROMK null mice with a high survival rate and varying severity of...
Direct Link | 27th June, 2008
| Dept. of Cellular and Molecular Physiology, Yale Univ. School of Medicine,
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Severe failure to thrive in infant.
Failure to thrive in an infant has multiple etiologies and at times, is...
Direct Link | 10th June, 2008
| Department of Pediatrics, Division of Critical Care, Lincoln Medical and
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Salt wasting and blood pressure.
Renal stone disease (nephrolithiasis) affects 3-5% of the population and...
Direct Link | 23rd May, 2008
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Genetic causes of hypercalciuric nephrolithiasis.
Renal stone disease (nephrolithiasis) affects 3-5% of the population and...
Direct Link | 1st May, 2008
| Academic Endocrine Unit, Nuffield Department of Clinical Medicine, Oxford
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