Works matching DE "BARTTER syndrome"
Results: 202
ACE2 and prognosis of COVID‐19: Insights from Bartter's and Gitelman's syndromes patients.
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- Journal of Medical Virology, 2020, v. 92, n. 11, p. 2308, doi. 10.1002/jmv.25978
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- Article
Effective medical treatment strategies to help cessation of purging behaviors.
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- International Journal of Eating Disorders, 2016, v. 49, n. 3, p. 324, doi. 10.1002/eat.22500
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- Article
What the emergency department needs to know when caring for your patients with eating disorders.
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- International Journal of Eating Disorders, 2012, v. 45, n. 8, p. 977, doi. 10.1002/eat.22035
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- Article
Early diagnosis of pseudo-Bartter syndrome in a hot climate region. Importance of suspecting the possibility of this diagnosis.
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- Paediatria Croatica, 2014, v. 58, n. 2, p. 155, doi. 10.13112/pc.636
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- Article
Medical Complications of Self-Induced Vomiting.
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- Eating Disorders, 2013, v. 21, n. 4, p. 287, doi. 10.1080/10640266.2013.797317
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- Article
Successful “Detoxing” From Commonly Utilized Modes of Purging in Bulimia Nervosa.
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- Eating Disorders, 2012, v. 20, n. 4, p. 312, doi. 10.1080/10640266.2012.689213
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- Article
Antenatal Bartter Syndrome: A Review.
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- International Journal of Pediatrics, 2012, p. 1, doi. 10.1155/2012/857136
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- Article
Pediatric Nephrology: Highlights for the General Practitioner.
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- International Journal of Pediatrics, 2012, p. 1, doi. 10.1155/2012/270725
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- Article
Standardized, systemic phenotypic analysis of Slc12a1<sup>I299F</sup> mutant mice.
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- Journal of Biomedical Science, 2014, v. 21, n. 1, p. 1, doi. 10.1186/s12929-014-0068-0
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- Article
Hypomagnesemia: An Evidence-Based Approach to Clinical Cases.
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- Iranian Journal of Kidney Diseases, 2010, v. 4, n. 1, p. 13
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- Article
NKCC2 activity is inhibited by the Bartter's syndrome type 5 gain-of-function CaR-A843E mutant in renal cells.
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- Biology of the Cell (Wiley-Blackwell), 2015, v. 107, n. 4, p. 98, doi. 10.1111/boc.201400069
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- Article
P149: Neonatal Variant of Bartter's Syndrome and Deafness.
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- 2006
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- Abstract
A missense mutation in solute carrier family 12, member 1 (SLC12A1) causes hydrallantois in Japanese Black cattle.
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- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3035-1
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- Article
Different roles of the RAAS affect bone metabolism in patients with primary aldosteronism, Gitelman syndrome and Bartter syndrome.
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- BMC Endocrine Disorders, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12902-022-00955-2
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- Article
Inherited Renal Diseases.
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- Current Pediatric Reviews, 2014, v. 10, n. 2, p. 95
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- Article
Bartter-like syndrome in patients with molecular defects of the insulin receptor gene.
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- 2014
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- Publication type:
- Letter
Molecular Genetics of Bartter Syndrome.
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- Journal of Pediatric Nephrology, 2014, v. 2, n. 1, p. 6
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- Article
A unique finding of normal aldosterone level in Bartter's syndrome.
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- Journal of Nephropathology, 2017, v. 6, n. 4, p. 359, doi. 10.15171/jnp.2017.59
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- Article
Genetic heterogeneity in patients with Bartter syndrome type 1.
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- Molecular Medicine Reports, 2017, v. 15, n. 2, p. 581, doi. 10.3892/mmr.2016.6063
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- Article
Gitelman Syndrome in a Case of Diabetic Kidney Disease: A Diagnostic and Therapeutic Dilemma.
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- Journal of Clinical & Diagnostic Research, 2018, v. 12, n. 1, p. 19, doi. 10.7860/JCDR/2018/29991.11121
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- Article
A Case of Bartter's Syndrome Presenting in Adulthood.
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- 2020
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- journal article
Association of Mucopolysaccharidosis Type 4A and Bartter Syndrome.
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- 2019
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- Publication type:
- journal article
Nephropathic Cystinosis Mimicking Bartter Syndrome: a Novel Mutation.
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- 2018
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- journal article
SÍNDROME DE BARTTER.
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- Acta Médica Portuguesa, 2011, v. 24, n. S3, p. 671
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- Article
Successful Rifampin Administration After Rifabutin-Induced Leukopenia.
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- 2020
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- Publication type:
- Letter
Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis.
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- 2019
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- Publication type:
- journal article
BARTTER SYNDROME MIMICKING HYPOPITUITARISM.
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- 2013
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- Publication type:
- Case Study
Does hypokalaemia cause nephropathy? an observational study of renal function in patients with Bartter or Gitelman syndrome.
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- QJM: An International Journal of Medicine, 2011, v. 104, n. 11, p. 939, doi. 10.1093/qjmed/hcr095
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- Article
Bartter syndrome presenting as poor weight gain and dehydration in an infant.
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- 2012
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- Publication type:
- Case Study
Pseudo-Bartter as an initial presentation of cystic fibrosis. A case report and review of the literature.
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- 2010
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- Publication type:
- Case Study
Colistin-induced Bartter-like Syndrome: Ponder before Treatment!
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- Indian Journal of Critical Care Medicine, 2022, v. 26, n. 2, p. 239, doi. 10.5005/jp-journals-10071-24117
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- Article
Acquired Bartter-like Syndrome Presenting with Polyuria and Reversible Hypokalemia Associated with Colistin Use in a Critically Ill Pediatric Patient.
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- Indian Journal of Critical Care Medicine, 2021, v. 25, n. 7, p. 822
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- Publication type:
- Article
Colistin-induced Acquired Bartter-like Syndrome: A Rare Cause of Difficult Weaning.
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- Indian Journal of Critical Care Medicine, 2020, v. 24, n. 8, p. 739, doi. 10.5005/jp-journals-10071-23551
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- Publication type:
- Article
Renal outer medullary potassium channel knockout models reveal thick ascending limb function and dysfunction.
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- Clinical & Experimental Nephrology, 2012, v. 16, n. 1, p. 49, doi. 10.1007/s10157-011-0495-0
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- Article
A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH) vitamin D levels.
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- Clinical & Experimental Nephrology, 2011, v. 15, n. 4, p. 572, doi. 10.1007/s10157-011-0431-3
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- Article
Hereditary renal tubular disorders in Turkey: demographic, clinical, and laboratory features.
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- Clinical & Experimental Nephrology, 2011, v. 15, n. 1, p. 108, doi. 10.1007/s10157-010-0367-z
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- Article
A patient with Bartter syndrome accompanying severe growth hormone deficiency and focal segmental glomerulosclerosis.
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- Clinical & Experimental Nephrology, 2010, v. 14, n. 3, p. 278, doi. 10.1007/s10157-009-0262-7
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- Article
CLCNKB mutations causing mild Bartter syndrome profoundly alter the pH and Ca dependence of ClC-Kb channels.
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- Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 9, p. 1713, doi. 10.1007/s00424-013-1401-2
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- Article
Physiology and pathophysiology of SLC12A1/2 transporters.
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- Pflügers Archiv: European Journal of Physiology, 2014, v. 466, n. 1, p. 91, doi. 10.1007/s00424-013-1370-5
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- Article
Paradoxical hypertension and salt wasting in Type II Bartter syndrome.
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- Nephrology Dialysis Transplantation, 2012, v. 5, n. 3, p. 217
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- Article
Genetic basis of Bartter syndrome in Korea.
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- Nephrology Dialysis Transplantation, 2012, v. 27, n. 4, p. 1516, doi. 10.1093/ndt/gfr475
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- Article
Long-term follow-up of patients with Bartter syndrome type I and II.
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- Nephrology Dialysis Transplantation, 2010, v. 25, n. 9, p. 2976, doi. 10.1093/ndt/gfq119
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- Article
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
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- Nephrology Dialysis Transplantation, 2009, v. 24, n. 5, p. 1455, doi. 10.1093/ndt/gfn689
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- Article
Basic science in hypertension or diabetes.
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- 2007
- Publication type:
- Abstract
Unusual Complication of Multidrug Resistant Tuberculosis.
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- 2017
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- Publication type:
- Case Study
Bartter sendromlu hastada anestezi yaklaşımı: Olgu sunumu.
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- Dicle Medical Journal / Dicle Tip Dergisi, 2012, v. 39, n. 3, p. 449, doi. 10.5798/diclemedj.0921.2012.03.0179
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- Article
Neonatal Bartter Syndrome.
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- Journal of Nepal Paediatric Society, 2016, v. 36, n. 2, p. 204, doi. 10.3126/jnps.v36i2.14818
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- Article
Rare Variant of Bartter Syndrome with Sensorineural Deafness.
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- 2015
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- Publication type:
- Case Study
Case of Pseudo-Bartter's Syndrome: An atypical presentation of cystic fibrosis.
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- 2011
- By:
- Publication type:
- Case Study
Correction: Alkalosis in Critically Ill Patients with Severe Sepsis and Septic Shock.
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- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0175530
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- Publication type:
- Article