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ALLMedicine™ Bartter Syndrome Center

Research & Reviews  245 results

Type-5 Bartter syndrome presenting with metabolic seizure in adulthood.
https://doi.org/10.1136/bcr-2020-235349
BMJ Case Reports; Hussain A, Atlani M et. al.

Feb 18th, 2021 - Bartter syndrome is a very rare and heterogeneous disease with variable age of onset and symptom severity. Genotypically they have inherited disorders of the thick ascending limb in the renal tubular system, which manifest phenotypically as electr...

Diagnosis and management of Bartter syndrome: executive summary of the consensus and re...
https://doi.org/10.1016/j.kint.2020.10.035
Kidney International; Konrad M, Nijenhuis T et. al.

Jan 29th, 2021 - Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hypokalemic and hypochloremic metabolic alkalosis and low to normal blood pressure. The primary pathogenic mechanism is defe...

Prenatal biochemical diagnosis of two forms of congenital diarrheal disorders (congenit...
https://doi.org/10.1002/pd.5878
Prenatal Diagnosis REFERENCES; Macraigne L, Allaf B et. al.

Dec 22nd, 2020 - Congenital diarrheal disorders (CDDs) are a group of rare diseases among which some present as inherited disorders of intestinal electrolyte transportation: congenital chloride diarrhea (CCD) and congenital sodium diarrhea (CSD) with prenatal mani...

A highly unusual case of osmotic demyelination syndrome and extrapontine myelinolysis i...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645388
The Journal of International Medical Research; Gargano G, Manfredi M et. al.

Oct 27th, 2020 - Bartter syndrome (BS) is a rare autosomal recessive renal tubular disorder characterized by acute electrolyte imbalance, and similarly, osmotic demyelination syndrome (ODS) is a rather rare complication occurring during electrolyte imbalance. The ...

Late-Onset Bartter Syndrome Type II Due to a Homozygous Mutation in KCNJ1 Gene: A Case ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534490
The American Journal of Case Reports; Elfert KA, Geller DS et. al.

Sep 30th, 2020 - BACKGROUND Bartter syndrome is a rare genetic disease characterized by hypokalemia, metabolic alkalosis, and hyperreninemic hyperaldosteronism. Five different subtypes have been described based on the genetic defect identified. Bartter syndrome ty...

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Guidelines  1 results

Diagnosis and management of Bartter syndrome: executive summary of the consensus and re...
https://doi.org/10.1016/j.kint.2020.10.035
Kidney International; Konrad M, Nijenhuis T et. al.

Jan 29th, 2021 - Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hypokalemic and hypochloremic metabolic alkalosis and low to normal blood pressure. The primary pathogenic mechanism is defe...

see more →

Clinicaltrials.gov  247 results

Type-5 Bartter syndrome presenting with metabolic seizure in adulthood.
https://doi.org/10.1136/bcr-2020-235349
BMJ Case Reports; Hussain A, Atlani M et. al.

Feb 18th, 2021 - Bartter syndrome is a very rare and heterogeneous disease with variable age of onset and symptom severity. Genotypically they have inherited disorders of the thick ascending limb in the renal tubular system, which manifest phenotypically as electr...

Diagnosis and management of Bartter syndrome: executive summary of the consensus and re...
https://doi.org/10.1016/j.kint.2020.10.035
Kidney International; Konrad M, Nijenhuis T et. al.

Jan 29th, 2021 - Bartter syndrome is a rare inherited salt-losing renal tubular disorder characterized by secondary hyperaldosteronism with hypokalemic and hypochloremic metabolic alkalosis and low to normal blood pressure. The primary pathogenic mechanism is defe...

Prenatal biochemical diagnosis of two forms of congenital diarrheal disorders (congenit...
https://doi.org/10.1002/pd.5878
Prenatal Diagnosis REFERENCES; Macraigne L, Allaf B et. al.

Dec 22nd, 2020 - Congenital diarrheal disorders (CDDs) are a group of rare diseases among which some present as inherited disorders of intestinal electrolyte transportation: congenital chloride diarrhea (CCD) and congenital sodium diarrhea (CSD) with prenatal mani...

A highly unusual case of osmotic demyelination syndrome and extrapontine myelinolysis i...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645388
The Journal of International Medical Research; Gargano G, Manfredi M et. al.

Oct 27th, 2020 - Bartter syndrome (BS) is a rare autosomal recessive renal tubular disorder characterized by acute electrolyte imbalance, and similarly, osmotic demyelination syndrome (ODS) is a rather rare complication occurring during electrolyte imbalance. The ...

Late-Onset Bartter Syndrome Type II Due to a Homozygous Mutation in KCNJ1 Gene: A Case ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7534490
The American Journal of Case Reports; Elfert KA, Geller DS et. al.

Sep 30th, 2020 - BACKGROUND Bartter syndrome is a rare genetic disease characterized by hypokalemia, metabolic alkalosis, and hyperreninemic hyperaldosteronism. Five different subtypes have been described based on the genetic defect identified. Bartter syndrome ty...

see more →

News  1 results

Are Medical Blogs Important? Survey Says…
https://www.medscape.com/viewarticle/702514

May 11th, 2009 - In a nondescript hospital somewhere, an attending physician -- bald, not quite as spry as he once was -- sits down at a computer and does something that he could not have imagined 35 years ago in medical school. He pulls up PubMed or eMedicine, or...

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