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Bartter Syndrome Presenting as Arginine-Vasopressin Resistance: A Report of 2 Cases.

• Authors : Sousa M; Department of Pediatrics, Hospital Divino Espírito Santo, Ponta Delgada, Portugal.; Medeiros R

Subjects: Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/diagnosis ; Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/genetics; Humans

• Source: The American journal of case reports [Am J Case Rep] 2024 Jun 17; Vol. 25, pp. e942872. Date of Electronic Publication: 2024 Jun 17.Publisher: International Scientific Information, Inc Country of Publication: United States NLM ID: 101489566 Publication Model: Electronic Cited Medium:

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Protein Quality Control of NKCC2 in Bartter Syndrome and Blood Pressure Regulation.

• Authors : Laghmani K; Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université de Paris, F-75006 Paris, France.; CNRS, ERL8228, F-75006 Paris, France.

Subjects: Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/metabolism ; Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/genetics ; Solute Carrier Family 12, Member 1*/Solute Carrier Family 12, Member 1*/Solute Carrier Family 12, Member 1*/metabolism

• Source: Cells [Cells] 2024 May 10; Vol. 13 (10). Date of Electronic Publication: 2024 May 10.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409

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Expert Consensus for the Diagnosis and Treatment of Bartter Syndrome in China(2023)

• Authors : Chinese Society of Rare Diseases; Rare Diseases Society of Chinese Research Hospital Association; China Alliance for Rare Diseases

Subjects: bartter syndrome; diagnosis; treatment

• Source: 罕见病研究, Vol 3, Iss 1, Pp 87-101 (2024)

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Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome.

• Authors : Yan X; Reproductive Medicine Center, Renmin Hospital, Hubei University of Medicine, Shiyan, 442000, China.; Biomedical Engineering College, Hubei University of Medicine, Shiyan, 442000, China.

Subjects: Bartter Syndrome*/Bartter Syndrome*/Bartter Syndrome*/genetics; Humans ; Female

• Source: BMC medical genomics [BMC Med Genomics] 2024 Jan 18; Vol. 17 (1), pp. 23. Date of Electronic Publication: 2024 Jan 18.Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794

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Functional analysis of compound heterozygous variations in the CLCNKB gene in a patient with Bartter syndrome type Ⅲ

• Authors : Yu-wen Cai; Xue-qin Cheng; Ruo-chen Che

Subjects: iii bartter syndrome; clcnkb gene; genotype

• Source: Linchuang shenzangbing zazhi, Vol 24, Iss 5, Pp 385-392 (2024)

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Adult classic Bartter syndrome: a case report with 5-year follow-up and literature review

• Authors : Le Jiang; Dongmei Li; Qiansha Guo

Subjects: hypokalemia; bartter syndrome type 3; adult-onset

• Source: Endocrine Journal, Vol 71, Iss 5, Pp 537-542 (2024)

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A Case of Childhood-Onset Bartter Syndrome Type 1 with Renal Dysfunction

• Authors : PENG Xiaoyan; CHEN Chaoying; YANG Hongxian

Subjects: bartter syndrome type 1; antenatal bartter syndrome; renal dysfunction

• Source: 罕见病研究, Vol 3, Iss 1, Pp 124-130 (2024)

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A Rare Diagnosis in A Pediatric Case Without Metabolic Alkalosis; Bartter Syndrome

• Authors : Demet Tosun; Sebahat Tülpar; Rümeysa Yasemin Çiçek

Subjects: bartter syndrome; hypokalemia; metabolic alkalosis

• Source: Bagcilar Medical Bulletin, Vol 9, Iss 1, Pp 71-73 (2024)

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Nephrogenic Diabetes Insipidus or Bartter Syndrome? A Dilemma of Refractory Hypokalemia in Pregnancy: A Case Report from Soedono Regional Public Hospital in Madiun.

• Authors : Aditya, Bayu¹ ; Wardhana, Manggala Pasca^2,3; Islamy, Tauhid⁴

• Source: Pharmacognosy Journal. Mar/Apr2024, Vol. 16 Issue 2, p495-497. 3p.

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Identification of a novel intronic mutation of MAGED2 gene in a Chinese family with antenatal Bartter syndrome

• Authors : Xu Yan; Yueyue Hu; Xin Zhang

Subjects: Antenatal Bartter syndrome; Whole exome sequencing; MAGED2

• Source: BMC Medical Genomics, Vol 17, Iss 1, Pp 1-6 (2024)

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