المؤلفون: Giri K; Resident, Department of Nephrology, Osmania Medical College, Hyderabad, Telangana, India, Corresponding Author., Sahay M; Professor and Head, Department of Nephrology, Osmania Medical College, Hyderabad, Telangana, India., Ismal K; Professor, Department of Nephrology, Osmania Medical College, Hyderabad, Telangana, India., Gowrishankar S; Head of Department, Department of Pathology, Apollo Hospitals, Hyderabad, Telangana, India., Swain M; Consultant, Department of Pathology, Apollo Hospitals, Hyderabad, Telangana, India., Kavadi A; Assistant Professor, Department of Nephrology, Osmania Medical College, Hyderabad, Telangana, India., Rama E; Assistant Professor, Department of Nephrology, Osmania Medical College, Hyderabad, Telangana, India., Manocha A; Pathologist, Department of Pathology, Apollo Hospitals, Hyderabad, Telangana, India.

المصدر: The Journal of the Association of Physicians of India [J Assoc Physicians India] 2024 Sep; Vol. 72 (9), pp. e19-e21.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Association of Physicians of India Country of Publication: India NLM ID: 7505585 Publication Model: Print Cited Medium: Print ISSN: 0004-5772 (Print) Linking ISSN: 00045772 NLM ISO Abbreviation: J Assoc Physicians India Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/diagnosis , Bartter Syndrome*/genetics , Bartter Syndrome*/complications , Acute Kidney Injury*/etiology , Acute Kidney Injury*/diagnosis , Myoglobin*/blood, Humans ; Male ; Child, Preschool

المؤلفون: Dutta P; Department of Applied Mathematics, University of Waterloo, Waterloo, Ontario, Canada., Layton AT; Department of Applied Mathematics, University of Waterloo, Waterloo, Ontario, Canada.; Department of Biology, University of Waterloo, Waterloo, Ontario, Canada.; Cheriton School of Computer Science, University of Waterloo, Waterloo, Ontario, Canada.; School of Pharmacology, University of Waterloo, Waterloo, Ontario, Canada.

المصدر: American journal of physiology. Renal physiology [Am J Physiol Renal Physiol] 2024 Sep 01; Vol. 327 (3), pp. F386-F396. Date of Electronic Publication: 2024 Jul 11.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: American Physiological Society Country of Publication: United States NLM ID: 100901990 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1522-1466 (Electronic) Linking ISSN: 15221466 NLM ISO Abbreviation: Am J Physiol Renal Physiol Subsets: MEDLINE

مواضيع طبية MeSH: Gitelman Syndrome*/metabolism , Gitelman Syndrome*/genetics , Gitelman Syndrome*/physiopathology , Magnesium*/metabolism , Bartter Syndrome*/metabolism , Bartter Syndrome*/genetics, Animals ; Female ; Male ; Calcium/metabolism ; Rats ; Nephrons/metabolism ; Computer Simulation ; Solute Carrier Family 12, Member 3/metabolism ; Solute Carrier Family 12, Member 3/genetics ; Sex Factors ; Models, Biological ; Solute Carrier Family 12, Member 1/metabolism ; Solute Carrier Family 12, Member 1/genetics

المؤلفون: Chen G, Hong P

المصدر: Clinical laboratory [Clin Lab] 2024 Aug 01; Vol. 70 (8).

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Clinical Laboratory Publications Country of Publication: Germany NLM ID: 9705611 Publication Model: Print Cited Medium: Internet ISSN: 1433-6510 (Print) Linking ISSN: 14336510 NLM ISO Abbreviation: Clin Lab Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/genetics , Bartter Syndrome*/diagnosis , Chloride Channels*/genetics , Heterozygote*, Humans ; Mutation ; Adult ; Male ; Female ; Exons/genetics ; DNA Mutational Analysis ; Codon, Nonsense

SCR Disease Name: Bartter syndrome, type 3

المؤلفون: Vergine G; UOC Pediatria, Ospedale Infermi, Rimini, ASL Romagna., Fressola G; Scuola di Specializzazione in Pediatria, Università degli Studi di Ferrara., Ambroni M; Centro Regionale Fibrosi Cistica, Ospedale Bufalini, Cesena, ASL Romagna., Gessaroli M; Scuola di Specializzazione in Pediatria, Università degli Studi di Bologna., Bigucci B; UOC Pediatria, Ospedale Infermi, Rimini, ASL Romagna., Mazzocco M; UOC Pediatria, Ospedale Infermi, Rimini, ASL Romagna., Conte ML; UOC Pediatria, Ospedale Infermi, Rimini, ASL Romagna.

المصدر: Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia [G Ital Nefrol] 2024 Jun 28; Vol. 41 (3). Date of Electronic Publication: 2024 Jun 28.

نوع المنشور: Case Reports; English Abstract; Journal Article

بيانات الدورية: Publisher: Società Italiana di Nefrologia Country of Publication: Italy NLM ID: 9426434 Publication Model: Electronic Cited Medium: Internet ISSN: 1724-5990 (Electronic) Linking ISSN: 03935590 NLM ISO Abbreviation: G Ital Nefrol Subsets: MEDLINE

مواضيع طبية MeSH: Cystic Fibrosis*/complications , Cystic Fibrosis*/genetics , Cystic Fibrosis*/diagnosis , Bartter Syndrome*/complications , Bartter Syndrome*/diagnosis , Bartter Syndrome*/genetics, Humans ; Male ; Female ; Hyponatremia/etiology ; Alkalosis/etiology ; Child, Preschool ; Child

المؤلفون: Jiang L; Department of Endocrinology, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010000, China., Li D; Department of Endocrinology, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010000, China., Guo Q; Department of Endocrinology, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010000, China., Li Y; Department of Endocrinology, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010000, China., Zan L; Department of Endocrinology, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010000, China., Ao R; Department of Endocrinology, Inner Mongolia Autonomous Region People's Hospital, Hohhot 010000, China.

المصدر: Endocrine journal [Endocr J] 2024 May 23; Vol. 71 (5), pp. 537-542. Date of Electronic Publication: 2024 Mar 19.

نوع المنشور: Case Reports; Journal Article; Review

بيانات الدورية: Publisher: Japan Endocrine Society Country of Publication: Japan NLM ID: 9313485 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1348-4540 (Electronic) Linking ISSN: 09188959 NLM ISO Abbreviation: Endocr J Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/genetics , Bartter Syndrome*/diagnosis , Bartter Syndrome*/complications , Chloride Channels*/genetics, Humans ; Male ; Young Adult ; Follow-Up Studies ; Gitelman Syndrome/genetics ; Gitelman Syndrome/diagnosis ; Gitelman Syndrome/complications ; Mutation

SCR Disease Name: Bartter syndrome, type 3

عنوان ترانسليتريتد: 以假性Bartter综合征为主要表现的囊性纤维化患儿3例并文献复习.

المؤلفون: Zhang JY; Department of Respiratory Medicine,Hunan Children's Hospital, Changsha 410001, China., Sun LJ, Duan XJ; Department of Respiratory Medicine,Hunan Children's Hospital, Changsha 410001, China., Zhang ZM, Xiao ZH, Chen YP; Department of Respiratory Medicine,Hunan Children's Hospital, Changsha 410001, China., You JY

المصدر: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics [Zhongguo Dang Dai Er Ke Za Zhi] 2024 May 15; Vol. 26 (5), pp. 506-511.

نوع المنشور: Journal Article; Case Reports; Review; English Abstract

بيانات الدورية: Publisher: Zhongguo dang dai er ke za zhi she Country of Publication: China NLM ID: 100909956 Publication Model: Print Cited Medium: Print ISSN: 1008-8830 (Print) Linking ISSN: 10088830 NLM ISO Abbreviation: Zhongguo Dang Dai Er Ke Za Zhi Subsets: MEDLINE

مواضيع طبية MeSH: Cystic Fibrosis*/genetics , Cystic Fibrosis*/complications , Cystic Fibrosis Transmembrane Conductance Regulator*/genetics , Bartter Syndrome*/genetics , Bartter Syndrome*/diagnosis , Bartter Syndrome*/complications , Mutation*, Humans ; Male ; Female ; Infant ; Child, Preschool ; Child ; Retrospective Studies

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

المصدر: Cells [Cells] 2024 May 10; Vol. 13 (10). Date of Electronic Publication: 2024 May 10.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101600052 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4409 (Electronic) Linking ISSN: 20734409 NLM ISO Abbreviation: Cells Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/metabolism , Bartter Syndrome*/genetics , Solute Carrier Family 12, Member 1*/metabolism , Blood Pressure*, Humans ; Animals ; Endoplasmic Reticulum-Associated Degradation

المؤلفون: Sousa M; Department of Pediatrics, Hospital Divino Espírito Santo, Ponta Delgada, Portugal., Medeiros R; Department of Endocrinology and Nutrition, Hospital Divino Espírito Santo, Ponta Delgada, Portugal., Rodrigues AL; Department of Pediatrics, Hospital Divino Espírito Santo, Ponta Delgada, Portugal., Dias Pereira B; Department of Endocrinology and Nutrition, Hospital Divino Espírito Santo, Ponta Delgada, Portugal.

المصدر: The American journal of case reports [Am J Case Rep] 2024 Jun 17; Vol. 25, pp. e942872. Date of Electronic Publication: 2024 Jun 17.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: International Scientific Information, Inc Country of Publication: United States NLM ID: 101489566 Publication Model: Electronic Cited Medium: Internet ISSN: 1941-5923 (Electronic) Linking ISSN: 19415923 NLM ISO Abbreviation: Am J Case Rep Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/diagnosis , Bartter Syndrome*/genetics, Humans ; Male ; Infant ; Child ; Arginine Vasopressin

المؤلفون: Mohan Lal B; Department of Medicine, All India Institute of Medical Sciences, New Delhi, Delhi, India., Musthafa Hafeesa N; Department of Medicine, All India Institute of Medical Sciences, New Delhi, Delhi, India., Vikram NK; Department of Medicine, All India Institute of Medical Sciences, New Delhi, Delhi, India., Ray A; Department of Medicine, All India Institute of Medical Sciences, New Delhi, Delhi, India doctoranimeshray@gmail.com.

المصدر: BMJ case reports [BMJ Case Rep] 2024 May 03; Vol. 17 (5). Date of Electronic Publication: 2024 May 03.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: BMJ Pub. Group Country of Publication: England NLM ID: 101526291 Publication Model: Electronic Cited Medium: Internet ISSN: 1757-790X (Electronic) Linking ISSN: 1757790X NLM ISO Abbreviation: BMJ Case Rep Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/chemically induced , Bartter Syndrome*/diagnosis , Polymyxin B*/adverse effects , Anti-Bacterial Agents*/adverse effects, Humans ; Male ; Middle Aged

المؤلفون: Kieszek B; Department of Nephrology, Hypertension and Kidney Transplantation, Medical University of Lodz, Central University Hospital, Łódź, Poland, Cichocki P; Department of Nuclear Medicine, Medical University of Lodz, Łódź, Poland, Adamczewski Z; Department of Nephrology, Hypertension and Kidney Transplantation, Medical University of Lodz, Central University Hospital, Łódź, Poland. nefro@wp.pl, Nowicki M; Department of Nephrology, Hypertension and Kidney Transplantation, Medical University of Lodz, Central University Hospital, Łódź, Poland. nefro@wp.pl, Masajtis-Zagajewska A; Department of Nephrology, Hypertension and Kidney Transplantation, Medical University of Lodz, Central University Hospital, Łódź, Poland

المصدر: Polish archives of internal medicine [Pol Arch Intern Med] 2024 Apr 26; Vol. 134 (4). Date of Electronic Publication: 2024 Apr 04.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Medycyna Praktyczna Country of Publication: Poland NLM ID: 101700960 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1897-9483 (Electronic) Linking ISSN: 00323772 NLM ISO Abbreviation: Pol Arch Intern Med Subsets: MEDLINE

مواضيع طبية MeSH: Bartter Syndrome*/therapy , Embolization, Therapeutic*/methods , Renal Artery*/diagnostic imaging, Adult ; Female ; Humans