bartter szindróma - dofaq.co
Long-read sequencing reveals new details of Bartter syndrome type 3
News-Medical.Net - 23 Aug 2023
Long-read sequencing reveals new details of Bartter syndrome type 3 ...
MAGED2 mutations in transient antenatal Bartter syndrome
Nature - 16 May 2016
MAGED2 mutations in transient antenatal Bartter syndrome ...
Bartter syndrome-like phenotype in a patient with diabetes: a case report
springermedizin.de - 26 May 2019
Bartter syndrome-like phenotype in a patient with diabetes: a case report ...
Florida woman survives traumatic crash after getting blood transfusion on the scene, deputies say
AOL.com - 17 Apr 2024
Florida woman survives traumatic crash after getting blood transfusion on the scene, deputies say ...
Cyclooxygenase-2 expression is associated with the renal macula densa of patients with Bartter-like syndrome
ScienceDirect.com - 13 Jan 2018
Cyclooxygenase-2 expression is associated with the renal macula densa of patients with Bartter-like syndrome ...
Bartter Syndrome Prenatal Diagnosis Based on Amniotic Fluid Biochemical Analysis | Pediatric Research
Nature - 25 May 2018
Bartter Syndrome Prenatal Diagnosis Based on Amniotic Fluid Biochemical Analysis | Pediatric Research ...
Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome
ScienceDirect.com - 29 Nov 2017
Role of cyclooxygenase-2 in hyperprostaglandin E syndrome/antenatal Bartter syndrome ...
MAGED2 mutation causes antenatal Bartter's syndrome
Medical Xpress - 28 Apr 2016
MAGED2 mutation causes antenatal Bartter's syndrome ...
Case study of Bartter Syndrome-a rare Renal Tubulopathy
Medical Dialogues - 04 Sep 2018
Case study of Bartter Syndrome-a rare Renal Tubulopathy ...
In Need of a Second Transplant, Remy Marceau Fights On
Mayo Clinic - 07 Sep 2017
In Need of a Second Transplant, Remy Marceau Fights On ...
Transient antenatal Bartter's Syndrome and X-linked polyhydramnios: insights from the genetics of a rare condition
ScienceDirect.com - 27 Dec 2017
Transient antenatal Bartter's Syndrome and X-linked polyhydramnios: insights from the genetics of a rare condition ...
Inherited salt-losing tubulopathies are associated with immunodeficiency due to impaired IL-17 responses
Nature - 31 Aug 2020
Inherited salt-losing tubulopathies are associated with immunodeficiency due to impaired IL-17 responses ...
MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells
ScienceDirect.com - 10 Feb 2022
MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells ...
Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome | Journal of Human Genetics
Nature - 30 May 2018
Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome | Journal of Human Genetics ...
Gitelman syndrome caused by a novel hemiallelic missense mutation in SLC12A3 revealed by 16q12.2q21 ...
Nature - 27 May 2020
Gitelman syndrome caused by a novel hemiallelic missense mutation in SLC12A3 revealed by 16q12.2q21 ... ...
Sclerochoroidal calcification in a patient with classic Bartter's syndrome
ScienceDirect.com - 27 Sep 2017
Sclerochoroidal calcification in a patient with classic Bartter's syndrome ...
The Urinary Excretion of Uromodulin is Regulated by the Potassium Channel ROMK | Scientific Reports
Nature - 20 Dec 2019
The Urinary Excretion of Uromodulin is Regulated by the Potassium Channel ROMK | Scientific Reports ...
Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype | Pediatric Research
Nature - 01 Dec 2000
Mutations in the Chloride Channel Gene, CLCNKB, Leading to a Mixed Bartter-Gitelman Phenotype | Pediatric Research ...
In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening ...
Nature - 03 Aug 2017
In silico model of the human ClC-Kb chloride channel: pore mapping, biostructural pathology and drug screening ... ...