about
Salt handling and hypertensionEpithelial sodium channel (ENaC) family: Phylogeny, structure-function, tissue distribution, and associated inherited diseasesLocalisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mappingNovel mutations in the SCNN1A gene causing Pseudohypoaldosteronism type 1Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.Salt restriction induces pseudohypoaldosteronism type 1 in mice expressing low levels of the beta-subunit of the amiloride-sensitive epithelial sodium channelGlucocorticoid hormone resistance during primate evolution: receptor-mediated mechanisms.A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene.Pseudohypoaldosteronism.GPR48 increases mineralocorticoid receptor gene expression.Mineralocorticoid receptor mutations and a severe recessive pseudohypoaldosteronism type 1.Dermal and Ophthalmic Findings in Pseudohypoaldosteronism.A salt-losing syndrome in infancy. Pseudo-hypoadrenocorticalism.A REVERSIBLE SALT-WASTING SYNDROME OF THE NEWBORN AND INFANT: POSSIBLE INFANTILE HYPOALDOSTERONISMThe adrenal cortex in childhood. 2. Pathological aspects.The mineralocorticoid receptor: insights into its molecular and (patho)physiological biologyPseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene.A mouse model for the renal salt-wasting syndrome pseudohypoaldosteronismPseudohypoaldosteronism type 1: clinical features and management in infancy.Hypertension, dietary salt intake, and the role of the thiazide-sensitive sodium chloride transporter NCCT.Molecular insights from dysregulation of the thiazide-sensitive WNK/SPAK/NCC pathway in the kidney: Gordon syndrome and thiazide-induced hyponatraemia.Pathophysiology, diagnosis, and treatment of mineralocorticoid disorders.Severe hyperkalemia is rescued by low-potassium diet in renal βENaC-deficient mice.Systemic Pseudohypoaldosteronism Type I: A Case Report and Review of the Literature.The function and regulation of acid-sensing ion channels (ASICs) and the epithelial Na(+) channel (ENaC): IUPHAR Review 19.Clinical features and molecular basis of pseudohypoaldosteronism type 1.Glucocorticoid and mineralocorticoid resistance.Pseudohypoaldosteronism: case report and discussion of the syndrome.Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes.Case report of two children with pseudohypoaldosteronism.Erythrocyte Na+,K+-ATPase and nasal potential in pseudohypoaldosteronism.Pseudohypoaldosteronism type 1 and respiratory distress syndrome.A novel nonsense mutation of the mineralocorticoid receptor gene in the renal form of pseudohypoaldosteronism type 1.Revealing a subclinical salt-losing phenotype in heterozygous carriers of the novel S562P mutation in the alpha subunit of the epithelial sodium channel.Genetic mechanisms of human hypertension and their implications for blood pressure physiology.A new syndrome: hearing loss and familial salivary gland insensitivity to aldosterone in two brothers.Rare Cause of Hyperkalemia in the Newborn Period: Report of Two Cases of Pseudohypoaldosteronism Type 1.Pseudohypoaldosteronism type 1: the index case revisitedPseudohypoaldosteronism: kidney, lungs and colon*
P2860
Q24631439-8143BDD1-573A-4C18-AFF5-84C74F02FBC5Q28272095-7E1B83DF-C052-4C01-9216-0E0725FC85D1Q28291215-368DC7E1-2E9A-4F35-B484-DEA3AB0EB671Q28533708-CD74BDD4-5834-4DE8-8F25-D6CAA39B313AQ30884885-798335B7-8EDC-40EA-A402-6A12A32B5A98Q31904160-0FC1CFC8-99F2-49ED-8BC4-1BF7618E1EB0Q34714009-E223E863-9485-4C28-9B7D-85B057040EFDQ34799197-EA6A4394-C5BD-4464-ADF0-656C23257E07Q35114478-8F5DFB11-C3A3-4DD7-A6A2-431BE5A5662AQ35715750-0C38FE63-2240-4615-8BFE-5C32C32DC81FQ35758441-8520F871-BA1E-4EC3-A77A-003BE3C8F7ECQ36038857-7766496A-19CB-4F52-9F82-DE6B51A8C0D1Q36050613-1AD285C1-53C1-4F4C-8600-92FA0E86624EQ36060148-368431E5-93D1-4333-9BD8-1DBB3077A875Q36061200-D09BACC8-12CD-4BA1-9675-176F8BC15D7CQ36238325-DEF5470E-1152-4518-BB2F-BCCD33D6D02AQ36488880-F0F8739B-3BF9-463E-A6E0-5F3516832DEEQ36611582-24E1ABA0-4FF9-42A2-B4AB-CAEADBB58A74Q37580096-EB7703AD-50D0-4BEB-9B7A-846AEA0241D4Q37821983-D62CA641-CF9D-46E4-8A22-F61207F37814Q38107545-E895B387-00BC-48C2-A931-D855796BF45CQ38221451-986F59E6-CB1D-4F27-9CDF-4A9CD143AC30Q38752148-F5AA2E35-75EF-4B0C-BFD0-FAE0E1D187C0Q38796714-A446841E-6639-4848-99B7-C9BE4867A6CDQ38859500-2309EF97-2626-4FFE-99C3-F3B58D26B2CAQ40095277-CBCE47EA-ECC0-40BA-959F-41BEEB59E6E4Q41530418-FDD8ACBC-958C-4787-A6D2-38CB197CF890Q41564697-A09A4C75-301B-49B5-8856-426E13F54471Q41822493-4EB40767-458A-4A4A-AD99-C66F97744C0AQ43831617-A01696E9-F853-4ACD-A1F2-F4A450EFE4A3Q44006166-4A469206-E1D9-422A-A9F8-AF0D3606A234Q44263591-1E2CAED0-3110-423E-9F5B-F18C838F86EDQ44984942-F938B221-ED55-40C2-B7B6-389220127659Q46960945-8E69F72D-2CD2-4427-BA57-794E685013F3Q48100826-CD31E3C7-4B6C-47CE-8F14-9B9E68EA5A88Q50547974-855D8393-06AF-4615-8847-27F17E42B6C0Q53703887-9E19F5CE-F689-42DD-99ED-327A16736F1AQ56983689-4C9B24F7-69FF-4D33-9686-3C380BEF5039Q58433832-3389430E-4878-4741-955E-68BB7BC5BA8A
P2860
description
1958 nî lūn-bûn
@nan
1958 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1958 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1958年の論文
@ja
1958年論文
@yue
1958年論文
@zh-hant
1958年論文
@zh-hk
1958年論文
@zh-mo
1958年論文
@zh-tw
1958年论文
@wuu
name
A salt wasting syndrome in infancy
@ast
A salt wasting syndrome in infancy
@en
A salt wasting syndrome in infancy
@nl
type
label
A salt wasting syndrome in infancy
@ast
A salt wasting syndrome in infancy
@en
A salt wasting syndrome in infancy
@nl
prefLabel
A salt wasting syndrome in infancy
@ast
A salt wasting syndrome in infancy
@en
A salt wasting syndrome in infancy
@nl
P2860
P356
P1476
A salt wasting syndrome in infancy
@en
P2093
P2860
P356
10.1136/ADC.33.169.252
P407
P577
1958-06-01T00:00:00Z