BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 27639857)

  • 1. Hyperkalemia in young children: blood pressure checked?
    Hollander R; Mortier G; van Hoeck K
    Eur J Pediatr; 2016 Dec; 175(12):2011-2013. PubMed ID: 27639857
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pseudohypoaldosteronism Type II: A Young Girl Presented with Hypertension, Hyperkalemia and Metabolic Acidosis.
    Sethar GH; Almoghawi A; Khan N; Altourah W; Ashour NM
    J Coll Physicians Surg Pak; 2018 Mar; 28(3):S21-S22. PubMed ID: 29482694
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hypercalciuria in familial hyperkalemia and hypertension with KLHL3 mutations.
    Mayan H; Carmon V; Oleinikov K; London S; Halevy R; Holtzman EJ; Tenenbaum-Rakover Y; Farfel Z; Hanukoglu A
    Nephron; 2015; 130(1):59-65. PubMed ID: 25925082
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Insights into the diverse mechanisms and effects of variant CUL3-induced familial hyperkalemic hypertension.
    Sharma P; Chatrathi HE
    Cell Commun Signal; 2023 Oct; 21(1):286. PubMed ID: 37845702
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial Hyperkalemia and Hypertension (FHHt) and KLHL3: Description of a Family with a New Recessive Mutation (S553L) Compared to a Family with a Dominant Mutation, Q309R, with Analysis of Urinary Sodium Chloride Cotransporter.
    Kliuk-Ben Bassat O; Carmon V; Hanukoglu A; Ganon L; Massalha E; Holtzman EJ; Farfel Z; Mayan H
    Nephron; 2017; 137(1):77-84. PubMed ID: 28511177
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life.
    Etges A; Hellmig N; Walenda G; Haddad BG; Machtens JP; Morosan T; Rump LC; Scholl UI
    Nephron; 2022; 146(4):418-428. PubMed ID: 35093948
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hyperkalemia and hypertension: is this a "chloride-shunt" disorder?
    Hirsch DJ
    Clin Invest Med; 1990 Dec; 13(6):360-6. PubMed ID: 2078915
    [No Abstract]   [Full Text] [Related]  

  • 8. Association of Familial Hyperkalemia and Hypertension with Proximal Renal Tubular Acidosis and Epileptic Seizures.
    Shirin N; Rabinowitz G; Blatt I; Karlish SJD; Farfel Z; Mayan H
    Nephron; 2024; 148(3):179-184. PubMed ID: 37666233
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.
    Mansfield TA; Simon DB; Farfel Z; Bia M; Tucci JR; Lebel M; Gutkin M; Vialettes B; Christofilis MA; Kauppinen-Makelin R; Mayan H; Risch N; Lifton RP
    Nat Genet; 1997 Jun; 16(2):202-5. PubMed ID: 9171836
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome).
    Glover M; Ware JS; Henry A; Wolley M; Walsh R; Wain LV; Xu S; Van't Hoff WG; Tobin MD; Hall IP; Cook S; Gordon RD; Stowasser M; O'Shaughnessy KM
    Clin Sci (Lond); 2014 May; 126(10):721-6. PubMed ID: 24266877
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Salt-Losing Syndrome in a Girl with Type I and II Pseudohypoaldosteronism.
    Szmigielska A
    Am J Case Rep; 2022 Oct; 23():e937536. PubMed ID: 36303414
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Classification of pseudohypoaldosteronism type II as type IV renal tubular acidosis: results of a literature review.
    Adachi M; Motegi S; Nagahara K; Ochi A; Toyoda J; Mizuno K
    Endocr J; 2023 Jul; 70(7):723-729. PubMed ID: 37081692
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Gordon syndrome: The importance of measuring blood pressure in children].
    Bruel A; Vargas-Poussou R; Jeunemaitre X; Labbe A; Merlin E; Bessenay L
    Arch Pediatr; 2016 Aug; 23(8):827-31. PubMed ID: 27369102
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A Spanish Family with Gordon Syndrome Due to a Variant in the Acidic Motif of
    Peces R; Peces C; Espinosa L; Mena R; Blanco C; Tenorio-Castaño J; Lapunzina P; Nevado J
    Genes (Basel); 2023 Sep; 14(10):. PubMed ID: 37895227
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel
    Chatrathi HE; Collins JC; Wolfe LA; Markello TC; Adams DR; Gahl WA; Werner A; Sharma P
    Hypertension; 2022 Jan; 79(1):60-75. PubMed ID: 34878901
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pseudohypoaldosteronism Type II or Gordon Syndrome: A Rare Syndrome of Hyperkalemia and Hypertension With Normal Renal Function.
    Manas F; Singh S
    Cureus; 2024 Jan; 16(1):e52594. PubMed ID: 38374860
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension.
    Disse-Nicodème S; Achard JM; Desitter I; Houot AM; Fournier A; Corvol P; Jeunemaitre X
    Am J Hum Genet; 2000 Aug; 67(2):302-10. PubMed ID: 10869238
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A case report of pseudohypoaldosteronism type II with a homozygous KLHL3 variant accompanied by hyperthyroidism.
    Zhang R; Zhang S; Luo Y; Li M; Wen X; Cai X; Han X; Ji L
    BMC Endocr Disord; 2021 May; 21(1):103. PubMed ID: 34022862
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Dwarfism, arterial hypertension and hyperkalemic acidosis corrected with thiazides. A case of type II pseudohypoaldosteronism].
    Poujol A; Rimet Y; Cournelle MA; Cornus P; Frayssinet R; Zarrouk F; Brusquet Y
    Arch Fr Pediatr; 1993 Feb; 50(2):127-30. PubMed ID: 8343018
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.