These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

74 related articles for article (PubMed ID: 1962852)

  • 21. Rare cause of severe hypertension in an adolescent boy presenting with short stature: Answers.
    Yavas Abali Z; Yesil G; Kirkgoz T; Cicek N; Alpay H; Turan S; Bereket A; Guran T
    Pediatr Nephrol; 2020 Mar; 35(3):405-407. PubMed ID: 31529157
    [No Abstract]   [Full Text] [Related]  

  • 22. 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]  

  • 23. Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism.
    Sartorato P; Khaldi Y; Lapeyraque AL; Armanini D; Kuhnle U; Salomon R; Caprio M; Viengchareun S; Lombès M; Zennaro MC
    Mol Cell Endocrinol; 2004 Mar; 217(1-2):119-25. PubMed ID: 15134810
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prospective diagnosis of pseudohypoaldosteronism.
    Schindler AM; Bergman GE
    Pediatrics; 1986 Sep; 78(3):516-8. PubMed ID: 3529026
    [No Abstract]   [Full Text] [Related]  

  • 25. [Pseudohypoaldosteronism: a special form of sodium loss in infancy].
    Limbowo D; Monnens L; Wels C
    Tijdschr Kindergeneeskd; 1984 Oct; 52(5):200-4. PubMed ID: 6393425
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Pseudohypoaldosteronism (type I)].
    Endoh A; Igarashi Y
    Ryoikibetsu Shokogun Shirizu; 1993; (1):416-8. PubMed ID: 7757627
    [No Abstract]   [Full Text] [Related]  

  • 27. Plasma aldosterone regulation in anephric and non-nephrectomized patients on regular haemodialysis. A survey.
    Olgaard K
    Dan Med Bull; 1980 Feb; 27(1):22-35. PubMed ID: 6249547
    [No Abstract]   [Full Text] [Related]  

  • 28. Renin, aldosterone and electrolytes in idiopathic orthostatic hypotension.
    Bliddal J; Nielsen I
    Dan Med Bull; 1970 May; 17(5):153-7. PubMed ID: 5421365
    [No Abstract]   [Full Text] [Related]  

  • 29. [Transient neonatal pseudo-hypoaldosteronism].
    Trentesaux AS; Roussel B; Bednarek N; Pietrement C; Morville P
    Arch Pediatr; 1998 Oct; 5(10):1171-2. PubMed ID: 9809169
    [No Abstract]   [Full Text] [Related]  

  • 30. [Neonatal pseudohypoaldosteronism: when a denied truth can delay a diagnosis].
    Bagna R; Tonetto P; Spola R; Martano C; Ferrero L; Becchino L; Nicocia M; Ciaccia R; Giuliano V; Lala R; Fabris C
    Acta Biomed Ateneo Parmense; 2000; 71 Suppl 1():769-71. PubMed ID: 11424844
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fluid-solute regulation systems in patients with Meniere's disease.
    Colletti V; Sittoni V; Bonnanni G; Pavarin A
    Am J Otol; 1983 Apr; 4(4):315-7. PubMed ID: 6305200
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation.
    Tanaka T; Oki E; Mori T; Tsuruga K; Sohara E; Uchida S; Tanaka H
    Nephrology (Carlton); 2019 Apr; 24(4):489-490. PubMed ID: 30919533
    [No Abstract]   [Full Text] [Related]  

  • 33. [Pseudohypoaldosteronism in a premature newborn infant].
    González González MJ; Muro Brussi M; Sarria Osés J; Cabanillas Vilaplana L; Uribarri Zarranz F; Sáez Pérez E
    An Esp Pediatr; 1996 May; 44(5):517-9. PubMed ID: 8928980
    [No Abstract]   [Full Text] [Related]  

  • 34. A novel mutation of the epithelial Na+ channel causes type 1 pseudohypoaldosteronism.
    Bonny O; Knoers N; Monnens L; Rossier BC
    Pediatr Nephrol; 2002 Oct; 17(10):804-8. PubMed ID: 12376807
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Salt wasting disorder in the newborn.
    Ranjith G; Uthup S; Satish B; Jain N
    Indian J Pediatr; 2006 Jan; 73(1):95-6. PubMed ID: 16444070
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Hypercalcemia in pseudohypoaldosteronism].
    Lamireau T; Sarlangue J; Martin C
    Pediatrie; 1986; 41(5):419-24. PubMed ID: 3808846
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Adrenal insufficiency in Smith-Lemli-Opitz syndrome.
    Andersson HC; Frentz J; Martínez JE; Tuck-Muller CM; Bellizaire J
    Am J Med Genet; 1999 Feb; 82(5):382-4. PubMed ID: 10069708
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Salt losing syndrome in the new-born. New diagnostic approach. Report of our experience between 1960 and 1976].
    Limal JM; Rappaport R; Lenoir G
    Ann Pediatr (Paris); 1977 Jan; 24(1):49-55. PubMed ID: 16211944
    [No Abstract]   [Full Text] [Related]  

  • 39. Elevated plasma asymmetric dimethyl-L-arginine in a patient with Gordon syndrome.
    Wieczorek-Surdacka E; Surdacki A; Bode-Böger SM; Schubert B; Sulowicz W
    Nephrol Dial Transplant; 2007 Jan; 22(1):268-71. PubMed ID: 16998213
    [No Abstract]   [Full Text] [Related]  

  • 40. [Hemodynamics, various aspects of aldosterone metabolism and renin activity in children with cerebral palsy].
    Bankova VV; Iurkov Iua ; Shelkovskiĭ VI; Znamenskaia EN; Dvoriakovskaia GM
    Vestn Akad Med Nauk SSSR; 1985; (6):37-40. PubMed ID: 2992181
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.