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 *

107 related articles for article (PubMed ID: 74536)

  • 21. Lack of effect of aldosterone on intracellular sodium and potassium in mononuclear leucocytes from patients with pseudohypoaldosteronism.
    Wehling M; Kuhnle U; Witzgall H; Weber PC; Armanini D
    Clin Endocrinol (Oxf); 1988 Jan; 28(1):67-74. PubMed ID: 3168302
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Lowe's syndrome in 2 sisters].
    Klempous T; Prusek W; Zylka W
    Pediatr Pol; 1976 Nov; 51(11):1347-50. PubMed ID: 980579
    [No Abstract]   [Full Text] [Related]  

  • 23. [Arterial hypertension with hyperkalemia, tubular acidosis and normal renal function: Gordon syndrome and/or pseudohypoaldosteronism type II?].
    Ader JL; Waeber B; Suc JM; Brunner HR; Tran-Van T; Durand D; Praddaude F
    Arch Mal Coeur Vaiss; 1988 Jun; 81 Spec No():193-7. PubMed ID: 2973296
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Renin-aldosterone response, urinary Na/K ratio and growth in pseudohypoaldosteronism patients with mutations in epithelial sodium channel (ENaC) subunit genes.
    Hanukoglu A; Edelheit O; Shriki Y; Gizewska M; Dascal N; Hanukoglu I
    J Steroid Biochem Mol Biol; 2008 Sep; 111(3-5):268-74. PubMed ID: 18634878
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Urinary salt wastage in the adult: a form of pseudohypoaldosteronism].
    Brautbar N; Litwin JJ
    Harefuah; 1976 Oct; 91(7):182-4. PubMed ID: 1002035
    [No Abstract]   [Full Text] [Related]  

  • 26. Coincidence of pseudohypoaldosteronism with gluten-enteropathy.
    Dumić M; Mardesić D; Plavsić V; Brkljacić L; Novak M; Pal D; Kastelan A
    J Endocrinol Invest; 1984 Aug; 7(4):395-8. PubMed ID: 6389661
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary tubular disorders.
    Woolf LI
    Monogr Pathol; 1979; 20():218-38. PubMed ID: 388203
    [No Abstract]   [Full Text] [Related]  

  • 28. Hereditary tubular disorders of the Fanconi type and the idiopathic Fanconi syndrome.
    Bickel H; Manz F
    Prog Clin Biol Res; 1989; 305():111-35. PubMed ID: 2668968
    [No Abstract]   [Full Text] [Related]  

  • 29. [Pseudohypoaldosteronism: a case report (author's transl)].
    Carballo Pérez A; Martín Govantes J; Luque Hinojosa C; del Valle Núñez CJ; Gómez de Terreros I
    An Esp Pediatr; 1975; 8(4):443-8. PubMed ID: 1147418
    [No Abstract]   [Full Text] [Related]  

  • 30. [Pseudohypoaldosteronism in a male infant].
    Harayama N; Kato S; Shimizu S; Iwagaki H; Oyama K
    Horumon To Rinsho; 1975 Jun; 23(6):581-5. PubMed ID: 1170978
    [No Abstract]   [Full Text] [Related]  

  • 31. Renal urate excretion in five cases of hypouricemia with an isolated renal defect of urate transport.
    Akaoka I; Nishizawa T; Yano E; Kamtani N; Nishida Y; Sasaki S
    J Rheumatol; 1977; 4(1):86-94. PubMed ID: 886556
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. [Presentation of a case of oculo-cerebro-renal syndrome in a newborn].
    Canki N; Debevec M; Kenda S; Rainer S
    J Genet Hum; 1976 Nov; 24 Suppl():269-77. PubMed ID: 1025279
    [No Abstract]   [Full Text] [Related]  

  • 34. Inborn hypouricemia due to isolated defect in renal tubular uric acid transport.
    Garty BZ; Nitzan M; Sperling O
    Isr J Med Sci; 1981 Apr; 17(4):295-7. PubMed ID: 7239879
    [No Abstract]   [Full Text] [Related]  

  • 35. Molecular pathophysiology of inborn renal Na+ transport defects.
    Greger R
    Kidney Blood Press Res; 1998; 21(2-4):222-5. PubMed ID: 9762839
    [No Abstract]   [Full Text] [Related]  

  • 36. Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure.
    Ohtsuka Y; Zaitsu M; Ichida K; Isomura N; Tsuji K; Sato T; Hamasaki Y
    Pediatr Int; 2007 Apr; 49(2):235-7. PubMed ID: 17445045
    [No Abstract]   [Full Text] [Related]  

  • 37. [Renal tubular hypomagnesemia of familial origin].
    Rapado A; Pedraza M; Torrijos A; Moreno F; Aparicio A; Sánchez-Alarcón J
    Rev Clin Esp; 1985 Apr; 176(6):302-4. PubMed ID: 4001489
    [No Abstract]   [Full Text] [Related]  

  • 38. [Bartter's disease associated with hypercorticism, phosphate and magnesium deficiencies and familial renal tubular disease].
    Sann L; Moreau P; Longin B; Sassard J; François R
    Arch Fr Pediatr; 1975 Apr; 32(4):350-66. PubMed ID: 1164148
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Successful indomethacin treatment of two paediatric patients with severe tubulopathies. A boy with an unusual hypercalciuria and a girl with cystinosis.
    Bétend B; David L; Vincent M; Hermier M; François R
    Helv Paediatr Acta; 1979 Sep; 34(4):339-44. PubMed ID: 391773
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Type I pseudohypoaldosteronism includes two clinically and genetically distinct entities with either renal or multiple target organ defects.
    Hanukoglu A
    J Clin Endocrinol Metab; 1991 Nov; 73(5):936-44. PubMed ID: 1939532
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.