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Journal Abstract Search

145 related items for PubMed ID: 3800569

  • 1. [Oculocerebrorenal syndrome in a girl].
    Frézal J, Hors-Cayla MC, Szpiro-Tapia S.
    Arch Fr Pediatr; 1986; 43(7):537. PubMed ID: 3800569
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic transmission of Lowe's oculo-cerebro-renal syndrome in girl].
    Bétend B, Scherrer M, Evrard A, Votan-Bonnamour B, Hermier M.
    Arch Fr Pediatr; 1978 Mar; 35(3):269-79. PubMed ID: 666523
    [Abstract] [Full Text] [Related]

  • 3. Lowe's syndrome.
    Tripathi RC, Cibis GW, Harris DJ, Tripathi B.
    Birth Defects Orig Artic Ser; 1982 Mar; 18(6):629-44. PubMed ID: 6890859
    [No Abstract] [Full Text] [Related]

  • 4. A balanced de novo X/autosome translocation in a girl with manifestations of Lowe syndrome.
    Hodgson SV, Heckmatt JZ, Hughes E, Crolla JA, Dubowitz V, Bobrow M.
    Am J Med Genet; 1986 Mar; 23(3):837-47. PubMed ID: 3953680
    [Abstract] [Full Text] [Related]

  • 5. [Sex-related neurologic diseases. Duchenne muscular dystrophy. Lowe's disease].
    Castro-Gago M.
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():51-4. PubMed ID: 6517412
    [No Abstract] [Full Text] [Related]

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

  • 7. [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]

  • 8. Update: Lowe's syndrome.
    Wappner RS.
    Compr Ther; 1987 Apr; 13(4):3-4. PubMed ID: 3568601
    [No Abstract] [Full Text] [Related]

  • 9. [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]

  • 10. Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms.
    Silver DN, Lewis RA, Nussbaum RL.
    J Clin Invest; 1987 Jan; 79(1):282-5. PubMed ID: 2878939
    [Abstract] [Full Text] [Related]

  • 11. [Hereditary renal diseases].
    Norio R, Visakorpi JK.
    Duodecim; 1972 Jan; 88(1):109-18. PubMed ID: 5013564
    [No Abstract] [Full Text] [Related]

  • 12. Opacities of the lens indicating carrier status in the oculo-cerebro-renal (Lowe) syndrome.
    Delleman JW, Bleeker-Wagemakers EM, van Veelen AW.
    J Pediatr Ophthalmol; 1977 Jan; 14(4):205-12. PubMed ID: 894443
    [Abstract] [Full Text] [Related]

  • 13. Familial hypouricemia due to isolated renal tubular abnormality.
    Benjamin D, Sperling O, Weinberg A, Pinkhas J.
    Biomedicine; 1978 Apr; 29(2):54-6. PubMed ID: 667288
    [Abstract] [Full Text] [Related]

  • 14. [The Lyon effect of the lens: findings in the carriers of X chromosome-linked cataract and in Lowe syndrome].
    Koniszewski G, Rott HD.
    Klin Monbl Augenheilkd; 1985 Dec; 187(6):525-8. PubMed ID: 4094364
    [Abstract] [Full Text] [Related]

  • 15. [Oculo-cerebro-renal syndrome in a newborn].
    Dick J, Ashkenazi A, Chamke M.
    Harefuah; 1985 Jun 16; 108(12):592-3. PubMed ID: 4065726
    [No Abstract] [Full Text] [Related]

  • 16. [Oculo-cerebro-renal syndrome in a girl. Clinical, genetic and biological reevaluation at the age of 10 years].
    Lachaux A, David L, Descos B, Scherrer M, Hermier M.
    Arch Fr Pediatr; 1986 Jan 16; 43(1):68-9. PubMed ID: 3707282
    [No Abstract] [Full Text] [Related]

  • 17. Oculo-cerebro-renal syndrome (Lowe's syndrome)--a report of three cases.
    Curtis JA, Goel KM.
    Practitioner; 1982 Jun 16; 226(1368):1159-64. PubMed ID: 7111150
    [No Abstract] [Full Text] [Related]

  • 18. [Contribution of molecular biology to the study of renal tubular diseases].
    Rodríguez Soriano J.
    An Esp Pediatr; 1997 Jun 16; Spec No 1():40-2. PubMed ID: 9382265
    [No Abstract] [Full Text] [Related]

  • 19. Oculocerebrorenal syndrome in a female child.
    Svorc J, Masopust J, Komárková A, Macek M, Hyánek J.
    Am J Dis Child; 1967 Aug 16; 114(2):186-90. PubMed ID: 4951545
    [No Abstract] [Full Text] [Related]

  • 20. Familial iminoglycinuria. An inborn error of renal tubular transport.
    Rosenberg LE, Durant JL, Elsas LJ.
    N Engl J Med; 1968 Jun 27; 278(26):1407-13. PubMed ID: 5652624
    [No Abstract] [Full Text] [Related]

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