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Journal Abstract Search

96 related items for PubMed ID: 890096

  • 1. "Aldolase A" deficiency with syndrome of growth and developmental retardation, midfacial hypoplasia, hepatomegaly, and consanguineous parents.
    Lowry RB, Hanson JW.
    Birth Defects Orig Artic Ser; 1977; 13(3B):222-8. PubMed ID: 890096
    [No Abstract] [Full Text] [Related]

  • 2. A syndrome of mental retardation, short stature, hemolytic anemia, delayed puberty, and abnormal facial appearance: similarities to a report of aldolase A deficiency.
    Hurst JA, Baraitser M, Winter RM.
    Am J Med Genet; 1987 Dec; 28(4):965-70. PubMed ID: 3688035
    [Abstract] [Full Text] [Related]

  • 3. Larsen syndrome in siblings with consanguineous parents.
    Topley JM, Varady E, Lestringant GG.
    Clin Dysmorphol; 1994 Jul; 3(3):263-5. PubMed ID: 7526939
    [Abstract] [Full Text] [Related]

  • 4. Two cases of red cell aldolase deficiency associated with hereditary hemolytic anemia in a Japanese family.
    Miwa S, Fujii H, Tani K, Takahashi K, Takegawa S, Fujinami N, Sakurai M, Kubo M, Tanimoto Y, Kato T, Matsumoto N.
    Am J Hematol; 1981 Dec; 11(4):425-37. PubMed ID: 7331996
    [Abstract] [Full Text] [Related]

  • 5. [Aldolase A deficiency].
    Tsujino S.
    Ryoikibetsu Shokogun Shirizu; 2001 Dec; (36):35-6. PubMed ID: 11596407
    [No Abstract] [Full Text] [Related]

  • 6. Red cell enzymopathies in the newborn. II. Inherited deficiencies of red cell enzymes.
    Travis SF.
    Ann Clin Lab Sci; 1982 Dec; 12(3):163-77. PubMed ID: 6284015
    [No Abstract] [Full Text] [Related]

  • 7. Red cell aldolase deficiency and hemolytic anemia: a new syndrome.
    Beutler E, Scott S, Bishop A, Margolis N, Matsumoto F, Kuhl W.
    Trans Assoc Am Physicians; 1973 Dec; 86():154-66. PubMed ID: 4788792
    [No Abstract] [Full Text] [Related]

  • 8. [Anesthesia for a patient with red cell aldolase deficiency].
    Kiriyama T, Wakamatsu M, Furuta M, Kato H, Ono K.
    Masui; 1993 May; 42(5):750-2. PubMed ID: 8515555
    [Abstract] [Full Text] [Related]

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  • 10. [The lesions associated with leprechaunism (author's transl)].
    Lebreuil G, Pizzi M, Sebaoun M, Oddou JH.
    Arch Anat Cytol Pathol; 1980 May; 28(5):310-6. PubMed ID: 7447519
    [No Abstract] [Full Text] [Related]

  • 11. Growth in the high-risk infant.
    Manser JI.
    Clin Perinatol; 1984 Feb; 11(1):19-40. PubMed ID: 6370547
    [No Abstract] [Full Text] [Related]

  • 12. [Baller-Gerold syndrome].
    Satokata I.
    Ryoikibetsu Shokogun Shirizu; 2000 Feb; (30 Pt 5):136-7. PubMed ID: 11057169
    [No Abstract] [Full Text] [Related]

  • 13. Mild growth retardation and developmental delay, microcephaly, and a distinctive facial appearance.
    Partington M, Anderson D.
    Am J Med Genet; 1994 Jan 15; 49(2):247-50. PubMed ID: 7509568
    [Abstract] [Full Text] [Related]

  • 14. Bladder carcinoma in Costello syndrome: report on a patient born to consanguineous parents and review.
    Franceschini P, Licata D, Di Cara G, Guala A, Bianchi M, Ingrosso G, Franceschini D.
    Am J Med Genet; 1999 Sep 10; 86(2):174-9. PubMed ID: 10449656
    [Abstract] [Full Text] [Related]

  • 15. Anterior segment anomalies of the eye, clefting and skeletal abnormalities in two sibs of consanguineous parents: Michels syndrome or new syndrome?
    al Gazali LI, al Talabani J, Mosawi A, Lytle W.
    Clin Dysmorphol; 1994 Jul 10; 3(3):238-44. PubMed ID: 7981860
    [Abstract] [Full Text] [Related]

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  • 17. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
    [Abstract] [Full Text] [Related]

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  • 19. A new autosomal recessive disorder resembling Weaver syndrome.
    Teebi AS, Sundareshan TS, Hammouri MY, al-Awadi SA, al-Saleh QA.
    Am J Med Genet; 1989 Aug 01; 33(4):479-82. PubMed ID: 2596508
    [Abstract] [Full Text] [Related]

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