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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]
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]
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]