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Journal Abstract Search

129 related items for PubMed ID: 2624273

  • 1. Familial hyperinsulinism with nesidioblastosis of the pancreas: further evidence for autosomal recessive inheritance.
    Moreno LA, Turck D, Gottrand F, Fabre M, Manouvrier-Hanu S, Farriaux JP.
    Am J Med Genet; 1989 Dec; 34(4):584-6. PubMed ID: 2624273
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  • 2. Persistent hyperinsulinemic hypoglycemia of infancy ("nesidioblastosis"): autosomal recessive inheritance in 7 pedigrees.
    Glaser B, Phillip M, Carmi R, Lieberman E, Landau H.
    Am J Med Genet; 1990 Dec; 37(4):511-5. PubMed ID: 2260597
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  • 3. Familial nesidioblastosis: more evidence for autosomal recessive inheritance.
    Cherian MP, Haddad MJ, Sa'di AR, Mathew PM.
    Ann Trop Paediatr; 1994 Dec; 14(4):287-91. PubMed ID: 7880090
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  • 4. [Nesidioblastosis and persistent neonatal hyperinsulinism].
    Rahier J, Sempoux C, Poggi F, Brunelle F, Saudubray JM, Fekete C.
    Journ Annu Diabetol Hotel Dieu; 1995 Dec; ():73-82. PubMed ID: 7602894
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  • 6. Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literature.
    Koppel R, Friedman S, Fallet S.
    Am J Med Genet; 1996 Aug 23; 64(3):485-7. PubMed ID: 8862626
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  • 7. A case of familial nesidioblastosis: prenatal diagnosis of foetal hyperinsulinism.
    Bianchi C, Corbella E, Beccaria L, Bolla P, Chiumello G.
    Acta Paediatr; 1992 Oct 23; 81(10):853-5. PubMed ID: 1421899
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  • 8. [Familial hyperinsulinism].
    Lásztity N, Balogh L.
    Orv Hetil; 1995 Jul 23; 136(30):1611-3. PubMed ID: 7637980
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  • 9. Unilateral isolated microphthalmia inherited as an autosomal recessive trait.
    Fleckenstein M, Maumenee IH.
    Ophthalmic Genet; 2005 Dec 23; 26(4):163-8. PubMed ID: 16352476
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  • 11. Autosomal recessive primary generalized dystonia in two siblings from a consanguineous family.
    Moretti P, Hedera P, Wald J, Fink J.
    Mov Disord; 2005 Feb 23; 20(2):245-7. PubMed ID: 15390074
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  • 12. Probable autosomal recessive inheritance of polysplenia, situs inversus and cardiac defects in an Amish family.
    Arnold GL, Bixler D, Girod D.
    Am J Med Genet; 1983 Sep 23; 16(1):35-42. PubMed ID: 6638068
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  • 14. Additional case of opsismodysplasia supporting autosomal recessive inheritance.
    Beemer FA, Kozlowski KS.
    Am J Med Genet; 1994 Feb 01; 49(3):344-7. PubMed ID: 8209898
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  • 15. Familial hydrocephalus of prenatal onset.
    Zlotogora J, Sagi M, Cohen T.
    Am J Med Genet; 1994 Jan 15; 49(2):202-4. PubMed ID: 8116668
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  • 16. Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder.
    Thornton PS, Sumner AE, Ruchelli ED, Spielman RS, Baker L, Stanley CA.
    J Pediatr; 1991 Nov 15; 119(5):721-4. PubMed ID: 1941377
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  • 20. Hunting for a hypoglycemia gene: severe neonatal hypoglycemia in a consanguineous family.
    Molven A, Rishaug U, Matre GE, Njølstad PR, Søvik O.
    Am J Med Genet; 2002 Nov 15; 113(1):40-6. PubMed ID: 12400064
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