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Journal Abstract Search

61 related items for PubMed ID: 2867557

  • 1. Familial deficiency of growth hormone and spinal muscular atrophy.
    Leroy JG, Craen MM.
    Prog Clin Biol Res; 1985; 200():113-21. PubMed ID: 2867557
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  • 2. Hereditary polyneuropathy, oligophrenia, premature menopause and acromicria. A new syndrome.
    Lundberg PO.
    Eur Neurol; 1971; 5(2):84-98. PubMed ID: 5117105
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  • 4. Molecular analysis of familial human growth hormone disorders.
    Repaske DR, Phillips JA.
    Bioessays; 1986 Mar; 4(3):114-8. PubMed ID: 3827887
    [No Abstract] [Full Text] [Related]

  • 5. [Familial male hypogonadism in spinal and bulbar muscular atrophy of late onset (Kennedy's disease). A new cause of hypogonadism].
    Gómez JM, Arbizu T, Santamaría J, Quilez A, Soler J, Peres J.
    Arch Esp Urol; 1984 Mar; 37(1):49-55. PubMed ID: 6721595
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  • 7. Convergence of two types of familial short stature in a pedigree.
    Mollica F, Li Volti S, Pavone L, Vigo R, Raiti S.
    Acta Endocrinol (Copenh); 1981 Jul; 97(3):315-9. PubMed ID: 7020316
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  • 8. [Growth deficiency: concept and classification].
    González Vergaz A, Pérez Jurado LA.
    An Esp Pediatr; 1992 Jun; 36 Suppl 50():35-9. PubMed ID: 1416505
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  • 9. Regulation of growth hormone secretion. Relevance to the pediatrician.
    Bercu BB, Diamond FB.
    Pediatrician; 1987 Jun; 14(3):94-108. PubMed ID: 2899314
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  • 11. [Molecular genetic study of a severe growth hormone deficiency in a Chilean family].
    Aguirre E, Benítez R, Youlton R, Carvallo P.
    Rev Med Chil; 1993 Sep; 121(9):982-6. PubMed ID: 7910700
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  • 14. Familial combined hyperlipoproteinemia. Evidence for a role of growth hormone deficiency in effecting its manifestation.
    Merimee TJ.
    J Clin Invest; 1980 Apr; 65(4):829-35. PubMed ID: 6987267
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  • 15. Juvenile spinal muscular atrophy--a new hexosaminidase deficiency phenotype.
    Johnson WG, Wigger HJ, Karp HR, Glaubiger LM, Rowland LP.
    Trans Am Neurol Assoc; 1981 Apr; 106():215-8. PubMed ID: 7348998
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