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Journal Abstract Search

149 related items for PubMed ID: 16372230

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  • 2. Short stature and decreased insulin-like growth factor I (IGF-I)/growth hormone (GH)-ratio in an adult GH-deficient patient pointing to additional partial GH insensitivity due to a R179C mutation of the growth hormone receptor.
    Meyer S, Ipek M, Keth A, Minnemann T, von Mach MA, Weise A, Ittner JR, Nawroth PP, Plöckinger U, Stalla GK, Tuschy U, Weber MM, Kann PH, German KIMS Board, German KIMS Pharmacogenetics Study Group.
    Growth Horm IGF Res; 2007 Aug; 17(4):307-14. PubMed ID: 17462934
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  • 4. Molecular defects of the growth hormone receptor gene, including a new mutation, in Laron syndrome patients in Israel: relationship between defects and ethnic groups.
    Shevah O, Rubinstein M, Laron Z.
    Isr Med Assoc J; 2004 Oct; 6(10):630-3. PubMed ID: 15473594
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  • 6. Effects of heterozygosity for the E180 splice mutation causing growth hormone receptor deficiency in Ecuador on IGF-I, IGFBP-3, and stature.
    Guevara-Aguirre J, Rosenbloom AL, Guevara-Aguirre M, Yariz K, Saavedra J, Baumbach L, Shuster J.
    Growth Horm IGF Res; 2007 Jun; 17(3):261-4. PubMed ID: 17350302
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  • 10. Natural history of the classical form of primary growth hormone (GH) resistance (Laron syndrome).
    Laron Z.
    J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():231-49. PubMed ID: 10698588
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  • 12. Do deficiencies in growth hormone and insulin-like growth factor-1 (IGF-1) shorten or prolong longevity?
    Laron Z.
    Mech Ageing Dev; 2005 Feb; 126(2):305-7. PubMed ID: 15621211
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  • 13. Novel growth hormone receptor mutation in a Chinese patient with Laron syndrome.
    Hui HN, Metherell LA, Ng KL, Savage MO, Camacho-Hübner C, Clark AJ.
    J Pediatr Endocrinol Metab; 2005 Feb; 18(2):209-13. PubMed ID: 15751611
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  • 16. [Growth hormone receptor and dwarfism].
    Postel-Vinay MC.
    Rev Prat; 1994 May 15; 44(10):1281-5. PubMed ID: 7939185
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  • 17. Growth hormone insensitivity and severe short stature in siblings: a novel mutation at the exon 13-intron 13 junction of the STAT5b gene.
    Hwa V, Camacho-Hübner C, Little BM, David A, Metherell LA, El-Khatib N, Savage MO, Rosenfeld RG.
    Horm Res; 2007 May 15; 68(5):218-24. PubMed ID: 17389811
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  • 19. Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism.
    Arman A, Ozon A, Isguven PS, Coker A, Peker I, Yordam N.
    J Pediatr Endocrinol Metab; 2008 Jan 15; 21(1):47-58. PubMed ID: 18404972
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  • 20. Endocrine assessment, molecular characterization and treatment of growth hormone insensitivity disorders.
    Savage MO, Attie KM, David A, Metherell LA, Clark AJ, Camacho-Hübner C.
    Nat Clin Pract Endocrinol Metab; 2006 Jul 15; 2(7):395-407. PubMed ID: 16932322
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