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Journal Abstract Search

137 related items for PubMed ID: 10946881

  • 21. GH transcription factors.
    Pfaffle RW, Kim C, Blankenstein O, Kentrup H.
    J Pediatr Endocrinol Metab; 1999 Apr; 12 Suppl 1():311-7. PubMed ID: 10698595
    [Abstract] [Full Text] [Related]

  • 22. A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty.
    Arroyo A, Pernasetti F, Vasilyev VV, Amato P, Yen SS, Mellon PL.
    Clin Endocrinol (Oxf); 2002 Aug; 57(2):283-91. PubMed ID: 12153609
    [Abstract] [Full Text] [Related]

  • 23. Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency.
    Paracchini R, Giordano M, Corrias A, Mellone S, Matarazzo P, Bellone J, Momigliano-Richiardi P, Bona G.
    Clin Genet; 2003 Aug; 64(2):142-7. PubMed ID: 12859410
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  • 24. Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene.
    Rosenbloom AL, Almonte AS, Brown MR, Fisher DA, Baumbach L, Parks JS.
    J Clin Endocrinol Metab; 1999 Jan; 84(1):50-7. PubMed ID: 9920061
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  • 25. Combined pituitary hormone deficiency due to the F135C human Pit-1 (pituitary-specific factor 1) gene mutation: functional and structural correlates.
    Vallette-Kasic S, Pellegrini-Bouiller I, Sampieri F, Gunz G, Diaz A, Radovick S, Enjalbert A, Brue T.
    Mol Endocrinol; 2001 Mar; 15(3):411-20. PubMed ID: 11222742
    [Abstract] [Full Text] [Related]

  • 26. Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency.
    Kandemir N, Vurallı D, Taşkıran E, Gönç N, Özön A, Alikaşifoğlu A, Yılmaz E.
    Turk J Pediatr; 2012 Mar; 54(6):570-5. PubMed ID: 23692781
    [Abstract] [Full Text] [Related]

  • 27. High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.
    Navardauskaite R, Dusatkova P, Obermannova B, Pfaeffle RW, Blum WF, Adukauskiene D, Smetanina N, Cinek O, Verkauskiene R, Lebl J.
    J Clin Endocrinol Metab; 2014 Jan; 99(1):299-306. PubMed ID: 24178788
    [Abstract] [Full Text] [Related]

  • 28. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
    Halász Z.
    Orv Hetil; 2011 Feb 06; 152(6):221-32. PubMed ID: 21278027
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  • 30. Cellular determination in the anterior pituitary gland: PIT-1 and PROP-1 mutations as causes of human combined pituitary hormone deficiency.
    Rodriguez R, Andersen B.
    Minerva Endocrinol; 2003 Jun 06; 28(2):123-33. PubMed ID: 12717343
    [Abstract] [Full Text] [Related]

  • 31. Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency.
    Fofanova O, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S.
    J Clin Endocrinol Metab; 1998 Jul 06; 83(7):2601-4. PubMed ID: 9661653
    [Abstract] [Full Text] [Related]

  • 32. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
    Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM.
    Clin Endocrinol (Oxf); 2005 Feb 06; 62(2):163-8. PubMed ID: 15670191
    [Abstract] [Full Text] [Related]

  • 33. Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene.
    Pernasetti F, Toledo SP, Vasilyev VV, Hayashida CY, Cogan JD, Ferrari C, Lourenço DM, Mellon PL.
    J Clin Endocrinol Metab; 2000 Jan 06; 85(1):390-7. PubMed ID: 10634415
    [Abstract] [Full Text] [Related]

  • 34. Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion.
    Agarwal G, Bhatia V, Cook S, Thomas PQ.
    J Clin Endocrinol Metab; 2000 Dec 06; 85(12):4556-61. PubMed ID: 11134108
    [Abstract] [Full Text] [Related]

  • 35. Pituitary transcription factor Prop-1 stimulates porcine pituitary glycoprotein hormone alpha subunit gene expression.
    Sato T, Kitahara K, Susa T, Kato T, Kato Y.
    J Mol Endocrinol; 2006 Oct 06; 37(2):341-52. PubMed ID: 17032749
    [Abstract] [Full Text] [Related]

  • 36. PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.
    Vallette-Kasic S, Barlier A, Teinturier C, Diaz A, Manavela M, Berthezène F, Bouchard P, Chaussain JL, Brauner R, Pellegrini-Bouiller I, Jaquet P, Enjalbert A, Brue T.
    J Clin Endocrinol Metab; 2001 Sep 06; 86(9):4529-35. PubMed ID: 11549703
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  • 40. Suprasellar mass mimicking a hypothalamic glioma in a patient with a complete PROP1 deletion.
    Akcay A, Ulucan K, Taskin N, Boyraz M, Akcay T, Zurita O, Gomez A, Heath KE, Campos-Barros A.
    Eur J Med Genet; 2013 Aug 06; 56(8):445-51. PubMed ID: 23831233
    [Abstract] [Full Text] [Related]

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