These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

298 related items for PubMed ID: 17587179

  • 1. Genetics of septo-optic dysplasia.
    Kelberman D, Dattani MT.
    Pituitary; 2007; 10(4):393-407. PubMed ID: 17587179
    [Abstract] [Full Text] [Related]

  • 2. Septo-optic dysplasia - novel insights into the aetiology.
    Kelberman D, Dattani MT.
    Horm Res; 2008; 69(5):257-65. PubMed ID: 18259104
    [Abstract] [Full Text] [Related]

  • 3. Septo-optic dysplasia and other midline defects: the role of transcription factors: HESX1 and beyond.
    McCabe MJ, Alatzoglou KS, Dattani MT.
    Best Pract Res Clin Endocrinol Metab; 2011 Feb; 25(1):115-24. PubMed ID: 21396578
    [Abstract] [Full Text] [Related]

  • 4. The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.
    Kelberman D, Dattani MT.
    Ann Med; 2006 Feb; 38(8):560-77. PubMed ID: 17438671
    [Abstract] [Full Text] [Related]

  • 5. 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; 62(2):163-8. PubMed ID: 15670191
    [Abstract] [Full Text] [Related]

  • 6. HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
    McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, Papadimitriou A, Keller E, Keller A, Haufs N, Krude H, Shalet SM, Dattani MT.
    J Clin Endocrinol Metab; 2007 Feb; 92(2):691-7. PubMed ID: 17148560
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Septo-optic dysplasia complex: a heterogeneous malformation syndrome.
    Polizzi A, Pavone P, Iannetti P, Manfré L, Ruggieri M.
    Pediatr Neurol; 2006 Jan; 34(1):66-71. PubMed ID: 16376284
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. New insights into septo-optic dysplasia.
    Saranac L, Gucev Z.
    Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2014 Jan; 35(1):123-7. PubMed ID: 24802313
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Novel Genetic Diagnoses in Septo-Optic Dysplasia.
    Reis LM, Seese S, Maheshwari M, Basel D, Weik L, McCarrier J, University Of Washington Center For Mendelian Genomics, Semina EV.
    Genes (Basel); 2022 Jun 28; 13(7):. PubMed ID: 35885948
    [Abstract] [Full Text] [Related]

  • 16. [Natural course of septo-optic dysplasia: retrospective analysis of 20 cases].
    León-Gonzalez M, García-Peñas JJ, Puertas-Bordallo D, López-Pino MA, Argente-Oliver J, Cantarín-Extremera V.
    Rev Neurol; 2012 Mar 16; 54(6):321-31. PubMed ID: 22403144
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.