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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 25781531)

  • 1. Triple A syndrome with a novel indel mutation in the AAAS gene and delayed puberty.
    Bustanji H; Sahar B; Huebner A; Ajlouni K; Landgraf D; Hamamy H; Koehler K
    J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):933-6. PubMed ID: 25781531
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Allgrove syndrome in the mainland of China: clinical report and mutation analysis].
    Gong CX; Wen YR; Zhao XL; Su C; Cao BY; Zhang X
    Zhonghua Er Ke Za Zhi; 2007 Jun; 45(6):422-5. PubMed ID: 17880786
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Triple A or Allgrove syndrome. A case report with ophthalmic abnormalities and a novel mutation in the AAAS gene.
    Villanueva-Mendoza C; artínez-Guzmán O; Rivera-Parra D; Zenteno JC
    Ophthalmic Genet; 2009 Mar; 30(1):45-9. PubMed ID: 19172511
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutation spectra of the AAAS gene in Iranian families with Allgrove Syndrome.
    Yassaee VR; Soltani Z; Ardakani BM
    Arch Med Res; 2011 Feb; 42(2):163-8. PubMed ID: 21565631
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous deletion of the entire AAAS gene in a triple A syndrome patient.
    Koehler K; Hackmann K; Landgraf D; Schubert T; Shakiba M; Kariminejad A; Huebner A
    Eur J Med Genet; 2019 Jul; 62(7):103665. PubMed ID: 31071487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The genetic basis of triple A (Allgrove) syndrome in a Greek family.
    Papageorgiou L; Mimidis K; Katsani KR; Fakis G
    Gene; 2013 Jan; 512(2):505-9. PubMed ID: 23073554
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy.
    Jayant SS; Gupta R; Agrawal K; Das L; Dutta P; Bhansali A
    Hormones (Athens); 2021 Mar; 20(1):197-205. PubMed ID: 32700293
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Two patients with an identical novel mutation in the AAAS gene and similar phenotype of triple A (Allgrove) syndrome.
    Krull I; M-Woelfle M; Bärlocher K; Koehler K; Huebner A; Brändle M
    Exp Clin Endocrinol Diabetes; 2010 Aug; 118(8):530-6. PubMed ID: 20200814
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Two novel truncating variants of the AAAS gene causative of the triple A syndrome.
    Vezzoli V; Duminuco P; Pogliaghi G; Saccone M; Cangiano B; Rosatelli MC; Meloni A; Persani L; Bonomi M
    J Endocrinol Invest; 2020 Jul; 43(7):973-982. PubMed ID: 31939195
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Allgrove syndrome (triple A). Finding of a mutation not described in the AAAS gene].
    Capataz Ledesma M; Méndez Pérez P; Rodríguez López R; Galán Gómez E
    An Pediatr (Barc); 2013 Feb; 78(2):109-12. PubMed ID: 22824007
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases.
    Singh K; Puri RD; Bhai P; Arya AD; Chawla G; Saxena R; Verma IC
    J Pediatr Endocrinol Metab; 2018 Jul; 31(7):799-807. PubMed ID: 29874194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Allgrove syndrome.
    Kilicli F; Acibucu F; Senel S; Dokmetas HS
    Singapore Med J; 2012 May; 53(5):e92-4. PubMed ID: 22584989
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and genetic characterisation of a series of patients with triple A syndrome.
    Kurnaz E; Duminuco P; Aycan Z; Savaş-Erdeve Ş; Muratoğlu Şahin N; Keskin M; Bayramoğlu E; Bonomi M; Çetinkaya S
    Eur J Pediatr; 2018 Mar; 177(3):363-369. PubMed ID: 29255950
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.
    Kallabi F; Belghuith N; Aloulou H; Kammoun T; Ghorbel S; Hajji M; Gallas S; Chemli J; Chabchoub I; Azzouz H; Ben Chehida A; Sfaihi L; Makni S; Amouri A; Keskes L; Tebib N; Ben Becher S; Hachicha M; Kamoun H
    Arch Med Res; 2016 Feb; 47(2):105-10. PubMed ID: 27133709
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [From gene to disease; adrenocortical insufficiency, achalasia and disrupted tear secretion: Allgrove syndrome].
    van Daele PL; de Herder WW; Huebner A
    Ned Tijdschr Geneeskd; 2002 Nov; 146(48):2295-7. PubMed ID: 12497758
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel AAAS gene mutation (p.R194X) in a patient with triple A syndrome.
    Dusek T; Korsic M; Koehler K; Perkovic Z; Huebner A; Korsic M
    Horm Res; 2006; 65(4):171-6. PubMed ID: 16543750
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiency.
    Luigetti M; Pizzuti A; Bartoletti S; Houlden H; Pirro C; Bottillo I; Madia F; Conte A; Tonali PA; Sabatelli M
    J Neurol Sci; 2010 Mar; 290(1-2):150-2. PubMed ID: 20051279
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutant WD-repeat protein in triple-A syndrome.
    Tullio-Pelet A; Salomon R; Hadj-Rabia S; Mugnier C; de Laet MH; Chaouachi B; Bakiri F; Brottier P; Cattolico L; Penet C; Bégeot M; Naville D; Nicolino M; Chaussain JL; Weissenbach J; Munnich A; Lyonnet S
    Nat Genet; 2000 Nov; 26(3):332-5. PubMed ID: 11062474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spinal cord atrophy in triple A syndrome associated with a novel compound heterozygous mutation.
    Kunte H; Trendelenburg G; Matzen J; Ventz M; Kornak U; Harms L
    Neuro Endocrinol Lett; 2010; 31(3):301-3. PubMed ID: 20588230
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa.
    Kallabi F; Ben Rebeh I; Felhi R; Sellami D; Masmoudi S; Keskes L; Kamoun H
    Horm Res Paediatr; 2016; 85(1):18-21. PubMed ID: 26595337
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.