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 *

146 related articles for article (PubMed ID: 15625433)

  • 1. The triple "a" syndrome confirmed by molecular analysis: a case report of 7-year-old boy.
    Iwanczak F; Smigiel R; Blitek A; Huebner A
    J Pediatr Gastroenterol Nutr; 2005 Jan; 40(1):87-9. PubMed ID: 15625433
    [No Abstract]   [Full Text] [Related]  

  • 2. Triple-A syndrome with prominent ophthalmic features and a novel mutation in the AAAS gene: a case report.
    Brooks BP; Kleta R; Caruso RC; Stuart C; Ludlow J; Stratakis CA
    BMC Ophthalmol; 2004 Jun; 4():7. PubMed ID: 15217518
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Progressive bulbospinal amyotrophy in triple A syndrome with AAAS gene mutation.
    Goizet C; Catargi B; Tison F; Tullio-Pelet A; Hadj-Rabia S; Pujol F; Lagueny A; Lyonnet S; Lacombe D
    Neurology; 2002 Mar; 58(6):962-5. PubMed ID: 11914417
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Late-onset triple A syndrome: a risk of overlooked or delayed diagnosis and management.
    Salmaggi A; Zirilli L; Pantaleoni C; De Joanna G; Del Sorbo F; Koehler K; Krumbholz M; Huebner A; Rochira V
    Horm Res; 2008; 70(6):364-72. PubMed ID: 18953174
    [TBL] [Abstract][Full Text] [Related]  

  • 5. AAA syndrome--adrenal insufficiency, alacrima and achalasia.
    Wallace IR; Hunter SJ
    QJM; 2012 Aug; 105(8):803-4. PubMed ID: 21865313
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Phenotypic heterogeneity in AAAS gene mutation.
    Barat P; Goizet C; Tullio-Pelet A; Puel O; Labessan C; Barthelemy A
    Acta Paediatr; 2004 Sep; 93(9):1257-9. PubMed ID: 15384895
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. Esophageal achalasia and alacrima in siblings.
    Singh A; Shah A
    Indian Pediatr; 2006 Feb; 43(2):161-3. PubMed ID: 16528113
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ALADIN, but where's the genie?
    Orrell RW; Clark AJ
    Neurology; 2002 Mar; 58(6):847-8. PubMed ID: 11914396
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [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]  

  • 17. 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]  

  • 18. Muscle Pathology as a Diagnostic Clue to Allgrove Syndrome.
    Reimann J; Kohlschmidt N; Tolksdorf K; Weis J; Kuchelmeister K; Roos A
    J Neuropathol Exp Neurol; 2017 May; 76(5):337-341. PubMed ID: 28371804
    [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. Triple A (Allgrove) syndrome: an unusual association with syringomyelia.
    Bizzarri C; Benevento D; Terzi C; Huebner A; Cappa M
    Ital J Pediatr; 2013 Jun; 39():39. PubMed ID: 23800107
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.