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 *

150 related articles for article (PubMed ID: 31230109)

  • 21. Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome.
    Bayram Y; Pehlivan D; Karaca E; Gambin T; Jhangiani SN; Erdin S; Gonzaga-Jauregui C; Wiszniewski W; Muzny D; ; Elcioglu NH; Yildirim MS; Bozkurt B; Zamani AG; Boerwinkle E; Gibbs RA; Lupski JR
    Am J Med Genet A; 2014 Sep; 164A(9):2328-34. PubMed ID: 25045128
    [TBL] [Abstract][Full Text] [Related]  

  • 22. GAPO syndrome associated with pyoderma vegetans: an unreported co-existence.
    Karadag AS; Calka O; Bilgili SG; Karadag R; Bulut G
    Genet Couns; 2013; 24(2):133-9. PubMed ID: 24032282
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Consequences of cranial vault expansion surgery for craniosynostosis.
    Thompson DN; Jones BM; Harkness W; Gonsalez S; Hayward RD
    Pediatr Neurosurg; 1997 Jun; 26(6):296-303. PubMed ID: 9485157
    [TBL] [Abstract][Full Text] [Related]  

  • 24. GAPO syndrome: first patients with partially empty sella.
    Orbak Z; Orbak R; Ozkan B; Okten A
    J Pediatr Endocrinol Metab; 2002 Jun; 15(6):865-8. PubMed ID: 12099399
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Growth retardation, alopecia, pseudoanodontia, and optic atrophy (GAPO syndrome) with congenital glaucoma.
    Mullaney PB; Jacquemin C; al-Rashed W; Smith W
    Arch Ophthalmol; 1997 Jul; 115(7):940-1. PubMed ID: 9230846
    [No Abstract]   [Full Text] [Related]  

  • 26. GAPO syndrome: four new patients with congenital glaucoma and myelinated retinal nerve fiber layer.
    Bozkurt B; Yildirim MS; Okka M; Bitirgen G
    Am J Med Genet A; 2013 Apr; 161A(4):829-34. PubMed ID: 23494824
    [TBL] [Abstract][Full Text] [Related]  

  • 27. ANTXR1 deficiency promotes fibroblast senescence: implications for GAPO syndrome as a progeroid disorder.
    Przyklenk M; Karmacharya S; Bonasera D; Pasanen-Zentz AL; Kmoch S; Paulsson M; Wagener R; Liccardi G; Schiavinato A
    Sci Rep; 2024 Apr; 14(1):9321. PubMed ID: 38653789
    [TBL] [Abstract][Full Text] [Related]  

  • 28. GAPO syndrome: a new case.
    Sandgren G
    Am J Med Genet; 1995 Jul; 58(1):87-90. PubMed ID: 7573163
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Value of imaging in GAPO syndrome].
    Goucha S; Mnif N; Bouhala T; Tenzakhti F; El Andaloussi H; Fazaa B; Hamza R; Kamoun MR
    J Radiol; 2002 Feb; 83(2 Pt 1):153-6. PubMed ID: 11965163
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Evaluating Trends in Headache and Revision Surgery following Cranial Vault Remodeling for Craniosynostosis.
    Pellicer E; Siebold BS; Birgfeld CB; Gallagher ER
    Plast Reconstr Surg; 2018 Mar; 141(3):725-734. PubMed ID: 29481403
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Management of craniosynostoses.
    Renier D; Lajeunie E; Arnaud E; Marchac D
    Childs Nerv Syst; 2000 Nov; 16(10-11):645-58. PubMed ID: 11151714
    [TBL] [Abstract][Full Text] [Related]  

  • 32. GAPO syndrome with the novel features of pulmonary hypertension, ankyloglossia, and prognathism.
    Demirgüneş EF; Ersoy-Evans S; Karaduman A
    Am J Med Genet A; 2009 Feb; 149A(4):802-5. PubMed ID: 19291762
    [No Abstract]   [Full Text] [Related]  

  • 33. GAPO syndrome: first Egyptian case with ultrastructural changes in the gingiva.
    Meguid NA; Afifi HH; Ramzy MI; Hindawy A; Temtamy SA
    Clin Genet; 1997 Aug; 52(2):110-5. PubMed ID: 9298746
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Ophthalmic findings in GAPO syndrome.
    Ilker SS; Oztürk F; Kurt E; Temel M; Gül D; Sayli BS
    Jpn J Ophthalmol; 1999; 43(1):48-52. PubMed ID: 10197743
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [GAPO syndrome].
    Goucha S; Fazaa B; Ezzine N; Jaber K; Elandaloussi H; Abid R; Kamoun MR
    Ann Dermatol Venereol; 2000 May; 127(5):501-4. PubMed ID: 10863181
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Two siblings with GAPO syndrome: a novel missense variant in ANTXR1.
    Yildiz O; Taşdelen E; Karakaya T; Taşdelen H
    Clin Dysmorphol; 2022 Oct; 31(4):191-195. PubMed ID: 36094357
    [No Abstract]   [Full Text] [Related]  

  • 37. Surgical correction of craniosynostosis in malignant osteopetrosis.
    Krimmel M; Niemann G; Will B; Reinert S
    J Craniofac Surg; 2004 Mar; 15(2):218-20; discussion 221. PubMed ID: 15167232
    [TBL] [Abstract][Full Text] [Related]  

  • 38. GAPO syndrome: a report of two siblings and a review of literature.
    Nanda A; Al-Ateeqi WA; Al-Khawari MA; Alsaleh QA; Anim JT
    Pediatr Dermatol; 2010; 27(2):156-61. PubMed ID: 20537066
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The GAPO syndrome.
    Manouvrier-Hanu S; Largilliere C; Benalioua M; Farriaux JP; Fontaine G
    Am J Med Genet; 1987 Mar; 26(3):683-8. PubMed ID: 3565482
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Growth retardation, alopecia, pseudo-anodontia, and optic atrophy--the GAPO syndrome: report of a patient and review of the literature.
    Tipton RE; Gorlin RJ
    Am J Med Genet; 1984 Oct; 19(2):209-16. PubMed ID: 6507471
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.