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Table representation of search results timeline featuring number of search results per year.

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1988 1
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11 results

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Page 1
GAPO syndrome: a report of two siblings and a review of literature.
Nanda A, Al-Ateeqi WA, Al-Khawari MA, Alsaleh QA, Anim JT. Nanda A, et al. Pediatr Dermatol. 2010 Mar-Apr;27(2):156-61. doi: 10.1111/j.1525-1470.2010.01100.x. Pediatr Dermatol. 2010. PMID: 20537066 Review.
Growth retardation, alopecia, pseudoanodontia, optic atrophy (GAPO) syndrome is a rare autosomal recessive disorder. ...
Growth retardation, alopecia, pseudoanodontia, optic atrophy (GAPO) syndrome is a ra …
GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature.
Goloni-Bertollo EM, Ruiz MT, Goloni CB, Muniz MP, Valério NI, Pavarino-Bertelli EC. Goloni-Bertollo EM, et al. Am J Med Genet A. 2008 Jun 15;146A(12):1523-9. doi: 10.1002/ajmg.a.32157. Am J Med Genet A. 2008. PMID: 18470892 Review.
The GAPO syndrome is an extremely rare autosomal recessive disease that presents as main characteristics evident growth retardation, alopecia, pseudoanodontia, progressive optic atrophy and a typical face. Until now, only 30 …
The GAPO syndrome is an extremely rare autosomal recessive disease that presents as main characteristics evident growth …
GAPO Syndrome-A Rare Cause of Osteomyelitis of Jaws; Report of 4 Cases With a Brief Review of the Literature.
Puranik RS, Puranik SR, Hallur N, Venkatesh D. Puranik RS, et al. J Oral Maxillofac Surg. 2018 Jun;76(6):1216-1225. doi: 10.1016/j.joms.2017.12.002. Epub 2017 Dec 12. J Oral Maxillofac Surg. 2018. PMID: 29304326 Review.
GAPO syndrome is characterized by growth retardation, alopecia, pseudoanodontia, and ophthalmic abnormalities. ...Pseudoanodontia is a rare clinical and radiologic manifestation that is always associated with GAPO syndrom …
GAPO syndrome is characterized by growth retardation, alopecia, pseudoanodontia, and ophthalmic ab …
Converging physiological roles of the anthrax toxin receptors.
Sergeeva OA, van der Goot FG. Sergeeva OA, et al. F1000Res. 2019 Aug 12;8:F1000 Faculty Rev-1415. doi: 10.12688/f1000research.19423.1. eCollection 2019. F1000Res. 2019. PMID: 31448094 Free PMC article. Review.
In the last few years, insight into their endogenous roles has come from two rare diseases: hyaline fibromatosis syndrome, caused by mutations in CMG2, and growth retardation, alopecia, pseudo-anodontia, and optic atrophy (GAPO) …
In the last few years, insight into their endogenous roles has come from two rare diseases: hyaline fibromatosis syndrome, caused by …
GAPO syndrome: a new case of this rare syndrome and a review of the relative importance of different phenotypic features in diagnosis.
Bacon W, Hall RK, Roset JP, Boukari A, Tenenbaum H, Walter B. Bacon W, et al. J Craniofac Genet Dev Biol. 1999 Oct-Dec;19(4):189-200. J Craniofac Genet Dev Biol. 1999. PMID: 10731088 Review.
The case of GAPO syndrome reported here is the 24th recorded case, 23 cases having been published previously. The 29-year-old male under discussion presents all the typical features of the syndrome, having short stature, dysmorphic craniofacial features, tota …
The case of GAPO syndrome reported here is the 24th recorded case, 23 cases having been published previously. The 29-year-old …
GAPO syndrome: a new case.
Sandgren G. Sandgren G. Am J Med Genet. 1995 Jul 31;58(1):87-90. doi: 10.1002/ajmg.1320580117. Am J Med Genet. 1995. PMID: 7573163 Review.
The fifteenth known case of GAPO syndrome is presented: a probable autosomal-recessive condition of growth retardation, alopecia, pseudoanodontia (failure of tooth eruption), and optic atrophy. This article contains the clin …
The fifteenth known case of GAPO syndrome is presented: a probable autosomal-recessive condition of growth retardati …
[Tooth eruption disturbances and syndromes].
Oosterkamp BC, Ockeloen CW, Carels CE, Kuijpers-Jagtman AM. Oosterkamp BC, et al. Ned Tijdschr Tandheelkd. 2014 Apr;121(4):233-8. Ned Tijdschr Tandheelkd. 2014. PMID: 24881265 Review. Dutch.
There are 5 syndromes which involve the complete failure of several or even all teeth to erupt, specifically: cleidocranial dysplasia, Gardner's syndrome, osteopetrosis, mucopolysaccharidosis and GAPO syndrome. Some are very rare and will seldom be encountere …
There are 5 syndromes which involve the complete failure of several or even all teeth to erupt, specifically: cleidocranial dysplasia, Gardn …
Fell-Muir Lecture: Regulatory mechanisms of skeletal and connective tissue development and homeostasis - lessons from studies of human disorders.
Olsen BR, Berendsen AD, Besschetnova TY, Duan X, Hu K. Olsen BR, et al. Int J Exp Pathol. 2016 Aug;97(4):296-302. doi: 10.1111/iep.12198. Epub 2016 Sep 1. Int J Exp Pathol. 2016. PMID: 27581728 Free PMC article. Review.
Studies of proliferative hemangiomas have led to the discovery that interactions of endothelial cells with extracellular matrix and/or Vascular Endothelial Growth Factor (VEGF)-A stimulate the expression of VEGFR1, the VEGF decoy receptor, and suppress VEGF-dependent VEGFR …
Studies of proliferative hemangiomas have led to the discovery that interactions of endothelial cells with extracellular matrix and/or Vascu …
[Ocular manifestation in GAPO syndrome. Report of the first tunisian case].
Touzri RA, Goucha S, Kriaa L, Beltaif O, Fazaa B, El Andolsi H, Kamoun MR, Ouertani A. Touzri RA, et al. J Fr Ophtalmol. 2003 Dec;26(10):1067-70. J Fr Ophtalmol. 2003. PMID: 14691402 Review. French.
GAPO syndrome is a rare autosomal recessive disorder whose main manifestations are: growth retardation, alopecia, pseudoanodontia and optic atrophy. We report here the ophthalmological findings in a 12-year-old Tunisian boy …
GAPO syndrome is a rare autosomal recessive disorder whose main manifestations are: growth retardation, alope …
[Ophthalmological anomalies of the GAPO syndrome (growth retardation, alopecia, pseudo-anodontia, optic atrophy). Apropos of a case].
Dellac M, Manouvrier-Hanu S, Rouland JF. Dellac M, et al. J Fr Ophtalmol. 1990;13(11-12):547-50. J Fr Ophtalmol. 1990. PMID: 2081845 Review. French.
G.A.P.O. syndrome is a rare autosomal recessive disorder whose main manifestations are growth retardation, alopecia, pseudo-anodontia, and optic atrophy. Optic atrophy has been reported in 30% of affected patients, along wit …
G.A.P.O. syndrome is a rare autosomal recessive disorder whose main manifestations are growth retardation, alopecia …
11 results