Signs, complications, and platelet aggregation in familial exudative vitreoretinopathy.

No abstract is available for this paper.

• Publication year

  1991

• Venue

  American journal of ophthalmology-glaucoma

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  PMID 1985487
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Familial exudative vitreoretinopathy

  2004cited by this paper
• Surgical management of late-onset retinal detachments associated with regressed retinopathy of prematurity.

  1990cited by this paper
• Juvenile retinal detachment as a complication of familial exudative vitreoretinopathy.

  1989cited by this paper
• Is irradiation a justifiable treatment of choroidal melanoma?

  1989cited by this paper
• The histopathology of familial exudative vitreoretinopathy. A report of two cases.

  1985cited by this paper
• Description and pathogenesis of late stages of retinopathy of prematurity.

  1985cited by this paper
• [Familial exudative vitreoretinopathy, rhegmatogenous retinal detachment and postoperative uveitis with massive subretinal exudation].

  1984cited by this paper
• Criswick-Schepens syndrome (familial exudative vitreoretinopathy). Study of a Colombian kindred.

  1984cited by this paper
• Retinal vascular pattern in familial exudative vitreoretinopathy.

  1984cited by this paper
• Familial exudative vitreoretinopathy associated with familial thrombocytopathy.

  1983cited by this paper
• Falciform retinal fold as sign of familial exudative vitreoretinopathy.

  1983cited by this paper
• Autosomal dominant exudative vitreoretinopathy.

  1983cited by this paper
• Retinal involvement in familial exudative vitreoretinopathy.

  1982cited by this paper
• Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina.

  1982cited by this paper
• Congenital retinal fold as a sign of dominant exudative vitreoretinopathy.

  1981cited by this paper
• Pathologic findings in familial exudative vitreoretinopathy.

  1981cited by this paper
• Autosomal dominant exudative vitreoretinopathy.

  1980cited by this paper
• Familial exudative vitreo-retinopathy.

  1979cited by this paper
• Flourescein angiography in mild stages of dominant exudative vitreoretinopathy.

  1979cited by this paper
• Familial exudative vitreoretinopathy.

  1979cited by this paper
• An improved method for preparing platelet-rich plasma.

  1977cited by this paper
• Fluorescein angiographic findings in familial exudative vitreoretinopathy.

  1976cited by this paper
• The pleomorphism and complications of posterior hyperplastic primary vitreous.

  1975cited by this paper
• Familial exudative vitreoretinopathy. An expanded view.

  1971cited by this paper
• Familial exudative vitreoretinopathy.

  1969cited by this paper
• Intertissue vascular relationships in the fundus of the eye=.

  1965cited by this paper
• CONGENITAL RETINAL FOLD

  1935cited by this paper

• KIF11-related MCLMR presenting with FEVR-like retinopathy: first report in an Indian child

  2025cites this paper
• Fluorescein Angiography May Predict Surgical Outcomes of Tractional Retinal Detachment in Familial Exudative Vitreoretinopathy.

  2025cites this paper
• Temporal Retinal Vessel Angle as a Biomarker for Familial Exudative Vitreoretinopathy.

  2025cites this paper
• Angiographic characteristics in mild familial exudative vitreoretinopathy with genetically confirmed autosomal dominant inheritance.

  2024cites this paper
• LONG-TERM FUNCTIONAL AND CLINICAL OUTCOMES IN FAMILIAL EXUDATIVE VITREORETINOPATHY

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• Cyanoacrylate glue for iatrogenic retinal breaks during vitrectomy in stage 5 familial exudative vitreoretinopathy

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• Novel Exon 7 Deletions in TSPAN12 in a Three-Generation FEVR Family: A Case Report and Literature Review

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• Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy

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• Long-term clinical prognosis of 335 infant single-gene positive FEVR cases

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• Whole-Exome Sequencing Reveals Novel TSPAN12 Variants in Autosomal Dominant Familial Exudative Vitreoretinopathy

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• Pathogenic variants and associated phenotypic spectrum of TSPAN12 based on data from a large cohort

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• Reaching a FEVR Pitch: A Case Series of Familial Exudative Vitreoretinopathy in Northern Ireland.

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• Severe exudative vitreoretinopathy as a common feature for CTNNB1, KIF11 and NDP variants plus sector degeneration for KIF11.

  2021cites this paper
• Outcomes of surgery in eyes with familial exudative vitreoretinopathyassociated retinal detachment.

  2020cites this paper
• Clinical and whole-exome sequencing findings in Individuals from Yunnan Province with Familial Exudative Vitreoretinopathy

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• A start codon mutation of the TSPAN12 gene in Chinese families causes clinical heterogeneous familial exudative vitreoretinopathy

  2019cites this paper
• Retinal detachments in the pediatric population

  2018cites this paper
• Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

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• Familial Exudative Vitreoretinopathy: Pathophysiology, Diagnosis, and Management

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• Wnt-Spectrum Vitreoretinopathy Masquerading as Congenital Toxoplasmosis.

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• Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.

  2017cites this paper
• Characteristics of Retinal Breaks and Surgical Outcomes in Rhegmatogenous Retinal Detachment in Familial Exudative Vitreoretinopathy.

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• LONGITUDINAL CHANGES IN THE OPTIC NERVE HEAD AND RETINA OVER TIME IN VERY YOUNG CHILDREN WITH FAMILIAL EXUDATIVE VITREORETINOPATHY

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• Mutations in LRP 5 , FZD 4 , TSPAN 12 , NDP , ZNF 408 , or KIF 11 Genes Account for 38 . 7 % of Chinese Patients With Familial Exudative Vitreoretinopathy

  2017cites this paper
• Genetics Mutations in LRP 5 , FZD 4 , TSPAN 12 , NDP , ZNF 408 , or KIF 11 Genes Account for 38 . 7 % of Chinese Patients With Familial Exudative Vitreoretinopathy

  2017cites this paper
• Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy

  2017cites this paper
• FEVR-like Presentation in an 11q Deletion Syndrome and 16p13.11 Microdeletion.

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• Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12

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• DISTINCTIVE WHITE FUNDUS LESIONS IN FAMILIAL EXUDATIVE VITREORETINOPATHY: A NEWLY CHARACTERIZED CLINICAL FEATURE

  2016cites this paper
• SURGICAL MANAGEMENT OF ADVANCED FAMILIAL EXUDATIVE VITREORETINOPATHY WITH COMPLICATIONS

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• Anatomical and functional outcomes following vitrectomy for advanced familial exudative vitreoretinopathy: a single surgeon's experience

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• Fzd4 Haploinsufficiency Delays Retinal Revascularization in the Mouse Model of Oxygen Induced Retinopathy

  2016cites this paper
• ELUCIDATION OF THE CELLULAR AND MOLECULAR MECHANISMS OF MISSENSE MUTATIONS ASSOCIATED WITH FAMILIAL EXUDATIVE VITREORETINOPATHY AND CONGENITAL MYASTHENIC SYNDROME

  2015influential citation
• Familial exudative vitreoretinopathy and related retinopathies

  2015cites this paper
• Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy

  2015cites this paper
• KIF11 mutations are a common cause of autosomal dominant familial exudative vitreoretinopathy

  2015cites this paper
• Identification of two novel LRP5 mutations in families with familial exudative vitreoretinopathy

  2014cites this paper
• Identification of the cellular mechanisms that modulate trafficking of frizzled family receptor 4 (FZD4) missense mutants associated with familial exudative vitreoretinopathy.

  2014cites this paper
• Familial exudative vitreoretinopathy presenting with unilateral rhegmatogenous retinal detachment in a Malay teenager

  2013cites this paper
• Retinal exsudative Gefäßerkrankungen im Kindesalter: Morbus Coats und familiär exsudative Vitreoretinopathie (FEVR)

  2013cites this paper
• Familial exudative vitreoretinopathy in a premature child.

  2013cites this paper
• Traction retinal detachment under silicone oil treated with two-port, 25-gauge pars plana vitrectomy and scissor segmentation in a child with familial exudative vitreoretinopathy.

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• CLINICAL CHARACTERISTICS AND SURGICAL MANAGEMENT OF FAMILIAL EXUDATIVE VITREORETINOPATHY–ASSOCIATED RHEGMATOGENOUS RETINAL DETACHMENT

  2012cites this paper
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• Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy

  2012cites this paper
• Clinical presentation of familial exudative vitreoretinopathy.

  2011cites this paper
• Pediatric Rhegmatogenous Retinal Detachment

  2011cites this paper
• Familiäre exsudative Vitreoretinopathie

  2010cites this paper
• An Essential Role of the Cysteine-rich Domain of FZD4 in Norrin/Wnt Signaling and Familial Exudative Vitreoretinopathy*

  2010cites this paper
• FAMILIAL EXUDATIVE VITREORETINOPATHY: OUR EXPERIENCE VITREORRETINOPATÍA EXUDATIVA FAMILIAR: NUESTRA EXPERIENCIA

  2009cites this paper
• Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused by FZD4 Mutations in two Distinct Pedigrees

  2009cites this paper
• Estudio de las distrofias vitreorretinianas en población mexicana

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• VITREORRETINOPATÍA EXUDATIVA FAMILIAR: NUESTRA EXPERIENCIA FAMILIAL EXUDATIVE VITREORETINOPATHY: OUR EXPERIENCE

  2008cites this paper
• A rare association of familial exudative vitreoretinopathy and Turner's syndrome.

  2008cites this paper
• [Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy].

  2008cites this paper
• Retinal detachments in the pediatric population: part I.

  2007cites this paper
• Parameters of LRP5 from a structural and molecular perspective.

  2005cites this paper
• Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree

  2005cites this paper
• Identification of a fourth locus (EVR4) for familial exudative vitreoretinopathy (FEVR).

  2004cites this paper
• [Criswick-Schepens syndrome -- familial exudative vitreoretinopathy. Report of six cases in two consanguineous families].

  2004cites this paper
• Retinal capillary angioma in familial exudative vitreoretinopathy treated with photodynamic therapy.

  2004cites this paper
• Spectrum and frequency of FZD4 mutations in familial exudative vitreoretinopathy.

  2004cites this paper
• Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

  2004cites this paper
• Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity

  2003cites this paper
• Excessive myopia and anisometropia associated with familial exudative vitreoretinopathy.

  2002cites this paper
• [Vitreoretinal surgery in children].

  1999cites this paper
• Familial exudative vitreoretinopathy associated with monocular axial myopia.

  1999cites this paper
• Vitreoretinale Chirurgie bei Kindern

  1999cites this paper
• Peripheral retinal nonperfusion associated with essential thrombocytosis.

  1999cites this paper
• Autosomal recessive familial exudative vitreoretinopathy: evidence for genetic heterogeneity

  1998cites this paper
• High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population.

  1998cites this paper
• Familial exudative vitreoretinopathy. Results of surgical management.

  1998cites this paper
• COMBINED TRACTIONAL RHEGMATOGENOUS RETINAL DETACHMENT IN FAMILIAL EXUDATIVE VITREORETINOPATHY ASSOCIATED WITH POSTERIOR RETINAL HOLES: Surgical Therapy

  1998cites this paper
• Familial exudative vitreoretinopathy linked to D11S533 in a large Asian family with consanguinity.

  1996cites this paper
• Familial exudative vitreoretinopathy.

  1995cites this paper
• Improved surgical treatment of familial exudative vitreoretinopathy in children.

  1995cites this paper
• Molecular genetics of inherited eye disorders.

  1994cites this paper
• Recent developments in certain X-linked genetic eye disorders.

  1993cites this paper
• X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis.

  1993cites this paper
• Spontaneous and traumatic vitreous hemorrhage.

  1993cites this paper
• Retinal telangiectasis and proliferation of the retinal vessels in a family.

  1993cites this paper
• The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533.

  1992cites this paper
• Ultrastructural study of Norrie's disease.

  1991cites this paper