Borruat, François-Xavier
François-Xavier Borruat
VIAF ID: 31458714 (Personal)
Permalink: http://viaf.org/viaf/31458714
Preferred Forms
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- 100 1 _ ‡a Borruat, François-Xavier
- 100 1 _ ‡a Borruat, François-Xavier
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- 100 1 _ ‡a Borruat, François-Xavier
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- 100 0 _ ‡a François-Xavier Borruat
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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Acquired unilateral pseudoptosis: a presentation of silent sinus syndrome | |
Acute posterior multifocal placoid pigment epitheliopathy following mumps | |
Acute reversible Charles Bonnet syndrome precipitated by sudden severe anemia. | |
Altered vision during motion: an unusual symptom of cerebellar dysfunction, quantifiable by a simple clinical test | |
Aspergillosis: an unusual case of orbital apex syndrome | |
Central nervous system involvement in Guillain-Barré-like syndrome: clinical and magnetic resonance imaging evidence | |
Comment mieux vieillir | |
Congruous quadrantanopia and optic radiation lesion. | |
Corneal penetration of diclofenac from a fixed combination of diclofenac-gentamicin eyedrops | |
Differential effect of long versus short wavelength light exposure on pupillary re-dilation in patients with outer retinal disease. | |
Diplopia revealing unsuspected orbital foreign bodies | |
Double concentric autofluorescence ring in NR2E3-p.G56R-linked autosomal dominant retinitis pigmentosa. | |
Étiopathogénie des nystagmus verticaux du nourrisson | |
Evanescent white linear flecks and posterior microphthalmos: new features of a recently established disease. | |
Exigences visuelles pour la conduite : y voir plus clair | |
Extraconal orbital sarcoidosis: an unusual cause of optic neuropathy | |
False negative apraclonidine test in two patients with Horner syndrome | |
Favourable outcome of progressive multifocal leucoencephalopathy in two patients with dermatomyositis. | |
Herpes zoster ophthalmicus. Anterior ischemic optic neuropathy and acyclovir | |
Hypertension artérielle et oeil | |
Idiopathic orbital inflammation (orbital inflammatory pseudotumour): an unusual cause of transient ischaemic attack | |
[Indocyanine green angiography in posterior uveitis] | |
Isolated internal ophthalmoplegia associated with IgG anti-GQ1b antibody | |
Large deletion (7.2 kb) of mitochondrial DNA with novel boundaries in a case of progressive external ophthalmoplegia | |
[Multiple evanescent white dot syndrome] | |
Multiple intraorbital neurofibromas: a rare cause of proptosis | |
Mutation analysis of KIF21A in congenital fibrosis of the extraocular muscles (CFEOM) patients | |
Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness | |
Natural history of diffuse uveal melanocytic proliferation. Case report | |
[Neuro-ophthalmologic complications of disseminated lupus erythematosus] | |
New finding: transitory horizontal pendular nystagmus secondary to neonatal abstinence syndrome | |
Novel maculopathy in patients with spinocerebellar ataxia type 1 autofluorescence findings and functional characteristics. | |
Novel TULP1 mutation causing leber congenital amaurosis or early onset retinal degeneration | |
[Ocular mitochondrial myopathies: a spectrum of clinical presentations] | |
Optic nerve massaging: an extremely rare cause of self-inflicted blindness | |
[Optic neuropathy caused by alcoholism and smoking: a diagnostic pitfall of Leber's optic neuropathy] | |
Optic neuropathy in patients using amiodarone | |
Orbital infarction syndrome | |
Pathophysiology of vertical nystagmus in infancy. | |
Patient with Fanconi Syndrome (FS) and retinitis pigmentosa (RP) caused by a deletion and duplication of mitochondrial DNA (mtDNA) | |
Pediatric Ophthalmology, Neuro-Ophthalmology, Genetics | |
Perioperative visual loss: a rare complication of general surgery | |
Peripapillary neovascular membrane: a rare cause of acute vision loss in pediatric idiopathic intracranial hypertension | |
Persisting visual hallucinations and illusions in previously drug-addicted patients | |
Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene | |
Photophobia associated with a demyelinating lesion of the retrochiasmal visual pathway. | |
[Post-actinic retrobulbar optic neuropathy] | |
[Prevention of ocular complications of herpes zoster ophthalmicus by adequate treatment with acyclovir] | |
The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy. | |
Pseudotumor cerebri as a complication of amiodarone therapy | |
Pupillary dilation lag is intermittently present in patients with a stable oculosympathetic defect (Horner syndrome) | |
Rapid onset of visual recovery following acute visual loss due to leber's hereditary optic neuropathy | |
Retinal dystrophy in the oculo-auricular syndrome due to HMX1 mutation | |
Retinopathy in Danon disease | |
[Rhino-orbito-cerebral mucormycosis: clinical presentation] | |
[Role of the ophthalmologic examination in etiologic diagnosis of infantile spasms] | |
Selective and sequential therapy of oculomotor and palpebral sequelae resulting from biopsy of dorsal midbrain sarcoidosis | |
[Skew deviation] | |
Spasm of accommodation in a patient with increased intracranial pressure and pineal cyst. | |
Teaching Video NeuroImages: Minimal anomalies of dorsal midbrain syndrome (Parinaud syndrome). | |
Tocilizumab for giant cell arteritis with corticosteroid-resistant progressive anterior ischemic optic neuropathy. | |
Transient trochlear nerve palsy as the presenting neurological sign of panarteritis nodosa | |
[Transitory visual loss, amaurosis fugax : diagnostic and therapeutic approach] | |
Unsatisfactory outcomes in myasthenia gravis: influence by care providers | |
An unusual presentation of herpes zoster ophthalmicus: orbital myositis preceding vesicular eruption | |
Visual disturbances and transurethral resection of the prostate: the TURP syndrome. | |
Visual loss after orthopedic procedures | |
Visual recovery from radiation-induced optic neuropathy. The role of hyperbaric oxygen therapy | |
Visual signs and symptoms in patients with the visual variant of Alzheimer disease | |
Visual vertigo: an observational case series of eleven patients | |
Visualizing the skip lesions of giant cell arteritis with CT arteriography |