Citation Impact
Citing Papers
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.
2000
Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
2008 Standout
The multifunctional choroid
2009 Standout
Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species
2002
Guidelines for the use of immunosuppressive drugs in patients with ocular inflammatory disorders: recommendations of an expert panel
2000 Standout
The Retinal Pigment Epithelium in Visual Function
2005 Standout
The Natural History of Leber's Congenital Amoaurosis
1992
Leber Congenital Amaurosis
1999
The molecular basis of human retinal and vitreoretinal diseases
2010 Standout
Keratoconus
1998 Standout
Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype-phenotype correlations as a strategy for molecular diagnosis
2004
Retinitis Pigmentosa: Genes and Disease Mechanisms
2011 Standout
Tranexamic Acid
1999 Standout
TFOS DEWS II pathophysiology report
2017 Standout
Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer
2015 Standout
Human Corneal Thickness and Its Impact on Intraocular Pressure Measures
2000 Standout
The Hippo Signaling Pathway in Development and Cancer
2010 Standout
Toxoplasmosis: A history of clinical observations
2009 Standout
Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis
1996
TEAD mediates YAP-dependent gene induction and growth control
2008 Standout
The Phenotype of Leber Congenital Amaurosis in Patients With AIPL1 Mutations
2004
Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
1989
Leber congenital amaurosis: Genes, proteins and disease mechanisms
2008 Standout
Purification of component A of Rab geranylgeranyl transferase: Possible identity with the choroideremia gene product
1992 StandoutNobel
Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis
2001
Long-term Follow-up of the Physiologic Abnormalities and Fundus Changes in Fundus Albipunctatus
1990
Toxoplasma gondii: from animals to humans
2000 Standout
Review of Ophthalmic Findings in 204 Patients With Epidermolysis Bullosa
1994
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration)
2004
ERG and VEP follow-up study in children with Leber's congenital amaurosis
1999
Ocular Involvement in Epidermolysis Bullosa Acquisita
1989
Retinopathy induced in mice by targeted disruption of the rhodopsin gene
1997 StandoutNobel
The eye in dystrophic epidermolysis bullosa: Clinical and immunopathological findings
1989
EVALUATION OF GENOTYPE–PHENOTYPE ASSOCIATIONS IN LEBER CONGENITAL AMAUROSIS
2005
Retinitis pigmentosa
1988
Ichthyosis Follicularis With Alopecia and Photophobia
1985
A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype
1998
Isolation of a candidate gene for choroideremia.
1992
Eye Lesions of Epidermolysis Bullosa
1988
Fundus albipunctatus: A clinical study of the fundus lesions, the physiologic deficit, and the vitamin a metabolism
1977
Keratoconus and related noninflammatory corneal thinning disorders
1984 Standout
Causes and frequency of blindness in patients with intraocular inflammatory disease.
1996 Standout
Guanylyl Cyclases and Signaling by Cyclic GMP
2000 Standout
The Ocular Signs and Complications of Epidermolysis Bullosa
1988
Zur Genetik des Keratoconus
1974
Ocular phenotypes of three genetic variants of Bardet–Biedl syndrome
2004
Tissue plasminogen activator activity in human aqueous humor.
1994
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
2000 Standout
TRANEXAMIC ACID (AMCA) AND LATE HYPHAEMA
1976
Cardiac abnormalities in familial palmoplantar keratosis.
1986
Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis: Detection of Modifier Alleles
2005
Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel‐Feil, and Möbius anomalies
1986 Standout
High Hyperopia in Leber's Congenital Amaurosis
1985
The Clinical Course of Serpiginous Choroidopathy
1979
Ocular toxoplasmosis.
1973
Otological findings in cervico-oculo-auditory dysplasia
1980
Hornhautdickenmessung
1968
Mutational analysis and clinical correlation in Leber congenital amaurosis
2000
Works of A. Franceschetti being referenced
Histologic Aspect of Corneal Changes
1959
[Cervico-oculo-facial dysmorphia with familial deafness: Klippel-Feil, retractio bulbi, craniofacial asymetry and other congenital anomalies].
1954
A new instrument for taking lamellar grafts.
1957
Une nouvelle forme de fundus albipunctatus cum hemeralopia
1963
Isolement de Toxoplasma gondii dans un cas de choriorétinite séro-négative
1963
Fundus albipunctatus cum hemeralopia (Cas stationnaire depuis 49 ans)
1951
Manifestations cornéennes dans la keratosis follicularis spinulosa decalvans (Siemens)
1957
A curious affection of the Fundus oculi: Helicoid peripapillar chorioretinal degeneration. Its relation to pigmentary paravenous chorioretinal degeneration
1962
[2 Pairs of identical twins with concordant keratoconus].
1958
Importance diagnostique et pronostique de l'électrorétinogramme (ERG) dans les dégénérescences tapéto-rétiniennes avec rétrécissement du champ visuel et héméralopie
1954
Choroideremia : Clinical and Genetic Aspects
1952
Dégénérescence tapéto-rétinienne infantile (type Leber) avec aspect marbré du fond de l’œil périphérique
1958
Zur Differentialdiagnose zwischen Fundus albipunctatus cum hemeralopia congenital und Oguchi’scher Krankheit
1957
Fibrinolyse im Kammerwasser menschlicher und tierischer Augen
1959
[Meleda disease].
1972
A special form of tapetoretinal degeneration: fundus flavimaculatus.
1966