F. Munier

Discipline

Sociologie (2) Anthropologie biologique (1)

Type de document

Articles (10) Recensions (1) Colloques et conférences (1)

Co-auteur

Date

Source

Mot-clé

Human beings (7) Eye (6) gène (5) région (4) mutation (4) Treatment (4) Retinal (Visual pigment) (4) Patients (4) Patients (4) Mutation (4) famille (3) ADN (3) Case (3) Retinoblastoma (3) Mice (3) Grammar, Comparative and general--Case (3) Families (3) Expression (3) DNA (3) Case (3) Abnormalities, Human (3) Family (3) puits (2) thérapie (2) spectacle (2) analyse (2) acide aminé (2) maladie (2) adulte (2) Diagnosis (2)

Documents écrit par F. Munier (10) | parle de F. Munier (0)

Enhancer of Zeste Homolog 2 (EZH2) Contributes to Rod Photoreceptor Death Process in Several Forms of Retinal Degeneration and Its Activity Can Serve as a Biomarker for Therapy Efficacy.
M. Mbefo et al. (28 août 2021)
Protonentherapie für Bindehautkarzinom in der anophthalmischen Höhle 41 Jahre nach Enukleation wegen sporadischen Retinoblastoms [Proton Therapy of a Conjunctival Carcinoma in the Anophthalmic Socket, 41 Years after Enucleation for a Sporadic Retinoblastoma. A Case Report and Review of the Literature]
A. Moulin et al.
Juvenile xanthogranuloma involving concurrent iris and skin: Clinical, pathological and molecular pathological evaluations.
P. Meyer et al.
Multimodale Bildgebung eines retinalen Astrozyten-Hamartoms assoziert mit angeborener Hypertrophie des retinalen Pigmentepithels [Multimodal Imaging of Retinal Astrocytic Hamartoma Associated with Congenital Hypertrophy of Retinal Pigment Epithelium]
C. Trojman et al.
Congenital Nystagmus Gene FRMD7 Is Necessary for Establishing a Neuronal Circuit Asymmetry for Direction Selectivity.
K. Yonehara et al.
Treatment of Recurrent or Progressive Intraocular Retinoblastoma: Preliminary Results of A National Phase Ii Study of The Swiss Pediatric Oncology Group
M Beck Popovic et al.
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities
A. Dansault et al. (2007)
Differential diagnosis of leukocoria and strabismus, first presenting signs of retinoblastoma.
A. Balmer et al. (2007)
Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: relevance to ocular dysgenesis and hearing impairment.
D.B. Gould et al. (2004)
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma
R. V. Jamieson et al.