Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("BREZIN, A.-P")

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 12 of 12

  • Page / 1
Export

Selection :

  • and

Applications de l'amplification génique (réaction en chaîne à la polymérase) à la détection d'agents infectieux en ophtalmologie = DNA amplification (polymerase chain reaction) for the detection of infectious agents in ophthalmologyBREZIN, A. P; NUSSENBLATT, R. B.Journal français d'ophtalmologie. 1991, Vol 14, Num 8-9, pp 488-495, issn 0181-5512Article

Uvéites et médecine in terne: stratégies diagnostique et thérapeutique = Guidelines for the management of uveitis in Internal MedicineABAD, S; SEVE, P; DHOTE, R et al.La Revue de médecine interne (Paris). 2009, Vol 30, Num 6, pp 492-500, issn 0248-8663, 9 p.Article

Le syndrome de Vogt-Koyanagi-Harada : aspects cliniques, traitement et suivi à long terme dans une population caucasienne et africaine = Vogt-Koyanagi-Harada Disease: clinical features, therapy and long-term visual outcome in a Caucasian and African populationGUENOUN, J.-M; PARC, C; DHOTE, R et al.Journal français d'ophtalmologie. 2004, Vol 27, Num 9, pp 1013-1016, issn 0181-5512, 4 p., CAH1Conference Paper

Blindness, low vision, and other handicaps as risk factors attached to institutional residenceBREZIN, A. P; LAFUMA, A; FAGNANI, F et al.British journal of ophthalmology. 2004, Vol 88, Num 10, pp 1330-1337, issn 0007-1161, 8 p.Article

CYP1B1 mutations in French patients with early-onset primary open-angle glaucomaMELKI, R; COLOMB, E; LEFORT, N et al.Journal of medical genetics. 2004, Vol 41, Num 9, pp 647-651, issn 0022-2593, 5 p.Article

FACTORS OF OCCURRENCE OF OCULAR TOXOPLASMOSIS. A REVIEWTALABANI, H; MERGEY, T; YERA, H et al.Parasite (Paris). 2010, Vol 17, Num 3, pp 177-182, issn 1252-607X, 6 p.Conference Paper

Macular oedema following rituximab infusion in two patients with Wegener's granulomatosisBUSSONE, G; KASWIN, G; DE MENTHON, M et al.Clinical and experimental rheumatology (Testo stampato). 2010, Vol 28, Num 1, issn 0392-856X, S90-S92, SUP57Article

Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucomaCOLOMB, E; NGUYEN, T. D; GARCHON, H-J et al.Clinical genetics. 2001, Vol 60, Num 3, pp 220-225, issn 0009-9163Article

Genetic heterogeneity of primary open angle glaucoma and ocular hypertension : linkage to GLC1A associated with an increased risk of severe glaucomatous optic neuropathyBREZIN, A. P; BECHETOILLE, A; HAMARD, P et al.Journal of medical genetics. 1997, Vol 34, Num 7, pp 546-552, issn 0022-2593Article

Recurrent mutations in a single exon encoding the evolutionarily conserved olfactomedin-homology domain of TIGR in familial open-angle glaucomaADAM, M. F; BELMOUDEN, A; BACH, J.-F et al.Human molecular genetics (Print). 1997, Vol 6, Num 12, pp 2091-2097, issn 0964-6906Article

Association of peripheral multifocal choroiditis with sarcoidosis: A study of thirty-seven patientsABAD, S; MEYSSONIER, V; PESCE, F et al.Arthritis care and research. 2004, Vol 51, Num 6, pp 974-982, issn 0893-7524, 9 p.Article

Founder effect in GLc1A-linked familial open-angle glaucoma in Northern FranceBREZIN, A. P; ADAM, M. F; ROULAND, J.-F et al.American journal of medical genetics. 1998, Vol 76, Num 5, pp 438-445, issn 0148-7299Article

  • Page / 1