Françoise Meire
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UNILATERAL CYTOMEGALOVIRUS RETINITIS IN A PATIENT WITH IMMUNOGLOBULIN G2 DEFICIENCY.
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Pseudoglioma: a clinico-pathological report
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Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON)
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Ocular anomalies in an unbalanced translocation between chromosomes 7 and 8
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Fibromuscular dysplasia of the arteries: an arterial occlusive disease with severe neurological complications at young age
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Familial exudative vitreoretinopathy.
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Chromosome aberations in fibrous dysplasia
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Megalocornea: clinical and genetic-aspects
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DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY.
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Identification of a key recombinient which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.
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Biometry in X-linked megalocornea: pathognomic findings.
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X-linked progressive cone dystrophy.
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Features of mitochondrial DNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.
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Lens dislocation and optic-nerve hypoplasia in ring chromosome-21 mosaicism.
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Treatment of long term complications of toxoplasma chorioretinal scars
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Congenital ectropion uveae with glaucoma
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Osteoporosis-pseudoglioma syndrome
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HETEROGENEITY VERSUS VARIABILITY IN MEGALOCORNEA-MENTAL RETARDATION (MMR) SYNDROMES - REPORT OF NEW CASES AND DELINEATION OF 4 PROBABLE TYPES.
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ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3.
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Leber's hereditary optic neuropathy. Clinical and molecular genetic aspects. Preliminary results in our families