-
1
-
-
0033943782
-
Regional variation in blindness in children due to microphthalmos, anophthalmos and coloboma
-
Hornby SJ, Gilbert CE, Rahi JK, et al. Regional variation in blindness in children due to microphthalmos, anophthalmos and coloboma. Ophthalmic Epidemiol 2000;7:127-138.
-
(2000)
Ophthalmic Epidemiol
, vol.7
, pp. 127-138
-
-
Hornby, S.J.1
Gilbert, C.E.2
Rahi, J.K.3
-
2
-
-
0032480566
-
Geographical variation in anophthalmia and microphthalmia in England, 1988-94
-
Dolk H, Busby A, Armstrong BG, et al. Geographical variation in anophthalmia and microphthalmia in England, 1988-94. BMJ 1998;317:905-909.
-
(1998)
BMJ
, vol.317
, pp. 905-909
-
-
Dolk, H.1
Busby, A.2
Armstrong, B.G.3
-
3
-
-
0027293603
-
Classification of microphthalmos and coloboma
-
Warburg M. Classification of microphthalmos and coloboma. J Med Genet 1993;30:664-669.
-
(1993)
J Med Genet
, vol.30
, pp. 664-669
-
-
Warburg, M.1
-
4
-
-
0034010851
-
Ophthalmological and intracranial anomalies in patients with clinical anophthalmos
-
Jacquemin C, Mullaney PB, Bosley TM. Ophthalmological and intracranial anomalies in patients with clinical anophthalmos. Eye 2000;14(pt 1):82-87.
-
(2000)
Eye
, vol.14
, Issue.PART 1
, pp. 82-87
-
-
Jacquemin, C.1
Mullaney, P.B.2
Bosley, T.M.3
-
5
-
-
28544444511
-
Progressive cavitating leukoencephalopathy: A novel childhood disease
-
Naidu S, Bibat G, Lin D, et al. Progressive cavitating leukoencephalopathy: a novel childhood disease. Ann Neurol 2005;58:929-938.
-
(2005)
Ann Neurol
, vol.58
, pp. 929-938
-
-
Naidu, S.1
Bibat, G.2
Lin, D.3
-
6
-
-
0035112634
-
Micro syndrome in Muslim Pakistan children
-
Ainsworth JR, Morton JE, Good P, et al. Micro syndrome in Muslim Pakistan children. Ophthalmology 2001;108:491-497.
-
(2001)
Ophthalmology
, vol.108
, pp. 491-497
-
-
Ainsworth, J.R.1
Morton, J.E.2
Good, P.3
-
8
-
-
0042326078
-
An evaluation of selected human eye dimensions at different periods of the foetal life
-
Tomasik E, Czepita D, Zejmo M, et al. An evaluation of selected human eye dimensions at different periods of the foetal life. Folia Morphol (Warsz) 2003;62:297-299.
-
(2003)
Folia Morphol (Warsz)
, vol.62
, pp. 297-299
-
-
Tomasik, E.1
Czepita, D.2
Zejmo, M.3
-
9
-
-
16544388112
-
Diffusion magnetic resonance imaging patterns in metabolic and toxic brain disorders
-
Sener RN. Diffusion magnetic resonance imaging patterns in metabolic and toxic brain disorders. Acta Radiol 2004;45:561-570.
-
(2004)
Acta Radiol
, vol.45
, pp. 561-570
-
-
Sener, R.N.1
-
10
-
-
0030975392
-
A new leukoencephalopathy with vanishing white matter
-
van der Knaap MS, Barth PG, Gabreels FJ, et al. A new leukoencephalopathy with vanishing white matter. Neurology 1997;48:845-855.
-
(1997)
Neurology
, vol.48
, pp. 845-855
-
-
Van Der Knaap, M.S.1
Barth, P.G.2
Gabreels, F.J.3
-
12
-
-
33645777926
-
Perspective in research for undefined leukoencephalopathies
-
Uziel G, Taroni F, eds. Mariani Foundation Paediatric Neurology Series. London-Paris: John Libbey Eurotext
-
Schiffmann R. Perspective in research for undefined leukoencephalopathies. In: Uziel G, Taroni F, eds. Hereditary leukoencephalopathies in demyelinating neuropathies in children. Mariani Foundation Paediatric Neurology Series. Vol. 12. London-Paris: John Libbey Eurotext, 2004:43-47.
-
(2004)
Hereditary Leukoencephalopathies in Demyelinating Neuropathies in Children
, vol.12
, pp. 43-47
-
-
Schiffmann, R.1
-
13
-
-
0242322773
-
The genetic and molecular basis of congenital eye defects
-
Graw J. The genetic and molecular basis of congenital eye defects. Nat Rev Genet 2003;4:876-888.
-
(2003)
Nat Rev Genet
, vol.4
, pp. 876-888
-
-
Graw, J.1
-
14
-
-
21044452878
-
Heterozygous mutations of OTX2 cause severe ocular malformations
-
Ragge NK, Brown AG, Poloschek CM, et al. Heterozygous mutations of OTX2 cause severe ocular malformations. Am J Hum Genet 2005;76:1008-1022.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1008-1022
-
-
Ragge, N.K.1
Brown, A.G.2
Poloschek, C.M.3
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