Evaluation of the Child with Idiopathic Mental Retardation
Tài liệu tham khảo
Abel, 1986, Fetal alcohol syndrome is now leading cause of mental retardation, Lancet, 2, 1222, 10.1016/S0140-6736(86)92234-8
Akesson, 1986, The biologic origin of mild mental retardation, Acta Psychiatr Scand, 74, 3, 10.1111/j.1600-0447.1986.tb06218.x
Altherr, 1991, Molecular confirmation of Wolf-Hirschorn syndrome with subtle translocation of chromosome 4, Am J Hum Genet, 49, 1235
Astley, 1992, Analysis of facial shape in children gestationally exposed to marijuana, alcohol and/or cocaine, Pediatrics, 89, 67, 10.1542/peds.89.1.67
Barabas, 1986, The early signs and differential diagnosis of cerebral palsy, Pediatr Ann, 15, 203, 10.3928/0090-4481-19860301-06
Blair, 1988, Intrapartum asphyxia: A rare cause of cerebral palsy, J Pediatr, 112, 515, 10.1016/S0022-3476(88)80161-6
Bodensteiner, 1988, Macro cisterna magna: A marker for maldevelopment of the brain?, Pediatr Neurol, 4, 284, 10.1016/0887-8994(88)90067-7
Bodensteiner, 1990, The wide cavum septum pellucidum: A marker of disturbed development, Pediatr Neurol, 6, 391, 10.1016/0887-8994(90)90007-N
Breeding, 1991, The cavum septum pellucidum: An MRI study of prevalence and clinical associations in a pediatric population, Journal of Neuroimaging, 1, 115, 10.1111/jon199113115
Brown, 1990, The Fragile X: Progress toward solving the puzzle, Am J Hum Genet, 47, 175
Brown, 1991, Conference report: Fourth International Workshop on the Fragile X and X-linked mental retardation, Am J Med Genet, 38, 158, 10.1002/ajmg.1320380202
Byrne, 1990, Serial magnetic resonance imaging in neonatal hypoxic-ischemic encephalopathy, J Pediatr, 117, 694, 10.1016/S0022-3476(05)83323-2
Clarren, 1987, Facial effects of fetal alcohol exposure: Assessment of photographs by morphometric analysis, Am J Med Genet, 26, 651, 10.1002/ajmg.1320260321
Cohen, 1991, Why are autism and the Fragile X syndrome associated? Conceptual and methodological issues, Am J Hum Genet, 48, 195
Cohen, 1986, 89
Coorsen, 1991, Marker for prenatal etiology of cerebral palsy, Dev Med Child Neurol, 33, 730, 10.1111/j.1469-8749.1991.tb14952.x
Courchesne, 1991, Neuroanatomic imaging in autism, Pediatr, 87, 781, 10.1542/peds.87.5.781
DiLiberti, 1991, Application of D’Arcy Thompson’s coordinate transformation approach to clinical genetics photographs using image processing techniques, J Med Genet, 28, 472, 10.1136/jmg.28.7.472
DiLiberti, 1991, Photogrammetric evaluation in clinical genetics: Theoretical considerations and experimental results, Am J Med Genet, 39, 161, 10.1002/ajmg.1320390209
Edmond, 1989, Cerebral palsy in two national cohort studies, Arch Dis Child, 64, 848, 10.1136/adc.64.6.848
Ellis, 1988, Neuropathologic documentation of prenatal brain damage, Am J Dis Child, 142, 858
Escanol, 1991, In vivo stereological assessment of human cerebellar volume, American Journal of Neuroradiology, 12, 927
Filipek, 1989, Magnetic resonance imaging-based brain morphometry: Development and application to normal subjects, Ann Neurol, 25, 61, 10.1002/ana.410250110
Freeman, 1988, Intrapartum asphyxia and cerebral palsy, Pediatrics, 82, 240, 10.1542/peds.82.2.240
Frias, 1991
Gillerot, 1989, The geneticist and the so-called “sociocultural” familial mental retardation, J Genet Hum, 37, 103
Gorlin, 1990
Greenberg, 1991, Molecular analysis of the Smith-Magenis syndrome: A possible contiguous gene syndrome associated with del(17)(pll.2), Am J Hum Genet, 49, 1207
1977
Hagberg, 1982, Mild mental retardation in Swedish school children: II. Etiologic and pathogenetic aspects, Acta Pediatr Scand, 70, 445, 10.1111/j.1651-2227.1981.tb05721.x
Hagerman, 1991, Fragile X checklist, Am J Med Genet, 38, 283, 10.1002/ajmg.1320380223
Harper, 1981, Localization of single copy DNA sequences on G-banded human chromosomes by in situ hybridization, Chromosoma, 83, 431, 10.1007/BF00327364
Hunter, 1980, A study of institutionalized mentally retarded patients in Manitoba: I. Classification and preventability, Dev Med Child Neurol, 22, 145, 10.1111/j.1469-8749.1980.tb04324.x
Jernigan, 1990, Methods for measuring brain morphologic features on magnetic resonance images, Arch Neurol, 47, 27, 10.1001/archneur.1990.00530010035015
Jones, 1988
Knoll, 1990, Angelman syndrome: Three molecular classes identified with chromosome 15qllq13q-specific DNA markers, Am J Hum Genet, 47, 149
Koeda, 1990, MR imaging of spastic diplegia, Neuroradiology, 32, 187, 10.1007/BF00589108
Kolvraa, 1991, Application of fluorescence in situ hybridization techniques in clinical genetics: Use of two alphoid repeat probes detecting the centromeres of chromosomes 13 and 21 or chromosomes 14 and 22 respectively, Clin Genet, 39, 278, 10.1111/j.1399-0004.1991.tb03026.x
Laing, 1991, Clinical screening for the Fragile X (MartinBell) syndrome, Am J Med Genet, 38, 256, 10.1002/ajmg.1320380219
Lingam, 1983, Computed tomography in non-specific mental retardation and idiopathic epilepsy, Arch Dis Child, 58, 628, 10.1136/adc.58.8.628
Lingam, 1982, Value of computerized tomography in children with non-specific mental subnormality, Arch Dis Child, 57, 381, 10.1136/adc.57.5.381
Lubs, 1969, A marker X chromosome, Am J Hum Genet, 21, 231
Lüdecke, 1991, Molecular definition of the shortest region of deletion overlap in the Langer-Giedeon syndrome, Am J Hum Genet, 49, 1197
Lutz, 1989, X-linked olivopontocerebellar atrophy, Clin Genet, 35, 417, 10.1111/j.1399-0004.1989.tb02966.x
May, 1983, Epidemiology of fetal alcohol syndrome among American Indians of the Southwest, Soc Biol, 30, 374
McCabe, 1991, Maternal phenylketonuria, Pediatrics, 88, 1284, 10.1542/peds.88.6.1284
McKusick, 1966
McKusick, 1990
McLaren, 1987, Review of recent epidemiological studies of mental retardation: Prevalence, associated disorders, and etiology, Am J Ment Retard, 92, 243
Miller, 1989, Minor congenital anomalies and ataxic cerebral palsy, Arch Dis Child, 64, 557, 10.1136/adc.64.4.557
Moser, 1983, Mental retardation, 352
Nolin, 1991, Fragile X screening in New York state, Am J Med Genet, 38, 251, 10.1002/ajmg.1320380218
1991, Special issue: X-linked mental retardation 4, Am J Med Genet, 38, 173
Polednak, 1977, Post-mortem neuropathology in a mentally retarded population, Lancet, 26, 492, 10.1016/S0140-6736(77)91988-2
Punnett, 1990, Old syndromes new cytogenetics, Devel Med Child Neurol, 32, 820
Rapin, 1991, Autistic children: Diagnosis and clinical features, Pediatrics, 87, 751
Reiss, 1991, Neuroanatomy in Fragile X females: The posterior fossa, Am J Hum Genet, 49, 279
Robinson, 1991, Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients, Am J Hum Genet, 49, 1219
Rousseau, 1991, Direct diagnosis by DNA analysis of the Fragile X syndrome of mental retardation, N Engl J Med, 325, 1673, 10.1056/NEJM199112123252401
Saksena, 1990, Facial morphometrics in the identification of gene carriers of X-linked hypohydrotic ectodermal dysplasia, Am J Med Genet, 35, 105, 10.1002/ajmg.1320350120
Schaefer, 1991, Subtle markers of cerebral dysgenesis, 109
Schaefer, 1991, Clinical and morphometric analysis of the hypoplastic corpus callosum, Arch Neurol, 48, 933, 10.1001/archneur.1991.00530210059024
Schaefer, 1991, Age-related changes in the relative growth of the posterior fossa, J Child Neurol, 6, 15, 10.1177/088307389100600103
Schaefer, 1990, Morphometric analysis of brain growth utilizing quantitative analysis of magnetic resonance imaging, J Child Neurol, 5, 127, 10.1177/088307389000500211
Schinzel, 1984
Schmickel, 1986, Contiguous gene syndrome: A component of recognizable syndromes, J Pediatr, 109, 231, 10.1016/S0022-3476(86)80377-8
Shah, 1991, Assessment of posterior fossa structures with midsagittal MRI: The effects of age, Neurobiol Aging, 12, 371, 10.1016/0197-4580(91)90025-F
Shanks, 1988, Lobar holoprosencephaly presenting as spastic diplegia, Dev Med Child Neurol, 30, 378
Smith, 1964, Congenital anomalies associated with idiopathic mental retardation, J Pediatr, 65, 189, 10.1016/S0022-3476(64)80519-9
Stanley, 1987, The changing face of cerebral palsy, Dev Med Child Neurol, 29, 263, 10.1111/j.1469-8749.1987.tb02145.x
Suddath, 1990, Anatomic abnormalities in the brains of monozygotic twins discordant for schizophrenia, N Engl J Med, 322, 789, 10.1056/NEJM199003223221201
Sutherland, 1977, Fragile sites on human chromosomes: Demonstration of their dependence on the type of tissue culture medium, Science, 197, 265, 10.1126/science.877551
Sybert, 1990, Pigmentary abnormalities and mosaicism for chromosomal aberration: Association with clinical features similar to hypomelanosis of Ito, J Pediatr, 116, 581, 10.1016/S0022-3476(05)81606-3
Tharapel, 1991, Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with α-satellite DNA probes, Am J Med Genet, 40, 117, 10.1002/ajmg.1320400125
Thomas, 1989, Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism, Am J Hum Genet, 45, 193
Thomas, 1989, New methods for quantitative arid qualitative facial studies: An overview, J Craniofac Genet Dev Biol, 9, 107
Torfs, 1990, Prenatal and perinatal factors in the etiology of cerebral palsy, J Pediatr, 116, 615, 10.1016/S0022-3476(05)81615-4
Ward, 1989, Facial morphometry as determined by anthropometry: Keeping it simple, J Craniofac Genet Dev Biol, 9, 45
Warkany, 1981, 3
Webb, 1991, Molecular genetics of Fragile X: A cytogenetics viewpoint. Report of the Fifth International Symposium on X-linked Mental Retardation, J Med Genet, 28, 814, 10.1136/jmg.28.12.814
Wiklund, 1990, Morphology of cerebral lesions in children with congenital hemiplegia, Neuroradiology, 32, 179, 10.1007/BF00589107
Williams, 1990, Placental examination can help determine cause of brain damage in neonates, Tex Med, 86, 33
Yokoch, 1991, MRI of children with spastic diplegia, Dev Med Child Neurol, 33, 18