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Developmental disorders
Citations 91-100 of 105 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Diffusion tensor imaging of periventricular leukomalacia shows affected sensory cortex white matter pathways
- A. H. Hoon, Jr., W. T. Lawrie, Jr., E. R. Melhem, E. M. Reinhardt, P. C.M. van Zijl, M. Solaiyappan, H. Jiang, M. V. Johnston, and S. Mori
Neurology 2002; 59: 752-756.
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- BRIEF COMMUNICATIONS
Valproate embryopathy in three sets of siblings: Further proof of hereditary susceptibility
- H. Malm, E. Kajantie, S. Kivirikko, H. Kääriäinen, M. Peippo, and M. Somer
Neurology 2002; 59: 630-633.
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- CLINICAL/SCIENTIFIC NOTES
Abnormal cortical development shown by 3D MRI in Prader–Willi syndrome
- Akira Yoshii, Kalpathy S. Krishnamoorthy, and P. Ellen Grant
Neurology 2002; 59: 644.
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- VIEWS & REVIEWS
The neurogenetics of mucolipidosis type IV
- G. Altarescu, M. Sun, D. F. Moore, J. A. Smith, E. A. Wiggs, B. I. Solomon, N. J. Patronas, K. P. Frei, S. Gupta, C. R. Kaneski, O. W. Quarrell, S. A. Slaugenhaupt, E. Goldin, and R. Schiffmann
Neurology 2002; 59: 306-313.
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- ARTICLES
Developmental language disorder associated with polymicrogyria
- M. M. Guerreiro, S. R.V. Hage, C. A. Guimarães, D. V. Abramides, W. Fernandes, P. S. Pacheco, A. M.S.G. Piovesana, M. A. Montenegro, and F. Cendes
Neurology 2002; 59: 245-250.
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- BRIEF COMMUNICATIONS
Intractable epilepsy in vascular congenital hemiparesis: Clinical features and surgical options
- M. Carreño, P. Kotagal, A. Perez Jiménez, T. Mesa, W. Bingaman, and E. Wyllie
Neurology 2002; 59: 129-131.
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- CLINICAL/SCIENTIFIC NOTES
Loss of doublecortin in heterotopic gray matter of a fetus with subcortical laminar heterotopia
- M. Mizuguchi, S. Takashima, K. Ikeda, M. Kato, and A. Hori
Neurology 2002; 59: 143-144.
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- VIEWS & REVIEWS
Classification system for malformations of cortical development: Update 2001
- A. J. Barkovich, R. I. Kuzniecky, G. D. Jackson, R. Guerrini, and W. B. Dobyns
Neurology 2001; 57: 2168-2178.
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- ARTICLES
Head growth and neurodevelopment of infants born to HIV-1–infected drug-using women
- C. Macmillan, L.S. Magder, P. Brouwers, C. Chase, J. Hittelman, T. Lasky, K. Malee, C.A. Mellins, and J. Velez–Borras
Neurology 2001; 57: 1402-1411.
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- BRIEF COMMUNICATIONS
Congenital muscular dystrophy with primary partial laminin  2 chain deficiency: Molecular study
- Y. He, K. J. Jones, N. Vignier, G. Morgan, M. Chevallay, A. Barois, B. Estournet–Mathiaud, H. Hori, T. Mizuta, F. M.S. Tomé, K. N. North, and P. Guicheney
Neurology 2001; 57: 1319-1322.
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