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발행년	- (예 : 2010-2015)

Myelopathy in neonatal and infantile lupus erythematosus.

Academic Journal

Kaye, E M; Butler, I J; Conley, S

Journal of Neurology, Neurosurgery & Psychiatry; Jul1987, Vol. 50 Issue 7, p923-926, 4p

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Familial lethal cardiomyopathy with mental retardation and scapuloperoneal muscular dystrophy.

Academic Journal

Bergia, B; Sybers, H D; Butler, I J

Journal of Neurology, Neurosurgery & Psychiatry; Dec1986, Vol. 49 Issue 12, p1423-1426, 4p

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Congenital hypomyelinating neuropathy.

Academic Journal

Harati, Y; Butler, I J

Journal of Neurology, Neurosurgery & Psychiatry; Dec1985, Vol. 48 Issue 12, p1269-1276, 8p

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Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot-Marie-Tooth disease.

Periodical

Jordanova, A; De Jonghe, P; Boerkoel, C F; Takashima, H; De Vriendt, E; Ceuterick, C; Martin, J-J; Butler, I J; Mancias, P; Papasozomenos, S Ch; Terespolsky, D; Potocki, L; Brown, C W; Shy, M; Rita, D A; Tournev, I; Kremensky, I; Lupski, J R; Timmerman, V

Brain: A Journal of Neurology; March 2003, Vol. 126 Issue: 3 p590-597, 8p

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The effect of disuse on cholinergic enzymes.

Periodical

Butler, I J; Drachman, D B; Goldberg, A M

Journal of Physiology; January 1978, Vol. 274 Issue: 1 p593-600, 8p

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Long-term neurological sequelae in achondroplasia.

Academic Journal

Hecht, Jacqueline; Butler, Ian; Scott, Charles; Hecht, J T; Butler, I J; Scott, C I Jr

European Journal of Pediatrics; 1984, Vol. 143 Issue 1, p58-60, 3p

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Foramen magnum stenosis in homozygous achondroplasia.

Academic Journal

Hecht, J.; Horton, W.; Butler, I.; Goldie, W.; Miner, M.; Shannon, R.; Pauli, R.; Hecht, J T; Horton, W A; Butler, I J; Goldie, W D; Miner, M E; Pauli, R M

European Journal of Pediatrics; 1986, Vol. 145 Issue 6, p545-547, 3p

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Infantile herpes zoster ophthalmicus and acute hemiparesis following intrauterine chickenpox.

Academic Journal

Leis, Angel A.; Butler, Ian J.; Leis, A A; Butler, I J

Neurology; Sep1987, Vol. 37 Issue 9, p1537-1538, 2p

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Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cells.

Academic Journal

Milstien, S; Holtzman, N A; O'Flynn, M E; Thomas, G H; Butler, I J; Kaufman, S

Journal of Pediatrics (J PEDIATR), 1976 Nov; 89: 763-766. (4p)

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