Neurology & Neurotherapeutics - NE Neuro Pediatrics Section

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Deficiencia del transportador de glucosa tipo 1 (Glut1): Manifestaciones de un síndrome neurológico hereditario

Translated title of the contribution: Type 1 glucose transporter (Glut1) deficiency: Manifestations of a hereditary neurological syndromePascual, J. M., Lecumberri, B., Wang, D., Yang, R., Engelstad, K. & De Vivo, D. C., May 1 2004, In : Revista de Neurologia. 38, 9, p. 860-864 5 p.

Research output: Contribution to journalReview article

7 Scopus citations

Epilepsy in children

Arnold, S. T. & Dodson, W. E., Dec 1 1996, In : Bailliere's Clinical Neurology. 5, 4, p. 783-802 20 p.

Research output: Contribution to journalReview article

7 Scopus citations

Epilepsy in inherited metabolic disorders

Pascual, J. M., Campistol, J. & Gil-Nagel, A., Nov 1 2008, In : Neurologist. 14, 6 SUPPL. 1, p. S2-S14

Research output: Contribution to journalReview article

24 Scopus citations

Fenocopias neurológicas

Translated title of the contribution: Neurological phenocopyingPascual, J. M., Dec 1 2006, In : Revista de Neurologia. 43, 12, p. 753-757 5 p.

Research output: Contribution to journalReview article

Glucose transporter protein syndromes

De Vivo, D. C., Wang, D., Pascual, J. M. & Ho, Y. Y., 2002, In : International Review of Neurobiology. 51, p. 259-288 30 p.

Research output: Contribution to journalReview article

25 Scopus citations

GLUT1 deficiency and other glucose transporter diseases

Pascual, J. M., Wang, D., Lecumberri, B., Yang, H., Mao, X., Yang, R. & De Vivo, D. C., May 2004, In : European Journal of Endocrinology. 150, 5, p. 627-633 7 p.

Research output: Contribution to journalReview article

90 Scopus citations

Indications and methodology for video-electroencephalographic studies in the epilepsy monitoring unit

Shih, J. J., Fountain, N. B., Herman, S. T., Bagic, A., Lado, F., Arnold, S., Zupanc, M. L., Riker, E. & Labiner, D. M., Jan 1 2018, In : Epilepsia. 59, 1, p. 27-36 10 p.

Research output: Contribution to journalReview article

14 Scopus citations

Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype

Kaufmann, P., Engelstad, K., Wei, Y., Kulikova, R., Oskoui, M., Sproule, D. M., Battista, V., Koenigsberger, D. Y., Pascual, J. M., Shanske, S., Sano, M., Mao, X., Hirano, M., Shungu, D. C., DiMauro, S. & De Vivo, D. C., Nov 29 2011, In : Neurology. 77, 22, p. 1965-1971 7 p.

Research output: Contribution to journalReview article

77 Scopus citations

Pyruvate carboxylase deficiency: Mechanisms, mimics and anaplerosis

Marin-Valencia, I., Roe, C. R. & Pascual, J. M., Sep 1 2010, In : Molecular genetics and metabolism. 101, 1, p. 9-17 9 p.

Research output: Contribution to journalReview article

64 Scopus citations

Síndromes hereditarios del transporte de glucosa

Translated title of the contribution: Glucose transport hereditary diseasesPascual, J. M., Nov 11 2006, In : Medicina Clinica. 127, 18, p. 709-714 6 p.

Research output: Contribution to journalReview article

5 Scopus citations