-
1
-
-
1542564547
-
Infantile spasms and West syndrome
-
Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Wolf P, eds. 3rd Ed. London: John Libbey and Co. Ltd
-
Dulac O, Tuxhorn I. Infantile spasms and West syndrome. In: Roger J, Bureau M, Dravet C, Genton P, Tassinari CA, Wolf P, eds. Epileptic Syndromes, 3rd Ed. London: John Libbey and Co. Ltd., 2002; 48-63.
-
(2002)
Epileptic Syndromes
, pp. 48-63
-
-
Dulac, O.1
Tuxhorn, I.2
-
4
-
-
0023474709
-
Neuroradiological aspects of infantile spasms
-
Ludwig B. Neuroradiological aspects of infantile spasms. Brain Dev 1987; 9: 358-360.
-
(1987)
Brain Dev.
, vol.9
, pp. 358-360
-
-
Ludwig, B.1
-
6
-
-
7244224097
-
Hypoglycemia in the infant and child
-
Sperling MA, ed. Philadelphia, PA: Saunders-Elsevier Science
-
Thornton PS, Finegold DN, Stanley CA, Sperling MA. Hypoglycemia in the infant and child. In: Sperling MA, ed. Pediatric Endocrinology. Philadelphia, PA: Saunders-Elsevier Science, 2002; 367-384.
-
(2002)
Pediatric Endocrinology
, pp. 367-384
-
-
Thornton, P.S.1
Finegold, D.N.2
Stanley, C.A.3
Sperling, M.A.4
-
7
-
-
0031802399
-
Genetic heterogeneity in familial hyperinsulinism
-
Nestorowicz A, Glaser B, Wilson BA, Shyng SL, Nichols CG, Stanley CA, Thornton PS, Permutt MA. Genetic heterogeneity in familial hyperinsulinism. Hum Mol Genet 1998; 7: 1119-1128.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1119-1128
-
-
Nestorowicz, A.1
Glaser, B.2
Wilson, B.A.3
Shyng, S.L.4
Nichols, C.G.5
Stanley, C.A.6
Thornton, P.S.7
Permutt, M.A.8
-
8
-
-
0029021696
-
Mutations in sulfonylurea receptor gene familial persistent hyperinsulinemic hypoglycemia of infancy
-
Thomas PM, Cote GJ, Wohlik N, Haddad B, Mathew PM, Rabl W, Aguilar-Bryan L, Gagel RF, Bryan J. Mutations in sulfonylurea receptor gene familial persistent hyperinsulinemic hypoglycemia of infancy. Science 1995; 268: 426-429.
-
(1995)
Science
, vol.268
, pp. 426-429
-
-
Thomas, P.M.1
Cote, G.J.2
Wohlik, N.3
Haddad, B.4
Mathew, P.M.5
Rabl, W.6
Aguilar-Bryan, L.7
Gagel, R.F.8
Bryan, J.9
-
9
-
-
0035219051
-
A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene
-
Yasuda K, Koda N, Kadowaki H, Ogawa Y, Kimura S, Kadowaki T, Akanuma Y. A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene. Intern Med 2002; 40: 32-37.
-
(2002)
Intern. Med.
, vol.40
, pp. 32-37
-
-
Yasuda, K.1
Koda, N.2
Kadowaki, H.3
Ogawa, Y.4
Kimura, S.5
Kadowaki, T.6
Akanuma, Y.7
-
11
-
-
0037387691
-
Persistent hyperinsulinemic hypoglycemia followed as benign infantile convulsion
-
Yoshikawa H, Honma T, Abe T. Persistent hyperinsulinemic hypoglycemia followed as benign infantile convulsion. Seizure 2003; 12: 186-187.
-
(2003)
Seizure
, vol.12
, pp. 186-187
-
-
Yoshikawa, H.1
Honma, T.2
Abe, T.3
-
12
-
-
0035120388
-
Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
-
Menni F, Lonlay P, Sevin C, Touati G, Peigne C, Barbier V, Nihoul-Fekete C, Saudubray JM, Roert JJ. Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia. Pediatrics 2001; 3: 476-479.
-
(2001)
Pediatrics
, vol.3
, pp. 476-479
-
-
Menni, F.1
Lonlay, P.2
Sevin, C.3
Touati, G.4
Peigne, C.5
Barbier, V.6
Nihoul-Fekete, C.7
Saudubray, J.M.8
Roert, J.J.9
-
13
-
-
0017108682
-
Etiology of convulsions in neonatal and infantile period
-
Kurokawa T, Yokata K, Takashima S, Nambu Y, Hanai T. Etiology of convulsions in neonatal and infantile period. Folia Psychiatr Neurol Jpn 1976; 30: 365-378.
-
(1976)
Folia. Psychiatr. Neurol. Jpn.
, vol.30
, pp. 365-378
-
-
Kurokawa, T.1
Yokata, K.2
Takashima, S.3
Nambu, Y.4
Hanai, T.5
-
15
-
-
0034782069
-
Epidemiological data of West syndrome in Finland
-
Riikonen R. Epidemiological data of West syndrome in Finland. Brain Dev 2001; 23: 539-541.
-
(2001)
Brain Dev.
, vol.23
, pp. 539-541
-
-
Riikonen, R.1
-
16
-
-
0033929961
-
Epileptic syndromes in the first year of life and congenital errors of metabolism
-
Campistol J. Epileptic syndromes in the first year of life and congenital errors of metabolism. Rev Neurol 2000; 30 (Suppl 1): S60-74.
-
(2000)
Rev. Neurol.
, vol.30
, Issue.SUPPL. 1
-
-
Campistol, J.1
|