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153 related items for PubMed ID: 3287208
21. Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment. Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, Bastos AC, Palmini A, Fernandes W, Montenegro MA, Cendes F, Andermann F. Ann Neurol; 2000 Jul; 48(1):39-48. PubMed ID: 10894214 [Abstract] [Full Text] [Related]
22. [Idiopathic cerebral and cerebrovascular calcifications as a cause of disturbed psychosomatic development in children]. Stepień A, Wilgoszyńska B. Pediatr Pol; 1976 Apr; 51(4):445-8. PubMed ID: 1264531 [No Abstract] [Full Text] [Related]
23. Clinical characteristics of children with cerebral white matter abnormalities. Kristjánsdóttir R, Uvebrant P, Wiklund LM. Eur J Paediatr Neurol; 2000 Apr; 4(1):17-26. PubMed ID: 10701100 [Abstract] [Full Text] [Related]
24. Evidence of brain ischemia in early neonatal sudden death syndrome. Obonai T, Asanuma M, Mizuta R, Horie H, Tanaka J, Takashima S. Neuropediatrics; 1997 Jun; 28(3):145-8. PubMed ID: 9266551 [Abstract] [Full Text] [Related]
25. Analysis of glial fibrillary acidic protein in the cerebrospinal fluid of children investigated for encephalopathy. Ehlers S, Kyllerman M, Rosengren L. Neuropediatrics; 1994 Jun; 25(3):129-33. PubMed ID: 7969795 [Abstract] [Full Text] [Related]
26. The widespread but silent cerebral mineralization: a case report. Kuchna I, Laure-Kamionowska M, Walkiewicz W. Acta Neurobiol Exp (Wars); 1993 Jun; 53(1):285-8. PubMed ID: 8317261 [Abstract] [Full Text] [Related]
27. [Symmetrical pseudocalcium deposits in the basal ganglia and white matter of the brain with moderate leukoencephalopathy in Down's syndrome]. Murofushi K. Neuropadiatrie; 1974 Feb; 5(1):103-8. PubMed ID: 4274397 [No Abstract] [Full Text] [Related]
28. Astrocytes in the postnatal central nervous system. From birth to 14 years of age. An immunohistochemical study on paraffin-embedded material. Reske-Nielsen E, Gregersen M, Lund E. Acta Pathol Microbiol Immunol Scand A; 1987 Nov; 95(6):347-56. PubMed ID: 3687438 [Abstract] [Full Text] [Related]
29. Glial fibrillary acidic protein mutations in infantile, juvenile, and adult forms of Alexander disease. Li R, Johnson AB, Salomons G, Goldman JE, Naidu S, Quinlan R, Cree B, Ruyle SZ, Banwell B, D'Hooghe M, Siebert JR, Rolf CM, Cox H, Reddy A, Gutiérrez-Solana LG, Collins A, Weller RO, Messing A, van der Knaap MS, Brenner M. Ann Neurol; 2005 Mar; 57(3):310-26. PubMed ID: 15732097 [Abstract] [Full Text] [Related]
38. The Aircardi-Goutières syndrome: variable clinical expression in two siblings. Verrips A, Hiel JA, Gabreëls FJ, Wesseling P, Rotteveel JJ. Pediatr Neurol; 1997 May; 16(4):323-5. PubMed ID: 9258967 [Abstract] [Full Text] [Related]
39. Juvenile ceroid-lipofuscinosis and calcifications of the CNS. Bruun I, Reske-Nielsen E, Oster S. Acta Neurol Scand; 1991 Jan; 83(1):1-8. PubMed ID: 2011942 [Abstract] [Full Text] [Related]
40. Familial idiopathic brain calcification with autosomal dominant inheritance. Kobari M, Nogawa S, Sugimoto Y, Fukuuchi Y. Neurology; 1997 Mar; 48(3):645-9. PubMed ID: 9065541 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]