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Journal Abstract Search
78 related items for PubMed ID: 5865055
1. Familial tuberous sclerosis: a review with report of three cases. Verma BS, Tailor MH. Indian Pediatr; 1965 Nov; 2(11):401-10. PubMed ID: 5865055 [No Abstract] [Full Text] [Related]
2. Familial tuberous sclerosis (report of two cases in family with intra-abdominal tumors). Singh SV, Goyal SK, Chowdhury BL, Shrimali R, Bansal NK. J Assoc Physicians India; 1972 Jul; 20(7):529-32. PubMed ID: 4655742 [No Abstract] [Full Text] [Related]
3. [Familial tuberous sclerosis in 2 successive generations with jacksonian crisis and grand-mal epilepsy]. Serbănescu G, Neagoe S, Serbănescu C, Mălăescu G, Colceriu N, Davidescu C, Ruxanda M. Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1982 Jul; 27(2):119-24. PubMed ID: 6216566 [No Abstract] [Full Text] [Related]
4. [Tuberous sclerosis. Case report of a family]. Rasore-Quartino A, Bertamino F, Giunta E, Massone L, Piccardo A. Pathologica; 1983 Jul; 75 Suppl():163-6. PubMed ID: 6680420 [No Abstract] [Full Text] [Related]
5. [Acoustic neuroma and tuberous sclerosis. Familial inquiry (author's transl)]. Rousseaux M, Leys D, Petit H. Rev Otoneuroophtalmol; 1980 Jul; 52(3):245-53. PubMed ID: 6967618 [No Abstract] [Full Text] [Related]
6. Mutation analysis of TSC2 gene in 33 Turkish familial cases with tuberous sclerosis. Apak A, Haliloğlu G, Köse G, Yilmaz E, Anlar B, Aysun S. Turk J Pediatr; 2003 Jul; 45(1):1-5. PubMed ID: 12718362 [Abstract] [Full Text] [Related]
7. [Clinical and genetic study of tuberous sclerosis in a pediatric hospital]. del Castillo V, Carnevale A, Ruiz-Maldonado R, Tamayo L. Rev Invest Clin; 1983 Jul; 35(2):135-9. PubMed ID: 6622872 [No Abstract] [Full Text] [Related]
8. Analysis of all exons of TSC1 and TSC2 genes for germline mutations in Japanese patients with tuberous sclerosis: report of 10 mutations. Yamashita Y, Ono J, Okada S, Wataya-Kaneda M, Yoshikawa K, Nishizawa M, Hirayama Y, Kobayashi E, Seyama K, Hino O. Am J Med Genet; 2000 Jan 17; 90(2):123-6. PubMed ID: 10607950 [Abstract] [Full Text] [Related]
9. [Tuberous sclerosis]. Amir N, Oren N, Shalev RS. Harefuah; 1981 May 15; 100(10):457-8. PubMed ID: 7308883 [No Abstract] [Full Text] [Related]
10. Clinical and genotype studies of cardiac tumors in 154 patients with tuberous sclerosis complex. Jóźwiak S, Kotulska K, Kasprzyk-Obara J, Domańska-Pakieła D, Tomyn-Drabik M, Roberts P, Kwiatkowski D. Pediatrics; 2006 Oct 15; 118(4):e1146-51. PubMed ID: 16940165 [Abstract] [Full Text] [Related]
11. Intrafamilial phenotypic variability in tuberous sclerosis complex. Lyczkowski DA, Conant KD, Pulsifer MB, Jarrett DY, Grant PE, Kwiatkowski DJ, Thiele EA. J Child Neurol; 2007 Dec 15; 22(12):1348-55. PubMed ID: 18174550 [Abstract] [Full Text] [Related]
12. Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis. Beauchamp RL, Banwell A, McNamara P, Jacobsen M, Higgins E, Northrup H, Short P, Sims K, Ozelius L, Ramesh V. Hum Mutat; 1998 Dec 15; 12(6):408-16. PubMed ID: 9829910 [Abstract] [Full Text] [Related]
13. [Tuberous sclerosis. Description of a family study]. Trinidad JC, Iraburu M, Martínez A, Espiñeira M, Bañales T, Alvarez I. An Med Interna; 1997 Jul 15; 14(7):351-4. PubMed ID: 9410122 [Abstract] [Full Text] [Related]
14. Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex. Zhang H, Nanba E, Yamamoto T, Ninomiya H, Ohno K, Mizuguchi M, Takeshita K. J Hum Genet; 1999 Jul 15; 44(6):391-6. PubMed ID: 10570911 [Abstract] [Full Text] [Related]
15. [Cytogenetic study of tuberous sclerosis]. Suzuki Y. No To Shinkei; 1977 May 15; 29(5):537-42. PubMed ID: 559508 [No Abstract] [Full Text] [Related]
16. Tuberose sclerosis--a report of three cases in a family. Seth HC, Hazra LK, Kishore B, Trehon OP, Saxena DK. J Assoc Physicians India; 1969 Jun 15; 17(6):375-7. PubMed ID: 5347675 [No Abstract] [Full Text] [Related]
17. Management of tuberous sclerosis. Webb DW, Osborne JP. Ir Med J; 1991 Mar 15; 84(1):7-8. PubMed ID: 2045272 [No Abstract] [Full Text] [Related]
18. A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients. Young JM, Burley MW, Jeremiah SJ, Jeganathan D, Ekong R, Osborne JP, Povey S. Ann Hum Genet; 1998 May 15; 62(Pt 3):203-13. PubMed ID: 9803264 [Abstract] [Full Text] [Related]