147 related articles for article (PubMed ID: 16506130)
1. [Autosomal dominant mental retardation].
Sánchez-Díaz A; Morales-Peydró C; Madrigal-Bajo I
Rev Neurol; 2006 Jan; 42 Suppl 1():S33-7. PubMed ID: 16506130
[TBL] [Abstract][Full Text] [Related]
2. Neurocutaneous syndromes: neurofibromatosis 1, neurofibromatosis 2, and tuberous sclerosis.
Korf BR
Curr Opin Neurol; 1997 Apr; 10(2):131-6. PubMed ID: 9146993
[TBL] [Abstract][Full Text] [Related]
3. Tuberous sclerosis complex with polycystic kidney disease of the adult type: the TSC2/ADPKD1 contiguous gene syndrome.
Bisceglia M; Galliani C; Carosi I; Simeone A; Ben-Dor D
Int J Surg Pathol; 2008 Oct; 16(4):375-85. PubMed ID: 18611938
[TBL] [Abstract][Full Text] [Related]
4. [Common types of neurofibromatosis. Elements of a mental syndrome (apropos of 5 cases].
Imache C
Ann Med Psychol (Paris); 1974 Jun; 2(1):19-59. PubMed ID: 4217115
[No Abstract] [Full Text] [Related]
5. Genes, plasticity and mental retardation.
Vaillend C; Poirier R; Laroche S
Behav Brain Res; 2008 Sep; 192(1):88-105. PubMed ID: 18329113
[TBL] [Abstract][Full Text] [Related]
6. Epileptic fit: the most dramatic sign of tuberous sclerosis.
Isichei HU; Obafunwa
Trop Geogr Med; 1993; 45(3):137-9. PubMed ID: 8362458
[TBL] [Abstract][Full Text] [Related]
7. Tuberous sclerosis: presentation of a clinical case with oral manifestations.
López E; Escovich L; Vigna A
Med Oral; 2003; 8(2):122-8. PubMed ID: 12618672
[TBL] [Abstract][Full Text] [Related]
8. Macrosomia and mental retardation: evidence of autosomal dominant inheritance in four generations.
Mangano L; Palmeri S; Dotti MT; Moschini F; Federico A
Am J Med Genet; 1989 Jan; 32(1):67-71. PubMed ID: 2705485
[TBL] [Abstract][Full Text] [Related]
9. The tuberous sclerosis genes and regulation of the cyclin-dependent kinase inhibitor p27.
Rosner M; Freilinger A; Hengstschläger M
Mutat Res; 2006 Sep; 613(1):10-6. PubMed ID: 16713332
[TBL] [Abstract][Full Text] [Related]
10. [Simultaneous occurrence of neurofibromatosis and tuberous sclerosis, acquired as neo-mutations].
Janeiro PC; Cunha MS; Cordeiro I; Santos HG; Antunes NL
Rev Neurol; 2008 Mar 16-31; 46(6):347-50. PubMed ID: 18368679
[TBL] [Abstract][Full Text] [Related]
11. Simultaneous occurrence of neurofibromatosis type 1 and tuberous sclerosis in a young girl.
Wheeler PG; Sadeghi-Nejad A
Am J Med Genet A; 2005 Feb; 133A(1):78-81. PubMed ID: 15637706
[TBL] [Abstract][Full Text] [Related]
12. [Difficulties in genetic counseling in phakomatosis].
Francois J
J Genet Hum; 1975 Mar; 23(1):17-27. PubMed ID: 809545
[TBL] [Abstract][Full Text] [Related]
13. [Genetic mental retardation. Presentation of the GIRMOGEN network].
Tejada MI
Rev Neurol; 2006 Jan; 42 Suppl 1():S1-6. PubMed ID: 16506122
[TBL] [Abstract][Full Text] [Related]
14. A case of neurofibromatosis-Noonan syndrome with a central giant cell granuloma.
Yazdizadeh M; Tapia JL; Baharvand M; Radfar L
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2004 Sep; 98(3):316-20. PubMed ID: 15356469
[TBL] [Abstract][Full Text] [Related]
15. Molecular and clinical analyses of 84 patients with tuberous sclerosis complex.
Hung CC; Su YN; Chien SC; Liou HH; Chen CC; Chen PC; Hsieh CJ; Chen CP; Lee WT; Lin WL; Lee CN
BMC Med Genet; 2006 Sep; 7():72. PubMed ID: 16981987
[TBL] [Abstract][Full Text] [Related]
16. Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disorders.
Carey JC; Viskochil DH
Am J Med Genet; 1999 Mar; 89(1):7-13. PubMed ID: 10469431
[TBL] [Abstract][Full Text] [Related]
17. [Phacomatosis and genetically determined tumors: the transition from childhood to adulthood].
de Ribaupierre S; Vernet O; Vinchon M; Rilliet B
Neurochirurgie; 2008 Oct; 54(5):642-53. PubMed ID: 18752812
[TBL] [Abstract][Full Text] [Related]
18. Mutational analysis of TSC1 and TSC2 in Korean patients with tuberous sclerosis complex.
Choi JE; Chae JH; Hwang YS; Kim KJ
Brain Dev; 2006 Aug; 28(7):440-6. PubMed ID: 16554133
[TBL] [Abstract][Full Text] [Related]
19. Genetics and pathophysiology of mental retardation.
Chelly J; Khelfaoui M; Francis F; Chérif B; Bienvenu T
Eur J Hum Genet; 2006 Jun; 14(6):701-13. PubMed ID: 16721406
[TBL] [Abstract][Full Text] [Related]
20. [Hyperparathyroidism in a patient with neurofibromatosis associated with Steinert's disease].
Duquenne M; Klein M; Duriez T; Hadjadj S; Weryha G; Leclère J
Ann Med Interne (Paris); 1994; 145(7):505-7. PubMed ID: 7864524
[No Abstract] [Full Text] [Related]
[Next] [New Search]