106 related articles for article (PubMed ID: 9686256)
1. [Neurofibromatosis I and multiple sclerosis. Apropos of a case].
Masson C; Colombani JM
Rev Neurol (Paris); 1997 Nov; 153(11):684-6. PubMed ID: 9686256
[TBL] [Abstract][Full Text] [Related]
2. [Multiple sclerosis and neurofibromatosis 1].
Alfonso S; Roquer J; Pou A
Neurologia; 1996; 11(6):233-5. PubMed ID: 8768681
[TBL] [Abstract][Full Text] [Related]
3. Neurofibromatosis 1 and multiple sclerosis.
Ferner RE; Hughes RA; Johnson MR
J Neurol Neurosurg Psychiatry; 1995 May; 58(5):582-5. PubMed ID: 7745407
[TBL] [Abstract][Full Text] [Related]
4. Detailed analysis of the oligodendrocyte myelin glycoprotein gene in four patients with neurofibromatosis 1 and primary progressive multiple sclerosis.
Johnson MR; Ferner RE; Bobrow M; Hughes RA
J Neurol Neurosurg Psychiatry; 2000 May; 68(5):643-6. PubMed ID: 10766898
[TBL] [Abstract][Full Text] [Related]
5. Learning disability and oligodendrocyte myelin glycoprotein (OMGP) gene in neurofibromatosis type 1.
Terzi YK; Oğuzkan-Balci S; Anlar B; Erdoğan-Bakar E; Ayter S
Turk J Pediatr; 2011; 53(1):75-8. PubMed ID: 21534343
[TBL] [Abstract][Full Text] [Related]
6. Neurofibromatosis type I associated multiple sclerosis.
Pipatpajong H; Phanthumchinda K
J Med Assoc Thai; 2011 Apr; 94(4):505-10. PubMed ID: 21591539
[TBL] [Abstract][Full Text] [Related]
7. A case of neurofibromatosis and breast cancer: loss of heterozygosity of NF1 in breast cancer.
Güran S; Safali M
Cancer Genet Cytogenet; 2005 Jan; 156(1):86-8. PubMed ID: 15588864
[TBL] [Abstract][Full Text] [Related]
8. Increased dental caries in people with neurofibromatosis 1.
Tucker T; Birch P; Savoy DM; Friedman JM
Clin Genet; 2007 Dec; 72(6):524-7. PubMed ID: 18001351
[TBL] [Abstract][Full Text] [Related]
9. Absence of c-kit gene mutations in gastrointestinal stromal tumours from neurofibromatosis type 1 patients.
Kinoshita K; Hirota S; Isozaki K; Ohashi A; Nishida T; Kitamura Y; Shinomura Y; Matsuzawa Y
J Pathol; 2004 Jan; 202(1):80-5. PubMed ID: 14694524
[TBL] [Abstract][Full Text] [Related]
10. A patient severely affected by spinal neurofibromas carries a recurrent splice site mutation in the NF1 gene.
Wimmer K; Mühlbauer M; Eckart M; Callens T; Rehder H; Birkner T; Leroy JG; Fonatsch C; Messiaen L
Eur J Hum Genet; 2002 May; 10(5):334-8. PubMed ID: 12082509
[TBL] [Abstract][Full Text] [Related]
11. Constitutional NF1 mutations in neurofibromatosis 1 patients with malignant peripheral nerve sheath tumors.
Kluwe L; Friedrich RE; Peiper M; Friedman J; Mautner VF
Hum Mutat; 2003 Nov; 22(5):420. PubMed ID: 14517963
[TBL] [Abstract][Full Text] [Related]
12. [Polymorphism of length of tetranucleotide repeat from the 5'-side from the myelin basic protein gene in multiple sclerosis in Russians].
Andreevskiĭ TV; Guérini FR; Sudomoina MA; Boĭko AN; Alekseenkov AD; Kulakova OG; Kitsuake K; Ferrabte O; Gusev EI; Favorova OO
Mol Biol (Mosk); 2003; 37(6):999-1006. PubMed ID: 14714495
[TBL] [Abstract][Full Text] [Related]
13. Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletions.
Lopez Correa C; Brems H; Lázaro C; Estivill X; Clementi M; Mason S; Rutkowski JL; Marynen P; Legius E
Hum Mutat; 1999; 14(5):387-93. PubMed ID: 10533064
[TBL] [Abstract][Full Text] [Related]
14. SNP mapping and candidate gene sequencing in the class I region of the HLA complex: searching for multiple sclerosis susceptibility genes in Tasmanians.
Burfoot RK; Jensen CJ; Field J; Stankovich J; Varney MD; Johnson LJ; Butzkueven H; Booth D; Bahlo M; Tait BD; Taylor BV; Speed TP; Heard R; Stewart GJ; Foote SJ; Kilpatrick TJ; Rubio JP
Tissue Antigens; 2008 Jan; 71(1):42-50. PubMed ID: 17971048
[TBL] [Abstract][Full Text] [Related]
15. Clinically aggressive central giant cell granulomas in two patients with neurofibromatosis 1.
Edwards PC; Fantasia JE; Saini T; Rosenberg TJ; Sachs SA; Ruggiero S
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Dec; 102(6):765-72. PubMed ID: 17138179
[TBL] [Abstract][Full Text] [Related]
16. Three different pathological lesions in the NF1 gene originating de novo in a family with neurofibromatosis type 1.
Upadhyaya M; Majounie E; Thompson P; Han S; Consoli C; Krawczak M; Cordeiro I; Cooper DN
Hum Genet; 2003 Jan; 112(1):12-7. PubMed ID: 12483293
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. A nonsense mutation at Arg-1947 in the NF1 gene in a case of neurofibromatosis type 1 in a Korean patient.
Park KC; Choi HO; Park KH; Kim KH; Eun HC
J Hum Genet; 2000; 45(2):84-5. PubMed ID: 10721668
[TBL] [Abstract][Full Text] [Related]
19. Neurofibromatosis 1 associated with embryonal rhabdomyosarcoma of the urinary bladder.
Reich S; Overberg-Schmidt US; Leenen A; Henze G
Pediatr Hematol Oncol; 1999; 16(3):263-6. PubMed ID: 10326226
[TBL] [Abstract][Full Text] [Related]
20. Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: further evidence for a contiguous gene syndrome in 17q11.2.
Streubel B; Latta E; Kehrer-Sawatzki H; Hoffmann GF; Fonatsch C; Rehder H
Am J Med Genet; 1999 Nov; 87(1):12-6. PubMed ID: 10528240
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
