Homozygosity of MSH2 c.1906G→C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I

2008 ◽  
Vol 8 (3) ◽  
pp. 187-194 ◽  
Author(s):  
Helen Toledano ◽  
Yael Goldberg ◽  
Inbal Kedar-Barnes ◽  
Hagit Baris ◽  
Rinnat M. Porat ◽  
...  
Keyword(s):  
Colon Cancer ◽  
Germline Mutation ◽  
Neurofibromatosis Type ◽  
Type I ◽  
Neurofibromatosis Type I

Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?

2006 ◽  
Vol 37 (06) ◽  
Author(s):  
J Neinert ◽  
E Fastnacht ◽  
R Larisch ◽  
E Legius ◽  
R Engelskirchen ◽  
...  
Keyword(s):  
Malignant Transformation ◽  
Neurofibromatosis Type ◽  
Type I ◽  
Neurofibromatosis Type I ◽  
18Fdg Pet

scholarly journals Folliculosebaceous Cystic Hamartoma in a Patient with Neurofibromatosis Type I

2011 ◽  
Vol 23 (Suppl 2) ◽  
pp. S185 ◽  
Author(s):  
Seongmin Noh ◽  
Ji Eun Kwon ◽  
Kwang Gil Lee ◽  
Mi Ryung Roh
Keyword(s):  
Neurofibromatosis Type ◽  
Type I ◽  
Neurofibromatosis Type I ◽  
Cystic Hamartoma

Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndrome

1996 ◽  
Vol 8 (1) ◽  
pp. 51-56 ◽  
Author(s):  
Rina Wu ◽  
Eric Legius ◽  
Wim Robberecht ◽  
Monique Dumoulin ◽  
Jean-Jacques Cassiman ◽  
...  
Keyword(s):  
Gene Mutation ◽  
Neurofibromatosis Type ◽  
Type I ◽  
Neurofibromatosis Type I ◽  
Leopard Syndrome ◽  
I Gene
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