Neurofibromatosis type 1 (NF1) associated with tumor of the corpus callosum

[1]  A. Thurm,et al.  Observations on intelligence and behavior in 15 patients with Legius syndrome , 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

[2]  D. Viskochil,et al.  NF1 exon 22 analysis of individuals with the clinical diagnosis of neurofibromatosis type 1 , 2010, American journal of medical genetics. Part A.

[3]  S. Pascual-Pascual,et al.  Posterior fossa tumors in children with neurofibromatosis type 1 (NF1) , 2010, Child's Nervous System.

[4]  J. Viano,et al.  Tumores de los hemisferios cerebrales en la neurofibromatosis tipo 1 durante la infancia , 2010 .

[5]  A. Fanaroff Clinical and Mutational Spectrum of Neurofibromatosis Type 1–like Syndrome , 2010 .

[6]  G. Leverger,et al.  SPRED1 disorder and predisposition to leukemia in children. , 2009, Blood.

[7]  R. Fahsold,et al.  Independent NF1 and PTPN11 mutations in a family with neurofibromatosis‐Noonan syndrome , 2009, American journal of medical genetics. Part A.

[8]  E. Haan,et al.  SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotype , 2009, Journal of Medical Genetics.

[9]  A. Shuper,et al.  Lesions of the corpus callosum in children with neurofibromatosis 1. , 2008, Pediatric neurology.

[10]  García-Segura Jm,et al.  Neurofibromatosis tipo 1 y gliomas de vías ópticas. Una serie de 80 pacientes , 2008 .

[11]  B. O'neill,et al.  Gliomas in Neurofibromatosis Type 1: A Clinicopathologic Study of 100 Patients , 2008, Journal of neuropathology and experimental neurology.

[12]  M. Upadhyaya,et al.  Neurofibromatosis type 1 & Related Disorders , 2008 .

[13]  G. Thomas,et al.  Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype , 2007, Nature Genetics.

[14]  J. Echeveste,et al.  Actualización sobre la biología molecular de los gliomas: hacia una clasificación patomolecular de los gliomas , 2007 .

[15]  J. Viano,et al.  Tumores de tronco cerebral asociados con neurofibromatosis tipo 1. Presentaciôn de 20 pacientes infantiles , 2007 .

[16]  Kathryn N North,et al.  Learning disabilities in children with neurofibromatosis type 1: subtypes, cognitive profile, and attention-deficit-hyperactivity disorder. , 2006, Developmental medicine and child neurology.

[17]  D. Stevenson,et al.  Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotype , 2006, Clinical genetics.

[18]  A. Battaglia,et al.  NF1 gene mutations represent the major molecular event underlying neurofibromatosis-Noonan syndrome. , 2005, American journal of human genetics.

[19]  J. Krieger,et al.  Neurofibromatosis–Noonan syndrome: Molecular evidence of the concurrence of both disorders in a patient , 2005, American journal of medical genetics. Part A.

[20]  Arie Perry,et al.  Comparative gene expression profile analysis of neurofibromatosis 1-associated and sporadic pilocytic astrocytomas. , 2002, Cancer research.

[21]  L. Kluwe,et al.  Treatment of ADHD in neurofibromatosis type 1 , 2002, Developmental medicine and child neurology.

[22]  C. James,et al.  Cancer-related gene expression profiles in NF1-associated pilocytic astrocytomas , 2001, Neurology.

[23]  G. Vezina,et al.  MR imaging of the corpus callosum in pediatric patients with neurofibromatosis type 1. , 2001, AJNR. American journal of neuroradiology.

[24]  P. Griffiths,et al.  Neurofibromatosis Bright Objects in Children With Neurofibromatosis Type 1: A Proliferative Potential? , 1999, Pediatrics.

[25]  B. Zuckerman,et al.  Restraining Orders: A Frequent Marker of Adverse Maternal Health , 1999, Pediatrics.

[26]  J. Carey,et al.  Neurofibromatosis-Noonan syndrome. , 1998, American journal of medical genetics.

[27]  D. Evans,et al.  Neurofibromatosis/Noonan phenotype: a variable feature of type 1 neurofibromatosis , 1996, Clinical genetics.

[28]  J R Hesselink,et al.  MR imaging of the corpus callosum. , 1993, AJR. American journal of roentgenology.

[29]  S. Bundey Fetal and Perinatal Neurology , 1992 .

[30]  I. Pascual‐Castroviejo Complications of Neurofibromatosis Type 1 in a Series of 197 Children , 1992 .

[31]  J. Charrow,et al.  Optic gliomas in children with neurofibromatosis type 1. , 1989, The Journal of pediatrics.

[32]  M. Eliason Neurofibromatosis: implications for learning and behavior. , 1986, Journal of developmental and behavioral pediatrics : JDBP.