Recent Publications on : |  |
Multiple gastrointestinal stromal tumors in neurofibromatosis type 1: Report of a case.
This report presents a case of multiple gastrointestinal stromal tumors...
Direct Link | 3rd November, 2009
| Department of Gastroenterological Surgery, Kumamoto University, 1-1-1
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[Usefulness of systematic brain magnetic resonance imaging in children with neurofibromatosis type 1.]
BACKGROUND AND AIM: The aim of this study was to evaluate the usefulness...
Direct Link | 30th October, 2009
| Service de neurologie pediatrique, hopital Femme-Mere-Enfant, hospices
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Multiple spinal ganglioneuromas in a patient harboring a pathogenic NF1 mutation.
Bacci C, Sestini R, Ammannati F, Bianchini E, Palladino T, Carella M,...
Direct Link | 30th October, 2009
| Department of Clinical Physiopathology, Medical Genetics Unit, University
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| [Hereditary diseases with propensity to myeloid malignancy]
| 29th October, 2009
| Department of Pediatrics, Nihon University School of Medicine.
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Plurifocal malignant peripheral nerve sheath tumor demonstrated by 18F-fluorodeoxyglucose positron emission tomography/computed tomography.
Malignant peripheral nerve sheath tumors (MPNSTs) are sarcomas that derive...
Direct Link | 27th October, 2009
| Department of Nuclear Medicine, Spedali Civili di Brescia, Piazza Spedali
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The neurofibromatosis type I pre-mRNA is a novel target of CELF protein-mediated splicing regulation.
The CUG-BP and ETR-3 like factors (CELF) are a family of six highly...
Direct Link | 27th October, 2009
| Department of Genetics, School of Medicine, Case Western Reserve
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PTEN dosage is essential for neurofibroma development and malignant transformation.
Patients with neurofibromatosis type 1 (NF1) carry approximately a 10%...
Direct Link | 23rd October, 2009
| Department of Molecular and Medical Pharmacology, Department of Pathology
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Noonan syndrome and neurofibromatosis type I in a family with a novel mutation in NF1.
Nystrom AM, Ekvall S, Allanson J, Edeby C, Elinder M, Holmstrom G,...
Direct Link | 23rd October, 2009
| Department of Genetics and Pathology, Uppsala University Hospital, 751 85
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Characteristics of children enrolled in treatment trials for NF1-related plexiform neurofibromas.
OBJECTIVE: To describe the characteristics of children enrolled in...
Direct Link | 21st October, 2009
| National Cancer Institute, Pediatric Oncology Branch, NIH, Bethesda, MD
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| A novel mutation of the IL12RB1 gene in a child with nocardiosis, recurrent salmonellosis and neurofibromatosis type I: first case report from Thailand.
| 21st October, 2009
| Department of Immunology, Faculty of Medicine Siriraj Hospital, Mahidol
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Malignant peripheral nerve sheath tumour (MPNST): the clinical implications of cellular signalling pathways.
Malignant peripheral nerve sheath tumour (MPNST) is a rare malignancy...
Direct Link | 20th October, 2009
| Department of Surgical Oncology and Sarcoma Research Center, The
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Spontaneous rupture of an intercostal artery in a patient with neurofibromatosis type 1.
A 48-year-old man with neurofibromatosis type 1 (NF1) presented with a...
Direct Link | 17th October, 2009
| Jichi Medical University, Shimotsuke, Japan.
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Surgical strategies for managing foraminal nerve sheath tumors: the emerging role of CyberKnife ablation.
Sixteen Stanford University Medical Center (SUMC) patients with foraminal...
Direct Link | 3rd October, 2009
| Department of Neurosurgery, Stanford University Medical Center, Stanford,
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Alterations of BRAF and HIPK2 loci predominate in sporadic pilocytic astrocytoma.
OBJECTIVE: Independent studies have previously demonstrated that both the...
Direct Link | 2nd October, 2009
| From the Departments of Pathology (J.Y., H.D., M.A.W., R.N.) and Neurology
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Juvenile xanthogranuloma in a child with previously unsuspected neurofibromatosis type 1 and juvenile myelomonocytic leukemia.
The association of neurofibromatosis 1 (NF1), juvenile xanthogranulomas...
Direct Link | 29th September, 2009
| Eunice Kennedy Shriver National Institute of Child Health and Human
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