Disease: Neurofibromatosis- familial intestinal
- "Wild type" GIST: Clinicopathological features and clinical practice
- A case of neurofibromatosis complicated with small bowel obstruction
- A Rare Case of Multiple Gastrointestinal Stromal Tumors Coexisting with a Rectal Adenocarcinoma in a Patient with Attenuated Familial Adenomatous Polyposis Syndrome and a Mini Review of the Literature
- A rare case of retroperitoneal malignant Triton tumor invading renal vein and small intestine
- Appendiceal schwannoma - report of a case and literature review
- Case Report: Multiple gastrointestinal stromal tumors along with numerous cutaneous neurofibromas: a case description and literature analysis
- Caucasian familial moyamoya syndrome with rare multisystemic malformations
- Current status of familial gastrointestinal polyposis syndromes
- Diagnosis and Management of Hereditary Carcinoids
- Epithelial and neuroendocrine tumors of the duodenum
- Extra-intestinal manifestations of familial adenomatous polyposis
- Familial cancer syndromes: a survey
- Familial enteric neurofibromatosis
- Familial ganglioneuromatous polyposis of the large bowel. Report of a family with associated juvenile polyposis
- Ganglioneuromas of the gastrointestinal tract. Relation to Von Recklinghausen disease and other multiple tumor syndromes
- Gastrointestinal aspects of cutaneous and familial diseases
- Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium
- Gastrointestinal manifestations of neurofibromatosis in childhood
- Gastrointestinal polyposis syndromes
- Gastrointestinal stromal tumors: review on morphology, molecular pathology, prognosis, and differential diagnosis
- Gastrointestinal stromal tumour
- Genetic counseling in cancerology
- Glioblastoma multiforme in four siblings: a cytogenetic and molecular genetic study
- Hereditary intestinal neurofibromatosis. I. A distinctive genetic disease
- Hereditary intestinal neurofibromatosis. II. Translocation between chromosomes 12 and 14
- Hereditary intestinal polyposis syndromes
- Inherited tumor syndromes of gastroenteropancreatic and thoracic neuroendocrine neoplasms
- Intestinal neurofibromatosis is a subtype of familial GIST and results from a dominant activating mutation in PDGFRA
- Intra-abdominal plexiform neurofibromatosis including periportal, mesentery, and gastrointestinal tract involvement in neurofibromatosis type 1: case report and review of the literature
- Involvement of the large intestine in neurofibromatosis type 1
- Isolated intestinal Ganglioneuromatosis: case report and literature review
- KIT and PDGFRA mutations in gastrointestinal stromal tumors (GISTs)
- Malignant peripheral nerve sheath tumor arising from the colon in a newborn: report of a case and review of the literatures
- Metachronous Wilms Tumor, Glioblastoma, and T-cell Leukemia in an Child With Constitutional Mismatch Repair Deficiency syndrome due to Novel Mutation in MSH6 (c.2590G>T)
- Microscopic gastrointestinal stromal tumors in esophageal and intestinal surgical resection specimens: a clinicopathologic, immunohistochemical, and molecular study of 19 lesions
- Molecular genetics of gastroenteropancreatic neuroendocrine tumors
- Multicentric malignant gastrointestinal stromal tumor
- Multiple Gastrointestinal Stromal Tumor with Neurofibromatosis Type :Report of One Case
- Multiple Gastrointestinal Stromal Tumor with Neurofibromatosis Type Ⅰ:Report of One Case
- Multiple gastrointestinal stromal tumors in type I neurofibromatosis: a pathologic and molecular study
- Multiple gastrointestinal stromal tumors: Clinicopathologic and genetic analysis of 12 patients
- Multiple non-metastatic gastrointestinal stromal tumors. Differential features
- Multiple schwannoma with digestive localizations (Von Recklinghausen's disease). Apropos of a familial case
- Neurofibromatosis and a tumor of Vater's papilla
- NHERF1/EBP50 controls morphogenesis of 3D colonic glands by stabilizing PTEN and ezrin-radixin-moesin proteins at the apical membrane
- PDGFRA-mutant syndrome
- Solitary ganglioneuromatosis of the descending colon, presenting as giant retroperitoneal tumour
- Solitary neurofibroma of the mesentery: report of a case and review of the literature
- Sporadic ampullary hamartoma simulating cancer
- Synchronous GIST with osteoclast-like giant cells and a well-differentiated neuroendocrine tumor in Ampula Vateri: coexistence of two extremely rare entities
- Tandem duplication within the neurofibromatosis type 1 gene (NF1) and reciprocal t(15;16)(q26.3;q12.1) translocation in familial association of NF1 with intestinal neuronal dysplasia type B (IND B)
- The different forms of neurofibromatosis
- The gardner syndrome. A study in cell culture
- The genetics of neuroendocrine tumors
- The hamartomatous polyposis syndromes: a clinical and molecular review
- The neurofibromatoses. An overview
- Volar melanotic macules in a gardener: a case report and review of the literature
- Von Recklinghausen's disease associated with malignant peripheral nerve sheath thmor presenting with constipation and urinary retention: a case report and review of the literature