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Literature DB >> 4340974

Mutation and cancer: neuroblastoma and pheochromocytoma.

A G Knudson, L C Strong.

Abstract

Entities: Disease

Mesh：

Year: 1972 PMID： 4340974 PMCID： PMC1762170

Source DB: PubMed Journal: Am J Hum Genet ISSN： 0002-9297 Impact factor: 11.025

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87 in total

1. Pheochromocytoma associated with multiple neurofibromatosis and intracranial hemangioma.

Authors: R C CHAPMAN; V E KEMP; I TALIAFERRO
Journal: Am J Med Date: 1959-06 Impact factor: 4.965

2. Pheochromocytoma in children; report of case.

Authors: A C SMID; J W DUSHANE
Journal: AMA Am J Dis Child Date: 1955-07

3. Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2.

Authors: A L Steiner; A D Goodman; S R Powers
Journal: Medicine (Baltimore) Date: 1968-09 Impact factor: 1.889

4. Phaeochromocytoma, neurofibromatosis and pregnancy.

Authors: R M Humble
Journal: Anaesthesia Date: 1967-04 Impact factor: 6.955

5. Neuroblastoma and ganglioneuroma in a child with multiple neurofibromatosis. Implications for the mutational origin of neuroblastoma.

Authors: A G Knudson; G D Amromin
Journal: Cancer Date: 1966-07 Impact factor: 6.860

6. Abnormal intradermal histamine reaction in the syndrome of pheochromocytoma, medullary carcinoma of the thyroid gland and multiple mucosal neuromas.

Authors: J L Baum
Journal: N Engl J Med Date: 1971-04-29 Impact factor: 91.245

7. [Medullary thyroid cancer and bilateral pheochromocytoma].

Authors: L Aubert; H Arroyo; G Godeffroi; J L de Gennes
Journal: Bull Mem Soc Med Hop Paris Date: 1967 Nov 3-10

8. Von Recklinghausen's disease associated with pheochromocytoma and carcinoid tumor.

Authors: H Y Lee; P E Garber
Journal: Ohio State Med J Date: 1970-06

9. Mutation and cancer: statistical study of retinoblastoma.

Authors: A G Knudson
Journal: Proc Natl Acad Sci U S A Date: 1971-04 Impact factor: 11.205

10. Neuroblastoma (sympathicoblastoma) in Northern Ireland: a review over a ten-year period.

Authors: W COCHRAN
Journal: Ulster Med J Date: 1963-06

66 in total

1. ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome.

Authors: Franck Bourdeaut; Sandrine Ferrand; Laurence Brugières; Marjorie Hilbert; Agnès Ribeiro; Ludovic Lacroix; Jean Bénard; Valérie Combaret; Jean Michon; Dominique Valteau-Couanet; Bertrand Isidor; Xavier Rialland; Maryline Poirée; Anne-Sophie Defachelles; Michel Peuchmaur; Gudrun Schleiermacher; Gaëlle Pierron; Marion Gauthier-Villars; Isabelle Janoueix-Lerosey; Olivier Delattre
Journal: Eur J Hum Genet Date: 2011-11-09 Impact factor: 4.246

9. Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

Authors: E R Maher; J R Yates; M A Ferguson-Smith
Journal: J Med Genet Date: 1990-05 Impact factor: 6.318

Review 10. Biology of pediatric peripheral neuroectodermal tumors.

Authors: C J Thiele
Journal: Cancer Metastasis Rev Date: 1991-12 Impact factor: 9.264

Mutation and cancer: neuroblastoma and pheochromocytoma.

1. Pheochromocytoma associated with multiple neurofibromatosis and intracranial hemangioma.

2. Pheochromocytoma in children; report of case.

3. Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2.

4. Phaeochromocytoma, neurofibromatosis and pregnancy.

5. Neuroblastoma and ganglioneuroma in a child with multiple neurofibromatosis. Implications for the mutational origin of neuroblastoma.

6. Abnormal intradermal histamine reaction in the syndrome of pheochromocytoma, medullary carcinoma of the thyroid gland and multiple mucosal neuromas.

7. [Medullary thyroid cancer and bilateral pheochromocytoma].

8. Von Recklinghausen's disease associated with pheochromocytoma and carcinoid tumor.

9. Mutation and cancer: statistical study of retinoblastoma.

10. Neuroblastoma (sympathicoblastoma) in Northern Ireland: a review over a ten-year period.

1. ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome.

2. The aetiology of cancer in the very young.

3. Increased predisposition to cancer in brothers and offspring of testicular tumor patients.

4. Familial occurrence of Wilms' tumor: nephroblastoma in one of monozygous twins and in another sibling.

5. Search for neuroblastoma loci: characterization of tumor cell lines that could facilitate their positional cloning.

6. Neurologic manifestations of von Hippel-Lindau disease.

Review 7. Genetics of neoplasia--impact of ecogenetics on oncogenesis. A review.

8. Neuroepithelioma (neuroblastoma) arising in an adult. A case report.

9. Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

Review 10. Biology of pediatric peripheral neuroectodermal tumors.