21/73US=27 / Clin/Médica
Arnaout MA. Doenças císticas do rim. In: Goldman L, Ausiello D, editors. Cecil medicina. 23ª ed. Rio de Janeiro: Elsevier, 2009. p. 1042-51. ISBN 85-3523677-4.

DOENCAS CISTICAS RENAIS; DOENCA RENAL POLICISTICA AUTOSSOMICA DOMINANTE; DOENCA RENAL POLICISTICA AUTOSSOMICA RECESSIVA; DOENCA RENAL CISTICA ADQUIRIDA; DOENCAS RENAIS CISTICAS MEDULARES; NEFRONOFTISE FAMILIAL; RIM ESPONJOSO MEDULAR


22/73US=27 / Clin/Médica
DuBois RN. Neoplasias do cólon e intestino delgado. In: Goldman L, Ausiello D, editors. Cecil medicina. 23ª ed. Rio de Janeiro: Elsevier, 2009. p. 1689-701. ISBN 85-3523677-4.

CANCER DE COLON; POLIPOS DO COLON; POLIPOS NAO ADENOMATOSOS; POLIPOS ADENOMATOSOS; POLIPOSE ADENOMATOSA FAMILIAL; SINDROME DE GARDNER; CANCER DE COLON E RETO HEREDITARIO NAO POLIPOIDE; SINDROME DE PEUTZ-JEGHERS; POLIPOSE JUVENIL; SINDROME DE COWDEN; ADENOCARCINOMA DE COLON E RETO; CANCER DE INTESTINO DELGADO


23/73US=72 / Câncer
Noronha S. Síndrome hereditária e rastreamento para diagnóstico precoce de neoplasia. In: Buzaid AC, Maluf FC, Lima CMR. MOC: manual oncologia clínica do Brasil. 10ª ed. São Paulo: Dendrix, 2012. p. 728-34. ISBN 85-99453-50-6.

CANCER DE MAMA HEREDITARIO; CANCER DE OVARIO HEREDITARIO; SINDROME DE COWDEN; SINDROME DE LI-FRAUMENI; SINDROME DE LYNCH; CANCER DE COLON HEREDITARIO NAO POLIPOMATOSO; POLIPOSE ADENOMATOSA FAMILIAR; CANCER GASTRICO HEREDITARIO; NEOPLASIA ENDOCRINA MULTIPLA TIPO 1; NEOPLASIA ENDOCRINO MULTIPLA TIPO 2; RETINOBLASTOMA HEREDITARIO; MELANOMA FAMILIAL


24/73US=48 / Biol/Mol
Cote ML. Study designs in genetic epidemiology. In: Tainsky MA. Tumor biomarker discovery: methods and protocols. New Jersey: Humana Press, 2009. p. 247-57. (Methods in Molecular Biology 520) ISBN 978-1-60327-810-2.

EPIDEMIOLOGIA GENETICA; AGREGACAO FAMILIAL; ANALISE DE LIGACAO; ANALISE DE SEGREGACAO


25/73US=45-B / Cab/Pesc
Gillenwater AM. Melanoma of the head and neck: general principles and management. In: Harrison LB, Sessions RB, Hong WK. Head and neck cancer: a multidisciplinary approach. 3rd ed. Philadelphia: J B Lippincott, 2009. p. 571-84. ISBN 978-0-7817-7136-8.

CANCER DE CABECA E PESCOCO; MELANOMA; PELE. ANATOMIA; MELANOMA FAMILIAL


26/73US=9 / Pediatria
Plon SE, Malkin D. Childhood cancer and heredity. In: Pizzo PA, Poplack DG. Principles and practice of pediatric oncology. 5th ed. Philadelphia: Lippincott Williams and Wilkins, 2006. p. 14-37. ISBN 978-0-7817-5492-7.

ONCOLOGIA PEDIATRICA; CANCER INFANTIL; CRIANCA; HEREDITARIEDADE; PREDISPOSICAO HEREDITARIA; ANORMALIDADES CROMOSSOMICAS; SINDROME DE DOWN; SINDROME DE BECKWITH-WIEDEMANN; PARAGANGLIOMA; DISTURBIOS AUTOSSOMICOS DOMINANTES; RETINOBLASTOMA; SINDROME DE LI-FRAUMENI; NEOPLASIA ENDOCRINA MULTIPLA; TERATOIDE ATIPICO; TUMORES MALIGNOS RABDOIDES; SINDROME DE PREDISPOSICAO RABDOIDE; LEUCEMIA FAMILIAL; CANCER DE COLON; POLIPOSE ADENOMATOSA FAMILIAR; POLIPOSE JUVENIL; CANCER COLO-RETAL HEREDITARIO NAO POLIPOSE; SINDROME DE TURCOT; NEUROFIBROMATOSE TIPO 1; NEUROFIBROMATOSE TIPO 2; ESCLEROSE TUBEROSA; DOENCA DE VON HIPPEL-LINDAU; FEOCROMOCITOMA; SINDROME DO CARCINOMA BASOCELULAR NEVOIDE; SINDROME DE GORLIN-GOLTZ; XERODERMA PIGMENTOSO; SINDROME DE COCKAYNE; TRICOTIODISTROFIA; ATAXIA-TELANGIECTASIA


27/73US=15 / Gastro
Brune KA, Klein AP. Familial pancreatic cancer. In: Lowy AM, Leach SD, Philip PA. Pancreatic cancer. New York: Springer, 2008. p. 65-79. ISBN 978-0-387-69250-0.

CANCER DE PANCREAS FAMILIAR; CANCER DE PANCREAS FAMILIAR. FATORES DE RISCO; CANCER DA MAMA HEREDITARIO; HEREDITARIO SEM POLIPOSE; SINDROME DE CANCER COLORRETAL; PANCREATITE HEREDITARIA


28/73US=17 / Gastro
Raut CP, Hornick JL, Bertagnolli MM. Gastrointestinal stromal tumors of gastric origin. In: Wang TC, Fox JG, Giraud AS. The biology of gastric cancers. New York: Springer, 2008. p. 135-63. ISBN 978-0-387-69181-7.

TUMORES ESTROMAIS GASTROINTESTINAIS; HISTOLOGICA; CLASSIFICACAO MOLECULAR; RECEPTORAS TIROSINA-QUINASES; TUMORES ESTROMAIS GASTROINTESTINAIS. EPIDEMIOLOGIA; TUMORES ESTROMAIS GASTROINTESTINAIS FAMILIAL; TUMORES ESTROMAIS GASTROINTESTINAIS. APRESENTACAO CLINICA; TUMORES ESTROMAIS GASTROINTESTINAIS. DIAGNOSTICO; TUMORES ESTROMAIS GASTROINTESTINAIS. FATORES PROGNOSTICOS; TUMORES ESTROMAIS GASTROINTESTINAIS. TRATAMENTO


29/73Câncer
Silva SRM, Matos D, Waitzberg AFL, Artigiani R, Saad SS. Study of APC and &*946;-catenin protein expression in polyps and colorectal adenocarcinoma. Applied Cancer Research, São Paulo: Tecmedd, v.31, n.3, p. 81-6, 2011. ISSN 1980-5578.

Disponível em: http://accamargo.phlnet.com.br/applied/ACR2011;31p.81-6.pdf

ADENOMATOSE; POLIPOSE FAMILIAL; NEOPLASIAS COLORRETAIS; BETA CADERIN


30/73US=23 / Câncer
Bult P, Hoogerbrugge N. Familial breast cancer: detection of prevalent high-risk epithelial lesions. In: Hayat MA. Methods of cancer diagnosis, therapy and prognosis: breast carcinoma. v.1. New York: Springer, 2008. p. 61-71. ISBN 978-1-4020-8368-6.

CANCER DE MAMA; CANCER DE MAMA FAMILIAR; CARCINOMA LOBULAR IN SITU; HIPERPLASIA LOBULAR ATIPICA; CARCINOMA DUCTAL IN SITU; HIPERPLASIA DUCTAL ATIPICA


31/73US=33 / Gastro
Hamilton JP, Meltzer SJ. The molecular genetics of esophageal cancer. In: Kelsen DP, Daly JM, Kern SE, Levin B, Tepper JE, Van Cutsem E. Principles and practice of gastrointestinal oncology. 2ª ed. Philadelphia: Lippincott Willians & Wilkins, 2008. p. 167-78. ISBN 978-0-7817-7617-2.

CANCER DE ESOFAGO; GENETICA MOLECULAR; CARCINOMA ESOFAGICO FAMILIAL; CARCINOMA ESOFAGICO ESPORADICO; GENETICA; EPIGENETICA; APOPTOSE; ESOFAGO DE BARRETT


32/73US=33 / Gastro
Kern SE, Gallmeier E, Goggins M, Hruban RH. Pancreatic cancer: molecular biology and genetics. In: Kelsen DP, Daly JM, Kern SE, Levin B, Tepper JE, Van Cutsem E. Principles and practice of gastrointestinal oncology. 2ª ed. Philadelphia: Lippincott Willians & Wilkins, 2008. p. 329-42. ISBN 978-0-7817-7617-2.

CANCER DE PANCREAS; BIOLOGIA MOLECULAR; GENETICA; NEOPLASIA DUCTAL DO PANCREAS; CITOGENETICA; PLOIDIA; GENETICA MOLECULAR; CANCER PANCREATICO FAMILIAL; NEOPLASIA INTRAEPITELIAL PANCREATICO


33/73US=4 / Gastro
Barrett T, Choyke PL. Familial and inherited renal cancers. In: Patel U. Carcinoma of the kidney. New York: Cambridge University Press, 2008. p. 38-63. (Contemporary Issues in Cancer Imaging) ISBN 978-0-521-87838-8.

CANCER DE RIM HEREDITARIO; GENETICA; SINDROME DE VON HIPPEL-LINDAU; SINDROME BIRT-HOGG-DUBE; CARCINOMA RENAL PAPILAR HEREDITARIO; LEIOMIOMATOSE HEREDITARIA; CARCINOMA DE CELULAS RENAIS; COMPLEXO DA ESCLEROSE TUBEROSA; SINDROME DE HIPERPARATIREOIDISMO; TUMOR DE MANDIBULA; ONCOCITOMA RENAL FAMILIAR; TRANSLOCACAO DO CROMOSSOMO 3; CARCINOMA MEDULAR DO RIM; CANCER RENAL HEREDITARIO. TERAPIA


34/73US=42 / Gastro
Greenhalf W, Vitone LJ, Neoptolemos JP. Familial pancreatic cancer. In: Beger H, Warshaw A, Büchler M, Kozarek RA, Lerch MM, Neoptolemos JP, Shiratori K, Whitcomb DC, Rau BM. The pancreas: an integrated textbook of basic science, medicine, and surgery. 2nd ed. Massachuetts: Blackwell Scientific Publications, 2008. p. 591-600. ISBN 978-1-4051-4664-7.

CANCER DE PANCREAS FAMILIAR


35/73US=53 / Biol/Mol
Sandberg A, Stone JF. Meningioma. In: ___. The genetics and molecular biology of neural tumors. New Jersey: Humana Press, 2008. p. 83-144. ISBN 978-1-59745-510-7.

MENINGIOMA; PERDA DO CROMOSSOMO 22; GENE NF2; MENINGIOMAS RADIOINDUZIDAS; MENINGIOMA PEDIATRICO; TELOMERASE; RECEPTORES HORMONAIS; MENINGIOMA FAMILIAL; MENINGIOMA MULTIPLO; MENINGIOANGIOMATOSE


36/73US=8 / Dermatologia
Graham-Brown RAC. Familial benign pemphigus (Hailey-Hailey Disease). In: Freedberg IM, Eisen AZ, Wolff K, Austen KF, Goldsmith LA, Katz SI, editores. Fitzpatrick's dermatology in general medicine. 6th ed. New York: McGraw-Hill, 2008. p. 622-4. ISBN 978-0-07138076-0.

PENFIGO FAMILIAR BENIGNO; DOENCA DE HAILEY-HAILEY; PENFIGO FAMILIAR BENIGNO. ETIOLOGIA; PENFIGO FAMILIAR BENIGNO. MANIFESTACOES CLINICAS; PENFIGO FAMILIAR BENIGNO. PATOLOGIA; PENFIGO FAMILIAR BENIGNO. DIAGNOSTICO; PENFIGO FAMILIAR BENIGNO. TRATAMENTO


37/73US=8 / Dermatologia
Burgdorf WHC. Erythema annulare centrifugum and other figurate erythemas. In: Freedberg IM, Eisen AZ, Wolff K, Austen KF, Goldsmith LA, Katz SI, editores. Fitzpatrick's dermatology in general medicine. 6th ed. New York: McGraw-Hill, 2008. p. 977-9. ISBN 978-0-07138076-0.

ERITEMA ANULAR CENTRIFUGO; ERITEMA ANULAR FAMILIAL


38/73US=1 / Patologia
von Deimling A, Perry A. Familial tumour syndromes involving the nervous system: neurofibromatosis type 1. In: Louis DN, Ohgaki H, Wistler OD, Cavenee WK, editors. WHO Classification of tumours of the central nervous system. 4th ed. Lyon: IARC, 2007. p. 205-9. (WHO Classification of Tumours, v. 1IARC WHO Classification of Tumours, nº 1) ISBN 978-92-832-2430-3.

SINDROMES TUMORAIS. SISTEMA NERVOSO; NEUROFIBROMATOSE TIPO 1


39/73US=1 / Patologia
Stemmer-Rachamimov AO, Wiestler OD, Louis DN. Familial tumour syndromes involving the nervous system: neurofibromatosis type 2. In: Louis DN, Ohgaki H, Wistler OD, Cavenee WK, editors. WHO Classification of tumours of the central nervous system. 4th ed. Lyon: IARC, 2007. p. 210-4. (WHO Classification of Tumours, v. 1IARC WHO Classification of Tumours, nº 1) ISBN 978-92-832-2430-3.

SINDROMES TUMORAIS. SISTEMA NERVOSO; NEUROFIBROMATOSE TIPO 2


40/73US=1 / Patologia
Plate KH, Vortmeyer AO, Zagzag D, Neumann HPH. Familial tumour syndromes involving the nervous system: von hipper-lindau disease and haemangioblastoma. In: Louis DN, Ohgaki H, Wistler OD, Cavenee WK, editors. WHO Classification of tumours of the central nervous system. 4th ed. Lyon: IARC, 2007. p. 215-7. (WHO Classification of Tumours, v. 1IARC WHO Classification of Tumours, nº 1) ISBN 978-92-832-2430-3.

SINDROMES TUMORAIS. SISTEMA NERVOSO; DOENCA DE VON HIPPER-LINDAU; HEMANGIOBLASTOMA


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