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1. Endocrine tumor syndromes and their genetics
by Stratakis, Constantine A
2013, Frontiers of hormone research, ISBN 3318023302, Volume 41., xi, 187
In these times, a book should aspire to present the most significant advances in the field, reflect the themes of the moment, and provide a useful compendium... 
genetics | Peutz-Jeghers Syndrome | Endocrine glands | Endocrine Gland Neoplasms | Neurofibromatosis 1 | von Hippel-Lindau Disease | Multiple Endocrine Neoplasia | Tumors | Genetic aspects | Cancer | Diseases
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2. Genetic/familial high-risk assessment: Breast and ovarian, version 2.2015 Featured updates to the NCCN guidelines
by Daly, Mary B and Pilarski, Robert and Axilbund, Jennifer E and Berry, Michael and Buys, Saundra S and Crawford, Beth and Farmer, Meagan and Friedman, Susan and Garber, Judy E and Khan, Seema and Klein, Catherine and Kohlmann, Wendy and Kurian, Allison and Litton, Jennifer K and Madlensky, Lisa and Marcom, P. Kelly and Merajver, Sofia D and Offit, Kenneth and Pal, Tuya and Rana, Huma and Reiser, Gwen and Robson, Mark E and Shannon, Kristen Mahoney and Swisher, Elizabeth and Voian, Nicoleta C and Weitzel, Jeffrey N and Whelan, Alison and Wick, Myra J and Wiesner, Georgia L and Dwyer, Mary and Kumar, Rashmi and Darlow, Susan
JNCCN Journal of the National Comprehensive Cancer Network, ISSN 1540-1405, 02/2016, Volume 14, Issue 2, pp. 153 - 162
The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast and Ovarian provide recommendations for genetic testing and counseling and risk... 
ANNULAR TUBULES | ONCOLOGY | PEUTZ-JEGHERS-SYNDROME | SEX CORD TUMOR | FAMILIES | PANCREATIC-CANCER | PATHOLOGICAL FINDINGS | BRCA2 GERMLINE MUTATIONS | PREVALENCE | SALPINGECTOMY | CARCINOMA
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3. Full Text Recent progress in pancreatic cancer
by Wolfgang, Christopher L and Herman, Joseph M and Laheru, Daniel A and Klein, Alison P and Erdek, Michael A and Fishman, Elliot K and Hruban, Ralph H
CA: A Cancer Journal for Clinicians, ISSN 0007-9235, 09/2013, Volume 63, Issue 5, pp. 318 - 348
Answer questions and earn CME/CNE Pancreatic cancer is currently one of the deadliest of the solid malignancies. However, surgery to resect neoplasms of the... 
molecular biology | medical oncology | radiation oncology | pancreatic neoplasms | radiology | PEUTZ-JEGHERS-SYNDROME | PAPILLARY MUCINOUS NEOPLASM | GEMCITABINE-BASED CHEMORADIATION | RANDOMIZED CONTROLLED-TRIAL | CELIAC PLEXUS BLOCK | TOTAL LAPAROSCOPIC PANCREATICODUODENECTOMY | PHASE-III TRIAL | CONTROL CONSORTIUM PANC4 | 3-DIMENSIONAL COMPUTED-TOMOGRAPHY | ONCOLOGY | SINGLE-INSTITUTION EXPERIENCE | Adenocarcinoma - therapy | Pancreatic Neoplasms - etiology | Adenocarcinoma - etiology | Humans | Risk Factors | Pancreatic Neoplasms - therapy | Care and treatment | Usage | Drug therapy, Combination | Radiotherapy | Pancreatic cancer | Radiation therapy | Drug therapy | Toxicity | Medical treatment | Index Medicus | Abridged Index Medicus
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4. Full Text ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes
by Syngal, Sapna and Brand, Randall E and Church, James M and Giardiello, Francis M and Hampel, Heather L and Burt, Randall W and American College of Gastroenterology
American Journal of Gastroenterology, ISSN 0002-9270, 02/2015, Volume 110, Issue 2, pp. 223 - 262
This guideline presents recommendations for the management of patients with hereditary gastrointestinal cancer syndromes. The initial assessment is the... 
COST-EFFECTIVENESS ANALYSIS | DOUBLE-BALLOON ENTEROSCOPY | GENOTYPE-PHENOTYPE CORRELATIONS | CADHERIN GERMLINE MUTATIONS | NONPOLYPOSIS COLORECTAL-CANCER | MUIR-TORRE-SYNDROME | PEUTZ-JEGHERS-SYNDROME | LYNCH SYNDROME CARRIERS | FAMILIAL ADENOMATOUS POLYPOSIS | GASTROENTEROLOGY & HEPATOLOGY | DIFFUSE GASTRIC-CANCER | Gastrointestinal Neoplasms - genetics | Humans | Peutz-Jeghers Syndrome - therapy | Intestinal Polyposis - diagnosis | Colorectal Neoplasms, Hereditary Nonpolyposis - therapy | Intestinal Polyposis - congenital | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnosis | Neoplastic Syndromes, Hereditary - genetics | Adenomatous Polyposis Coli - therapy | Adenomatous Polyposis Coli - genetics | Hamartoma Syndrome, Multiple - genetics | Intestinal Polyposis - therapy | Genetic Testing - standards | Intestinal Polyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Neoplastic Syndromes, Hereditary - diagnosis | Gastrointestinal Neoplasms - diagnosis | Gastrointestinal Neoplasms - therapy | Peutz-Jeghers Syndrome - genetics | Hamartoma Syndrome, Multiple - diagnosis | Hamartoma Syndrome, Multiple - therapy | Neoplastic Syndromes, Hereditary - therapy | Peutz-Jeghers Syndrome - diagnosis | Disease Management | Adenomatous Polyposis Coli - diagnosis
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5. Full Text Successful Endoscopic Reduction of an Ileocolonic Intussusception in an Adult With Peutz-Jeghers Syndrome
by AlSamman, Mohd Amer and Ferreira, Jason D and Moustafa, Abdelmoniem and Moveson, Jonathan and Akerman, Paul
Gastroenterology research, ISSN 1918-2805, 02/2019, Volume 12, Issue 1, pp. 40 - 42
Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by hamartomatous polyps throughout the gastrointestinal tract, mostly causing... 
Endoscopy | Intussusception | Peutz-Jeghers syndrome | Case Report
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6. Full Text Small-bowel capsule endoscopy and device-assisted enteroscopy for diagnosis and treatment of small-bowel disorders: European Society of Gastrointestinal Endoscopy (ESGE) Clinical Guideline
by Pennazio, Marco and Spada, Cristiano and Eliakim, Rami and Keuchel, Martin and May, Andrea and Mulder, Chris J and Rondonotti, Emanuele and Adler, Samuel N and Albert, Joerg and Baltes, Peter and Barbaro, Federico and Cellier, Christophe and Charton, Jean Pierre and Delvaux, Michel and Despott, Edward J and Domagk, Dirk and Klein, Amir and McAlindon, Mark and Rosa, Bruno and Rowse, Georgina and Sanders, David S and Saurin, Jean Christophe and Sidhu, Reena and Dumonceau, Jean-Marc and Hassan, Cesare and Gralnek, Ian M
Endoscopy, ISSN 0013-726X, 04/2015, Volume 47, Issue 4, pp. 352 - 386
This Guideline is an official statement of the European Society of Gastrointestinal Endoscopy (ESGE). The Guideline was also reviewed and endorsed by the... 
Guideline | DOUBLE-BALLOON ENTEROSCOPY | SURGERY | SUSPECTED CROHNS-DISEASE | SINGLE-CENTER EXPERIENCE | PEUTZ-JEGHERS-SYNDROME | REFRACTORY CELIAC-DISEASE | TERM-FOLLOW-UP | FAMILIAL ADENOMATOUS POLYPOSIS | IRON-DEFICIENCY ANEMIA | GASTROENTEROLOGY & HEPATOLOGY | MAGNETIC-RESONANCE ENTEROCLYSIS | COMPUTED-TOMOGRAPHY ENTEROCLYSIS | Anemia, Iron-Deficiency - etiology | Humans | Jejunal Diseases - diagnosis | Capsule Endoscopy | Gastrointestinal Hemorrhage - diagnosis | Duodenal Diseases - therapy | Jejunal Diseases - complications | Double-Balloon Enteroscopy | Ileal Diseases - therapy | Jejunal Diseases - therapy | Celiac Disease - diagnosis | Ileal Diseases - diagnosis | Gastrointestinal Hemorrhage - etiology | Crohn Disease - diagnosis | Gastrointestinal Hemorrhage - therapy | Peutz-Jeghers Syndrome - diagnosis | Ileal Diseases - complications | Duodenal Diseases - diagnosis | Intestinal Neoplasms - diagnosis | Duodenal Diseases - complications | Population Surveillance - methods | Adenomatous Polyposis Coli - diagnosis | Intestinal Neoplasms - complications
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7. Full Text Intracholecystic Papillary Neoplasms Are Distinct From Papillary Gallbladder Cancers: A Clinicopathologic and Exome-sequencing Study
by Akita, Masayuki and Fujikura, Kohei and Ajiki, Tetsuo and Fukumoto, Takumi and Otani, Kyoko and Hirose, Takanori and Tominaga, Masahiro and Itoh, Tomoo and Zen, Yoh
The American Journal of Surgical Pathology, ISSN 0147-5185, 06/2019, Volume 43, Issue 6, pp. 783 - 791
Although intracholecystic papillary neoplasms (ICPNs) have been increasingly recognized, their features remain unclear because of the lack of standardized... 
SURGERY | STK11 | APC | PEUTZ-JEGHERS-SYNDROME | BILIARY-TRACT | MUTATIONS | PATHOLOGY | intraductal papillary neoplasm | CARCINOMA | ADENOMAS | mucus | POLYPS
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8. Full Text Tumor suppressors and cell metabolism: A recipe for cancer growth
by Jones, Russell G and Thompson, Craig B
Genes and Development, ISSN 0890-9369, 03/2009, Volume 23, Issue 5, pp. 537 - 548
Growing tumors face two major metabolic challenges-how to meet the bioenergetic and biosynthetic demands of increased cell proliferation, and how to survive... 
Cancer biology | Cellular metabolism | Proliferation | Tumor suppressors | Oncogenes | Apoptosis | HYPOXIA-INDUCIBLE FACTOR | ATP CITRATE LYASE | ACTIVATED PROTEIN-KINASE | proliferation | PEUTZ-JEGHERS-SYNDROME | oncogenes | C-MYC | apoptosis | UPSTREAM KINASE | DEVELOPMENTAL BIOLOGY | ACETYL-COA CARBOXYLASE | PROLYL HYDROXYLASE | CELL BIOLOGY | LKB1-AMPK PATHWAY | cellular metabolism | AEROBIC GLYCOLYSIS | GENETICS & HEREDITY | tumor suppressors | AMP-Activated Protein Kinases - metabolism | Cell Proliferation | Humans | Mitochondria - metabolism | Oncogenes - physiology | Autophagy | Animals | Genes, Tumor Suppressor - physiology | Cells - metabolism | Glycolysis | Signal Transduction - physiology | Neoplasms - physiopathology | Cells - cytology | Cell proliferation | Cell metabolism | Tumor suppressor genes | Genetic aspects | Research | Cancer cells | Review
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9. Full Text Molecular genetics of colorectal cancer
by Fearon, Eric R
Annual Review of Pathology: Mechanisms of Disease, ISSN 1553-4006, 02/2011, Volume 6, Issue 1, pp. 479 - 507
Over the past three decades, molecular genetic studies have revealed some critical mutations underlying the pathogenesis of the sporadic and inherited forms of... 
adenoma-carcinoma sequence | KRAS mutation | adenomatous polyposis coli (APC) | mismatch repair | Wnt signaling | p53 tumor-suppressor gene (TSG) |