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The Long-Term Outcomes of the Second Generation of Familial Nonmedullary Thyroid Carcinoma Are More Aggressive than Sporadic Cases
Young Joo Park et al.
THYROID (2012)
A Clinical Scoring System for Selection of Patients for PTEN Mutation Testing Is Proposed on the Basis of a Prospective Study of 3042 Probands
Min-Han Tan et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Succinate Dehydrogenase-Deficient GISTs: A Clinicopathologic, Immunohistochemical, and Molecular Genetic Study of 66 Gastric GISTs With Predilection to Young Age
Markku Miettinen et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2011)
Pediatric-Type Gastrointestinal Stromal Tumors Are SDHB Negative (Type 2) GISTs
Anthony J. Gill et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2011)
Immunohistochemical Staining of Thyroidectomy Specimens for PTEN Can Aid in the Identification of Patients With Cowden Syndrome
Justine A. Barletta et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2011)
Renal Tumors Associated With Germline SDHB Mutation Show Distinctive Morphology
Anthony J. Gill et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2011)
Evidence for an hMSH3 Defect in Familial Hamartomatous Polyps
Sherry C. Huang et al.
CANCER (2011)
SDHA Immunohistochemistry Detects Germline SDHA Gene Mutations in Apparently Sporadic Paragangliomas and Pheochromocytomas
Esther Korpershoek et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)
Thyroid Nodules and Cancer in Children with PTEN Hamartoma Tumor Syndrome
Jessica R. Smith et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)
Bilateral Adrenal Medullary Hyperplasia Associated With an SDHB Mutation
Raymon H. Grogan et al.
JOURNAL OF CLINICAL ONCOLOGY (2011)
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
Inaki Comino-Mendez et al.
NATURE GENETICS (2011)
Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations
Katherine A. Janeway et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)
Clinical Characteristics and Outcome of Familial Nonmedullary Thyroid Cancer: A Retrospective Controlled Study
Eyal Robenshtok et al.
THYROID (2011)
Thyroid Pathology in PTEN-Hamartoma Tumor Syndrome: Characteristic Findings of a Distinct Entity
Anna Ray Laury et al.
THYROID (2011)
Prevalence, Clinicopathologic Features, and Somatic Genetic Mutation Profile in Familial Versus Sporadic Nonmedullary Thyroid Cancer
Willieford Moses et al.
THYROID (2011)
The Optimal Surgical Treatment for Primary Hyperparathyroidism in MEN1 Patients: A Systematic Review
Jennifer M. J. Schreinemakers et al.
WORLD JOURNAL OF SURGERY (2011)
Bilateral adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1 (MEN1) and a novel mutation in the MEN1 gene
John E. Griniatsos et al.
WORLD JOURNAL OF SURGICAL ONCOLOGY (2011)
Thyroid Cancer of Follicular Cell Origin in Inherited Tumor Syndromes
Vania Nose
ADVANCES IN ANATOMIC PATHOLOGY (2010)
Immunohistochemistry for SDHB Divides Gastrointestinal Stromal Tumors (GISTs) into 2 Distinct Types
Anthony J. Gill et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2010)
Bilateral papillary cystadenoma of the mesosalpinx: a rare manifestation of Von Hippel-Lindau disease
Diana Baetschmann Zanotelli et al.
ARCHIVES OF GYNECOLOGY AND OBSTETRICS (2010)
MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27Kip1 and p18INK4C) mutations
Marianthi Georgitsi
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM (2010)
Familial Follicular Cell Tumors: Classification and Morphological Characteristics
Vania Nose
ENDOCRINE PATHOLOGY (2010)
Periampullary and Duodenal Neoplasms in Neurofibromatosis Type 1: Two Cases and an Updated 20-Year Review of the Literature Yielding 76 Cases
Daniel Relles et al.
JOURNAL OF GASTROINTESTINAL SURGERY (2010)
Cribriform-Morular Variant of Papillary Thyroid Carcinoma Molecular Characterization of a Case With Neuroendocrine Differentiation and Aggressive Behavior
Jose Cameselle-Teijeiro et al.
AMERICAN JOURNAL OF CLINICAL PATHOLOGY (2009)
Pancreatic Endocrine Microadenomatosis in Patients With von Hippel-Lindau Disease
Martine Pé rigny et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2009)
Insulinomatosis A Multicentric Insulinoma Disease that Frequently Causes Early Recurrent Hyperinsulinemic Hypoglycemia
Martin Anlauf et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2009)
A Susceptibility Locus for Papillary Thyroid Carcinoma on Chromosome 8q24
Huiling He et al.
CANCER RESEARCH (2009)
Accuracy of Combined Protein Gene Product 9.5 and Parafibromin Markers for Immunohistochemical Diagnosis of Parathyroid Carcinoma
Viive M. Howell et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
A Germline Mutation (A339V) in Thyroid Transcription Factor-1 (TITF-1/NKX2.1) in Patients With Multinodular Goiter and Papillary Thyroid Carcinoma
Elly S. W. Ngan et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2009)
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
Francien H. van Nederveen et al.
LANCET ONCOLOGY (2009)
Hyperparathyroidism - jaw tumor syndrome: a report of three large kindred
Maurizio Iacobone et al.
LANGENBECKS ARCHIVES OF SURGERY (2009)
Biological behavior and prognosis of familial papillary thyroid carcinoma
Yasuhiro Ito et al.
SURGERY (2009)
Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: A SNP array-based linkage analysis of 38 families
Insoo Suh et al.
SURGERY (2009)
Familial Medullary Thyroid Carcinoma Associated with Cutaneous Lichen Amyloidosis
Amy E. Rothberg et al.
THYROID (2009)
Pituitary blastoma
Bernd W. Scheithauer et al.
ACTA NEUROPATHOLOGICA (2008)
Familial Thyroid Carcinoma A Diagnostic Algorithm
Jorge Dotto et al.
ADVANCES IN ANATOMIC PATHOLOGY (2008)
Somatostatin-producing neuroendocrine tumors of the duodenum and pancreas:: incidence, types, biological behavior, association with inherited syndromes, and functional activity
Nele Garbrecht et al.
ENDOCRINE-RELATED CANCER (2008)
Familial non-medullary thyroid carcinoma displays the features of clinical anticipation suggestive of a distinct biological entity
M. Capezzone et al.
ENDOCRINE-RELATED CANCER (2008)
Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism
Giulia Masi et al.
ENDOCRINE-RELATED CANCER (2008)
Familial non-medullary thyroid carcinoma (FNMTC):: analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations
Branca M. Cavaco et al.
ENDOCRINE-RELATED CANCER (2008)
Mapping a New Familial Thyroid Epithelial Neoplasia Susceptibility Locus to Chromosome 8p23.1-p22 by High-Density Single-Nucleotide Polymorphism Genome-Wide Linkage Analysis
Branca M. Cavaco et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
Familial hyperparathyroidism:: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations
Marta S. Sarquis et al.
SURGERY (2008)
Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma
Hugo Joao Prazeres et al.
FAMILIAL CANCER (2008)
Somatic SDHB mutation in an extraadrenal pheochromocytoma
Francien H. van Nederveen et al.
NEW ENGLAND JOURNAL OF MEDICINE (2007)
An evidence-based approach to familial nonmedullary thyroid cancer: Screening, clinical management, and follow-up
Rebecca S. Sippel et al.
WORLD JOURNAL OF SURGERY (2007)
Novel germline variants identified in the inner mitochondrial membrane transporter TIMM44 and their role in predisposition to oncocytic thyroid carcinomas
E. Bonora et al.
BRITISH JOURNAL OF CANCER (2006)
HRPT2 gene alterations in ossifying fibroma of the jaws
Flavio Juliano Pimenta et al.
ORAL ONCOLOGY (2006)
A new form of familial multi-nodular goitre with progression to differentiated thyroid cancer
A. Bakhsh et al.
ENDOCRINE-RELATED CANCER (2006)
A HIF1α regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
PLM Dahia et al.
PLOS GENETICS (2005)
Familial nonmedullary thyroid cancer
C Sturgeon et al.
THYROID (2005)
Somatic and germline mutation in GRIM-19, a dual function gene involved in mitochondrial metabolism and cell death, is linked to mitochondrion-rich (Hurthle cell) tumours of the thyroid
V Maximo et al.
BRITISH JOURNAL OF CANCER (2005)
Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome
KJ Bradley et al.
JOURNAL OF INTERNAL MEDICINE (2005)
Abnormal distribution and hyperplasia of thyroid C-cells in PTEN-associated tumor syndromes
E Zambrano et al.
ENDOCRINE PATHOLOGY (2004)
Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer
JD McKay et al.
JOURNAL OF MEDICAL GENETICS (2004)
Multiple endocrine neoplasia type 1 parathyroid adenoma development over time
GM Doherty et al.
WORLD JOURNAL OF SURGERY (2004)
Genetic analyses of the HRPT2 gene in primary hyperparathyroidism:: Germline and somatic mutations in familial and sporadic parathyroid tumors
F Cetani et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2004)
Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma
TM Shattuck et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)
Chromosome 2 (2p16) abnormalities in Carney complex tumours
L Matyakhina et al.
JOURNAL OF MEDICAL GENETICS (2003)
Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults
XP Zhou et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
JD Carpten et al.
NATURE GENETICS (2002)
Mutation cluster region, association between germline and somatic mutations and genotype phenotype correlation in upper gastrointestinal familial adenomatous polyposis
C Groves et al.
AMERICAN JOURNAL OF PATHOLOGY (2002)
Neurofibromin and NF1 gene analysis in composite pheochromocytoma and tumors associated with von Recklinghausen's disease
N Kimura et al.
MODERN PATHOLOGY (2002)
Clear cell carcinoid tumor of the gallbladder - Another distinctive manifestation of von Hippel-Lindau disease
PA Sinkre et al.
AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2001)
Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21
JD McKay et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Is familial non-medullary thyroid carcinoma more aggressive than sporadic thyroid cancer? A multicenter series
O Alsanea et al.
SURGERY (2000)
Familial papillary thyroid carcinoma: Genetics, criteria for diagnosis, clinical features, and surgical treatment
TJ Musholt et al.
WORLD JOURNAL OF SURGERY (2000)
Pancreatic involvement in von Hippel-Lindau disease
PR Hammel et al.
GASTROENTEROLOGY (2000)