| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/J.BEEM.2010.03.002 |
| P953 | full work available at URL | https://api.elsevier.com/content/article/PII:S1521690X10000291?httpAccept=text/plain |
| https://api.elsevier.com/content/article/PII:S1521690X10000291?httpAccept=text/xml | ||
| P698 | PubMed publication ID | 20833338 |
| P5875 | ResearchGate publication ID | 46219836 |
| P50 | author | Emilia Modolo Pinto | Q42780197 |
| P2093 | author name string | Gerard P. Zambetti | |
| Raul C. Ribeiro | |||
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| Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio | Q37204344 | ||
| The appearance of the adrenal glands on computed tomography in multiple endocrine neoplasia type 1. | Q37283052 | ||
| Adrenal incidentaloma: evaluation and management | Q37310048 | ||
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| Tissue selectivity in multiple endocrine neoplasia type 1-associated tumorigenesis. | Q37572229 | ||
| Congenital hemihypertrophy with adrenal adenoma and medullary sponge kidney | Q39533005 | ||
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| Congenital hemihypertrophy with adrenocortical adenoma | Q40531074 | ||
| Characterization of the human p53 gene | Q40669877 | ||
| Presence of a potent transcription activating sequence in the p53 protein | Q41724404 | ||
| Adrenocortical carcinoma in children: a study of 40 cases | Q41901795 | ||
| Open and laparoscopic adrenalectomy: analysis of the National Surgical Quality Improvement Program | Q42654968 | ||
| Paternal uniparental disomy in monozygotic twins discordant for hemihypertrophy | Q43074264 | ||
| The long-term survival in adrenocortical carcinoma with active surgical management and use of monitored mitotane | Q43212347 | ||
| Cyclical Cushing syndrome presenting in infancy: an early form of primary pigmented nodular adrenocortical disease, or a new entity? | Q44968721 | ||
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| Management of adrenocortical carcinoma. | Q45918783 | ||
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| Prenatal diagnosis of fetal bilateral adrenal carcinoma | Q47586136 | ||
| Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations | Q47645440 | ||
| Diagnosis: Novel molecular signatures for adrenocortical carcinoma | Q47734151 | ||
| Clinical genetic testing and early surgical intervention in patients with multiple endocrine neoplasia type 1 (MEN 1). | Q47768404 | ||
| Childhood Adrenocortical Tumors1 | Q50947804 | ||
| Prenatal sonographic findings of congenital adrenal cortical adenoma. | Q51118523 | ||
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| Constitutional UPD for chromosome 11p15 in individuals with isolated hemihyperplasia is associated with high tumor risk and occurs following assisted reproductive technologies. | Q53618272 | ||
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| Wilms's tumor in three children of a woman with congenital hemihypertrophy. | Q54102164 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient Evaluation | Q55982494 | ||
| Prevalence of adrenal incidentaloma in a contemporary computerized tomography series | Q57647831 | ||
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| Clinical studies of multiple endocrine neoplasia type 1 (MEN1) | Q71777163 | ||
| Correlation of pathologic features with clinical outcome in pediatric adrenocortical neoplasia. A study of a Brazilian population. Brazilian Group for Treatment of Childhood Adrenocortical Tumors | Q72410584 | ||
| Late relapse of adrenocortical carcinoma in Beckwith-Wiedemann syndrome. Clinical, endocrinological and genetic aspects | Q73512819 | ||
| Adrenal cortical neoplasms in the pediatric population: a clinicopathologic and immunophenotypic analysis of 83 patients | Q73575192 | ||
| Bilateral asynchronous adrenal adenoma in a girl with an incomplete form of Beckwith-Wiedemann syndrome | Q73678140 | ||
| Adrenocortical carcinoma: experience in 45 patients | Q73933750 | ||
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| Multiple endocrine neoplasia type 1: clinical and genetic topics | Q77292736 | ||
| Identification of a novel genetic locus for familial cardiac myxomas and Carney complex | Q77648653 | ||
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| Familial Cancer. Foreword | Q81525431 | ||
| Simultaneous occurrence of right adrenocortical tumor and left adrenal neuroblastoma in an infant with Beckwith-Wiedemann syndrome | Q81722096 | ||
| [Multiple endocrine neoplasia type 1 (MEN 1): clinical, biochemical and molecular diagnosis and treatment of the associated disturbances] | Q82413311 | ||
| Possible association between Carney complex and multiple endocrine neoplasia type 1 phenotypes | Q83238694 | ||
| Identification of a novel germ line variant hotspot mutant p53-R175L in pediatric adrenal cortical carcinoma | Q83364339 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 477-490 | |
| P577 | publication date | 2010-06-01 | |
| P1433 | published in | Best Practice and Research: Clinical Endocrinology and Metabolism | Q15755890 |
| P1476 | title | Familial predisposition to adrenocortical tumors: clinical and biological features and management strategies | |
| Familial predisposition to adrenocortical tumors: Clinical and biological features and management strategies | |||
| P478 | volume | 24 |
| Q90683505 | ADRENAL CARCINOMA IN CHILDREN: LONGITUDINAL STUDY IN MINAS GERAIS, BRAZIL |
| Q36745477 | Establishment and characterization of the first pediatric adrenocortical carcinoma xenograft model identifies topotecan as a potential chemotherapeutic agent |
| Q47616676 | Identification of Clinical and Biologic Correlates Associated With Outcome in Children With Adrenocortical Tumors Without Germline TP53 Mutations: A St Jude Adrenocortical Tumor Registry and Children's Oncology Group Study. |
| Q50186163 | Neonatal Cushing Syndrome: A Rare but Potentially Devastating Disease |
| Q37143014 | Network analysis reveals potential markers for pediatric adrenocortical carcinoma |
| Q38261745 | Perspectives in Pediatric Pathology, Chapter 22. Testicular Involvement in Systemic Diseases |
| Q34125931 | Prologue to the volume: Endocrine tumors and their genetics, a perspective |
| Q37064189 | Surgery for Li Fraumeni syndrome: pushing the limits of surgical oncology |
| Q38091770 | Testosterone exposure in childhood: discerning pathology from physiology |
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