Hereditary hyperparathyroidism—a consensus report of the European Society of Endocrine Surgeons (ESES)

Revised American Thyroid Association Guidelines for the Management of Medullary Thyroid Carcinoma

(2015) Samuel A. Wells et al.   THYROID

Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations ofCDC73gene in Chinese

(2014) Jing Kong et al.   CLINICAL ENDOCRINOLOGY

A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome

(2014) Francesco Tonelli et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

CDC73Intragenic Deletion in Familial Primary Hyperparathyroidism Associated With Parathyroid Carcinoma

(2014) Eeva Korpi-Hyövälti et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

The Surgical Management of Asymptomatic Primary Hyperparathyroidism: Proceedings of the Fourth International Workshop

(2014) Robert Udelsman et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Diagnosis of Asymptomatic Primary Hyperparathyroidism: Proceedings of the Fourth International Workshop

(2014) Richard Eastell et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Hyperparathyroidism 2 gene (HRPT2, CDC73) and parafibromin studies in two patients with primary hyperparathyroidism and uncertain pathological assessment

(2014) F. Cetani et al.   JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

Breast-Cancer Predisposition in Multiple Endocrine Neoplasia Type 1

(2014) Koen M.A. Dreijerink et al.   NEW ENGLAND JOURNAL OF MEDICINE

Characterization of a New CDC73 Missense Mutation that Impairs Parafibromin Expression and Nucleolar Localization

(2014) Giulia Masi et al.   PLoS One

A randomized, prospective trial of operative treatments for hyperparathyroidism in patients with multiple endocrine neoplasia type 1

(2014) Terry C. Lairmore et al.   SURGERY

Hyperparathyroidism-jaw tumor syndrome: Results of operative management

(2014) Amit Mehta et al.   SURGERY

A novel CDC73 gene mutation in an Italian family with hyperparathyroidism-jaw tumour (HPT-JT) syndrome

(2014) M. G. Chiofalo et al.   CELLULAR ONCOLOGY

Calcium-sensing receptor (CaSR) mutations and disorders of calcium, electrolyte and water metabolism

(2013) Fadil M. Hannan et al.   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Recurrent Hyperparathyroidism and a Novel Nonsense Mutation in a Patient with Hyperparathyriodism-Jaw Tumor Syndrome

(2013) Amer Abdulla et al.   Endocrine Practice

Hereditary Hyperparathyroidism Syndromes

(2013) Francesca Giusti et al.   JOURNAL OF CLINICAL DENSITOMETRY

Frequent Large GermlineHRPT2Deletions in a French National Cohort of Patients With Primary Hyperparathyroidism

(2013) Léopoldine Bricaire et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)

(2013) Rajesh V. Thakker   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Differences between sporadic and MEN related primary hyperparathyroidism; clinical expression, preoperative workup, operative strategy and follow-up

(2013) Bas A Twigt et al.   Orphanet Journal of Rare Diseases

Identification and Functional Characterization of Three NoLS (Nucleolar Localisation Signals) Mutations of the CDC73 Gene

(2013) Valerio Pazienza et al.   PLoS One

Minimally invasive parathyroidectomy provides a conservative surgical option for multiple endocrine neoplasia type 1–primary hyperparathyroidism

(2013) Mark Versnick et al.   SURGERY

Germline and Somatic Mutations in Cyclin-Dependent Kinase Inhibitor Genes CDKN1A, CDKN2B, and CDKN2C in Sporadic Parathyroid Adenomas

(2013) Jessica Costa-Guda et al.   Hormones & Cancer

Primary Hyperparathyroidism in MEN1 Patients

(2012) Carolina R. C. Pieterman et al.   ANNALS OF SURGERY

MENX and MEN4

(2012) NS Pellegata   Clinics

Hyperparathyroidism-jaw tumor syndrome

(2012) Matthew R. Kutcher et al.   HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK

Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)

(2012) Rajesh V. Thakker et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Successful Use of Bisphosphonate and Calcimimetic in Neonatal Severe Primary Hyperparathyroidism

(2012) A. Wilhelm-Bals et al.   PEDIATRICS

Forearm Bone Mineral Density in Familial Hypocalciuric Hypercalcemia and Primary Hyperparathyroidism: A Comparative Study

(2011) Troels Isaksen et al.   CALCIFIED TISSUE INTERNATIONAL

Identification of the first germline HRPT2 whole-gene deletion in a patient with primary hyperparathyroidism

(2011) Rita Domingues et al.   CLINICAL ENDOCRINOLOGY

Hereditäre Formen des primären Hyperparathyreoidismus

(2011) K Frank-Raue et al.   DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT

Identification of De Novo Germline Mutations in the HRPT2 Gene in Two Apparently Sporadic Cases with Challenging Parathyroid Tumor Diagnoses

(2011) Branca Maria Cavaco et al.   ENDOCRINE PATHOLOGY

Familial Hyperparathyroidism Due to a Germline Mutation of theCDC73Gene: Implications for Management and Age-Appropriate Testing of Relatives at Risk

(2011) Ariana Pichardo-Lowden et al.   Endocrine Practice

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors

(2011) Wai Kwan Siu et al.   Familial Cancer

Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family

(2011) Alberto Cascón et al.   GENES CHROMOSOMES & CANCER

Somatic Mutation and Germline Sequence Abnormalities inCDKN1B, Encoding p27Kip1, in Sporadic Parathyroid Adenomas

(2011) Jessica Costa-Guda et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

The Optimal Surgical Treatment for Primary Hyperparathyroidism in MEN1 Patients: A Systematic Review

(2011) Jennifer M. J. Schreinemakers et al.   WORLD JOURNAL OF SURGERY

Frequent Germ-Line Mutations of the MEN1, CASR, and HRPT2/CDC73 Genes in Young Patients with Clinically Non-familial Primary Hyperparathyroidism

(2011) Lee F. Starker et al.   Hormones & Cancer

HRPT2-related familial isolated hyperparathyroidism: could molecular studies direct the surgical approach?

(2010) Leticia G. Silveira et al.   Arquivos Brasileiros de Endocrinologia e Metabologia

Surgery for multiple endocrine neoplasia type 1-associated primary hyperparathyroidism

(2010) J. Waldmann et al.   BRITISH JOURNAL OF SURGERY

Benign Familial Hypocalciuric Hypercalcemia

(2010) Jeena Varghese et al.   Endocrine Practice

Defective nucleolar localization and dominant interfering properties of a parafibromin L95P missense mutant causing the hyperparathyroidism–jaw tumor syndrome

(2010) Leelamma M Panicker et al.   ENDOCRINE-RELATED CANCER

Update multiple endocrine neoplasia type 2

(2010) Friedhelm Raue et al.   Familial Cancer

A novel germline CDKN1B mutation causing multiple endocrine tumors: clinical, genetic and functional characterization

(2010) Sara Molatore et al.   HUMAN MUTATION

p27kip1: A New Multiple Endocrine Neoplasia Gene?

(2010) Ilaria Marinoni et al.   NEUROENDOCRINOLOGY

Results of cryopreserved parathyroid autografts: A retrospective multicenter study

(2010) Sophie Borot et al.   SURGERY

Causes and Treatment of Recurrent Hyperparathyroidism After Subtotal Parathyroidectomy in the Presence of Multiple Endocrine Neoplasia 1

(2010) Maria D. Balsalobre Salmeron et al.   WORLD JOURNAL OF SURGERY

Should Routine Analysis of the MEN1 Gene be Performed in all Patients with Primary Hyperparathyroidism Under 40 Years of Age?

(2010) Anita Skandarajah et al.   WORLD JOURNAL OF SURGERY

Una causa rara de hipercalcemia: carcinoma sincrónico de dos paratiroides en el contexto del síndrome de hiperparatiroidismo familiar-tumor mandibular

(2010) Brenda Veiguela et al.   Endocrinologia y Nutricion

Hyperparathyroidism-jaw tumor syndrome: A case report

(2009) N. Rekik et al.   ANNALES D ENDOCRINOLOGIE

Prospective Study of Surgery for Primary Hyperparathyroidism (HPT) in Multiple Endocrine Neoplasia-Type 1 and Zollinger-Ellison Syndrome

(2009) Jeffrey A. Norton et al.   ANNALS OF SURGERY

Surgical Approach in Hereditary Hyperparathyroidism

(2009) Francesco TONELLI et al.   ENDOCRINE JOURNAL

A Novel Loss-of-Function Mutation, Gln459Arg, of the Calcium-Sensing Receptor Gene Associated with Apparent Autosomal Recessive Inheritance of Familial Hypocalciuric Hypercalcemia

(2009) Steven A. Lietman et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Rare Germline Mutations in Cyclin-Dependent Kinase Inhibitor Genes in Multiple Endocrine Neoplasia Type 1 and Related States

(2009) Sunita K. Agarwal et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

DNA-based test: when and why to apply it to primary hyperparathyroidism clinical phenotypes

(2009) A. Falchetti et al.   JOURNAL OF INTERNAL MEDICINE

Hyperparathyroidism-Jaw Tumor Syndrome: A Case Report

(2009) Brian P. Schmidt et al.   JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY

Surgical strategy for sporadic primary hyperparathyroidism an evidence-based approach to surgical strategy, patient selection, surgical access, and reoperations

(2009) Radu Mihai et al.   LANGENBECKS ARCHIVES OF SURGERY

Hyperparathyroidism–jaw tumor syndrome: a report of three large kindred

(2009) Maurizio Iacobone et al.   LANGENBECKS ARCHIVES OF SURGERY

The extent of parathyroidectomy for HRPT2-related hyperparathyroidism

(2009) Maurizio Iacobone et al.   SURGERY

Symposium on Evidence-Based Endocrine Surgery (3: Hyperparathyroidism)

(2009) Göran Åkerström   WORLD JOURNAL OF SURGERY

Familial Parathyroid Tumors: Diagnosis and Management

(2009) Peter Stålberg et al.   WORLD JOURNAL OF SURGERY

Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations

(2008) Ogo I. Egbuna et al.   BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY

Discriminative power of three indices of renal calcium excretion for the distinction between familial hypocalciuric hypercalcaemia and primary hyperparathyroidism: a follow-up study on methods

(2008) Signe Engkjaer Christensen et al.   CLINICAL ENDOCRINOLOGY

Clinical, genetic, and histopathologic investigation of CDC73-related familial hyperparathyroidism

(2008) G. Masi et al.   ENDOCRINE-RELATED CANCER

Plasma 25-hydroxyvitamin D, 1,25-dihydroxyvitamin D, and parathyroid hormone in familial hypocalciuric hypercalcemia and primary hyperparathyroidism

(2008) Signe Engkjær Christensen et al.   EUROPEAN JOURNAL OF ENDOCRINOLOGY

Accuracy of Combined Protein Gene Product 9.5 and Parafibromin Markers for Immunohistochemical Diagnosis of Parathyroid Carcinoma

(2008) Viive M. Howell et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations

(2008) Marta S. Sarquis et al.   SURGERY

Re: Familial hyperparathyroidism: Surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations

(2008) Vito Guarnieri et al.   SURGERY

GRADE: an emerging consensus on rating quality of evidence and strength of recommendations

(2008) Gordon H Guyatt et al.   BMJ-British Medical Journal