Hereditary hyperparathyroidism--a consensus report of the European Society of Endocrine Surgeons (ESES). (Q38602740)

4 September 2017

Hereditary hyperparathyroidism--a consensus report of the European Society of Endocrine Surgeons (ESES). (English)

1 reference

4 September 2017

1 reference

4

Menno Vriens

1 reference

4 September 2017

Maurizio Iacobone

1

1 reference

4 September 2017

Bruno Carnaille

series ordinal

2

1 reference

4 September 2017

F Fausto Palazzo

series ordinal

3

1 reference

4 September 2017

language of work or name

English

0 references

publication date

8 October 2015

1 reference

Langenbeck's Archives of Surgery

4 September 2017

1 reference

4 September 2017

400

1 reference

4 September 2017

8

1 reference

4 September 2017

867-886

1 reference

https://scigraph.springernature.com/pub.10.1007/s00423-015-1342-7

4 September 2017

0 references

cites work

Revised American Thyroid Association guidelines for the management of medullary thyroid carcinoma

1 reference

12 December 2020

Surgical treatment of hyperparathyroidism in patients with multiple endocrine neoplasia type 1

1 reference

12 December 2020

Surgical approach in hereditary hyperparathyroidism.

1 reference

12 December 2020

Forearm bone mineral density in familial hypocalciuric hypercalcemia and primary hyperparathyroidism: a comparative study

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Long-term biochemical results after operative treatment of primary hyperparathyroidism associated with multiple endocrine neoplasia types I and IIa: is a more or less extended operation essential?

1 reference

12 December 2020

Familial isolated hyperparathyroidism: a distinct genetic entity with an increased risk of parathyroid cancer

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome: a case report

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Fine-needle aspiration cytology of parathyroid carcinoma mimic hürthle cell thyroid neoplasm

1 reference

12 December 2020

Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: a clinically and genetically distinct syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

[Hereditary variants of primary hyperparathyroidism--MEN1, MEN2, HPT-JT, FHH, FIHPT]

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypercalcaemic and hypocalcaemic conditions due to calcium-sensing receptor mutations

1 reference

12 December 2020

[Multiple endocrine neoplasia type 1. Surgical therapy of primary hyperparathyroidism].

1 reference

12 December 2020

Results of initial operation for hyperparathyroidism in patients with multiple endocrine neoplasia type 1

1 reference

12 December 2020

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

1 reference

12 December 2020

Guidelines for diagnosis and therapy of MEN type 1 and type 2.

1 reference

12 December 2020

Up-to-date on parathyroid carcinoma: analysis of an experience of 19 cases.

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome: a case report

1 reference

12 December 2020

Identification and functional characterization of three NoLS (nucleolar localisation signals) mutations of the CDC73 gene

1 reference

12 December 2020

Familial parathyroid tumors: diagnosis and management

1 reference

12 December 2020

[Prophylactic parathyroidectomy for familial parathyroid carcinoma]

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Casting new light on the clinical spectrum of neonatal severe hyperparathyroidism

1 reference

12 December 2020

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

1 reference

12 December 2020

Results of cryopreserved parathyroid autografts: a retrospective multicenter study

1 reference

12 December 2020

Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours.

1 reference

12 December 2020

Update multiple endocrine neoplasia type 2.

1 reference

12 December 2020

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

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome in Roma families from Portugal is due to a founder mutation of the HRPT2 gene.

1 reference

12 December 2020

Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome

1 reference

12 December 2020

Causes and treatment of recurrent hyperparathyroidism after subtotal parathyroidectomy in the presence of multiple endocrine neoplasia 1.

1 reference

12 December 2020

1 reference

12 December 2020

The MENX syndrome and p27: relationships with multiple endocrine neoplasia.

1 reference

12 December 2020

A molecular diagnosis of hyperparathyroidism-jaw tumor syndrome in an adolescent with recurrent kidney stones

1 reference

12 December 2020

p27kip1: a new multiple endocrine neoplasia gene?

1 reference

12 December 2020

Loss of parafibromin expression in a subset of parathyroid adenomas

1 reference

12 December 2020

Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states

1 reference

12 December 2020

Frequent germ-line mutations of the MEN1, CASR, and HRPT2/CDC73 genes in young patients with clinically non-familial primary hyperparathyroidism

1 reference

12 December 2020

Novel nonsense CDC73 mutations in Chinese patients with parathyroid tumors

1 reference

12 December 2020

Recurrent hyperparathyroidism and a novel nonsense mutation in a patient with hyperparathyriodism-jaw tumor syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of a new CDC73 missense mutation that impairs Parafibromin expression and nucleolar localization

1 reference

12 December 2020

Is total parathyroidectomy the treatment of choice for hyperparathyroidism in multiple endocrine neoplasia type 1?

1 reference

12 December 2020

Surveillance for early detection of aggressive parathyroid disease: carcinoma and atypical adenoma in familial isolated hyperparathyroidism associated with a germline HRPT2 mutation

1 reference

12 December 2020

[An uncommon cause of hypercalcemia: synchronous carcinoma of two parathyroids in the context of hyperparathyroidism-jaw tumor syndrome]

1 reference

12 December 2020

Uterine tumours are a phenotypic manifestation of the hyperparathyroidism-jaw tumour syndrome

1 reference

12 December 2020

Recessive transmission of a multiple endocrine neoplasia syndrome in the rat

1 reference

12 December 2020

Accuracy of combined protein gene product 9.5 and parafibromin markers for immunohistochemical diagnosis of parathyroid carcinoma

1 reference

12 December 2020

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

1 reference

12 December 2020

Clinical and laboratory features of calcium-sensing receptor disorders: a systematic review

1 reference

12 December 2020

Evidence-based treatment of acute pancreatitis: a look at established paradigms

1 reference

12 December 2020

Familial isolated primary hyperparathyroidism due to HRPT2 mutation

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome

1 reference

12 December 2020

Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas

1 reference

12 December 2020

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

1 reference

12 December 2020

The parathyroid glands in familial hypocalciuric hypercalcemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Benign familial hypocalciuric hypercalcemia

1 reference

12 December 2020

Parathyroid surgery in familial hyperparathyroid disorders

1 reference

12 December 2020

The outcome of subtotal parathyroidectomy for the treatment of hyperparathyroidism in multiple endocrine neoplasia type 1

1 reference

12 December 2020

A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemia

1 reference

12 December 2020

Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP)

1 reference

12 December 2020

Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapy

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Subtotal parathyroidectomy for primary chief cell hyperplasia of the multiple endocrine neoplasia type I syndrome

1 reference

12 December 2020

Symposium on evidence-based endocrine surgery (3: hyperparathyroidism)

1 reference

12 December 2020

A case of hyperparathyroidism-jaw tumour syndrome found in the treatment of an ossifying fibroma in the maxillary bone.

1 reference

12 December 2020

CDC73 intragenic deletion in familial primary hyperparathyroidism associated with parathyroid carcinoma

1 reference

12 December 2020

Surgical management of hyperparathyroidism in patients with multiple endocrine neoplasia type 2A

1 reference

12 December 2020

Predicting the risk of multiple endocrine neoplasia type 1 for patients with commonly occurring endocrine tumors.

1 reference

12 December 2020

The surgical management of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop.

1 reference

12 December 2020

Surgical approach to the patient with familial hyperparathyroidism

1 reference

12 December 2020

Hyperparathyroidism-jaw tumour syndrome detected by aggressive generalized osteitis fibrosa cystica.

1 reference

12 December 2020

Diagnosis of parathyroid tumors in familial isolated hyperparathyroidism with HRPT2 mutation: implications for cancer surveillance.

1 reference

12 December 2020

Familial hypercalcemia and hypercalciuria caused by a novel mutation in the cytoplasmic tail of the calcium receptor

1 reference

12 December 2020

HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours

1 reference

12 December 2020

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

1 reference

12 December 2020

Different somatic alterations of the HRPT2 gene in a patient with recurrent sporadic primary hyperparathyroidism carrying an HRPT2 germline mutation

1 reference

12 December 2020

Hyperparathyroidism-jaw tumor syndrome: Results of operative management

1 reference

12 December 2020

Familial hyperparathyroidism due to a germline mutation of the CDC73 gene: implications for management and age-appropriate testing of relatives at risk

1 reference

12 December 2020

Criteria for mutation analysis in MEN 1-suspected patients: MEN 1 case-finding

1 reference

12 December 2020

Diagnosis of asymptomatic primary hyperparathyroidism: proceedings of the Fourth International Workshop.

1 reference

12 December 2020

Dissecting the genetics of hyperparathyroidism--new clues from an old friend

1 reference

12 December 2020

Primary hyperparathyroidism in multiple endocrine neoplasia type IIa: retrospective French multicentric study. Groupe d'Etude des Tumeurs á Calcitonine (GETC, French Calcitonin Tumors Study Group), French Association of Endocrine Surgeons

1 reference

12 December 2020

Results of iterative surgery for persistent and recurrent parathyroid carcinoma

1 reference

12 December 2020

Primary and reoperative parathyroid operations in hyperparathyroidism of multiple endocrine neoplasia type 1

1 reference

12 December 2020

Immunohistochemical assessment of parafibromin in mouse and human tissues.

1 reference

12 December 2020

Breast-cancer predisposition in multiple endocrine neoplasia type 1.

1 reference

12 December 2020

Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age?

1 reference

12 December 2020

Subtotal parathyroidectomy as an adequate treatment for primary hyperparathyroidism in multiple endocrine neoplasia type 1.

1 reference

12 December 2020

Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutation

1 reference

12 December 2020

[Hyperparathyroidism-jaw tumor syndrome. A hereditary form of primary hyperparathyroidism with parathyroid carcinoma]

1 reference

12 December 2020

Genetic analyses of the HRPT2 gene in primary hyperparathyroidism: germline and somatic mutations in familial and sporadic parathyroid tumors

1 reference

12 December 2020

Primary hyperparathyroidism in MEN1 patients: a cohort study with longterm follow-up on preferred surgical procedure and the relation with genotype

1 reference

12 December 2020

Parafibromin expression, single-gland involvement, and limited parathyroidectomy in familial isolated hyperparathyroidism

1 reference

12 December 2020

Somatic and Germ-Line Mutations of theHRPT2Gene in Sporadic Parathyroid Carcinoma

1 reference

12 December 2020

Successful use of bisphosphonate and calcimimetic in neonatal severe primary hyperparathyroidism

1 reference

12 December 2020

Primary hyperparathyroidism in multiple endocrine neoplasia type 2A

1 reference

12 December 2020

Hyperparathyroidism in hereditary syndromes: special expressions and special managements.

1 reference

12 December 2020

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

1 reference

12 December 2020

Multiple endocrine neoplasia type 4.

1 reference

12 December 2020

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

1 reference

12 December 2020

Prospective study of surgery for primary hyperparathyroidism (HPT) in multiple endocrine neoplasia-type 1 and Zollinger-Ellison syndrome: long-term outcome of a more virulent form of HPT.

1 reference

12 December 2020

Should parafibromin staining replace HRTP2 gene analysis as an additional tool for histologic diagnosis of parathyroid carcinoma?

1 reference

12 December 2020

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

1 reference

12 December 2020

Surgical management of primary hyperparathyroidism in multiple endocrine neoplasia types 1 and 2.

1 reference

12 December 2020

Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia.

1 reference

12 December 2020

Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds

1 reference

12 December 2020

Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).

1 reference

12 December 2020

Parathyroid surgery in the multiple endocrine neoplasia type I syndrome: Choice of surgical procedure

1 reference

12 December 2020

Hereditary hyperparathyroidism syndromes

1 reference

12 December 2020

The optimal surgical treatment for primary hyperparathyroidism in MEN1 patients: a systematic review

1 reference

12 December 2020

The extent of parathyroidectomy for HRPT2-related hyperparathyroidism

1 reference

12 December 2020

A Novel IVS2-1G>A mutation causes aberrant splicing of the HRPT2 gene in a family with hyperparathyroidism-jaw tumor syndrome

1 reference

12 December 2020

Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

1 reference

12 December 2020

Primary hyperparathyroidism in familial multiple endocrine neoplasia type I. Long-term follow-up of serum calcium levels after parathyroidectomy

1 reference

12 December 2020

Parathyroid glands in familial benign hypercalcemia (familial hypocalciuric hypercalcemia)

1 reference

12 December 2020

Germline and somatic mutations in cyclin-dependent kinase inhibitor genes CDKN1A, CDKN2B, and CDKN2C in sporadic parathyroid adenomas.

1 reference

12 December 2020

Surgery for multiple endocrine neoplasia type 1-associated primary hyperparathyroidism

1 reference

12 December 2020

Familial isolated primary hyperparathyroidism/hyperparathyroidism-jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese.

1 reference

12 December 2020

Long-term results of less than total parathyroidectomy for hyperparathyroidism in multiple endocrine neoplasia type 1.

1 reference

12 December 2020

Hyperparathyroidism in multiple endocrine neoplasia type I: surgical trends and results of a 256-patient series from Groupe D'etude des Néoplasies Endocriniennes Multiples Study Group

1 reference

12 December 2020

Primary hyperparathyroidism in multiple endocrine neoplasia type 1: individualized management with low recurrence rates

1 reference

12 December 2020

Hyperparathyroidism in multiple endocrine neoplasia syndrome

1 reference

12 December 2020

10.1007/S00423-015-1342-7

Identifiers

DOI

1 reference

4 September 2017

1 reference