(Q37351692)

English

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

scientific article published on February 1996

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2. (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1 reference

based on heuristic

inferred from title

Georgios P. Chrousos

8

object named as

Chrousos GP

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Stratakis CA

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Carney JA

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Lin JP

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Papanicolaou DA

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Karl M

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Kastner DL

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Pras E

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

0 references

publication date

1 February 1996

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Europe PubMed Central

PMC publication ID

19 August 2017

Journal of Clinical Investigation

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Europe PubMed Central

PMC publication ID

19 August 2017

97

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

699-705

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Genetic mapping of a locus predisposing to human colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Faster sequential genetic linkage computations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Binding of mismatched microsatellite DNA sequences by the human MSH2 protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Localization of the human melanocortin-5 receptor gene (MC5R) to chromosome band 18p11.2 by fluorescence in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

A syndrome of various cutaneous pigmented lesions, myxoid neurofibromata and atrial myxoma: the NAME syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Mucocutaneous lentigines, cardiomucocutaneous myxomas, and multiple blue nevi: the "LAMB" syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

The complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

The significance of multiple, recurrent, and "complex" cardiac myxomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Familial cardiac myxoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Multiple cutaneous tumors: what do they mean?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Receptor-effector coupling by G proteins: implications for normal and abnormal signal transduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

The genetics of multiple endocrine neoplasia (MEN).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Cardio‐cutaneous syndrome (the “LEOPARD” syndrome). Review of the literature and a new family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

6 September 2017

Myxoma of the right ventricle in monozygotic twins: surgical ablation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

14 September 2017

Complete nucleotide sequence of the human corticotropin-β-lipotropin precursor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

14 September 2017

Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

28 September 2017

Clues to the pathogenesis of familial colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Psammomatous melanotic schwannoma. A new cutaneous marker for Carney's complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Microsatellite instability in human non-melanoma and melanoma skin cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Psammomatous melanotic schwannoma. A distinctive, heritable tumor with special associations, including cardiac myxoma and the Cushing syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Myxoid fibroadenoma and allied conditions (myxomatosis) of the breast. A heritable disorder with special associations including cardiac and cutaneous myxomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

The Carney complex with ocular signs suggestive of cardiac myxoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Bilateral eyelid myxomas in Carney's complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

[Heart-skin syndrome and cardiac myxoma: presentation of a case and clinical experience of 17 years.]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

The syndrome of right atrial myxoma, spotty skin pigmentation, and acromegaly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Cushing's syndrome due to primary pigmented nodular adrenocortical disease with cardiac myxomas and mucocutaneous lentigines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Left heart myxomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

26 June 2018

Avoiding recomputation in linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

2 September 2018

Hereditary gastrointestinal polyposis and nonpolyposis syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

2 September 2018

Bilateral primary pigmented nodular adrenocortical disease. Rare cause of the Cushing syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

2 September 2018

Generalized Intestinal Polyposis and Melanin Spots of the Oral Mucosa, Lips and Digits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

3 December 2018

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=507106

3 December 2018

Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by Fluorescence in situ hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

UNUSUAL CASE OF ADRENOCORTICAL HYPERFUNCTION

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary adrenocortical nodular dysplasia with Cushing's syndrome and cardiac myxomas. A peculiar familial disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pituitary-dependent Cushing disease and primary adrenocortical nodular dysplasia in childhood. Presentation of 4 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differences between nonfamilial and familial cardiac myxoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cutaneous myxomas. A major component of the complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mucocutaneous pigmented spots and oral myxomas: the oral manifestations of the complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adrenocortical micronodular dysplasia, cardiac myxomas, lentigines, and spindle cell tumors. Report of a kindred

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomally abnormal clones and nonrandom telomeric translocations in cardiac myxomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carney's complex of primary pigmented nodular adrenocortical disease and pigmentous and myxomatous lesions

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Cushing's syndrome due to primary pigmented nodular adrenocortical disease. Reinvestigation 50 years later

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Cushing's syndrome due to nodular adrenocortical dysplasia is an inherited disease of immunological origin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of mycosis fungoides

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methotrexate-nonsteroidal antiinflammatory drug interaction in children with arthritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ductal adenoma of the breast with tubular features. A probable component of the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple lentigines, myxoid tumours and endocrine overactivity; four cases of Carney's complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetics of a case of cardiac myxoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of a gene causing cystinuria to chromosome 2p

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief report: a familial syndrome of arterial dissections with lentiginosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cryptic trinucleotide repeat polymorphism in the POMC gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three dinucleotide repeat polymorphisms proximal to the D2S123 locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe osteopenia in young adults associated with Cushing's syndrome due to micronodular adrenal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Microadenomatosis of the adrenal cortex and hypercorticism in adolescents]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Cushing's syndrome with primary adrenocortical microadenomatosis (primary adrenocortical nodular dysplasia)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report and abstracts of the Second International Workshop on Human Chromosome 2 Mapping

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carney's complex in a patient with hormone-producing Sertoli cell tumor of the testicle

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac myxoma. A clinicopathologic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac myxoma characterized by clonal telomeric association

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myxomas of the external ear and their significance

1 reference

https://pubmed.ncbi.nlm.nih.gov/8609225

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI118467

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

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