Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes (Q34283507)

1 August 2017

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title

Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes (English)

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1 August 2017

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Stratakis CA

1

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1 August 2017

1 May 2001

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Journal of Endocrinological Investigation

1 August 2017

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1 August 2017

24

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1 August 2017

5

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1 August 2017

370-383

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https://scigraph.springernature.com/pub.10.1007/bf03343875

1 August 2017

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cites work

Genetic aspects of adenomatosis of endocrine glands

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https://api.crossref.org/works/10.1007%2FBF03343875

The association of pheochromocytoma with carcinoma of the thyroid gland

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03343875

Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03343875

The complex of myxomas, spotty pigmentation, and endocrine overactivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Positional cloning of the gene for multiple endocrine neoplasia-type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Identification of the von Hippel-Lindau disease tumor suppressor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Clinical significance of hyperparathyroidism in familial multiple endocrine adenomatosis type I (MEA I)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Results of treatment of pituitary disease in multiple endocrine neoplasia, type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

RET in human development and oncogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Genetics of Carney complex and related familial lentiginoses, and other multiple tumor syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex): breast imaging findings

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03343875

The epithelioid blue nevus. A multicentric familial tumor with important associations, including cardiac myxoma and psammomatous melanotic schwannoma.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03343875

Carney complex: the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas.

21 January 2018

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https://api.crossref.org/works/10.1007%2FBF03343875

Periodic Cushing syndrome in a short boy: usefulness of the ovine corticotropin releasing hormone test.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Neurosurgical implications of Carney complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Testicular ultrasound in Carney complex: report of three cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Cytogenetic analysis of intestinal polyps in polyposis syndromes: comparison with sporadic colorectal adenomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Chromosome instability in lymphocytes from patients affected by or genetically predisposed to colorectal cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Cyclic nucleotide-dependent protein kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits; a syndrome of diagnostic significance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

The molecular basis and clinical aspects of Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Increased risk for cancer in patients with the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Increased risk of cancer in the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Hereditary gastrointestinal polyposis and nonpolyposis syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Cancer and the Peutz-Jeghers syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Ovarian sex cord tumor with annular tubules: review of 74 cases including 27 with Peutz-Jeghers syndrome and four with adenoma malignum of the cervix

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Cloning and characterization of a novel serine/threonine protein kinase expressed in early Xenopus embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

The mouse Peutz-Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Identification of the von Hippel-Lindau (VHL) gene. Its role in renal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Molecular genetic analysis of von Hippel-Lindau disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Localization of the gene for Cowden disease to chromosome 10q22–23

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF03343875

Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene

21 January 2018

2 references

https://api.crossref.org/works/10.1007%2FBF03343875

21 January 2018

12 December 2020

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

1 reference

12 December 2020

Testing candidate loci on chromosomes 1 and 6 for genetic linkage to Peutz-Jeghers' disease

1 reference

12 December 2020

Hyperparathyroidism: a prerequisite for Zollinger-Ellison syndrome in multiple endocrine adenomatosis Type 1--report of a further family and a review of th literature

1 reference

12 December 2020

Prolactin secretion abnormalities in patients with the "syndrome of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex).

1 reference

12 December 2020

Peutz-Jeghers syndrome: risks of a hereditary condition.

1 reference

12 December 2020

The natural history of multiple endocrine neoplasia type 1. Highly uncommon or highly unrecognized?

1 reference

12 December 2020

Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan-Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci.

1 reference

12 December 2020

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

1 reference

12 December 2020

The Carney complex with ocular signs suggestive of cardiac myxoma

1 reference

12 December 2020

Cushing syndrome due to primary pigmented nodular adrenocortical disease: findings at CT and MR imaging

1 reference

12 December 2020

Peutz-Jeghers syndrome: a clinicopathologic survey of the "Harrisburg family" with a 49-year follow-up

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12 December 2020

Ductal adenoma of the breast and the Carney complex

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12 December 2020

Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families

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12 December 2020

UNUSUAL CASE OF ADRENOCORTICAL HYPERFUNCTION

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12 December 2020

Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel-Lindau and RET genes

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12 December 2020

Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.

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12 December 2020

Myxomas of the external ear and their significance

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12 December 2020

Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease

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12 December 2020

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

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12 December 2020

The development of bilateral adenomatous adrenal hyperplasia in a case of Cushing's syndrome of eighteen years' duration

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12 December 2020

Studies of the adrenal hyperfunction in 2 patients with atypical Cushing's syndrome

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12 December 2020

Multiple endocrine neoplasia type 2a associated with cutaneous lichen amyloidosis

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12 December 2020

Multiple endocrine neoplasias

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12 December 2020

Chromosome instability in cultured skin fibroblasts from patients with familial polyposis coli and Peutz-Jeghers' syndrome.

1 reference

12 December 2020

Genetics of Cowden syndrome: through the looking glass of oncology

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12 December 2020

Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

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12 December 2020

Multiple endocrine neoplasia type 1: clinical and genetic features of the hereditary endocrine neoplasias.

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12 December 2020

Multiple endocrine neoplasia--syndromes of the twentieth century

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12 December 2020

Multiple endocrine neoplasia type I: assessment of laboratory tests to screen for the gene in a large kindred.

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12 December 2020

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

1 reference

12 December 2020

Multiple endocrine neoplasia type 1: clinical and genetic topics

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12 December 2020

Ovarian lesions in Carney complex: clinical genetics and possible predisposition to malignancy.

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12 December 2020

Genetic heterogeneity in Peutz-Jeghers syndrome

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12 December 2020

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients

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12 December 2020

Cancer in Peutz-Jeghers syndrome

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12 December 2020

Screening for the multiple endocrine neoplasia syndrome type I. A study of 11 kindreds in The Netherlands

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12 December 2020

Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

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12 December 2020

Hirschsprung disease in MEN 2A: increased spectrum of RET exon 10 genotypes and strong genotype-phenotype correlation

1 reference

12 December 2020

Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex).

1 reference

12 December 2020

Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex)

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12 December 2020

Chromosomally abnormal clones and nonrandom telomeric translocations in cardiac myxomas

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12 December 2020

Cardiac myxoma characterized by clonal telomeric association

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12 December 2020

ret protooncogene mutations and endocrine neoplasia--a story intertwined with neural crest differentiation

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12 December 2020

Feminizing Sertoli cell tumors in boys with Peutz-Jeghers syndrome

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12 December 2020

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

1 reference

12 December 2020

Differences between nonfamilial and familial cardiac myxoma

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12 December 2020

Pituitary adenomas of the multiple endocrine neoplasia type I syndrome

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12 December 2020

Cytogenetics of a case of cardiac myxoma

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12 December 2020

STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer.

1 reference

12 December 2020

Bilateral small-node adenomatosis of the adrenal cortex in Cushing's syndrome

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12 December 2020

Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease

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12 December 2020

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

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12 December 2020

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

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12 December 2020

Mucinous ovarian tumors associated with mucinous adenocarcinomas of the cervix. A clinicopathological analysis of 16 cases

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12 December 2020

FAMILIAL MULTIPLE ENDOCRINE ADENOMA-PEPTIC ULCER COMPLEX

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12 December 2020

Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex)

1 reference

12 December 2020

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

1 reference

12 December 2020

Primary pigmented nodular adrenocortical disease: reevaluation of a patient with carney complex 27 years after unilateral adrenalectomy.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03343875

1 reference

PubMed ID

11407658

Dimensions Publication ID

1 August 2017

0 references

1 reference

PubMed ID

11407658